Saturday, November 28, 2009

CANCER TREATMENT

The following is a list of terms that descripe surgical procedures used in traeting cancer.

Cryosurgery

Maligant tissue is frozen and thus destroyed. This procedure is occasinonally used to treat bladder and prostatetumors.

Electrocauterization

Maligant tissue is destroyed by burning. Electrocauterization is often used in treating tumors of the rectum and colon, when surgical removal is not possible.

En bloc resection

Tumor is removed along with a large area of surrounding tissue containing lymph nodes. Modified radical mastectomy, colectomy, and gas-trectomy are examples.

Excisional biopsy

Removal of tumor and a margin of normal tissue. This procedure provides a specimen for diagnosis and may be curative for small tumors.

Exenteration

A wide resection involving removal of the tumor, its organ of origin, and all surrounding tissue in the body space. Pelvic exenteration may be performed to treat large primary tumors of the uterus.

Fulguration

Destruction of tissue by electric sparks generated by a high

Incisional biopsy

A piece of tumor is removed for examination to establish a diagnosis. A more extensive surgical procedure or other forms of treatment, such as chemotherapy or x – ray, may then be used to treat the bulk of the tumor.

MICROSCOPIC DESCRIPTIONS

Alveolar

Tumor cells from patterns resembling small, microscopic sacs; commonly found in tumors of muscle, bone, fat, and cartilarge.

Carcinoma in situ

Referring to localized tumor cells that have not invaded adjacent structures. Cancer of the cervix may begin as carcinoma in situ.

Diffuse

Spreading evenly throughout the affected tissue. Malignant lymphomas may display diffuse involvment of lymph nodes.

Dysplastic

Pertaining to abnormal formation of cells. These tumors display a highly abnormal but not clearly cancerous appearance. Dysplastic nevi (moles on skin) are an example.

Epidermoid

Resembling squamous epithelial cells (thin, plate-like), often occurring in the respiratory tract.

Follicular

Forming small, moicroscopic, gland-type sacs. Thyroid gland cancer is an example.

Nodular

Forming multiple areas of tightly packed clusters of cells with lightly populated areas in between. Maligant lymphomas may display a nodular pattern of lymph node involvement.

Papillary

Forming small, finger-like or nipple-like projections of cells. Bladder cancer may be described as papillary.

Pleomorphic

Composed of a varitey of types of cells. Mixed-cell tumors are examples.

Scirrhous

Densely packed (scirrhous means hard) tumors, overgrown with fibrous tissue; commonly found in breast or stomach cancers.

Undifferentiated

Lacking microscopic structures typical of normal mature cells.

Classification of Cancerous Tumors

It is possible to divide these types of cancer into three broad groups on the basis of histogenesis that is, by identifying the particular type of tissue (hist/o) from which the tumor cells arise ( -genesis ). These major groups are carcinomas , sarcomas , and mixed tissue tumors.

Carcinomas

Carcinomas, the Largest group , are solid Tumors that are derived from etithelial tissue that lines external and internal body surfaces, including skin , glands , and digestive , urinary , and reproductive organs.

Sarcomas

Sarcomas are less common (less than 5 percent of all malignant tumors ) than carcinomas and are derived from connective tissues in the body, such as bone, fat, muscle, cartilage, and bone marrow and from cells of the lymphatic system.


PATHOLOGICAL DESCRIPTIONS

The following terms are used to descripe the apperance of a maligant tumor, on either gross (visual) or on microscopic examination

Cystic

Forming large open spaces filled with fluid.Mucinous tumors are filled with mucus (thick, sticky fluid ), and serous tumors are filled with a thin, watery fluid resembling serum. The most common site of cystic tumors is in ovaries.

Fungating

Mushrooming pattern of growth in which tumor cells pile one on top another and project from a tissue surface. Tumors found in the colon are often of this type.

Inflammatory

Having the features of inflammation ; that is, redness, sweling, and heat. Inflammatory changes result from tumor blockage of the lymphatic drainage of the skin, as in breast cancer.

Medullary

Pertaining to large, soft, fleshy tumors. Thyroid and breast tumors may be medullary.

Necrotic

Containing dead tissue. Any type of tumor can outgrow its blood supply and undergo necrosis.

Polypoid

Growths that are like projecttions extending outward from a base. Sessile polypoid tumors extend from a broad base, and pedunculated polypoid tumors extend from a stem or stalk. Both benign and maligant tumors of the colon may grow as polyps

Ulcerating

Characterized by an open, exposed surface resulting from the death of overlying tissue. Ulcerating tumors are often found in the sromach, breast, colon, and skin.

Verrucous

Resembling a wart-like growth. Tumors of the gingiva (cheek ) are frequently verrucous.

Environmental Agents

Agents From the environment , such as chemicals drugs, depacco smoke, radiation, and viruses, can cause damage to DNA and thus produce cancer. These environmental agents are called carcinogens.

Heredity

Cancer may be caused not only by environmental factors but also by inherited factors examples are retinoblastoma (tumor of the retina of the eye ) polyposis coil syndrome (polyps that grow in the colon and rectum) and certain other forms of colon , breast , and kidney cancer

GENES IMPLICATED IN HEREDITARY CANCERS

Cancer

Gene

Chromosomal Location

Breast ; Ovarian

BRCA1

17q21

Breast

BRCA2

13q12-13

Polyposis Coil Sybdrome

APC

5q21

Li-Fraument(multiple cancers)

P53

17p13

Retinoblastoma

Rb1

13q14

Wilms tumor

WT1

11p13

The first number is the chromosome ; p is the short arm of the chromosome and q is the long arm of the chromosome ; the second number is the religion (band) of the chromosome

In many, it belived that these tumors arise because of inherited or acquired abnormalites in certain genes called suppressor genes. Examples of suppressor genes are the retinoblastoma gene (Rb-1) and the p53 gene

Friday, November 20, 2009

Follow testing for gastric cancer

Once someone completes treatment for gastric cancer (including surgery +/- radiation and chemotherapy), he or she needs to be closely followed by his or her cancer physicians. This close follow-up is required for a couple of reasons. First, it needs to be insured that the patient recovers from the cancer treatment itself. This includes ensuring that the patient has no vomiting or diarrhea and has healed from surgery. Also, symptoms of "dumping syndrome" need to be addressed with dietary modifications. In addition, because of the removal of the stomach or a portion of the stomach, gastric cancer patients are prone to a certain type of anemia, resulting from not having enough vitamin B-12. This will be monitored for the patient's entire life, as this anemia does not usually occur until years after the surgery.

The other major reason a patient needs to be followed closely is to make sure their cancer does not recur. Recurrence can be detected using physical exam, repeat, periodic endoscopies, and CT scans. At first, patients will have follow-up visits and tests fairly often. The longer the patient is free of disease, the less often he or she will have to go for check-ups.

What are the treatments for gastric cancer

Currently, all curative treatments for gastric cancer involve surgery (surgical resection of all of the cancer). The smallest amount of surgery that is possible while still taking out all of the cancer is what is normally performed. Generally, tumors which are localized to the part of the stomach closest to the esophagus (proximal stomach) are treated with a gastrectomy (removal of the entire stomach). A partial gastrectomy is the removal of only a portion of the stomach, in contrast to a total gastrectomy, which is done when the tumor is larger. Partial gastrectomies may be appropriate for those tumors located further from the esophagus, in the distal portion of the stomach. For partial gastrectomy, the surgical margin around the gastric cancer needs to be 5 cm, i.e., there needs to be 5 cm of normal stomach tissue around the tumor in the portion of the stomach removed. Diffuse disease involving the stomach is also an indication for a total gastrectomy. Also, the surgeon performs a complete dissection of the lymph nodes, removing as many as possible. How extensive of a lymph node dissection to perform is controversial, with contradictory data from the United States compared with Japan. However, it is import that an experienced surgeon perform the dissection as it is a difficult surgery. Obviously, when the stomach or a portion of the stomach is removed, the two ends must be rejoined. This is done by various procedures, all attempting to eliminate as many of the side effects of the surgery as possible, such as inability to eat larger meals and the so-called "dumping syndrome". Dumping syndrome results from the stomach being removed and the result of the small intestine filling too rapidly with undigested food. Symptoms include nausea, vomiting, bloating, diarrhea, and even shortness of breath. These symptoms can usually be managed with dietary modifications.

Although surgery is always required for curative treatment, it is often not enough to achieve cure in many cases. The majority of cases of early gastric cancer are cured by surgery alone. However, in most patients with more advanced cases of gastric cancer, such as those with positive lymph nodes or tumors which have invaded the deep layers of the stomach or beyond, the cancer will come back if only surgery is done. Up to two-thirds of these patients recur, with cancer coming back in their lymph nodes or other organs. To combat this, radiation therapy and chemotherapy are recommended in many patients. It is felt that any patient with stage IB or higher gastric cancer (involvement of deeper portions of the stomach wall or any lymph nodes involved with cancer) will benefit from additional therapy with concurrent radiation and chemotherapy.

Radiation therapy makes the use of high energy x-rays to kill cancer cells. It does this by damaging the DNA in tumor cells. Normal cells in our body can repair radiation damage much quicker than tumor cells, so while tumor cells are killed by radiation, many normal cells are not. This is the basis for the use of radiation therapy in cancer treatment. Radiation is delivered using large machines that produce the high energy x-rays. After radiation oncologists set up the radiation fields ("radiation fields" are the areas of the body that will be treated by radiation), treatment is begun. Radiation is given 5 days a week for approximately 5 weeks at a radiation treatment center. The treatment takes just a few minutes each day and is completely painless. The typical radiation field used in the treatment of gastric cancer includes portions of the upper abdomen. In other words, it is designed to kill tumor cells in the area that the surgery was performed. Typical side effects include nausea and vomiting (though this should be less of a problems since the stomach has already been removed) and diarrhea.

Chemotherapy is defined as drugs that are used to kill tumor cells. The large advantage in using chemotherapy is that, since it is a medicine, is travels through the entire body. Hence, if some tumor cells have spread outside of what surgery or radiation can treat, they can potentially be killed by chemotherapy. Similar to radiation, some normal cells are damaged during treatment, resulting in side effects. The standard chemotherapy used in the treatment of gastric cancer is called 5-FU, coupled with another drug called leucovorin. This type of chemotherapy is delivered through the vein. Side effects from 5-FU and leucovorin include nausea, diarrhea, skin changes, and sores of the mouth. Although other chemotherapy drugs (cisplatin, oxaloplatin, epirubicin) are being investigated for the treatment of gastric cancer, 5-FU plus leucovorin remains the standard. Sometimes chemotherapy and radiation are used prior to surgery, but a large trial has demonstrated that surgery follow by radiation with chemotherapy appears to be the best current treatment. The value of radiation and chemotherapy was demonstrated in a large study just reported in 2001 by MacDonald et al. These authors reported a much better outcome in patients with Stage IB or greater gastric cancer who were treated with radiation and chemotherapy after potentially curable surgery. This study has established the “standard of care” in the United States, and is detailed as follows:

Surgery- to remove all of the cancer, as well as removal of the lymph nodes in the area of the stomach

Radiation- to the area of the upper abdomen, 5 days per week for 5 weeks;usually starts 4-6 weeks after surgery, to allow for recovery from surgery, but may be delayed by a few weeks if chemotherapy is started first, prior to combining the two treatments.

Chemotherapy- using 5-FU and leucovorin combination therapy, given during the radiation and also after the radiation is completed; can sometimes be started for a few weeks prior to the start of radiation therapy, to allow for local healing if needed

There has also been a study which has demonstrated the benefit of postoperative chemotherapy alone in people who may not tolerate radiation with chemotherapy. The type of chemotherapy advised in this setting is epirubicin, cisplatin and 5-fluorouracil (ECF).

How is gastric cancer diagnosed and staged

Diagnosis

Upper endoscopy, as described above, is routinely used for the initial diagnosis and staging of patients with gastric cancer. Using endoscopy, the diagnosis can be obtained in over 95% of cases. Many times, ultrasound during endoscopy is used to attempt to identify how deep into the wall of the stomach the cancer has penetrated. In addition, ultrasound can identify spread to lymph nodes in many cases. Depth of wall invasion and presence of lymph node spread are two very important components of treatment, as the surgeon uses this information to determine if he or she can operate.
Other procedures are needed to determine the stage of the disease. CT scans ("CAT scans") of the abdomen and chest are done, not only to rule out spread to distant organs, like the liver and lungs, but also to determine the spread to lymph nodes close to the stomach that could not be identified by ultrasound. Other tests to rule out abdominal spread of disease outside of the stomach itself are PET scans, which use radioactive solutions to identify tumors, and laparoscopy. Laparoscopy is a surgical procedure that involves puncturing the abdominal cavity with a fiber optic camera and directly viewing the organs and tissues in the stomach's area and the entire abdominal cavity. Although PET scans and laparoscopy are fairly new introductions to the staging of gastric cancer, CT scans, endoscopy, and ultrasound are more generally accepted as required in order to properly identify the extent of disease, and all will likely be done in a patient diagnosed with gastric cancer.
Other, more routine tests done before treatment include blood screening tests, to insure that overall blood counts are within normal limits, and that a patient's liver, kidneys, and overall health are normal.

All of these test are important to determine the extent of the disease which allows the disease to be staged. The stage provides a guideline for the optimal treatment of the gastric cancer as well as the prognosis.

Staging

The staging of a cancer basically describes how much it has grown before the diagnosis has been made, documenting the extent of disease. Unfortunately, gastric cancer often presents as a more advanced disease because of lack of early diagnosis, due mainly to the lack of specific associated symptoms. Before the staging systems are introduced, here’s some background on how cancers grow and spread, and therefore become more advanced in stage.

Cancers cause problems because they spread and can disrupt the functioning of normal organs. One way gastric cancer can spread is by local extension to invade through the stomach wall and into adjacent structures. These surrounding structures include the soft tissues and fat surrounding the stomach as well as other organs such as the spleen, pancreas, large intestine, small intestine, liver, and large blood vessels.

Gastric cancer can also spread by accessing the lymphatic system. The lymphatic circulation is a complete circulation system in the body (somewhat like the blood circulatory system) that drains into various lymph nodes. When cancer cells access this lymphatic circulation, they can travel to lymph nodes and start new sites of cancer. This is called lymphatic spread. Gastric cancers have a propensity to undergo lymphatic spread because there are many small lymphatic vessels contained within the stomach wall. The first lymph nodes that cancer cells spread to are the "perigastric" nodes along the sides of the stomach itself. They can then spread to lymph nodes adjacent to the liver, spleen, pancreas, and aorta.

Gastric cancers can also spread through the bloodstream. Cancer cells gain access to distant organs via the bloodstream and the tumors that arise from these cells are called metastases. Because of the stomach's blood supply, the most common organ it spreads to is the liver, though tumors can also spread to the lung or other organs less commonly.

A fourth way gastric cancer can spread is throughout the entire abdomen, the so-called peritoneal cavity. Although rare, once cancer cells grow outside of the stomach itself, there is nothing stopping cells from spreading to any surface in the entire abdominal cavity.

There are two accepted staging systems in gastric cancer. They both detail the extent of disease by describing the growth of tumor in the stomach itself as well as the presence and extent of spread to the lymph nodes. The TNM systems are used to describe many types of cancers. They have three components: T-describing the extent of the "primary" tumor (the tumor in the stomach itself); N-describing the spread to the lymph nodes; M-describing the spread to other organs (i.e.-metastases).
The "T" stage is as follows:

• Tis-"in-situ cancer"-very superficial tumor, without invasion of the stomach wall

• T1-tumor invades into only the superficial portions of the stomach wall

• T2-tumor invades into the deeper layers of the stomach wall

• T3-tumor extends through the stomach wall into the fat outside of the stomach

• T4-tumor extends outside the stomach wall and invades into other organs
The "N" stage is as follows:

• N0-no spread to lymph nodes

• N1-tumor spread to 1-6 lymph nodes

• N2-tumor spread to 7-15 lymph nodes

• N3-tumor spread to more than 15 lymph nodes

The "M" stage is as follows:

• M0-no tumor spread to other organs

• M1-tumor spread to other organs

The overall stage is based on a combination of these T, N, and M parameters:

• Stage IA-T1N0M0
• Stage IB-T1N1M0 or T2N0M0
• Stage II-T1N2M0 or T2N1M0 or T3N0M0
• Stage IIIA-T2N2M0 or T3N1M0 or T4N0M0
• Stage IIIB-T3N2M0 or
• Stage IV-T4N2M0 or T1-3N3M0 or T4N1-3M0 or any M1

Though complicated, this staging systems help physicians determine the extent of the cancer, and therefore make treatment decisions regarding a patient's cancer. The stage of cancer, or extent of disease, is based on information gathered through various tests done as the diagnosis and work-up of the cancer is being performed.

What are the signs of gastric cancer

The symptoms of gastric cancer are often nonspecific, and the majority of people will unfortunately present with advanced disease. The vast majority of gastric cancer patients present with vague complaints such as upper abdominal discomfort or indigestion, loss of appetite, occasional vomiting, belching, or decreased ability to eat a large meal. Unfortunately, these symptoms are often the exact symptoms that patients experience when they have peptic ulcer disease or gastritis. Therefore, patients can be treated for benign diseases, such as ulcers, without the diagnosis of gastric cancers being made. This is not incorrect management, as gastritis and peptic ulcer disease are much more common than gastric cancer. However, if symptoms persist or do not respond to treatment, further investigations should follow.

Up to 25% of people with gastric cancer will have a history of gastric ulcers. Other symptoms, such as vomiting blood or problems with swallowing, are less common, but should be investigated without delay. Additional symptoms that generally apply to cancer patients are unexplained weight loss as well as fatigue and weakness, with or without anemia. Again, these symptoms are, unfortunately, nondescript, and do not necessarily apply to cancer in general or gastric cancer specifically.. Advanced disease can present with lymph node involvement with masses in the area of the belly button, the underarms, or the clavicle. People with advanced disease may also present with abdominal swelling.

How can I prevent gastric cancer

There is no one risk factor directly associated with gastric cancer, there is no strict lifestyle change that can greatly decrease a person's risk of developing gastric cancer. However, eating a "Western" type diet, without heavily smoked or salted foods and rich in fruits and vegetables will likely decrease a person's risk. Also, smoking cessation will likely decrease gastric cancer risk (though smoking should be stopped for numerous other health reasons). Some have advocated the consumption of foods with high level of antioxidants and vitamin C to prevent gastric cancers, though this has not been definitively proven. Since H. pylori infections have been linked to the development of gastric cancers, the quick treatment of H. pylori infections may decrease the numbers of gastric cancers, though whether treating H. Pylori actually reduces the risk ofgastic cancer remains controversial. The decision to treat H. pylori should be discussed with your physician.

What screening tests are available

There are no established programs for primary prevention of gastric cancer in the United States. There are no plans to initiate a screening program in the United States, simply because the incidence of gastric cancer is fairly low, and thus the yield from gastric cancer screening would be far too low to approach cost-effectiveness. A few populations may be exceptions (e.g.-patients with known atrophic gastritis), but overall screening for gastric cancer in the United States would likely cause more problems than it would solve (i.e. a lot of false positives, or false alarms). Currently, screening for H. Pylori is not recommended for areas with a relatively low incidence of gastric cancer, such as in the United States.

In some Japanese centers, where gastric cancer is much more prevalent, screening has been more successful. A variety of tests have been used in these screening programs, with the ability to accurately identify gastric cancers in over 90% of patients who actually have it. These tests include double-contrast barium radiographs (so-call "upper GIs" or "barium swallows") and upper endoscopies. An upper endoscopy (or an "EGD") is a test done using a camera at the end of a long tube that is placed down the patient's throat to the stomach itself. The physician performing the EGD is able to directly visualize the stomach. Many abnormalities can be detected with an EGD-most importantly, ulcers and cancers. Patients are sedated during the procedure, so discomfort is kept to a minimum.

More recently, studies have verified the use of a newer blood test that could be used for screening for gastric cancer. This analyzes the presence of enzymes in the blood called the serum pepsinogen I/II ratio, which is low in patients at risk for atrophic gastritis and gastric cancer. However, this is still in the earlier stage of testing and needs to be verified.

Risk for gastric cancer

In the United States, there are about 22,000 gastric cancers annually, with about 11,00 deaths attributed to this disease each year Interestingly, its incidence has drastically decreased since 1930. Although it is presumed that this is due to some sort of dietary or environmental factor(s), the exact reason behind this decrease is not known. One theory is that the advent of refrigeration led to decreased use of nitrites, “smoking” of foods, and other such forms of food preservation. It also decreased food contamination. Gastric cancer is approximately twice as common in men and more common in Blacks than Caucasians. It is rare to see gastric cancer before the age of 40, and its incidence increases with age thereafter. There are two types of gastric cancer, the intestinal type and the diffuse type; the latter carries a worse prognosis.

Although gastric cancer has greatly decreased in the United States, on a worldwide scale its incidence is still high, and it is the second leading cause of cancer death worldwide, behind lung cancer. Its highest incidence is in East Asia (e.g.-Japan, China), presumably because of a diet consisting of heavily smoked, salted, and pickled foods. Interestingly, first generation immigrants from these countries have a decreased incidence of stomach cancer after moving to the United States, but it is still higher than the general American population. However, the incidence greatly declines in second and third generation Japanese and Chinese immigrants to the United States, pointing to the fact that there does not appear to be an inherently genetic component in Eastern Asians’ preponderance to gastric cancer, but rather an environmental component.

As mentioned above, diets heavily salted, smoked, or pickled are associated with an increased risk of disease, while diets rich in fruits, vegetables, and dietary fiber are associated with a decreased risk of cancer. The incidence of gastric cancers also increases with decreasing socioeconomic status, likely due to a number of social, occupational, and cultural factors. Tobacco use has also been associated with an increase in gastric cancers. There does not appear to be a link with alcohol consumption.

There does appear to be a genetic link in some cases of gastric cancer, and there are some genetic diseases such as hereditary nonpolyposis colorectal cancer, familial adenomatous polyposis, and Peutz Jeghers syndrome which all predispose to gastric cancer. It also appears that people with blood type A are at increased risk for gastric caner for an unknown reason.

Studies have also linked infection with Helicobacter pylori with gastric cancer. H. pylori is associated with gastric ulcers and chronic atrophic gastritis, which may explain the high incidence of gastric cancer in patients infected with H. pylori. However, the exact role of H. pylori in the development of gastric cancer remains unclear. It is theorized that H. pylori causes a gastritis or inflammation of the stomach, which can lead to a loss of secretory cells in the stomach, also known as strophic gastritis. It is believed that this process of atrophy can lead to gastric cancer. H. pylori has also been linked to lymphomas of the stomach.

Pernicious anemia, an autoimmune disease where the stomach does not produce stomach acid, has also been linked to gastric cancer. Drugs which cause a decrease in stomach acid production have not been linked to an increased risk of gastric cancer.

It should be noted that, although these risk factors are listed above, the majority of gastric cancers develop without any one obvious predisposing cause. In other words, there is no extremely strong cause effect relationship with any risk factor, in contrast, for example, to that between smoking and lung cancer.

What are the treatments and survival for colon cancer

Surgery is the most common treatment for colorectal cancer. During surgery, the tumor, a small margin of the surrounding healthy bowel, and adjacent lymph nodes are removed. The surgeon then reconnects the healthy sections of the bowel. In patients with rectal cancer, the rectum is permanently removed. The surgeon then creates an opening (colostomy) on the abdomen wall through which solid waste in the colon is excreted. Specially trained nurses (enterostomal therapists) can help patients adjust to colostomies, and most patients with colostomies return to a normal lifestyle.

The long-term prognosis after surgery depends on whether the cancer has spread to other organs (metastasis). The risk of metastasis is proportional to the depth of penetration of the cancer into the bowel wall. In patients with early colon cancer which is limited to the superficial layer of the bowel wall, surgery is often the only treatment needed. These patients can experience long-term survival in excess of 80%. In patients with advanced colon cancer, wherein the tumor has penetrated beyond the bowel wall and there is evidence of metastasis to distant organs, the five-year survival rate is less than 10%.

In some patients, there is no evidence of distant metastasis at the time of surgery, but the cancer has penetrated deeply into the colon wall or reached adjacent lymph nodes. These patients are at risk of tumor recurrence either locally or in distant organs. Chemotherapy in these patients may delay tumor recurrence and improve survival.

Chemotherapy is the use of medications to kill cancer cells. It is a systemic therapy, meaning that the medication travels throughout the body to destroy cancer cells. After colon cancer surgery, some patients may harbor microscopic metastasis (small foci of cancer cells that cannot be detected). Chemotherapy is given shortly after surgery to destroy these microscopic cells. Chemotherapy given in this manner is called adjuvant chemotherapy. Recent studies have shown increased survival and delay of tumor recurrence in some patients treated with adjuvant chemotherapy within five weeks of surgery. Most drug regimens have included the use of 5-flourauracil (5-FU). On the other hand, chemotherapy for shrinking or controlling the growth of metastatic tumors has been disappointing. Improvement in the overall survival for patients with widespread metastasis has not been convincingly demonstrated.

Chemotherapy is usually given in a doctor's office, in the hospital as a outpatient, or at home. Chemotherapy is usually given in cycles of treatment periods followed by recovery periods. Side effects of chemotherapy vary from person to person, and also depend on the agents given. Modern chemotherapy agents are usually well tolerated, and side effects are manageable. In general, anticancer medications destroy cells that are rapidly growing and dividing. Therefore, red blood cells, platelets, and white blood cells are frequently affected by chemotherapy. Common side effects include anemia, loss of energy, easy bruising, and a low resistance to infections. Cells in the hair roots and intestines also divide rapidly. Therefore, chemotherapy can cause hair loss, mouth sores, nausea, vomiting, and diarrhea.

Radiation therapy in colorectal cancer has been limited to treating cancer of the rectum. There is a decreased local recurrence of rectal cancer in patients receiving radiation either prior to or after surgery. Without radiation, the risk of rectal cancer recurrence is close to 50%. With radiation, the risk is lowered to approximately 7%. Side effects of radiation treatment include fatigue, temporary or permanent pelvic hair loss, and skin irritation in the treated areas.

Other treatments have included the use of localized infusion of chemotherapeutic agents into the liver, the most common site of metastasis. This involves the insertion of a pump into the blood supply of the liver which can deliver high doses of medicine directly to the liver tumor. Response rates for these treatments have been reported to be as high as eighty percent. Side effects, however, can be serious. Additional experimental agents considered for the treatment of colon cancer include the use of cancer-seeking antibodies bound to cancer-fighting drugs. Such combinations can specifically seek and destroy tumor tissues in the body. Other treatments attempt to boost the immune system, the bodies' own defense system, in an effort to more effectively attack and control colon cancer. In patients who are poor surgical risks, but who have large tumors which are causing obstruction or bleeding, laser treatment can be used to destroy cancerous tissue and relieve associated symptoms. Still other experimental agents include the use of photodynamic therapy. In this treatment, a light sensitive agent is taken up by the tumor which can then be activated to cause tumor destruction.

Flexible sigmoidoscopy and colonoscopy

Beginning at age 50, a flexible sigmoidoscopy screening tests is recommended every three to five years. Flexible sigmoidoscopy is an exam of the rectum and the lower colon using a viewing tube (a short version of colonoscopy). Recent studies have shown that the use of screening flexible sigmoidoscopy can reduce mortality from colon cancer. This is a result of the detection of polyps or early cancers in people with no symptoms. If a polyp or cancer is found, a complete colonoscopy is recommended. The majority of colon polyps can be completely removed by colonoscopy without open surgery. Recently doctors are recommending screening colonoscopies instead of screening flexible sigmoidoscopies for healthy individuals starting at ages 50-55. Please read the Colon Cancer Screening article.

Patients with a high risk of developing colorectal cancer may undergo colonoscopies starting at earlier ages than 50. For example, patients with family history of colon cancer are recommended to start screening colonoscopies at an age 10 years before the earliest colon caner diagnosed in a first-degree relative, or five years earlier than the earliest precancerous colon polyp discovered in a first-degree relative. Patients with hereditary colon cancer syndromes such as FAP, AFAP, HNPCC, and MYH are recommended to begin colonoscopies early. The recommendations differ depending on the genetic defect, for example in FAP; colonoscopies may begin during teenage years to look for the development of colon polyps. Patients with a prior history of polyps or colon cancer may also undergo colonoscopies to exclude recurrence. Patients with a long history (greater than 10 years) of chronic ulcerative colitis have an increased risk of colon cancer, and should have regular colonoscopies to look for precancerous changes in the colon lining.

Genetic counseling and testing

Blood tests are now available to test for FAP, AFAP, MYH, and HNPCC hereditary colon cancer syndromes. Families with multiple members having colon cancers, members with multiple colon polyps, members having cancers at young ages, and having other cancers such as cancers of the ureters, uterus, duodenum, etc., should be referred for genetic counseling followed possibly by genetic testing. Genetic testing without prior counseling is discouraged because of the extensive family education that is involved and the complicated nature of interpreting the test results.

The advantages of genetic counseling followed by genetic testing include: (1) identifying family members at high risk of developing colon cancer to begin colonoscopies early; (2) identifying high risk members so that screening may begin to prevent other cancers such as ultrasound tests for uterine cancer, urine examinations for ureter cancer, and upper endoscopies for stomach and duodenal cancers; and (3) alleviating concern for members who test negative for the hereditary genetic defects.

Diet and colon cancer to prevent colon cancer

People can change their eating habits by reducing fat intake and increasing fiber (roughage) in their diet. Major sources of fat are meat, eggs, dairy products, salad dressings, and oils used in cooking. Fiber is the insoluble, nondigestible part of plant material present in fruits, vegetables, and whole-grain breads and cereals. It is postulated that high fiber in the diet leads to the creation of bulky stools which can rid the intestines of potential carcinogens. In addition, fiber leads to the more rapid transit of fecal material through the intestine, thus allowing less time for a potential carcinogen to react with the intestinal lining. For additional information, please read the Colon Cancer Prevention article.

How can colon cancer be prevented

Unfortunately, colon cancers can be well advanced before they are detected. The most effective prevention of colon cancer is early detection and removal of precancerous colon polyps before they turn cancerous. Even in cases where cancer has already developed, early detection still significantly improves the chances of a cure by surgically removing the cancer before the disease spreads to other organs. Multiple world health organizations have suggested general screening guidelines.

Digital rectal examination and stool occult blood testing

It is recommended that all individuals over the age of 40 have yearly digital examinations of the rectum and their stool tested for hidden or "occult" blood. During digital examination of the rectum, the doctor inserts a gloved finger into the rectum to feel for abnormal growths. Stool samples can be obtained to test for occult blood (see below). The prostate gland can be examined at the same time.
An important screening test for colorectal cancers and polyps is the stool occult blood test. Tumors of the colon and rectum tend to bleed slowly into the stool. The small amount of blood mixed into the stool is usually not visible to the naked eye. The commonly used stool occult blood tests rely on chemical color conversions to detect microscopic amounts of blood. These tests are both convenient and inexpensive. A small amount of stool sample is smeared on a special card for occult blood testing. Usually, three consecutive stool cards are collected. A person who tests positive for stool occult blood has a 30% to 45% chance of having a colon polyp and a 3% to 5% chance of having a colon cancer. Colon cancers found under these circumstances tend to be early and have a better long-term prognosis.

It is important to remember that having stool tested positive for occult blood does not necessarily mean the person has colon cancer. Many other conditions can cause occult blood in the stool. However, patients with a positive stool occult blood should undergo further evaluations involving barium enema x-rays, colonoscopies, and other tests to exclude colon cancer, and to explain the source of the bleeding. It is also important to realize that stool which has tested negative for occult blood does not mean the absence of colorectal cancer or polyps. Even under ideal testing conditions, at least 20% of colon cancers can be missed by stool occult blood screening. Many patients with colon polyps are tested negative for stool occult blood. In patients suspected of having colon tumors, and in those with high risk factors for developing colorectal polyps and cancer, flexible sigmoidoscopies or screening colonoscopies are performed even if the stool occult blood tests are negative.

What tests can be done to detect colon cancer

When colon cancer is suspected, either a lower GI series (barium enema x-ray) or colonoscopy is performed to confirm the diagnosis and to localize the tumor.

A barium enema involves taking x-rays of the colon and the rectum after the patient is given an enema with a white, chalky liquid containing barium. The barium outlines the large intestines on the x-rays. Tumors and other abnormalities appear as dark shadows on the x-rays. For more information, please read the Lower Gastrointestinal Series (Barium Enema) article.

Colonoscopy is a procedure whereby a doctor inserts a long, flexible viewing tube into the rectum for the purpose of inspecting the inside of the entire colon. Colonoscopy is generally considered more accurate than barium enema x-rays, especially in detecting small polyps. If colon polyps are found, they are usually removed through the colonoscope and sent to the pathologist. The pathologist examines the polyps under the microscope to check for cancer. While the majority of the polyps removed through the colonoscopes are benign, many are precancerous. Removal of precancerous polyps prevents the future development of colon cancer from these polyps. For more information, please read the Colonoscopy article.

If cancerous growths are found during colonoscopy, small tissue samples (biopsies) can be obtained and examined under the microscope to confirm the diagnosis. If colon cancer is confirmed by a biopsy, staging examinations are performed to determine whether the cancer has already spread to other organs. Since colorectal cancer tends to spread to the lungs and the liver, staging tests usually include chest x-rays, ultrasonography, or a CAT scan of the lungs, liver, and abdomen.

Sometimes, the doctor may obtain a blood test for CEA (carcinoembyonic antigen). CEA is a substance produced by some cancer cells. It is sometimes found in high levels in patients with colorectal cancer, especially when the disease has spread.

During the Procedure

• On the day of the colonoscopy, you will most likely be asked to arrive at the clinic up to an hour before the test is due to begin. This is to allow time to get ready for the test itself and to ask further questions. In addition, you will be asked the following questions:

* When did you last eat?

* What allergies do you have?

* Did you remember to take all your bowel preparation medication?

* Once you are undressed and changed into an examination gown, your vital signs (blood pressure, heart rate, respiration rate, and temperature) will be monitored and an intravenous line (IV) will be placed. This IV is necessary to give you sedation and pain medication that may be required during the test. Although you will not be fully asleep during the procedure, these medications will produce a sleepy state (sedation) and make the test more comfortable.

* The procedure will begin with you lying flat on your left side. The equipment used, the colonoscope, is lubricated to allow it to enter the anus. For a thorough investigation, air is required to gently open the folded colon. This may cause a temporary uncomfortable bloated sensation. When the doctor applies gentle pressure, the colonoscope moves further into the colon and is slowly advanced until the entire colon is seen.

* The colonoscope has a tiny camera on the end of it, which is connected to a monitor. This allows the physician to see the colon through the tip of the instrument even when it is far inside the body. As the scope passes the course of the colon, the normal turns and contours of the colon may impede the passage of the scope. You may be asked to change positions for better visualization. It is common for fluid and gas to escape through the rectum and anus; this should be expected. The entire procedure can take from 30 minutes up to 1 hour.
* In addition to simply viewing the bowel wall, the colonoscope has special attachments that allow the doctor to collect tissue samples or biopsies, remove small growths, and stop bleeding with laser, heat, or medication.

After the Procedure

When the colonoscopy is done as an outpatient procedure (without checking into the hospital), you will go home later that same day. But before you go home, you will be observed for some time and monitored until the effects of the medications are gone. It is a good idea to make arrangements for someone to come to the clinic and take you home, because nausea, bloating, and drowsiness can continue for some time after the procedure.

Colonoscopy Preparation

A colonoscopy can be carried out in a hospital, clinic, or in a doctor’s office, depending on the facility. You will be given an appointment and a set of instructions to follow before the test is performed.

• Although the exact instructions given may vary from clinic to clinic, their objective is the same: to clean out the contents of the bowel before the test.

• This allows the bowel wall to be seen during the test.

• This system of cleaning the bowel is often called bowel preparation.

• You will be given a combination of liquid diet, laxatives, or enemas for up to 2 days prior to the test with instructions on how to use them. Several medications are available for bowel cleansing, including polyethylene glycol 3350 (GoLYTELY, NuLYTELY), magnesium citrate (Citroma), and senna (X-Prep).

• These medications produce diarrhea, which can be uncomfortable, but unless the bowel is empty of stool, the test can be limited and may need to be repeated at a later date.

• On the night before the test is to be performed, nothing should be taken by mouth (food or liquids) until after the test is finished.

Stages of inflammatory breast cancer

Once the staging tests described above are completed, you doctor will describe the inflammatory breast cancer as stage IIIB, stage IIIC, or stage IV.

Stage IIIB means the cancer has spread to tissues near the breast, such as the skin or chest wall, including the ribs and muscles in the chest. The cancer may have spread to lymph nodes within the breast or under the arm.

Stage IIIC means the cancer has spread to lymph nodes beneath the collarbone and near the neck. The cancer also may have spread to lymph nodes within the breast or under the arm and to tissues near the breast.

Stage IV means that the cancer has spread to other organs. These can include the bones, lungs, liver, and/or brain, as well as the lymph nodes in the neck.

For more information about the staging, please visit the Stages of Breast Cancer section.

Tests for hormone-receptor and HER2-receptor status

In addition to figuring out the stage of the cancer, your doctor will test a sample of the cancerous tissue for estrogen, progesterone, and HER2 receptors.

Hormone-receptor status: This test is used to figure out whether or not the breast cancer has receptors for the hormones estrogen and progesterone. A positive result means that estrogen or progesterone (or both) is fueling the cancer cells’ growth. Most inflammatory breast cancers are hormone-receptor-negative. If the cancer is hormone-receptor-positive, however, your doctor can choose treatments that block or lower estrogen.

HER2-receptor status: Another test is done to find out whether the breast cancer cells make too much of a protein called HER2. If they do, then they also have too many HER2 receptors at the cell surface. With too many receptors, breast cancer cells pick up too many growth signals and start growing too much and too fast. One way to slow down or stop the growth of the cancer cells is to block the receptors so they don't pick up as many growth signals. That’s what the medication called Herceptin (chemical name: trastuzumab) does. Many inflammatory breast cancers are HER2-positive, which means they can be treated with Herceptin.

Tests for diagnosis and staging

To diagnose inflammatory breast cancer, your doctor will perform a biopsy. Biopsy is a surgical procedure that removes some of the suspicious breast tissue for examination under a microscope.
Because inflammatory breast cancer usually does not begin as a distinct lump, but instead as changes to the skin, a skin punch biopsy is often used to make the diagnosis. During this type of biopsy, the doctor uses a circular tool to remove a small section of the skin and its deeper layers, and then stitches the wound closed. If your doctor can see a distinct lesion, he or she may perform an ultrasound-guided core needle biopsy. Ultrasound is an imaging method that places a sound-emitting device on the breast to obtain images of the tissues inside. Guided by the ultrasound, the doctor inserts a hollow needle into the breast to remove several cylinder-shaped samples of tissue from the area of suspicion.

If the biopsy shows that inflammatory breast cancer is present, your doctor will order additional tests to figure out how much of the breast tissue and lymph nodes are involved, and whether or not the other breast is affected. Breast MRI, or magnetic resonance imaging, is considered the most reliable test for gathering more information about inflammatory breast cancer.

Once IBC is diagnosed, additional tests are used to determine whether the cancer has spread outside the breast to other organs, such as the lungs, bones, or liver. This is called staging. Tests that may be used include:

• chest X-ray

• CT scan (computerized tomography) of the chest, abdomen, and pelvis

• bone scan

• liver function tests

Some researchers are studying the usefulness of PET/CT scans in staging inflammatory breast cancer. A PET (positron emission tomography)/CT scan is a newer technology used to create images of the body’s cells as they work. First, you would be injected with a substance made up of sugar and a small amount of radioactive material. A special scanning machine then “highlights” any cancer cells throughout the body as they absorb the radioactive substance. Whether PET/CT is better than other tests at staging the cancer is yet to be determined.

Although PET/CT is still being studied, you may want to ask your doctor whether this test would be useful in your treatment planning. If the answer is “yes,” you can ask where PET/CT might be available in your area.

For more detailed information about these tests for diagnosing and staging breast cancer, please visit the Screening and Testing section.

Diagnosis and Staging of Inflammatory Breast Cancer

Inflammatory breast cancer forms in layers, your doctor may not feel a distinct lump during a breast exam and a mammogram may not detect one either. However, it is possible to see and feel the skin thickening that often happens with IBC. This skin thickening can also be detected on a mammogram.

In most cases, inflammatory breast cancer is diagnosed after you or your doctor can see or feel breast changes such as redness, swelling, warmth, or an orange-peel look to the skin. Because IBC grows quickly, it is usually found at a locally advanced stage, meaning that cancer cells have spread into nearby breast tissue or lymph nodes. Just about all people with IBC have evidence of cancer in the lymph nodes. In approximately 1 out of 3 people with IBC, the cancer has spread from the breast to other areas of the body.

If you’ve been diagnosed with inflammatory breast cancer, it’s completely understandable if you’re feeling overwhelmed. Keep in mind, though, that there are a variety of treatment options available for IBC.

Inflammatory Breast Cancer

Inflammatory breast cancer (IBC) is a rare and aggressive form of breast cancer. According to the National Cancer Institute, about 1-5% of all breast cancer cases in the United States are inflammatory breast cancers.

Inflammatory breast cancer usually starts with the reddening and swelling of the breast instead of a distinct lump. IBC tends to grow and spread quickly, with symptoms worsening within days or even hours. It’s important to recognize symptoms and seek prompt treatment. Although inflammatory breast cancer is a serious diagnosis, keep in mind that treatments today are better at controlling the disease than they used to be.

The average age at diagnosis for inflammatory breast cancer in the United States is 57 for white women and 52 for African American women. These ages are about 5 years younger than the average ages at diagnosis for other forms of breast cancer. According to the American Cancer Society, inflammatory breast cancer is more common in African American women. A 2008 study found that being overweight makes a person more likely to develop IBC. Like other forms of breast cancer, IBC can also affect men.

In this section, you can learn more about:


Symptoms of Inflammatory Breast Cancer

Diagnosis and Staging of Inflammatory Breast Cancer

Treating Inflammatory Breast Cancer

Follow-up Care for Inflammatory Breast Cancer

Types of Breast Cancer

Breast cancer can begin in different areas of the breast – the ducts, the lobules, or in some cases, the tissue in between. In this section, you can learn about the different types of breast cancer, including non-invasive, invasive, recurrent, and metastatic breast cancers. You can also read about breast cancer in men.

* DCIS – Ductal Carcinoma In Situ

* LCIS – Lobular Carcinoma In Situ

* IDC – Invasive Ductal Carcinoma

* Less Common Subtypes of Invasive Ductal Carcinoma

* ILC – Invasive Lobular Carcinoma

* Paget's Disease of the Nipple

* Inflammatory Breast Cancer

* Male Breast Cancer

* Recurrent and Metastatic Breast Cancer

Wednesday, November 18, 2009

How is lung cancer treated

Treatment for lung cancer can involve surgical removal of the cancer, chemotherapy, or radiation therapy, as well as combinations of these treatments. The decision about which treatments will be appropriate for a given individual must take into account the localization and extent of the tumor as well as the overall health status of the patient.

As with other cancers, therapy may be prescribed that is intended to be curative (removal or eradication of a cancer) or palliative (measures that are unable to cure a cancer but can reduce pain and suffering). More than one type of therapy may be prescribed. In such cases, the therapy that is added to enhance the effects of the primary therapy is referred to as adjuvant therapy. An example of adjuvant therapy is chemotherapy or radiotherapy administered after surgical removal of a tumor in order to be certain that all tumor cells are killed.

Surgery: Surgical removal of the tumor is generally performed for limited-stage (stage I or sometimes stage II) NSCLC and is the treatment of choice for cancer that has not spread beyond the lung. About 10% -35% of lung cancers can be removed surgically, but removal does not always result in a cure, since the tumors may already have spread and can recur at a later time. Among people who have an isolated, slow-growing lung cancer removed, 25% -40% are still alive five years after diagnosis. Surgery may not be possible if the cancer is too close to the trachea or if the person has other serious conditions (such as severe heart or lung disease) that would limit their ability to tolerate an operation. Surgery is less often performed with SCLC because these tumors are less likely to be localized to one area that can be removed.

The surgical procedure chosen depends upon the size and location of the tumor. Surgeons must open the chest wall and may perform a wedge resection of the lung (removal of a portion of one lobe), a lobectomy (removal of one lobe), or a pneumonectomy (removal of an entire lung). Sometimes lymph nodes in the region of the lungs are also removed (lymphadenectomy). Surgery for lung cancer is a major surgical procedure that requires general anesthesia, hospitalization, and follow-up care for weeks to months. Following the surgical procedure, patients may experience difficulty breathing, shortness of breath, pain, and weakness. The risks of surgery include complications due to bleeding, infection, and complications of general anesthesia.

Radiation: Radiation therapy may be employed as a treatment for both NSCLC and SCLC. Radiation therapy uses high-energy X-rays or other types of radiation to kill dividing cancer cells. Radiation therapy may be given as curative therapy, palliative therapy (using lower doses of radiation than with curative regimens), or as adjuvant therapy in combination with surgery or chemotherapy. The radiation is either delivered externally, by using a machine that directs radiation toward the cancer, or internally through placement of radioactive substances in sealed containers within the area of the body where the tumor is localized. Brachytherapy is a term used to describe the use of a small pellet of radioactive material placed directly into the cancer or into the airway next to the cancer. This is usually done through a bronchoscope.

Radiation therapy can be given if a person refuses surgery, if a tumor has spread to areas such as the lymph nodes or trachea making surgical removal impossible, or if a person has other conditions that make them too ill to undergo major surgery. Radiation therapy generally only shrinks a tumor or limits its growth when given as a sole therapy, yet in 10% -15% of people it leads to long-term remission and palliation of the cancer. Combining radiation therapy with chemotherapy can further increase the chances of survival when chemotherapy is administered. External radiation therapy can generally be carried out on an outpatient basis, while internal radiation therapy requires a brief hospitalization. A person who has severe lung disease in addition to a lung cancer may not be able to receive radiotherapy to the lung. A type of external radiation therapy called the "gamma knife" is sometimes used to treat single brain metastases. In this procedure, multiple beams of radiation are focused on the tumor over a few minutes to hours while the head is held in place by a rigid frame.

For external radiation therapy, a process called simulation is necessary prior to treatment. Using CT scans, computers, and precise measurements, simulation maps out the exact location where the radiation will be delivered, called the treatment field or port. This process usually takes 30 minutes to two hours. The external radiation treatment itself generally is done over four or five days a week for several weeks.

Radiation therapy does not carry the risks of major surgery, but it can have unpleasant side effects including fatigue and lack of energy. A reduced white blood cell count (rendering a person more susceptible to infection) and low blood platelet levels (making blood clotting more difficult) can also occur with radiation therapy. If the digestive organs are in the field exposed to radiation, patients may experience nausea, vomiting, or diarrhea. Radiation therapy can irritate the skin in the area that is treated, but this irritation generally improves with time after treatment has ended.

Chemotherapy: Both NSCLC and SCLC may be treated with chemotherapy. Chemotherapy refers to the administration of drugs that stop the growth of cancer cells by killing them or preventing them from dividing. Chemotherapy may be given alone, as an adjuvant to surgical therapy, or in combination with radiotherapy. While a number of chemotherapeutic drugs have been developed, the class of drugs known as the platinum-based drugs have been the most effective in treatment of lung cancers.

Chemotherapy is the treatment of choice for most SCLC, since these tumors are generally widespread in the body when they are diagnosed. Only half of people who have SCLC survive for four months without chemotherapy. With chemotherapy, their survival time is increased up to four-to fivefold. Chemotherapy alone is not particularly effective in treating NSCLC, but when NSCLC have metastasized, it can prolong survival in many cases.

Chemotherapy may be given as pills, as an intravenous infusion, or as a combination of the two. Chemotherapy treatments are usually given in an outpatient setting. A combination of drugs is given in a series of treatments, called cycles, over a period of weeks to months, with breaks in between cycles. Unfortunately, the drugs used in chemotherapy also kill normally dividing cells in the body, resulting in unpleasant side effects. Damage to blood cells can result in increased susceptibility to infections and difficulties with blood clotting (bleeding or bruising easily). Other side effects include fatigue, weight loss, hair loss, nausea, vomiting, diarrhea, and mouth sores. The side effects of chemotherapy vary according to the dosage and combination of drugs used and may also vary from individual to individual. Medications have been developed that can treat or prevent many of the side effects of chemotherapy. The side effects generally disappear during the recovery phase of the treatment or after its completion.

Brain prophylactic radiation: SCLC often spreads to the brain. Sometimes people with SCLC that is responding well to treatment are treated with radiation therapy to the head to treat very early spread to the brain (called micrometastasis) that is not yet detectable with CT or MRI scans and has not yet produced symptoms. Brain radiation therapy can cause short-term memory problems, fatigue, nausea, and other side effects.

Treatment of recurrence: Lung cancer that has returned following treatment with surgery, chemotherapy, and / or radiation therapy is called recurrent or relapsed. If a recurrent cancer is confined to one site in the lung, it may be treated with surgery. Relapsed tumors generally do not respond to the chemotherapeutic drugs that were previously administered. Since platinum-based drugs are generally used in initial chemotherapy of lung cancers, these agents are not useful in most cases of recurrence. A type of chemotherapy referred to as second-line chemotherapy is used to treat recurrent cancers that have previously been treated with chemotherapy, and a number of second-line chemotherapeutic regimens have been proven effective at prolonging survival. People with recurrent lung cancer who are well enough to tolerate therapy are also good candidates for experimental therapies (see below), including clinical trials.

Targeted therapy: One alternative to standard chemotherapy is the drug erlotinib (Tarceva) which may be used in patients with NSCLC who are no longer responding to chemotherapy. It is a so-called targeted drug, a drug that more specifically targets cancer cells, resulting in less damage to normal cells. Erlotinib targets a protein called the epidermal growth factor receptor (EGFR) that helps cells to divide. This protein is found at abnormally high levels on the surface of some types of cancer cells, including many cases of non-small cell lung cancer. Erlotinib is taken by mouth in pill form.

Other attempts at targeted therapy include drugs known as antiangiogenesis drugs, which block the development of new blood vessels within a cancer. Without adequate blood vessels to supply oxygenated blood, the cancer cells will die. The antiangiogenic drug bevacizumab (Avastin) has recently been found to prolong survival in advanced lung cancer when it is added to the standard chemotherapy regimen. Bevacizumab is given intravenously every two to three weeks. However, since this drug may cause bleeding, it is not appropriate for use in patients who are coughing up blood, if the lung cancer has spread to the brain, or in people who are receiving anticoagulation therapy ( "blood thinner" medications). Bevacizumab is also not used in cases of squamous cell cancer, because it leads to bleeding from this type of lung cancer.

Photodynamic therapy (PDT): One newer therapy used for different types and stages of lung cancer (as well as some other cancers) is photodynamic therapy. In photodynamic treatment, a photosynthesizing agent (such as a porphyrin, a naturally occurring substance in the body) is injected into the bloodstream a few hours prior to surgery. During this time, the agent deposits itself selectively in rapidly growing cells such as cancer cells. A procedure then follows in which the physician applies a certain wavelength of light through a handheld wand directly to the site of the cancer and surrounding tissues. The energy from the light activates the photosensitizing agent, causing the production of a toxin that destroys the tumor cells. PDT has the advantages that it can precisely target the location of the cancer, is less invasive than surgery, and can be repeated at the same site if necessary. The drawbacks of PDT are that it is only useful in treating cancers that can be reached with a light source and is not suitable for treatment of extensive cancers. Research is ongoing to further determine the effectiveness of PDT in lung cancer.

Radiofrequency ablation (RFA): Radiofrequency ablation is being studied as an alternative to surgery, particularly in cases of early stage lung cancer. In this newer type of treatment, a needle is inserted through the skin into the cancer, usually under guidance by CT scanning. Radiofrequency (electrical) energy is then transmitted to the tip of the needle where it produces heat in the tissues, killing the cancerous tissue and closing small blood vessels that supply the cancer. RFA usually is not painful and has been approved by the US Food and Drug Administration for the treatment of certain cancers including lung cancers. Studies have shown that this treatment can prolong survival similarly to surgery, when used to treat early stages of lung cancer, but without the risks of major surgery and the prolonged recovery time associated with major surgical procedures.