“I have kidney cancer. What now?”
This site contains information from scientists and physicians who are experts in understanding and treating kidney cancer. The goal is to help you beat cancer by making you smarter.
How is this possible? Your ability to think, to use information, and to make choices about treatment can help bend the odds in your favor. Visiting this website is the first step.
This page provides you with brief background information about kidney cancer and some immediate resources that may be helpful and information that follows is much more in-depth, ranging from current surgical and therapeutic approaches to practical advice for living with cancer day to day.
Improving your health starts right now!
You Are Not Alone
Last year, more than 1.3 million new cancers were diagnosed in the United States. According to the American Cancer Society, more than 50,000 of these individuals were diagnosed with kidney cancer. But there is hope: More than 200,000 kidney cancer survivors are living in the United States right now. Recent advances in diagnosis, surgical procedures, and treatment options will allow even more patients to live with the disease, continuing to maintain their normal schedules and lifestyles.
This marks the beginning of an important new era for kidney cancer patients, with the recent approval by the Food and Drug Administration (FDA) of new drugs to treat their advanced disease. These drugs target cancer cells in different ways than current drugs used to treat kidney cancer, and will have a very positive impact for many patients. Continued research efforts will improve our understanding of the disease even more and increase the options available to fight kidney cancer.
Each person diagnosed with kidney cancer goes through the shock of being told they have the disease. It is a difficult experience. Feelings of shock, loneliness, alienation, fear, frustration, anger, and hurt are natural parts of any life-threatening illness. It is okay to have these feelings, to cry, and to be upset.
After the shock of diagnosis, it’s time to start healing. Don’t let your emotions and your cancer destroy your home life or relations with the important people in your life. They may also be hurting inside, fearing for you and themselves. When cancer strikes, it hits the whole family. Your friends and family are rooting for you.
Sometimes kidney cancer is called by its medical name, renal cell carcinoma. Renal is from the Latin word renalis for kidneys. Kidney cancer includes various forms, including clear cell, papillary, sarcomatoid, transitional cell, and others. These will be explained in more detail later.
Some patients are diagnosed before the cancer has metastasized (spread) to other parts of the body, while others have metastatic disease when their cancer is initially diagnosed. Surgery may be the first course of treatment, or systemic treatment — that is, a treatment that is injected into the bloodstream or swallowed — may be recommended prior to surgery (though this tends to be rare). If surgery is done first, additional treatment may be recommended to delay the cancer’s return, or to treat metastatic disease.
The choice of treatment, where treatment is administered, the frequency of check-ups, and many other aspects of the management of your disease are determined with input from you. The more you know, the better your decisions, and the more you can feel in control of your illness. Knowledge about your disease will help you better communicate with your doctor and nurse, and increase your confidence in the treatment that you receive. Getting smarter about kidney cancer is an important step in effectively fighting your disease.
How to Learn More about Kidney Cancer
Your own doctor can be one of the best sources of information about your disease and its treatment. Doctors that specialize in treating cancer are known as oncologists. After an initial diagnosis is made, don’t be afraid to ask your oncologist many questions. You should also consider getting a second opinion from another doctor who is a kidney cancer specialist. If you do not know the name of a specialist, you may obtain names from the Kidney Cancer Association. Your doctor won’t be offended if you seek a second opinion. It is common practice. In fact, your doctor often gives second opinions to colleagues. You may not need to have tests repeated because often the results of your previous tests can be sent to the second doctor. Rarely will a second opinion change your diagnosis, but it can give you useful information and fresh insights about treatment alternatives. In addition, your insurance company may require a second opinion. If you are in a health maintenance organization (HMO), you should find out about its policy concerning second opinions. You’ll find more information about working with your doctor later.
The Kidney Cancer Association
The Kidney Cancer Association is available to assist you in many ways, including providing written information on the disease, treatment options, and resources. You can contact us by telephone to speak with a nurse who can help you. This website has valuable information that you can read, print, or share with family and friends.
Kidney cancer patients can learn a great deal from one another. The best way to do that is to attend a patient meeting sponsored by the Kidney Cancer Association or support groups sponsored by your local hospital. Support groups provide excellent open environments for frank exchange with other patients and professional counselors. Our message board and Facebook® Fan Page are good resources, too.
The National Cancer Information Service
No matter where you live in the United States, you can call 1-800-4-CANCER, the toll-free telephone number of the National Cancer Information Service. This information service is provided by the National Cancer Institute (NCI), which is part of the National Institutes of Health (NIH). The NIH is operated by the US Department of Health and Human Services. You can ask for a variety of free booklets.
There are many other websites that can help you understand the disease and its diagnosis, treatment options, dealing with the illness and side effects of treatment, work and coping with a life-threatening diagnosis. You must be careful because some medical information on the Internet is posted by nonprofessionals and is not reliable. Always check the site to learn more about the source of any information provided. Look for well-known, established sources online and don’t rely on any one website. Reputable sites with reliable information for patients are sometimes accredited (approved) by a governing body such as the “Health on the NET.” In any case, use common sense and compare sites carefully before considering online material.
Once you have a basic understanding of your disease, you may want to go to the library and dig into medical books and journals. More and more research is being done as scientists and physicians gain new knowledge about how kidney cancer develops and spreads, in order to improve our ability to treat and cure more patients. Nursing literature may be helpful to understand the treatment options and management of side effects. The amount of research on kidney cancer being presented at national and international physician and nursing conferences and published literature reporting research results has increased significantly in the past five years. There are many meetings devoted to education and open dialogue and researchers are continually discovering new information about kidney cancer. Doctors and nurses will provide you with this information as they discuss treatment options appropriate for you, and care for you during the course of your treatments.
Genetic Causes of Kidney Cancer
Genetic factors have been linked to an increased risk of developing kidney cancer. A hereditary disorder called von Hippel-Lindau (VHL) disease is associated with a high risk of developing kidney cancer, for example. Scientists have isolated the gene responsible for VHL disease, and this discovery offers exciting future possibilities for improved diagnosis and treatment of some kidney cancers. Another genetic mutation is thought to be responsible for tuberous sclerosis, a disease characterized by small tumors of the blood vessels that results in numerous bumps on the skin, mental retardation, seizures, and cysts in the kidneys, liver, and pancreas. In some cases, tuberous sclerosis has been associated with renal cell carcinoma. Birt Hogg Dube Syndrome (BHD) is another disorder associated with kidney cancer that is characterized by the presence of multiple small bumps (nodules) on the skin covering the nose, cheeks, forehead, ears, and neck. For more information about these genetic factors, as well as HLRCC and HPRCC, please click here.
Some external factors, such as smoking and obesity, have been related to a higher incidence of kidney cancer. In an attempt to answer the question “Why me?” some people want to determine such factors as a cause for their cancer. Although it is important for people to know what factors or behaviors are associated with an increased risk of kidney cancer, blaming yourself for past behavior is neither helpful nor healing. The fact that a person’s behavior included a risk factor such as smoking doesn’t necessarily mean the factor caused the cancer.
Information and Fear
Some patients don’t think that actively seeking information about their disease will do any good. They think that whatever their doctor says is all they want or need to know. Others are afraid to learn more about kidney cancer. Information about survival statistics particularly frightens them. It is important, however, to remember that these statistics are based on population averages and are often several years old by the time they are published. Therefore, the most up-to-date information and factors that affect the risks and benefits of treatment may not be published. Your doctor and nurse will give this information to you. Asking questions is a very important way to reduce fear and anxiety and is the only way to truly empower yourself to make the best decisions for you and your family.
Some patients believe that information about kidney cancer is presented in complicated medical terms they won’t be able to understanding. But a great deal of information, including the resources recommended in this booklet, is specifically written for patients in easy-to-read language that requires no specialized training to understand. Your doctors and nurses will be very willing to answer your questions, because the more you understand the better you will be able to participate as an active member of your health-care team.
We think that learning more about the disease and your treatment choices will help you. History has shown that assertive patients who actively work to overcome cancer often increase the odds of survival, live longer, and enjoy life more. You can be a passive victim or an active fighter. The choice is yours. Our recommendation is to fight.
A comprehensive look at types, symptoms, treatments and much more. Use this page to formulate questions for your physician about the status of your kidney cancer.
According to the American Cancer Society (ACS), well over one million new cases of cancer are diagnosed each year in the United States. In recent years, the percentage of cases involving kidney cancer have made up only about 3% of the total (in 2005 more than 36,000 new kidney cancer cases were diagnosed.)
Kidney cancer occurs roughly twice as often in males as in females. 12,660 people died from this disease in 2005. However, more than 100,000 kidney cancer survivors are living in the United States right now, according to ACS. These statistics include both adults and children and include all forms of kidney cancer.
Renal cell carcinoma (RCC) is the most common type of kidney cancer. In terms of all cancers, renal cell carcinoma is relatively rare, representing about 3% of all adult cancers. It is usually treated initially with surgery to remove the tumor. If caught in early stages, the chance that it will return is low. Unfortunately, it has few symptoms in its early stages so it is usually undiagnosed or misdiagnosed and not detected until the tumor has grown fairly large. At that point, it displaces other nearby organs, causing symptoms. Many kidney (renal) tumors are found incidentally on x-rays or ultrasound examinations performed for reasons that don’t relate to the tumor or any of its potential symptoms.
Thirty percent of kidney cancer patients show signs of advanced RCC when diagnosed. Fifteen to 25 percent of patients have metastatic disease at the time of their diagnosis, meaning their cancer has spread to other areas of the body.
The most common symptom of kidney cancer is painless urination of blood, a condition known as hematuria. This symptom occurs in 40% to 50% of patients. Often, blood in the urine will occur one day and not the next. (Note that blood in the urine can indicate other diseases besides kidney cancer, such as kidney stones. When blood in the urine does occur, a doctor should evaluate this symptom immediately.)
Other common symptoms of kidney cancer include the presence of an abdominal mass, a hard lump or a thickening or bulging under the skin that can be seen or felt as the tumor grows. There also may be back or flank pain or pressure. Kidney cancer occurs most often in men between the age of 40 and 60. Since back pain is common among people over 40 years of age, such pain is often ignored and the presence of kidney cancer can go undetected.
If the tumor has spread to distant organs, symptoms may vary, depending on the specific organ affected, though patients may notice unexplained weight loss, fevers, anemia, or high blood pressure. The following list includes symptoms patients describe at the time of their diagnosis. This demonstrates how common some symptoms are, and how infrequent others are.
Renal cell carcinoma symptoms
|Blood in the urine||59%|
|Back or flank pain||41%|
|Low blood counts (anemia)||21%|
|Tumor calcification on x-ray||13%|
|Symptoms of metastases||10%|
|High calcium in blood||7%|
|High blood counts||7%|
Subtypes of Renal Cell Carcinoma (RCC)
Not all kidney cancers are the same. There is an increasing understanding among clinicians and researchers that there are different subtypes of RCC and that they behave quite differently, both with regard to how aggressive they are in the patient and how they respond to treatment. Ten or fifteen years ago, it was common for a pathology report from a patient with kidney cancer to read simply “Renal Cell Carcinoma.” This simple diagnosis is now thought to be incomplete. Identification of the specific subtype or cell type (histology) of the kidney cancer can be as important in determining patient prognosis as knowing the stage or grade of the RCC. Your doctor should give you information regarding the histology, grade and stage of your kidney cancer. If not, you should feel comfortable asking for this information since it is an important part of your treatment planning.
The subtypes of RCC come from the description of the cell’s appearance and other characteristics. They include:
Clear Cell (conventional) RCC
This is the most common form of kidney cancer and represents between 66% and 75% of all cases. Clear cell RCC is the cell type associated with the von Hippel Lindau (VHL) gene mutation in hereditary kidney cancer. In fact, approximately 70% of non-hereditary cases of clear cell RCC also have aVHL mutation. Much of today’s research, which is attempting to identify new effective treatments for patients with locally advanced or metastatic disease, is focused on this disease subtype since it is the most common type of RCC. When the tumor has not spread, prognosis is very good following surgical excision. Prognosis for the patient is directly related to both the cancer’s stage (tumor size and rate of growth) and grade (the characteristics of a tumor’s cell structure). Staging and grading are both explained later in this chapter. Patients with metastatic clear cell RCC – or a tumor that has spread to other parts of the body – have a significantly poorer prognosis.
This is the second most common form of kidney cancer, making up approximately 15% of cases. Papillary RCC itself is divided into two subtypes based on cell appearance: Type I (5%) and Type II (10%). There is an increased incidence of papillary RCC in African Americans and an increased incidence of bilateral disease (involving both kidneys) associated with this subtype. There are also hereditary forms of both Type I and Type II papillary RCC. When papillary RCC has not spread, surgical removal is usually associated with an excellent prognosis. However, when papillary RCC metastasizes to other locations in the body, most conventional therapies for RCC, such as immunotherapy are ineffective.
This rare form of kidney cancer represents approximately 5% of RCC cases. This type of RCC is thought to originate from the same cell type as those that form renal oncocytomas (see below). Hybrid tumors that contain features of both chromophobe RCC and renal oncocytoma have also been diagnosed. There is a familial or inherited form of chromophobe RCC (in association with renal oncocytoma) called Birt Hogg Dubé syndrome, which is also associated with a specific genetic mutation. Chromophobe RCC rarely metastasizes until very late in its clinical course, and surgical removal of localized or even locally advanced disease is usually associated with an excellent prognosis. Metastatic chromophobe RCC is quite rare, and no standard therapy currently exists.
This is a benign tumor of the kidney that makes up approximately 5% of all kidney tumors. These tumors do not metastasize, although they can grow to a large size in the kidney and invade local structures, which can result in symptoms requiring surgery. They are thought to be related to chromophobe RCC, and it can be quite difficult to differentiate the two. The tumor is treated by a partial or complete removal of the kidney.
Less than 1% of renal cell carcinomas are an unclassified type and are very rare. They don’t fit into one of the more common subtypes of RCC listed above. When examined under a microscope, these unclassified cancer cells have a structure and genetic features that don’t match the description of the more common RCC subtypes. This category usually includes aggressive tumors that do not respond to traditional therapy for RCC.
Collecting Duct Carcinoma
This is a rare and very aggressive variant of kidney cancer that represents less than 1% of cases. This form of RCC is usually metastatic at the time of diagnosis, and is more common in younger individuals. Treatment has been directed at using chemotherapy-based regimens, similar to those used in the treatment of transitional cell carcinoma (see below), as these tumors do not respond to traditional RCC therapies such as bioimmunotherapy.
This condition, known as “differentiation,” can occur with any of the common RCC subtypes. The term refers to the fact that the RCC cells — when viewed under the microscope — have the appearance of sarcoma cells. The percentage of sarcomatoid differentiation is usually reflected in the tumor’s pathology report and relates to the tumor’s aggressiveness. The prognosis associated with Sarcomatoid RCC is usually poor. The condition is found frequently in patients whose kidney cancer has metastasized widely. This form of kidney cancer is sometimes treated with chemotherapy.
Transitional Cell Carcinoma of the Kidney
Transitional cell carcinoma (TCC) of the kidney is a rare and potentially very aggressive tumor that should not be considered a true kidney cancer, but instead should be grouped with those cancers that develop from cells that line the urinary tract. This includes TCC of the urinary bladder, which is far more common than TCC of the kidney. If the cancer has not spread, the tumor can be treated by surgical removal of both the kidney and its ureter, although recurrences of TCC in the bladder are common. When the tumor is large or has metastasized, the prognosis is extremely poor, and treatment options are similar to those for metastatic urinary bladder cancer, which includes chemotherapy.
Translocation renal cell carcinoma
Also described as TFE3 rearranged renal cell carcinoma, Xp11 translocation PEComa, melanotic Xp11 translocation cancer, t(6;11) translocation renal cell carcinoma, and TFEB rearranged renal cell carcinoma, and MiT family translocation carcinoma. There is so standard treatment protocol for patients with MiT family translocation RCC. Ongoing studies will work to identify prognostic factors and therapeutic targets.
Renal medullary carcinoma (RMC)
- Renal medullary carcinoma (RMC) is an extremely rare variant of kidney cancer that affects young patients who carry the sickle cell trait, or more rarely, have sickle cell disease. Typical presentations include young African Americans who present with flank pain and blood in their urine. Most commonly, these cancers are widely metastatic at presentation and patients may present with symptoms related to their metastatic disease. These cancers tend to behave in a very aggressive manner and prognosis often is poor, even with treatment. We, at the Kidney Cancer Association, would strongly urge patients with these symptoms and who harbor the sickle cell trait to contact a major tertiary cancer care center or a National Cancer Institute designated Cancer Center for a multidisciplinary treatment approach that may include surgery as well as chemotherapy. Because of the rarity of these tumors, uniform treatment guidelines have not been established. Please contact the Kidney Cancer Association for further information and an appropriate referral in your area.
Detection, Diagnosis and Staging
Because kidney cancer may spread to other parts of your body, it is important to be very thorough in testing for its presence. Your doctor may order some or all of a variety of tests that are available to determine the extent of your cancer and to develop your treatment plan.
Your doctor may use different approaches to diagnose RCC, depending on the symptoms you display. All approaches begin with a careful physical examination, combined with a complete discussion of past and present medical problems.
Certain tests may be done to assist your doctor in determining the correct diagnosis. The most common tests that may be ordered include:
Computed Tomography (CT scan)
A CT scan is a highly specialized x-ray that is used to visualize internal organs and provides a very accurate cross section picture of specific areas of the body. It is used as one of the primary imaging tools for the assessment of RCC. If the initial sign of the tumor is a mass or thickening in the kidney area detected on an x-ray taken for other reasons, or seen or felt from the outside of the body, a CT scan is often ordered.
CT scans are more detailed then ordinary x-rays, taking pictures of your organs one thin slice at a time from different angles. Then a computer puts the images together to show the size and location of any abnormalities. To enhance the image of the abdominal organs, dye may be taken orally (by mouth) before the scan. An IV may also be placed for injection of additional contrast dye. There is generally no pain associated with the CT scan, although the IV dye may cause a hot flushing sensation. Some people may also experience an allergic reaction to IV dye (also called IV contrast), especially individuals who are allergic to iodine. Depending on the part of the body visualized, dietary restrictions may be required prior to the procedure.
CT scanning technology has recently been improved by development of a method called spiral CT scanning. This type of CT scan is faster and gives a better image than older CT methods.
Magnetic resonance imaging (MRI)
An MRI is a highly specialized scan that is similar to a CT scan, but may be better suited for assessing certain areas of the body, such as the bones. It creates an accurate cross-section picture of specific organs within the body, to allow for a layer-by-layer examination. An MRI is usually not a painful procedure. Because it uses a powerful magnet to produce the images, people with metal within their body — such as prosthetic hip replacements, pacemakers, or metal plates — should discuss the use of an MRI with their physician and the MRI technician before the scan is performed. The test may require the patient to lie still for a long time usually in a narrow space, which may be difficult for some people who do not like closed in spaces. MRI scans are often used in cases where CT scans may not be able to view an area of the body well enough.
A bone scan is used to check for the spread of cancer to the bones. It is done by injecting small amounts of a special radioactive material through a vein into your bloodstream. This material is carried to the bone, where it collects in areas where there is a lot of bone activity. The test can identify both cancerous and non-cancerous diseases but the test can’t distinguish between cancer and other conditions such as arthritis when used it is used alone. Therefore other tests may be needed, such as x-rays or CT scans.
PET scan (Positron Emission Tomography)
A PET scan is a very specialized diagnostic study that provides information about how extensively a cancer has spread, based on certain activities of the cells. PET scans are typically used for breast, colorectal, ovarian, lymphoma, lung, melanoma, and head & neck cancer. The effectiveness of PET scans for kidney cancer is still being studied.
Unlike CT and MRI scans, which produce images of internal organs or other structures, a PET scan produces images based on the chemical and physiological changes related to a cell’s metabolism. This is important because chemical and physiological changes in the cells often occur before structural changes in tissues can be seen. The result is that PET scans can help distinguish benign from malignant tumors and help doctors determine the stage of cancer spread in the patient. PET scans can also measure whether or not treatment therapies are working. PET scans are quite often used in combination with CT and MRI scans. A PET scan can last from 15 minutes to 2 hours, depending on the area of the body being scanned.
Ultrasonography (ultrasound or US)
If there is blood in the urine, an ultrasound of the abdomen with special attention to the kidneys, ureters, and bladder may be ordered. Usually no preparation is needed for this test, and it is generally not uncomfortable. It utilizes sound waves to produce images of internal organs, helping the radiologist detect any masses that may be present. A wand called a transducer is passed over the skin, and emits sound waves that are detected as echoes bouncing back off internal organs. The echo-pattern images produced by kidney tumors look different from those of normal kidney tissue. This test may be used for initial diagnosis of a kidney mass or to help visualize a mass when a fine needle biopsy is done (see Biopsy Procedure).
Intravenous pyelogram (IVP)
An intravenous pyelogram (IVP) test may also be used. Special dye is injected into a blood vessel, usually in the arm. The dye circulates through the blood stream to the different organs of the body including the kidneys. X-rays are taken of the kidneys as the dye circulates through them. This will identify any abnormalities within the kidney. If either the ultrasound or IVP is abnormal, a CT scan may be ordered.
A plain x-ray of the chest may be done to see if the cancer has spread to the lungs. If something is seen on the x-ray, the doctor may order a CT scan of the chest to help determine what it is.
This procedure is used to visualize location and function of arteries. A catheter is usually threaded up a large artery in the leg into an artery leading to your kidney (renal artery). A contrast dye is then injected into the artery to outline blood vessels. Angiography can outline the blood vessels that supply a kidney tumor, which can help a surgeon better plan an operation. Angiography may also help diagnose renal cancers since the blood vessels supplying tumors usually look different than the normal blood supply to the kidney.
If, after diagnostic tests are completed, there is a strong clinical suspicion that the kidney mass is cancerous (malignant), surgical removal of the kidney (nephrectomy) will be performed immediately. If the diagnostic test results are not clear, a biopsy may be performed. During a biopsy procedure a small sample of tissue is removed from the mass and examined to determine whether it is benign or malignant. There are several ways to perform a biopsy of a kidney mass, though the most common method is a procedure called a fine needle aspiration (FNA) or fine needle biopsy. Using ultrasound or a CT scanner for guidance, the doctor will insert a long thin needle through the skin, directly into the mass, and remove the sample tissue. This is generally not an uncomfortable procedure. A pathologist will evaluate the biopsy tissue under a microscope to determine whether it is benign or malignant. If it is malignant, the pathologist also will identify the histology, or cell type.
If there is clear evidence of widespread metastasis at the time of the discovery of the kidney mass, a biopsy may be taken from an area of metastasis, instead of from the kidney. This may be recommended to reduce risk of bleeding, if the metastatic area is more easily accessible than the kidney.
In addition to the tests described above, your doctor may order one or more of the following lab tests to complete your evaluation.
Urinalysis is usually part of a complete physical exam. Microscopic and chemical tests are performed that will detect small amounts of blood and other substances not seen with the naked eye. About half of all patients with renal cell cancer will have blood in their urine. Microscopic examination of urine samples (called urine cytology) can also detect cancer cells in the urine.
A complete blood count and chemical test of the blood can detect findings associated with RCC. Anemia (too few red blood cells) is very common. Erythrocytosis (too many red blood cells) may also occur because some of these renal cancers produce a hormone (erythropoietin) that can increase red blood cell production by the bone marrow.
High levels of liver function enzymes in the blood (for reasons not known) and hypercalcemia (high calcium levels) sometimes occur.
The Role of Staging and Grading
Staging of a cancer is the process of classifying how far a cancer has spread, while grading determines the characteristics and make up of the cancer’s cells. The two systems play different roles, but both staging and grading are important predictors of the course of the disease and treatment effectiveness (prognosis). They are useful tools in determining what therapy is appropriate and the chance of treatment success.
Certain imaging tests, including CT and MRI scans, can help determine staging. Blood tests will also be done to evaluate your overall health and to detect whether the cancer has spread to certain organs.
A staging system is a standardized way in which the cancer care team describes the extent of the cancer. The most commonly used staging system was developed by the American Joint Committee on Cancer (AJCC)
American Joint Committee on Cancer (AJCC) TNM Staging System
The AJCC staging system is based on the evaluation of the tumor size on the kidney (T), the number of lymph nodes (N) and the extent of metastisis (M). Evaluation of the T, N and M components is followed by a stage grouping.
The T component designates the size of the tumor. The numerical value increases with tumor size and extent of invasiveness. The letter T followed by a number from 0 to 3 describes the tumor’s size and spread to nearby tissues. Some of these numbers are further subdivided with letters, such as T1a and T1b. Higher T numbers indicate a larger tumor and/or more extensive spread to tissues near the kidney.
The N component designates the presence or absence of tumor in the regional lymph nodes. In some sites there is an increasing numerical valued based on size, fixation, or capsular invasion. In other sites, numerical value is based on multiple node involvement or number of location and the regional lymph nodes. The letter N followed by a number from 0 to 2 indicates whether the cancer has spread to lymph nodes near the kidney and, if so, how many are affected. Lymph nodes are bean-sized collections of immune system cells that help fight infections and cancers.
The M component identifies the how distant the spread of the cancer has been, including lymph nodes that are not in the region of the original tumor. The letter M followed by a 0 or 1 indicates whether or not the cancer has spread (metastasized) to distant organs such as the lungs or bones, or to lymph nodes that are not near the kidneys.
Detailed Definitions of T, N, and M Categories
Primary tumor (T)
TX: Primary tumor cannot be assessed (information not available).
T0: No evidence of a primary tumor.
T1a: Tumor is 4 cm (about 11/2 inches) in diameter or smaller and is limited to the kidney.
T1b: Tumor is larger than 4 cm but smaller than 7 cm (about 2¾ inches) and is limited to the kidney.
T2: Tumor is larger than 7 cm but is still limited to the kidney.
T3a: Tumor has spread into the adrenal gland or into fatty tissue around the kidney, but not beyond a fibrous tissue called Gerota’s fascia, which surrounds the kidney and nearby fatty tissue.
T3b: Tumor has spread into the large vein leading out of the kidney (renal vein) and/or the part of the large vein leading into the heart (vena cava) that is within the abdomen.
T3c: Tumor has reached the part of the vena cava that is within the chest or invades the wall of the vena cava.
T4: Tumor has spread beyond Gerota’s fascia (fibrous tissue that surrounds the kidney and the fatty tissue next to the kidney).
Regional lymph nodes (N)
NX: Regional lymph nodes cannot be assessed (information not available).
N0: No regional lymph node metastasis.
N1: Metastasis to one regional (nearby) lymph node.
N2: Metastasis to more than one regional (nearby) lymph node. Distant metastasis (M):
Extent of Metastasis (M)
MX: Presence of distant metastasis cannot be assessed (information not available).
M0: No distant metastasis.
M1: Distant metastasis present; includes metastasis to non-regional (not near the kidney) lymph nodes and/or to other organs (such as the lungs, bones, or brain).
Renal Cell Cancer Stage Grouping
Once the T, N, and M categories have been determined, this information is combined in a process called stage grouping to determine a patient’s overall disease stage. This is expressed in Roman numerals from stage I (the least serious or earliest stage) to stage IV (the most serious or advanced stage).
Stage I: T1a-T1b, N0, M0. The tumor is 7 cm or smaller and limited to the kidney. There is no spread to lymph nodes or distant organs.
Stage II: T2, N0, M0. The tumor is larger than 7 cm but is still limited to the kidney. There is no spread to lymph nodes or distant organs.
Stage III: T1a-T3b, N1, M0 or T3a-T3c, N0, M0. Several combinations of T and N categories are included in this stage. These include any tumor that has spread to only one nearby lymph node but not to other organs. Stage III also includes tumors that have not spread to lymph nodes or distant organs but have spread to the adrenal glands, to fatty tissue around the kidney, and/or have grown into the large vein (vena cava) leading from the kidney to the heart.
Stage IV: T4, N0-N1, M0 or Any T, N2, M0 or Any T, Any N, M1. Several combinations of T, N, and M categories are included in this stage, which includes any cancers that have spread directly through the fatty tissue and beyond Gerota’s fascia, the fibrous tissue that surrounds the kidney. Stage IV also includes any cancer that has spread to more than one lymph node near the kidney, or to any lymph node distant from the kidney, or to any distant organs such as the lungs, bone, or brain.
The system for determining the characteristics of a cancer’s cells is called Fuhrman grading. The Fuhrman grade is determined by a pathologist, who will review the cellular details of your tumor. The grade is based on an examination of how closely the cancer cell’s nucleus (part of a cell in which DNA is stored) resembles a normal kidney cell’s nucleus.
Kidney cancers are usually given a Fuhrman grade on a scale of 1 through 4. Grade 1 kidney cancers have cell nuclei that look very much like a normal kidney cell nucleus. These cancers are usually slow growing and are slow to spread to other parts of the body (metastasize). They tend to have a good outlook (prognosis). Grade 4 kidney cancer, on the upper end of the Fuhrman scale, looks quite different from normal kidney cells and has a worse prognosis. Generally, the higher the Fuhrman grade the worse the