Facts on Childhood Extracranial Germ Cell Tumors
- Childhood extracranial germ cell tumors form from germ cells in parts of the body other than the brain.
- Childhood extracranial germ cell tumors may be benign or malignant.
- There are three types of extracranial germ cell tumors.
- Mature teratomas
- Immature teratomas
- Malignant berm cell tumors
- Childhood extracranial germ cell tumors are grouped as gonadal or extragonadal.
- Gonadal germ cell tumors
- Extragonadal extracranial germ cell tumors
- The cause of most childhood extracranial germ cell tumors is unknown.
- Having certain inherited disorders can increase the risk of an extracranial germ cell tumor.
- Signs of childhood extracranial germ cell tumors depend on the type of tumor and where it is in the body.
- Imaging studies and blood tests are used to detect (find) and diagnose childhood extracranial germ cell tumors.
- Certain factors affect prognosis (chance of recovery) and treatment options.
What Are Childhood Extracranial Germ Cell Tumors?
Childhood extracranial germ cell tumors form from germ cells in parts of the body other than the brain.
A germ cell is a type of cell that forms as a fetus (unborn baby) develops. These cells later become sperm in the testicles or eggs in the ovaries. Sometimes while the fetus is forming, germ cells travel to parts of the body where they should not be and grow into a germ cell tumor. The tumor may form before or after birth. This summary is about germ cell tumors that form in parts of the body that are extracranial (outside the brain).
Extracranial germ cell tumors usually form in the following areas of the body:
- Testicles.
- Ovaries.
- Sacrum or coccyx (bottom part of the spine).
- Retroperitoneum (the back wall of the abdomen).
- Mediastinum (area between the lungs).
Extracranial germ cell tumors are most common in adolescents.
Extracranial germ cell tumors may be benign (noncancer) or malignant (cancer).
What Are the Different Types of Extracranial Germ Cell Tumors?
There are three types of extracranial germ cell tumors. Extracranial germ cell tumors are grouped into mature teratomas, immature teratomas, and malignant germ cell tumors:
Mature Teratomas
Mature teratomas are the most common type of extracranial germ cell tumor. Mature teratomas are benign tumors and not likely to become cancer. They usually occur in the sacrum or coccyx (bottom part of the spine) in newborns or in the ovaries of girls at the start of puberty. The cells of mature teratomas look almost like normal cells under a microscope. Some mature teratomas release enzymes or hormones that cause signs and symptoms of disease.
Immature Teratomas
Immature teratomas also usually occur in the sacrum or coccyx (bottom part of the spine) in newborns or the ovaries of girls at the start of puberty. Immature teratomas have cells that look very different from normal cells under a microscope. Immature teratomas may be cancer. They often have several different types of tissue in them, such as hair, muscle, and bone. Some immature teratomas release enzymes or hormones that cause signs and symptoms of disease.
Malignant Germ Cell Tumors
Malignant germ cell tumors are cancer. There are two main types of malignant germ cell tumors:
- Germinomas: Tumors that make a hormone called beta-human chorionic gonadotropin (β-hCG). There are three types of germinomas.
- Dysgerminomas form in the ovary in girls.
- Seminomas form in the testicle in boys.
- Germinomas form in areas of the body that are not the ovary or testicle.
- Nongerminomas: There are four types of nongerminomas.
Yolk sac tumors make a hormone called alpha-fetoprotein (AFP). They can form in the ovary, testicle, or other areas of the body.
Choriocarcinomas make a hormone called beta-human chorionic gonadotropin (β-hCG). They can form in the ovary, testicle, or other areas of the body.
Embryonal carcinomas may make a hormone called β-hCG and/or a hormone called AFP. They can form in the testicle or other parts of the body, but not in the ovary.
Mixed germ cell tumors are made up of both malignant germ cell tumor and teratoma. They can form in the ovary, testicle, or other areas of the body.
Childhood extracranial germ cell tumors are grouped as gonadal or extragonadal. Malignant extracranial germ cell tumors are gonadal or extragonadal.
Gonadal Germ Cell Tumors
Gonadal germ cell tumors form in the testicles in boys or ovaries in girls.
Testicular Germ Cell Tumors
Testicular germ cell tumors are divided into two main types, seminoma and nonseminoma. Seminomas make a hormone called beta-human chorionic gonadotropin (β-hCG).
Nonseminomas are usually large and cause signs or symptoms. They tend to grow and spread more quickly than seminomas.
Testicular germ cell tumors usually occur before the age of 4 years or in adolescents and young adults. Testicular germ cell tumors in adolescents and young adults are different from those that form in early childhood. Boys older than 14 years with testicular germ cell tumors are treated in pediatric cancer centers, but the treatment is much like the treatment used in adults.
Ovarian Germ Cell Tumors
Ovarian germ cell tumors are more common in adolescent girls and young women. Most ovarian germ cell tumors are benign teratomas . Sometimes immature teratomas, dysgerminomas, yolk sac tumors, and mixed germ cell tumors (cancer) occur.
Extragonadal Extracranial Germ Cell Tumors
Extragonadal extracranial germ cell tumors form in areas other than the brain, testicles, or ovaries. Most extragonadal extracranial germ cell tumors form along the midline of the body. This includes the following:
- Sacrum (the large, triangle-shaped bone in the lower spine that forms part of the pelvis).
- Coccyx (the small bone at the bottom of the spine, also called the tailbone).
- Mediastinum (the area between the lungs).
- Back of the abdomen.
- Neck.
In younger children, extragonadal extracranial germ cell tumors usually occur at birth or in early childhood. Most of these tumors are teratomas in the sacrum or coccyx. In older children, adolescents, and young adults, extragonadal extracranial germ cell tumors are often in the mediastinum.
What Are Risk Factors for Childhood Extracranial Germ Cell Tumors?
The cause of most childhood extracranial germ cell tumors is unknown.
Having certain inherited disorders can increase the risk of an extracranial germ cell tumor.
Anything that increases your risk of getting a disease is called a risk factor. Having a risk factor does not mean that you will get cancer; not having risk factors doesn’t mean that you will not get cancer. Talk with your child’s doctor if you think your child may be at risk.
Possible risk factors for extracranial germ cell tumors include the following:
Having certain genetic syndromes:
- Klinefelter syndrome may increase the risk of germ cell tumors in the mediastinum.
- Swyer syndrome may increase the risk of germ cell tumors in the testicles or ovaries.
- Turner syndrome may increase the risk of germ cell tumors in the ovaries.
Having an undescended testicle may increase the risk of developing a testicular germ cell tumor.
What Are the Symptoms and Signs of Childhood Extracranial Germ Cell Tumors?
Signs of childhood extracranial germ cell tumors depend on the type of tumor and where it is in the body.
Different tumors may cause the following signs and symptoms. Other conditions may cause these same signs and symptoms. Check with a doctor if your child has any of the following:
- A lump in the abdomen or lower back.
- A painless lump in the testicle.
- Pain in the abdomen.
- Fever.
- Constipation.
- In females, no menstrual periods.
- In females, unusual vaginal bleeding.
How Are Childhood Extracranial Germ Cell Tumors Diagnosed?
Imaging studies and blood tests are used to detect (find) and diagnose childhood extracranial germ cell tumors.
The following tests and procedures may be used:
- Physical exam and history: An exam of the body to check general signs of health, including checking for signs of disease, such as lumps or anything else that seems unusual. The testicles may be checked for lumps, swelling, or pain. A history of the patient's health habits and past illnesses and treatments will also be taken.
- Serum tumor marker test: A procedure in which a sample of blood is checked to measure the amounts of certain substances released into the blood by organs, tissues, or tumor cells in the body. Certain substances are linked to specific types of cancer when found in increased levels in the blood. These are called tumor markers. Most malignant germ cell tumors release tumor markers. The following tumor markers are used to detect extracranial germ cell tumors:
- Alpha-fetoprotein (AFP). Beta-human chorionic gonadotropin (β-hCG). For testicular germ cell tumors, blood levels of the tumor markers help show if the tumor is a seminoma or nonseminoma.
- Blood chemistry studies: A procedure in which a blood sample is checked to measure the amounts of certain substances released into the blood by organs and tissues in the body. An unusual (higher or lower than normal) amount of a substance can be a sign of disease.
- Chest X-ray: An X-ray of the organs and bones inside the chest. An X-ray is a type of energy beam that can go through the body and onto film, making a picture of areas inside the body.
- CT scan (CAT scan): A procedure that makes a series of detailed pictures of areas inside the body, taken from different angles. The pictures are made by a computer linked to an x-ray machine. A dye may be injected into a vein or swallowed to help the organs or tissues show up more clearly. This procedure is also called computed tomography, computerized tomography, or computerized axial tomography.
- MRI (magnetic resonance imaging): A procedure that uses a magnet, radio waves, and a computer to make a series of detailed pictures of areas inside the body. This procedure is also called nuclear magnetic resonance imaging (NMRI).
- Ultrasound exam: A procedure in which high-energy sound waves (ultrasound) are bounced off internal tissues or organs and make echoes. The echoes form a picture of body tissues called a sonogram. The picture can be printed to be looked at later.
- Biopsy: The removal of cells or tissues so they can be viewed under a microscope by a pathologist to check for signs of cancer. In some cases, the tumor is removed during surgery and then a biopsy is done. The following tests may be done on the sample of tissue that is removed:
- Cytogenetic analysis: A laboratory test in which cells in a sample of tissue are viewed under a microscope to look for certain changes in the chromosomes.
- Immunohistochemistry: A test that uses antibodies to check for certain antigens in a sample of tissue. The antibody is usually linked to a radioactive substance or a dye that causes the tissue to light up under a microscope. This type of test may be used to tell the difference between different types of cancer.
What Are the Stages of Childhood Extracranial Germ Cell Tumors?
After a childhood extracranial germ cell tumor has been diagnosed, tests are done to find out if cancer cells have spread from where the tumor started to nearby areas or to other parts of the body.
The process used to find out if cancer has spread from where the tumor started to other parts of the body is called staging. The information gathered from the staging process determines the stage of the disease. It is important to know the stage in order to plan treatment. In some cases, staging may follow surgery to remove the tumor.
The results from tests and procedures used to detect and diagnose childhood extracranial germ cell tumors may also be used in staging.
There are three ways that cancer spreads in the body. Cancer can spread through tissue, the lymph system, and the blood:
- Tissue. The cancer spreads from where it began by growing into nearby areas.
- Lymph system. The cancer spreads from where it began by getting into the lymph system. The cancer travels through the lymph vessels to other parts of the body.
- Blood. The cancer spreads from where it began by getting into the blood. The cancer travels through the blood vessels to other parts of the body.
Cancer may spread from where it began to other parts of the body.
When cancer spreads to another part of the body, it is called metastasis. Cancer cells break away from where they began (the primary tumor) and travel through the lymph system or blood.
The metastatic tumor is the same type of cancer as the primary tumor. For example, if an extracranial germ cell tumor spreads to the liver, the cancer cells in the liver are actually cancerous germ cells. The disease is metastatic extracranial germ cell tumor, not liver cancer.
Stages are used to describe the different types of extracranial germ cell tumors.
Childhood nonseminoma testicular germ cell tumors
- Stage I: In stage I, the cancer is found in the testicle only and is completely removed by surgery.
- Stage II: In stage II, the cancer is removed by surgery and some cancer cells remain in the scrotum or cancer that can be seen with a microscope only has spread to the scrotum or spermatic cord. Tumor marker levels do not return to normal after surgery or the tumor marker levels increase.
- Stage III: In stage III, the cancer has spread to one or more lymph nodes in the abdomen and is not completely removed by surgery. The cancer that remains after surgery can be seen without a microscope.
- Stage IV: In stage IV, the cancer has spread to distant parts of the body such as the liver.
Childhood Ovarian Germ Cell Tumors
There are two types of stages used for childhood ovarian germ cell tumors.
Stages From the Children's Oncology Group
- Stage I: In stage I, the cancer is in the ovary and can be completely removed by surgery. and the capsule (outer covering) of the ovary has not ruptured (broken open).
- Stage II: In stage II, one of the following is true:
- The cancer is not completely removed by surgery. The remaining cancer can be seen with a microscope only.
- The cancer has spread to the lymph nodes and can be seen with a microscope only.
- The cancer has spread to the capsule (outer covering) of the ovary.
- Stage III: In stage III, one of the following is true:
- The cancer is not completely removed by surgery. The remaining cancer can be seen without a microscope.
- The cancer has spread to lymph nodes and the lymph nodes are 2 centimeters or larger. Cancer in the lymph nodes can be seen without a microscope.
- The cancer is found in fluid in the abdomen.
- Stage IV: In stage IV, the cancer has spread to the lung, liver, brain, or bone.
Stages From the International Federation of Gynecology and Obstetrics (FIGO)
- Stage I: In stage I, cancer is found in one or both of the ovaries and has not spread. Stage I is divided into stage IA, stage IB, and stage IC.
- Stage IA: Cancer is found in one ovary.
- Stage IB: Cancer is found in both ovaries.
- Stage IC: Cancer is found in one or both ovaries and one of the following is true:
- cancer is found on the outside surface of one or both ovaries;
- or the capsule (outer covering) of the tumor has ruptured (broken open) ; or cancer cells are found in fluid that has collected in the abdomen or cancer cells are found in washings of the peritoneal cavity (the body cavity that contains most of the organs in the abdomen).
- Stage II: In stage II, cancer is found in one or both ovaries and has spread into other areas of the pelvis. Stage II is divided into stage IIA stage IIB, and stage IIC.
- Stage IIA: Cancer has spread to the uterus and/or the fallopian tubes (the long slender tubes through which eggs pass from the ovaries to the uterus).
- Stage IIB: Cancer has spread to other tissue within the pelvis such as the bladder, rectum, or vagina.
- Stage IIC: Cancer has spread to the uterus and/or fallopian tubes and/or other tissue within the pelvis and one of the following is true: cancer is found on the outside surface of one or both ovaries; or the capsule (outer covering) of the tumor has ruptured (broken open); or cancer cells are found in fluid that has collected in the abdomen; or cancer cells are found in washings of the peritoneal cavity (the body cavity that contains most of the organs in the abdomen).
- Stage III: In stage III, cancer is found in one or both ovaries and has spread to other parts of the abdomen. Cancer that has spread to the surface of the liver is also stage III disease. Stage III is divided into stage IIIA, stage IIIB, and stage IIIC:
- Stage IIIA: The tumor is found in the pelvis only, but cancer cells that can only be seen with a microscope have spread to the surface of the peritoneum (tissue that lines the abdominal wall and covers most of the organs in the abdomen) or to the small bowel.
- Stage IIIB: Cancer has spread to the peritoneum and is 2 centimeters or smaller in diameter.
- Stage IIIC: Cancer has spread to the peritoneum and is larger than 2 centimeters in diameter and/or has spread to lymph nodes in the abdomen.
- Stage IV: In stage IV, cancer is found in one or both ovaries and has metastasized (spread) beyond the abdomen to other parts of the body. Cancer that has spread to tissues in the liver is also stage IV disease.
Childhood Extragonadal Extracranial Germ Cell Tumors
- Stage I: In stage I, the cancer is in one place and can be completely removed by surgery. For tumors in the sacrum or coccyx (bottom part of the spine), the sacrum and coccyx are completely removed by surgery. Tumor marker levels return to normal after surgery.
- Stage II: In stage II, the cancer has spread to the capsule (outer covering) and/or lymph nodes. The cancer is not completely removed by surgery and the cancer remaining after surgery can be seen with a microscope only. Tumor marker levels do not return to normal after surgery or increase.
- Stage III: In stage III, one of the following is true:
- The cancer is not completely removed by surgery. The cancer remaining after surgery can be seen without a microscope.
- The cancer has spread to lymph nodes and is larger than 2 centimeters in diameter.
- Stage IV: In stage IV, the cancer has spread to distant parts of the body, including the liver, brain, bone, or lung.
What Is the Treatment for Childhood Extracranial Germ Cell Tumors?
Different types of treatments are available for children with extracranial germ cell tumors. Some treatments are standard (the currently used treatment), and some are being tested in clinical trials. A treatment clinical trial is a research study meant to help improve current treatments or obtain information on new treatments for patients
with cancer. When clinical trials show that a new treatment is better than the standard treatment, the new treatment may become the standard treatment.
Because cancer in children is rare, taking part in a clinical trial should be considered. Some clinical trials are open only to patients who have not started treatment.
Children with extracranial germ cell tumors should have their treatment planned by a team of health care providers who are experts in treating cancer in children. Treatment will be overseen by a pediatric oncologist, a doctor who specializes in treating children with cancer. The pediatric oncologist works with other health care providers who are experts in treating children with extracranial germ cell tumors and who specialize in certain areas of medicine. These may include the following specialists:
- Pediatrician.
- Pediatric surgeon.
- Pediatric hematologist.
- Radiation oncologist.
- Endocrinologist.
- Pediatric nurse specialist.
- Rehabilitation specialist.
- Child life professional.
- Psychologist.
- Social worker.
- Geneticist.
Treatment for childhood extracranial germ cell tumors may cause side effects. Side effects from cancer treatment that begin after treatment and continue for months or years are called late effects. Late effects of cancer treatment may include the following:
- Physical problems.
- Changes in mood, feelings, thinking, learning, or memory.
- Second cancers (new types of cancer).
For example, late effects of surgery to remove tumors in the sacrum or coccyx include constipation, loss of bowel and bladder control, and scars. Some late effects may be treated or controlled. It is important to talk with your child's doctors about the effects cancer treatment can have on your child.
Standard treatment may involve:
Surgery
Surgery to completely remove the tumor is done whenever possible. If the tumor is very large, chemotherapy may be given first, to make the tumor smaller and decrease the amount of tissue that needs to be removed during surgery. A goal of surgery is to keep reproductive function. The following types of surgery may be used:
- Resection: Surgery to remove tissue or part or all of an organ.
- Radical inguinal orchiectomy: Surgery to remove one or both testicles through an incision (cut) in the groin.
- Unilateral salpingo-oophorectomy: Surgery to remove one ovary and one fallopian tube on the same side. Even if the doctor removes all the cancer that can be seen at the time of the surgery, some patients may be given chemotherapy after surgery to kill any cancer cells that are left. Treatment given after the surgery, to lower the risk that the cancer will come back, is called adjuvant therapy.
Observation
Observation is closely monitoring a patient’s condition without giving any treatment until signs or symptoms appear or change. For childhood extracranial germ cell tumors, this includes physical exams, imaging tests, and tumor marker tests.
Chemotherapy
Chemotherapy is a cancer treatment that uses drugs to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. When chemotherapy is taken by mouth or injected into a vein or muscle, the drugs enter the bloodstream and can reach cancer cells throughout the body (systemic chemotherapy). When chemotherapy is placed directly into the cerebrospinal fluid, an organ, or a body cavity such as the abdomen, the drugs mainly affect cancer cells in those areas (regional chemotherapy). Combination chemotherapy is treatment using more than one anticancer drug.
The way the chemotherapy is given depends on the type and stage of the cancer being treated. New types of treatment are being tested in clinical trials. This summary section describes treatments that are being studied in clinical trials. It may not mention every new treatment being studied.
High-dose Chemotherapy with Stem Cell Transplant
High-dose chemotherapy with stem cell transplant is a way of giving high doses of chemotherapy and replacing blood -forming cells destroyed by the cancer treatment. Stem cells (immature blood cells) are removed from the blood or bone marrow of the patient or a donor and are frozen and stored. After the chemotherapy is completed, the stored stem cells are thawed and given back to the patient through an infusion. These reinfused stem cells grow into (and restore) the body's blood cells.
Radiation Therapy
Radiation therapy is a cancer treatment that uses high-energy x-rays or other types of radiation to kill cancer cells or keep them from growing. There are two types of radiation therapy:
External radiation therapy uses a machine outside the body to send radiation toward the cancer. Internal radiation therapy uses a radioactive substance sealed in needles, seeds, wires, or catheters that are placed directly into or near the cancer.
The way the radiation therapy is given depends on the type of cancer and whether it has come back. External radiation therapy is being studied for the treatment of childhood extracranial germ cell tumors that have come back.
Clinical Trials
Patietns may want to think about taking part in a clinical trial.
For some patients, taking part in a clinical trial may be the best treatment choice. Clinical trials are part of the cancer research process. Clinical trials are done to find out if new cancer treatments are safe and effective or better than the standard treatment.
Many of today's standard treatments for cancer are based on earlier clinical trials. Patients who take part in a clinical trial may receive the standard treatment or be among the first to receive a new treatment. Patients who take part in clinical trials also help improve the way cancer will be treated in the future. Even when clinical trials do not lead to effective new treatments, they often answer important questions and help move research forward.
Patients can enter clinical trials before, during, or after starting their cancer treatment. Some clinical trials only include patients who have not yet received treatment. Other trials test treatments for patients whose cancer has not gotten better. There are also clinical trials that test new ways to stop cancer from recurring (coming back) or reduce the side effects of cancer treatment.
Clinical trials are taking place in many parts of the country. Clinical trials supported by other organizations can be found on the ClinicalTrials.gov website.
Follow-up Tests
Some of the tests that were done to diagnose the cancer or to find out the stage of the cancer may be repeated. Some tests will be repeated in order to see how well the treatment is working. Decisions about whether to continue, change, or stop treatment may be based on the results of these tests.
Some of the tests will continue to be done from time to time after treatment has ended. The results of these tests can show if your child's condition has changed or if the cancer has recurred (come back). These tests are sometimes called follow-up tests or check-ups.
For childhood extracranial germ cell tumors, alpha-fetoprotein (AFP) tests and beta-human chorionic gonadotropin (β-hCG) tests are done to see if treatment is working. Continued high levels of AFP or β-hCG may mean the cancer is still growing. For at least 3 years after surgery, follow-up will include regular physical exams, imaging tests, and tumor marker tests.
Treatment Options By Stage and Type for Childhood Extracranial Germ Cell Tumors
Mature and Immature Teratomas
Treatment of mature teratomas that are not in the sacrum or coccyx (bottom part of the spine) includes the following:
- Surgery to remove the tumor followed by observation.
Treatment of immature teratomas that are not in the sacrum or coccyx includes the following:
- Surgery to remove the tumor followed by observation for stage I tumors.
- Surgery to remove the tumor for stage II–IV tumors.
Treatment of immature teratomas that are in the sacrum or coccyx includes the following:
- Surgery (removal of the sacrum and coccyx) followed by observation.
- Sometimes a mature or immature teratoma also has malignant cells. The teratoma and malignant cells may need to be treated differently.
- Regular follow-up exams with imaging tests and the alpha-fetoprotein (AFP) tumor marker test will be done for at least 3 years.
Malignant Gonadal Germ Cell Tumors
Malignant Testicular Germ Cell Tumors: Treatment of malignant testicular germ cell tumors may include the following:
For boys younger than 15 years:
- Surgery (radical inguinal orchiectomy) followed by observation for stage I tumors.
- Surgery (radical inguinal orchiectomy) followed by combination chemotherapy for stage II-IV tumors. A
- A second surgery may be done to remove any tumor remaining after chemotherapy.
For boys 15 years and older:
- Malignant testicular germ cell tumors in boys 15 years and older are treated differently than they are in young boys. Surgery may include removal of lymph nodes in the abdomen.
Malignant Ovarian Germ Cell Tumors
Dysgerminomas
Treatment of stage I dysgerminomas in young girls may include the following:
- Surgery (unilateral salpingo-oophorectomy) followed by observation.
- Combination chemotherapy may be given if the tumor comes back.
Treatment of stages II–IV dysgerminomas in young girls may include the following:
- Surgery (unilateral salpingo-oophorectomy) followed by combination chemotherapy.
- Combination chemotherapy to shrink the tumor, followed by surgery (unilateral salpingo-oophorectomy).
Nongerminomas
Treatment of stage Inongerminomas in young girls may include the following:
- Surgery followed by observation.
- Surgery followed by combination chemotherapy.
Treatment of stages II–IV nongerminomas in young girls may include the following:
Surgery followed by combination chemotherapy. A second surgery may be done to remove any remaining cancer.
Biopsy followed by combination chemotherapy to shrink the tumor and sometimes surgery for tumors that cannot be removed by surgery when cancer is diagnosed.
The treatment for adolescents and young adults with ovarian germ cell tumor is much like the treatment for adults.
Malignant Extragonadal Extracranial Germ Cell Tumors
Treatment of childhood malignant extragonadal extracranial germ cell tumors extracranial germ cell tumors may include the following:
- Combination chemotherapy to shrink the tumor followed by surgery to remove the sacrum and coccyx (bottom part of the spine) for tumors that are in the sacrum or coccyx.
- Combination chemotherapy to shrink the tumor followed by surgery to remove tumors that are in the mediastinum.
- Biopsy followed by combination chemotherapy to shrink the tumor and surgery to remove tumors that are in the abdomen.
- Surgery to remove the tumor followed by combination chemotherapy for tumors of the head and neck.
- Treatment of malignant extragonadal extracranial germ cell tumors in places not already described includes the following:
- Surgery followed by combination chemotherapy.
Recurrent Childhood Malignant Extracranial Germ Cell Tumors
There is no standard treatment for recurrent childhood malignant extracranial germ cell tumors. Treatment depends on the following:
- The type of treatment given when the cancer was diagnosed.
- How the tumor responded to the initial treatment.
Treatment is usually within a clinical trial and may include the following:
Surgery
Surgery followed by combination chemotherapy, for most malignant extracranial germ cell tumors including immature teratomas, malignant testicular germ cell tumors, and malignant ovarian germ cell tumors. Surgery for tumors that come back in the sacrum or coccyx (bottom part of the spine), if surgery to remove the sacrum and coccyx was not done when the cancer was diagnosed.
Chemotherapy may be given before surgery, to shrink the tumor. If any tumor remains after surgery, radiation therapy may also be given. Combination chemotherapy for stage I malignant testicular germ cell tumors and stage I ovarian dysgerminomas.
High-dose chemotherapy and stem cell transplant
Radiation therapy followed by surgery to remove the tumor in the brain for cancer that has spread to the brain.
A clinical trial of combination chemotherapy alone compared with high-dose chemotherapy followed by stem cell transplant.
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Last updated May 4, 2018