Ovarian cancer is a cancer that develops in a woman's ovary. It can be difficult to detect in its early stages. Unlike cervical and breast cancers, there are currently no effective screening methods for ovarian cancer. The majority of women are diagnosed when the cancer is in an advanced stage.
If you are diagnosed with ovarian cancer, you should be referred to a gynecologic oncologist, a doctor who specializes in diagnosing and treating cancers of the female reproductive system. Outcomes are best when women receive care in hospitals and from doctors with experience treating ovarian cancer.
The main risk factors for ovarian cancer are:
Factors that may help reduce the risk for ovarian cancer include:
BRCA Genetic Mutations
Guidelines from the United States Preventive Service Task Force recommend screening for BRCA genetic mutations in women whose family history suggests a high risk for ovarian cancer. Mutations in the genes called BRCA1 and BRCA2 are among the strongest risk factors for ovarian and breast cancers. Women who do not have risk factors do not need to be screened for these gene mutations, but are still at risk of developing ovarian cancer.
Your health care provider may estimate your risk for these genes using a questionnaire. The Centers for Disease Control and Prevention has also developed an on-line screening resource (Know:BRCA Tool) that woman can use to understand their risks. Having several first-degree or second-degree relatives who have had breast, ovarian, fallopian tube, or peritoneal cancers is an indication of risk.
If you are at risk, you may be referred to a genetic counselor who can review your history and discuss with you whether you should be tested for these genetic mutations.
Targeted Therapy Drug Approval
In 2014, the FDA approved bevacizumab (Avastin) in combination with chemotherapy for treatment of resistant or recurrent ovarian cancer. Bevacizumab is a biologic drug that targets and blocks a protein associated with blood vessel growth.
Ovarian cancer is a cancer that begins in a woman's ovary, although there is information accumulating that many ovarian cancers may actually begin in the fallopian tube with very early spread to the ovary. The ovaries produce eggs (ova), and the hormones estrogen and progesterone. A woman's reproductive system includes the:
The ovaries are two small, almond-shaped organs located on either side of the uterus. Each ovary is attached to a fallopian tube. Both fallopian tubes connect to the uterus. During a woman's monthly reproductive cycle, an egg is released by an ovary, and travels down the fallopian tube towards the uterus to await fertilization.
The uterus, commonly called the womb, is a hollow muscular organ located in the female pelvis between the bladder and rectum. The ovaries produce the eggs that travel through the fallopian tubes. Once the egg has left the ovary it can be fertilized and implant itself in the lining of the uterus. The main function of the uterus is to nourish the developing fetus prior to birth.
Ovarian cancers begin when cells in an ovary that grow abnormally quickly and develop into a tumor. Some tumors are benign (non-cancerous). Others are malignant (cancerous.) Ovarian tumors may be either solid or cystic (fluid-filled sacs). They can look very similar in appearance to benign ovarian cysts, which are very common.
Ovarian cancers can develop in the different types of cells that make up the ovary. They are usually one of three types:
Ovarian Cancer Progression
Ovarian cancer progresses almost silently, usually with only vague, non-specific symptoms. By the time serious symptoms do appear, the ovarian tumor may have grown large enough to shed cancer cells throughout the abdomen. At such an advanced stage, the cancer is more difficult to cure.
As ovarian cancer advances, cells from the original tumor can spread (metastasize) throughout the pelvic and abdominal regions and travel to other parts of the body. Cancer cells are carried through the body through lymph vessels and the bloodstream.
Risk Factors and Prevention
Ovarian cancer is the fifth leading cause of cancer death in women. Each year in the United States, about 22,000 women are diagnosed with ovarian cancer. About 14,000 American women die each year from this disease.
Certain factors increase the risk for ovarian cancer, while other factors reduce risk. Inherited genetic mutations of BRCA genes are the strongest risk factor. A family history of breast or ovarian cancer is also a strong risk factor.
Many of the preventive factors are related to the number of times a woman ovulates during her lifetime, which is indicated by the number of menstrual periods she has. Fewer menstrual periods and ovulations appear to be associated with reduced risk for ovarian cancer.
Risk Factors for Ovarian Cancer
Older women have a higher risk for ovarian cancer than younger women. Ovarian cancer usually occurs after menopause, although it can develop in women of all ages. Most women diagnosed with ovarian cancer are older than age 55.
Ovarian cancer is more common in white women than in African American women. Women who are of Ashkenazi (Eastern European) Jewish descent have a higher risk of developing ovarian cancer.
Women are at high risk for ovarian cancer and for harboring a genetic mutation such as BRCA if they have a:
When a woman describes her family history to her doctor, she should include the history of cancer in women on both the mother's and the father's side. Both are significant.
Inherited mutations in the genes called BRCA1 and BRCA2 greatly increase the risk for ovarian and breast cancers. While these mutations are more common among women of Ashkenazi Jewish ancestry, they can occur in women of any ethnicity.
Women with a BRCA1 mutation have about a 40% to 60% lifetime risk for ovarian cancer. Women with a BRCA2 mutation have about a 10% to 30% lifetime risk for ovarian cancer. (By contrast, the lifetime ovarian cancer risk for women in the general public is about 1 in 55 or 1.8%.) These gene mutations are also associated with increased risks for breast cancer, fallopian tube cancer, pancreatic cancer, and prostate cancer in the male. In addition to an increased lifetime risk, women with these gene mutations tend to develop these cancers at an earlier age than that seen in the usual population of women with ovarian cancer.
Other genetic factors are also associated with increased risk. Women who have genetic mutations associated with hereditary non-polyposis colorectal cancer (HNPCC) have about a 10% to 15% lifetime risk of developing ovarian cancer.
Personal Medical History
Women who have been diagnosed with breast cancer are at increased risk for ovarian cancer, even if they do not have BRCA mutations. Endometriosis, a condition in which the cells that line the cavity of the uterus grow in other areas of the body such as on the ovaries or on the other pelvic structures, increases the risk for ovarian cancer.
Women are at increased risk for ovarian cancer if they began menstruating at an early age (before age 12), have not had any children, had their first child after age 35, or experienced early menopause (before age 50).
There are also preventive factors associated with reproductive history. The more times a woman gives birth, the less likely she is to develop ovarian cancer. Breast-feeding for a year or more after giving birth may also decrease ovarian cancer risk.
Tubal ligation, a method of sterilization that ties off the fallopian tubes, is associated with a decreased risk for ovarian cancer when it is performed after a woman has completed childbearing. Similarly, hysterectomy, the surgical removal of the uterus, may decrease risk.
Women who use hormone therapy (HT) after menopause for longer than 5 years may have an increased risk for ovarian cancer. The risk seems to be particularly significant for women who take estrogen-only HT. The risk is less clear for combination estrogen-progestin HT.
Oral contraceptives (birth control pills) significantly reduce the risk of ovarian cancer. The longer a woman takes oral contraceptives the greater the protection and the longer protection lasts after stopping oral contraceptives.
Women who are obese have an increased risk for ovarian cancer.
Preventive Strategies for Women at High Risk
Women with a strong family history of ovarian or related cancers should discuss preventive strategies with their providers.
Screening for BRCA Genetic Mutations
Guidelines from the U.S. Preventive Services Task Force (USPSTF) recommend BRCA screening for women at high risk for ovarian cancer due to persona or family history. The USPSTF does not recommend routine genetic screening or testing in women whose family history does not suggest BRCA mutations. Having several first-degree or second-degree relatives who have had breast, ovarian, fallopian tube, or peritoneal cancers is an indication of risk.
Your provider can screen you using a questionnaire that evaluates your family and personal medical history, and other factors. If your provider decides you are at risk, you may be referred to a genetic counselor who can review your history and discuss with you whether you should be tested for the BRCA1 and BRCA2 mutations, or for other genetic mutations that may be present and are also associated with increased risks.
The genetic test uses DNA from a blood or saliva sample to check for these mutations. A positive test means that the mutations are present. It does not, however, mean that a woman will definitely develop ovarian or breast cancer.
Removal of Ovaries (Oophorectomy)
Surgical removal of the ovaries called oophorectomy, significantly reduces the risk for ovarian cancer. When it is used to prevent cancer, the procedure is called a prophylactic oophorectomy.
Prophylactic oophorectomy is approximately 85% to 95% protective against ovarian cancer and is recommended for women at high risk for ovarian cancer. These women generally have the BRCA1 or BRCA2 genetic mutation, or have two or more first-degree relatives who have had ovarian cancer.
Bilateral oophorectomy is the removal of both ovaries. Bilateral salpingo-oophorectomy is the removal of both fallopian tubes plus both ovaries. Evidence is accumulating that many ovarian cancers actually arise in the fallopian tubes and secondarily involve the ovary. There is strong evidence that salpingo-oophorectomy is very effective in reducing risk for ovarian cancer in women who carry the BRCA1 or BRCA2 mutation.
Primary peritoneal carcinoma, a rare cancer that develops in the peritoneum (the thin membrane that lines the inside of the abdomen and gives rise to the epithelial lining of the ovary), can still develop in women who have their ovaries and tubes removed. Some of these peritoneal cancers may actually come from small tumors that originated in the fallopian tubes. Some evidence suggests that preventive salpingo-oophorectomy may reduce the risk for peritoneal cancer and fallopian tube cancers, in addition to ovarian cancer.
Oophorectomy causes immediate menopause, which can raise health concerns for premenopausal women. You should discuss all the risks and benefits of prophylactic oophorectomy with your health care team, as well as the option for hormone therapy after surgery.
Ovarian cancer used to be considered a "silent killer." Symptoms were thought to appear only when the cancer was in an advanced stage. Evidence now suggests that even early-stage ovarian cancer can produce symptoms.
Ovarian cancer grows quickly and can progress from early to advanced stages within a year. Paying attention to symptoms can help improve a woman's chances of being diagnosed and treated promptly. Detecting cancer while it is still in its earliest stages may help improve prognosis.
See your provider if you have the following symptoms on a daily basis for more than a few weeks:
Other symptoms that are sometimes associated with ovarian cancer include:
Be aware that these symptoms are very common in women who do not have cancer and are not specific for ovarian cancer. While prompt follow-up with your provider is important when one or more of these are present, there are many other explanations for these symptoms besides ovarian cancer.
Based on symptoms and physical examination, your provider may order pelvic imaging tests or blood tests. If these tests reveal possible signs of cancer, you should be referred to a gynecologic oncologist.
Ovarian cancer is difficult to detect in its early stages. Unlike Pap tests for cervical cancer or mammogram for breast cancer, there is currently no effective screening method for ovarian cancer.
Imaging tests, such as transvaginal ultrasound, and blood tests, such as CA-125 HE4 or OVA-1, have not proven to be useful screening tools. Studies indicate that screening with these tests does not reduce ovarian cancer mortality and may cause women to undergo unnecessary medical and surgical treatment due to their high rate of "false positives."
The United States Preventive Services Task Force and other medical associations do not recommend routine screening for ovarian cancer in women who do not have signs or symptoms of the disease. However, if your provider thinks you may have ovarian cancer, these tests can help in diagnosis. Some diagnostic tests are also used in the treatment process.
Physical signs indicating ovarian cancer may be detected during a pelvic exam. A pelvic exam is performed in two ways. The doctor inserts one or two fingers into the vagina while feeling the abdomen with the other hand. The doctor may also perform a rectovaginal exam, which involves the insertion of one finger into the vagina and another into the rectum.
Both exams enable the doctor to evaluate the size and shape of the ovaries. Enlarged ovaries and abdominal swelling can be signs of ovarian cancer. A mass felt during a pelvic exam often requires further evaluation by ultrasound and sometimes requires surgery to make a definitive diagnosis.
Not all masses felt are cancerous. They may be benign conditions such as ovarian cysts or uterine fibroids.
Transvaginal Ultrasound and Other Imaging Tests
Transvaginal ultrasound is a noninvasive diagnostic procedure that uses sound waves to bounce off tissues, organs, and masses in the pelvic area. It creates a visual picture of the ovaries, cervix, and uterus.
A probe, called a transducer, placed in the vagina sends out the sound waves. The echoes are collected and converted into a picture of the area. The image can help evaluate the size and internal structure of the ovaries and distinguish a solid mass (like ovarian cancer) from fluid-filled masses (like ovarian cysts.)
Transvaginal ultrasound does not provide enough specific information to reliably determine whether abnormal masses are cancerous. This test is not helpful as a screening tool for women who do not have signs of ovarian cancer.
Other Imaging Techniques
Other imaging tests are less common for the diagnosis or evaluation of suspected ovarian cancer but, in patients who appear to have ovarian cancer, they may help determine if cancer has spread to other parts of the body. They include:
CA-125 and Other Blood Tests
CA-125 Blood Test
CA-125 is a protein that is secreted by ovarian cancer cells and is elevated in over 80% of people with ovarian cancer. A blood test for this protein is usually ordered only if ovarian cancer is strongly suspected or has been diagnosed. In general, a CA-125 level is considered to be normal if it is less than 35 U/mL (microns per milliliter). The test may also be useful for evaluating tumor growth and predicting survival in people with recurrent cancer.
The test is not useful for diagnosis or early screening. In about one half of women with very early ovarian cancer, CA-125 levels are not elevated above the normal standard. Furthermore, an elevated level can be caused by a number of other conditions including:
A biopsy (tissue sample) is the only way to confirm a diagnosis of ovarian cancer. Biopsies for ovarian cancer are performed through exploratory surgery. A gynecological oncologist should perform this surgery. There are several surgical approaches:
The surgeon will take tissue samples and remove the tumor. The surgeon will also examine the organs and evaluate the spread of the cancer. Other surgical procedures, such as hysterectomy, removal or lymph nodes, appendectomy, omentectomy (removal of fatty tissue hanging from the colon) may also be performed.
The tissue samples are sent to a pathology lab for testing. If the test results indicate cancer, the woman may have additional imaging tests to see how far the cancer has spread. Based on biopsy and imaging tests, the cancer is staged.
Staging and Prognosis
Ovarian cancer is staged based on:
The TNM system is used to classify cancer in stages I to IV. Each stage is further divided into substages.
Stages of Ovarian Cancer
In stage I, the cancer has not spread. It is confined to one ovary (stage IA) or both ovaries (stage IB). In stages IA and IB, the ovarian capsules are intact, and there are no tumors on the surface. Stage IC can affect one or both ovaries, but the tumors are on the surface, or the capsule (outer covering of the ovary) has burst, or there is evidence of tumor cells in abdominal fluid (ascites).
In stage II, the cancer is in one or both ovaries and has spread to other areas in the pelvis. It may have advanced to the uterus or fallopian tubes (stage IIA), or other areas within the pelvis such as the bladder, colon or rectum (stage IIB), but is still limited to the pelvic area.
In stage III, the cancer is in one or both ovaries and has spread outside of the pelvis to nearby abdominal regions or lymph nodes. In Stage IIIA, microscopic amounts of cancer are in the peritoneum (the lining of the abdomen) or involve the lymph nodes. In Stage IIIB, the cancer is visually detectable in the peritoneum, with masses up to 2 cm in size with or without lymph node involvement. In Stage IIIC, the cancer has grown larger in the peritoneum, greater than 2 cm in size, with or without lymph node involvement.
Stage IV is the most advanced cancer stage. In Stage IVA, the cancer has spread to the fluid around the lungs. In Stage IVB, the cancer has spread to the liver or spleen or to other distant organs such as the lungs, brain, and bones.
Survival rates for ovarian cancer vary depending on many different factors, including the age of the woman and the stage at the time of diagnosis. Unfortunately, most cases with ovarian cancer are not diagnosed until the disease is advanced and has metastasized. In general, 75% of women survive ovarian cancer at least 1 year after diagnosis.
A 5-year survival rate is an estimate based on the percentage of people who are still alive 5 years after their cancer is diagnosed. In ovarian cancer:
Surgery is the initial treatment for most women with suspected ovarian cancer. Surgery is usually followed by chemotherapy. The course of treatment is determined by the stage of the cancer. Clinical trials investigating new types of treatments are an option for all stages of ovarian cancer.
It is very important that women with ovarian cancer seek care from a qualified gynecologic oncologist (a surgical specialist in female reproductive cancers) and a qualified medical oncologist with special expertise in the chemotherapeutic management of gynecologic cancer. Many gynecologic oncologists also have expertise in chemotherapeutics and provide this aspect of care as well.
Studies indicate that it is best for people, especially those with advanced-stage ovarian cancer, to receive care at medical centers that specialize in cancer treatment and surgery. Outcomes are best when women receive care from hospitals and doctors who treat a large number of ovarian cancer cases.
Women of child-bearing age should discuss with their cancer team any concerns and questions they may have about how various treatments could affect their fertility. They may also wish to have a consultation with a fertility specialist. Assisted reproductive technology such as embryo or oocyte (egg) cryopreservation ("freezing") may offer some women an option to later have children. It is very important that you have these discussions with your health care team before you begin cancer treatment.
Treatment for Stage I and Stage II Ovarian Cancers
Treatment options for stage I and stage II ovarian epithelial cancer may include:
Treatment for Stage III and Stage IV Ovarian Cancers
Treatment options for stage III and stage IV ovarian epithelial cancer may include:
Treatment for Recurrent Ovarian Cancer
If ovarian cancer returns or persists after treatment, chemotherapy is the main treatment. Surgery may also be performed to attempt an interval debulking, or to resolve such issues as urinary or intestinal blockages. Repeat surgical resections are best performed if limited areas of recurrent disease are seen and if the recurrence occurs longer than a year after completion of the last course of chemotherapy. Radiation therapy may be used to provide symptom relief. Clinical trials are investigating targeted therapy and hormone therapy.
Follow-Up after Treatment
After treatment is completed, you should have regular follow-up visits and tests to monitor your health and to check for any signs of cancer recurrence.
Recommended tests include:
Discuss with your cancer team how often you will need these tests. Some guidelines recommend follow-up visits:
You will usually have a CA-125 blood test at every visit. Your oncologist may also recommend imaging tests.
Surgery for ovarian cancer is used for both diagnostic and treatment purposes. Surgery has two goals:
It is extremely important that staging and debulking be performed by an experienced surgeon trained in cancer surgery techniques (usually a gynecologic oncologist). Accurate staging is essential for determining treatment options. Successful debulking will reduce the likelihood of repeat surgeries and increase the odds for survival.
Surgical staging involves taking biopsies (tissue samples) of:
An abdominal wash is performed by injecting a salt solution into the abdominal cavity to collect a fluid sample. The tissue and fluid samples are sent to a laboratory for evaluation. If immediate information is required, the pathologist may perform a frozen section of one of the tissue samples with a preliminary diagnosis available in 20 minutes.
The entire affected ovary is usually removed (oophorectomy) during surgical staging if the surgeon believes it might be cancerous. The surgeon will also examine the pelvic region, including the bowel and bladder, for signs of cancer invasion. If it appears the cancer has spread, the surgeon will remove the suspected cancer tissue (debulking).
Debulking, also called surgical cytoreduction, involves removing as much of the cancer as possible. The goal is to leave behind no tumor larger than 1 centimeter and preferably to leave behind no clearly visible tumor.
The surgery is typically performed as follows:
Hysterectomy results in infertility. A woman will no longer have menstrual periods and she can no longer become pregnant. Surgical removal of the ovaries (oophorectomy) causes immediate menopause. Symptoms, such as hot flashes, come on abruptly and may be more intense than those of natural menopause. Other menopausal symptoms include vaginal dryness, sleep problems, and weight gain.
The most important complications that occur in women who have had their ovaries removed are due to estrogen loss, which places women at risk for osteoporosis (loss of bone density) and a possible increase in risks for heart disease.
Hormone therapy after a hysterectomy is given as estrogen-only therapy (ET). It does have risks, including possibly increasing the chances for breast cancer and stroke. (Some recent data question these risks for women who do not receive estrogen in combination with progesterone.) It does not appear to increase the risk for ovarian cancer recurrence.
The decision to use estrogen therapy (ET) depends in part on a woman's age as well as other medical factors. For younger women (under age 40), the benefits of ET for bone and heart health may outweigh the risks. For women closer to the age of menopause, risks may outweigh benefits. Discuss with your oncologist whether hormone therapy is a safe or appropriate option for you.
Chemotherapy is drug therapy used to kill cancer cells that remain after surgery. Chemotherapy usually follows surgery (adjuvant chemotherapy). In some cases, it may also be used before surgery (neoadjuvant chemotherapy).
Chemotherapy is a systemic therapy. It uses drugs that are delivered into the bloodstream to reach and destroy cancer cells throughout the body.
Chemotherapy for ovarian cancer is administered:
Most women with stage I, II, and IV ovarian cancer receive intravenous chemotherapy. Women in stage III may receive a combination of intravenous and intraperitoneal chemotherapy. Side effects are more severe with intraperitoneal chemotherapy than when intravenous chemotherapy is used alone. However, the combination therapy may be more effective for women with later-stage cancer.
Clinical trials investigating new drugs and combinations of drugs are available for all stages of ovarian cancer. Discuss with your oncologist whether you may be an appropriate candidate for a clinical trial.
Drugs Used in Chemotherapy
Initial chemotherapy regimens commonly use a combination of:
Paclitaxel and docetaxel are taxane drugs. Carboplatin and cisplatin are platinum-based drugs. Carboplatin causes fewer side effects than cisplatin, and in general is easier to administer and better tolerated.
Drug Therapy for Resistant or Recurred Cancer
Some ovarian tumors are resistant to platinum drugs. In other cases, the cancer returns (recurs) after treatment. There are many different drug therapy approaches to treating resistant or recurrent cancer.
A different platinum chemotherapy drug, a new type of drug, or different combinations of drugs may be tried. Some of these drugs include gemcitabine, doxorubicin, and topotecan.
Bevacizumab (Avastin) is a biologic drug used in targeted therapy. It blocks a protein that helps blood vessels form. By targeting this protein, the drug slows the growth of cancer cells. Bevacizumab is approved to treat platinum-resistant or recurrent epithelial ovarian cancer. It is given by IV in combination with paclitaxel, pegylated liposomal doxorubicin (Doxyl), or topotecan.
Hormone therapy may be an option for women with recurrent cancer who cannot tolerate or who have not been helped by chemotherapy. Hormone therapy drugs include:
Some of these drugs are given by injection; others are taken orally as a pill.
Patients who have failed standard therapy may have their tumors evaluated for genetic abnormalities, called Next Generation Sequencing. If genetic changes are found, there may be specific biologic drugs that can be administered to target these genetic changes and kill the cancer cells or slow down or stop its growth.
Chemotherapy drugs go through a long testing process to see if they are active against various cancers and whether they are safe to use in humans. These tests are called clinical trials. When there is no well accepted treatment plan for a patient, she may be considered for a clinical trial where she may receive an experimental drug or treatment that is thought to be beneficial in fighting her cancer, but is still undergoing testing and evaluation. A good resource to find possible clinical trials for ovarian cancer as well as all others, is www.clinicaltrials.gov.
Administration of Chemotherapy
Chemotherapy drugs are given in cycles. You will receive an infusion of the drugs over the course of several days, followed by a rest period of several weeks, and then another cycle of infusion. The treatment is given in an outpatient clinic.
A chemotherapy infusion usually lasts about 3 to 6 hours. Treatment may be repeated every 3 weeks for a total of 6 cycles. Other dose schedules may require weekly treatment. The exact length of cycles varies depending on which drugs are used.
Side Effects of Chemotherapy
Side effects occur with all drugs and vary depending on the drug used. Side effects are more severe with higher doses and increase over the course of treatment. Most side effects go away after treatment is completed, but some may be long-lasting.
Common side effects may include:
Serious side effects may include:
Some side effects can sometimes be treated or prevented with other drugs or non-drug therapies. For example, yoga and acupuncture may be helpful for easing fatigue. Most patients receive premedication with anti-nausea to minimize that side effect. Discuss with your cancer care team strategies to help you cope.
Cancer support groups can help ease the stress of illness. Sharing with others who have common experiences and problems can help you not feel alone.
Radiation therapy is not typically used as a primary treatment for ovarian cancer. Radiation is sometimes used to as palliative treatment to help ease symptoms in recurrent ovarian cancer.
Aghajanian C, Goff B, Nycum LR, Wang YV, Husain A, Blank SV. Final overall survival and safety analysis of OCEANS, a phase 3 trial of chemotherapy with or without bevacizumab in patients with platinum-sensitive recurrent ovarian cancer. Gynecol Oncol. 2015;139(1):10-16. PMID: 26271155 www.ncbi.nlm.nih.gov/pubmed/26271155.
American College of Obstetricians and Gynecologists Committee on GynecologicPractice. Committee Opinion No. 477: the role of the obstetrician-gynecologist in the early detection of epithelial ovarian cancer. Obstet Gynecol. 2011;117(3):742-746. PMID: 21343791 www.ncbi.nlm.nih.gov/pubmed/21343791.
Berek JS, Chalas E, Edelson M, et al. Prophylactic and risk-reducing bilateral salpingo-oophorectomy: recommendations based on risk of ovarian cancer. Obstet Gynecol. 2010;116(3):733-743. PMID: 20733460 www.ncbi.nlm.nih.gov/pubmed/20733460.
Bevers TB, Brown PH, Maresso KC, Hawk ET. Cancer prevention, screening, and early detection. In: Niederhuber JE, Armitage JO, Doroshow JH, Kastan MB, Tepper JE, eds. Abeloff's Clinical Oncology. 5th ed. Philadelphia, PA: Elsevier Saunders; 2014:chap 23.
Bower JE, Bak K, Berger A, et al. Screening, assessment, and management of fatigue in adult survivors of cancer: an American Society of Clinical oncology clinical practice guideline adaptation. J Clin Oncol. 2014;32(17):1840-1850. PMID: 24733803 www.ncbi.nlm.nih.gov/pubmed/24733803.
Bristow RE, Chang J, Ziogas A, Anton-Culver H. Adherence to treatment guidelines for ovarian cancer as a measure of quality care. Obstet Gynecol. 2013;121(6):1226-1234. PMID: 23812456 www.ncbi.nlm.nih.gov/pubmed/23812456.
Burger RA, Brady MF, Bookman MA, et al. Incorporation of bevacizumab in the primary treatment of ovarian cancer. N Engl J Med. 2011;365(26):2473-2483. PMID: 22204724 www.ncbi.nlm.nih.gov/pubmed/22204724.
Buys SS, Partridge E, Black A, et al. Effect of screening on ovarian cancer mortality: the prostate, lung, colorectal and ovarian (PLCO) cancer screening randomized controlled trial. JAMA. 2011;305(22):2295-2303. PMID: 21642681 www.ncbi.nlm.nih.gov/pubmed/21642681.
Domchek SM, Friebel TM, Singer CF, et al. Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality. JAMA. 2010;304(9):967-975. PMID: 20810374 www.ncbi.nlm.nih.gov/pubmed/20810374.
Finch AP, Lubinski J, Møller P, et al. Impact of oophorectomy on cancer incidence and mortality in women with a BRCA1 or BRCA2 mutation. J Clin Oncol. 2014;32(15):1547-1553. PMID: 24567435 www.ncbi.nlm.nih.gov/pubmed/24567435.
Havrilesky LJ, Moorman PG, Lowery WJ, et al. Oral contraceptive pills as primary prevention for ovarian cancer: a systematic review and meta-analysis. Obstet Gynecol. 2013;122(1):139-147. PMID: 23743450 www.ncbi.nlm.nih.gov/pubmed/23743450.
Heintz AP, Odicino F, Maisonneuve P, et al. Carcinoma of the ovary. FIGO 26th annual report on the results of treatment in gynecological cancer. Int J Gynaecol Obstet. 2006;95 Suppl 1:S161-S192. PMID: 17161157 www.ncbi.nlm.nih.gov/pubmed/17161157.
Jacobs IJ, Menon U, Ryan A, et al. Ovarian cancer screening and mortality in the UK collaborative trial of ovarian cancer screening (UKCTOCS): a randomized controlled trial. Lancet. 2016;387(10022):945-956. PMID: 26707054 www.ncbi.nlm.nih.gov/pubmed/26707054.
Jensen A, Sharif H, Frederiksen K, Kjaer SK. Use of fertility drugs and risk of ovarian cancer: Danish population based cohort study. BMJ. 2009;338:b249. PMID: 19196744 www.ncbi.nlm.nih.gov/pubmed/19196744.
Loren AW, Mangu PB, Beck LN, et al. Fertility preservation for patients with cancer: American Society of Clinical Oncology clinical practice guideline update. J Clin Oncol. 2013;31(19):2500-2510. PMID: 23715580 www.ncbi.nlm.nih.gov/pubmed/23715580.
Mavaddat N, Peock S, Frost D, et al. Cancer risks for BRCA1 and BRCA2 mutation carriers: results from prospective analysis of EMBRACE. J Natl Cancer Inst. 2013;105(11):812-822. PMID: 23628597 www.ncbi.nlm.nih.gov/pubmed/23628597.
Morch LS, Lokkegaard E, Andreasen AH, Kruger-Kjaer, Lidegaard O. Hormone therapy and ovarian cancer. JAMA. 2009;302(3):298-305. PMID: 19602689 www.ncbi.nlm.nih.gov/pubmed/19602689.
Moyer VA; U.S. Preventive Services Task Force. Risk assessment, genetic counseling, and genetic testing for BRCA-related cancer in women: U.S. Preventive Services Task Force recommendation statement. Ann Intern Med. 2014;160(4):271-281. PMID: 24366376 www.ncbi.nlm.nih.gov/pubmed/24366376.
Moyer VA; U.S. Preventive Services Task Force. Screening for ovarian cancer: U.S. Preventive Services Task Force reaffirmation recommendation statement. Ann Intern Med. 2012;157(12):900-904. PMID: 22964825 www.ncbi.nlm.nih.gov/pubmed/22964825.
National Cancer Institute website. Ovarian, fallopian tube, and primary peritoneal cancer prevention (PDQ) - health professional version. www.cancer.gov/types/ovarian/hp/ovarian-prevention-pdq. Updated February 4, 2016. Accessed January 1, 2017.
National Comprehensive Cancer Network website. Genetic/Familial High-Risk Assessment: Breast and Ovarian. Version 2.2016. www.nccn.org/professionals/physician_gls/PDF/genetics_screening.pdf. Updated March 15, 2016. Accessed January 1, 2017.
National Comprehensive Cancer Network website. Ovarian cancer including fallopian tube cancer and primary peritoneal cancer. Version 2.2017. www.nccn.org/professionals/physician_gls/PDF/ovarian.pdf. Updated June 27, 2017. Accessed August 7, 2017.
Oza AM, Cook AD, Pfisterer J, et al. Standard chemotherapy with or without bevacizumab for women with newly diagnosed ovarian cancer (ICON7): overall survival results of a phase 3 randomised trial. Lancet Oncol. 2015;16(8):928-936. PMID: 26115797 www.ncbi.nlm.nih.gov/pubmed/26115797.
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