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Ovarian Cancer Early Detection, Diagnosis, and Staging

Catching cancer early often allows for more treatment options. Some early cancers may have signs and symptoms that can be noticed, but that is not always the case. Only about 20% of ovarian cancers are found at an early stage. When ovarian cancer is found early, about 94% of patients live longer than 5 years after diagnosis.

Why is it hard to find ovarian cancer early?

Ovarian cancer is hard to find early because it often does not cause symptoms until the cancer is advanced. Even regular pelvic exams usually can’t detect small tumors in the ovaries. Unlike for some other cancers, there’s no screening test that works well enough to find ovarian cancer early in most people. Researchers are still working to develop better ways to find it sooner.

What you can do to help find ovarian cancer early

Although there are no sure ways to find ovarian cancer early, it can help to be aware of symptoms and see your doctor regularly.

A pelvic exam allows your health care provider to feel the ovaries and uterus for size, shape, and consistency. Pelvic exams may help find other cancers or conditions, but most early ovarian tumors are difficult or impossible to feel. Talk to your doctor about whether you should have regular pelvic exams.

While Pap tests and HPV tests are important to screen for cervical cancer, they only rarely detect ovarian cancer.

Early ovarian cancer often causes no symptoms. More often, by the time ovarian cancer causes symptoms, it has already spread. This can happen rapidly in some types of ovarian cancer. The most common symptoms are:

  • Bloating
  • Pelvic or abdominal (belly) pain
  • Trouble eating or feeling full quickly
  • Urinary symptoms such as urgency (always feeling like you have to urinate) or frequency (having to often urinate)

If you have these symptoms on a consistent basis for more than a few weeks, report them right away to your health care provider. Prompt attention to symptoms may improve the odds of early diagnosis and successful treatment.

What to know about ovarian cancer screening

Screening tests and exams are used to detect a disease in people who don’t have any symptoms. (For example, a mammogram can often detect breast cancer in its earliest stage, even before a doctor can feel the cancer.)

Limitations of current screening tests for ovarian cancer

There has been a lot of research to develop a screening test for ovarian cancer, but there hasn’t been much success so far. The 2 tests used most often (in addition to a complete pelvic exam) to screen for ovarian cancer are transvaginal ultrasound (TVUS) and the CA-125 blood test.

  • TVUS (transvaginal ultrasound) uses sound waves to look at the uterus, fallopian tubes, and ovaries by putting an ultrasound wand into the vagina. It can help find a mass (tumor) in the ovary, but  it can't tell whether it’s cancer or benign. In fact, most masses found during screening are not cancer.
  • The CA-125 blood test measures a protein in the blood that’s often high in women with ovarian cancer. It can help track how well treatment is working if you have ovarian cancer, but it’s not a reliable screening test. Many common benign conditions such as endometriosis and pelvic inflammatory disease can also raise CA-125 levels. And not all ovarian cancers cause a high CA-125 level. If your CA-125 level is high and you don’t have a cancer diagnosis, your doctor might repeat the test or suggest a transvaginal ultrasound test.

Should I be screened for ovarian cancer?

There are no recommended screening tests for ovarian cancer for women without symptoms or high risk. Studies show that using TVUS and CA-125 to screen average-risk women leads to more testing and surgeries but doesn’t lower ovarian cancer deaths. That’s why no major medical or professional organization recommends these tests for routine screening.

Some organizations state that TVUS and CA-125 may be offered to screen women who have a high risk of ovarian cancer due to an inherited genetic syndrome such as Lynch syndrome, BRCA gene mutations, or a strong family history of breast and ovarian cancer. Even in these women, it has not been proven that using these tests for screening lowers their chances of dying from ovarian cancer.

Screening tests for germ cell tumors/stromal tumors

There are no recommended screening tests for germ cell tumors or stromal tumors. Some germ cell cancers release proteins such as human chorionic gonadotropin (HCG) and alpha-fetoprotein (AFP) into the blood. For women who have been treated for these tumors, doctors can use blood tests for these markers to see how well treatment has worked or to see whether the cancer is coming back.

Future screening tests for ovarian cancer

Although there are no reliable screening tests for ovarian cancer yet, researchers are still looking for better tests. One method being researched involves looking at the pattern of proteins in the blood (called proteomics) to find ovarian cancer early. Hopefully, improvements in screening tests will eventually lead to fewer deaths from ovarian cancer.


How is ovarian cancer diagnosed?

If you have symptoms or your doctor finds something suspicious during a pelvic exam, they will recommend exams and tests to find the cause.

Medical history and physical exam

Your doctor will:

  • Ask about your personal and family medical history, including any risk factors.
  • Ask about symptoms, when they started, and how long you've had them.
  • Likely do a pelvic exam to check for an enlarged ovary or signs of fluid in the abdomen (ascites).

If these findings suggest possible ovarian cancer, your doctor will order more tests and may refer you to a specialist.

Seeing a specialist

If ovarian cancer is suspected, it’s important to see a gynecologic oncologist – a doctor trained to treat cancers of the female reproductive system. This specialist can help ensure that you get the best kind of surgery and treatment for your cancer. It’s important to meet with a gynecologic oncologist before having surgery.

Tests for ovarian cancer

Tests for ovarian cancer typically include a combination of imaging, biopsy, and blood tests. Imaging studies such as ultrasound, CT, MRI, or PET scan help detect masses or abnormalities in the ovaries. A biopsy, often done during surgery or guided by imaging, is needed to confirm the presence of cancer and determine its type. Blood tests, like tumor markers, may be used to help guide both diagnosis and treatment of the cancer.

Transvaginal ultrasound uses sound waves to create images of the ovaries and nearby organs. A small probe is placed in the vagina and a transducer sends out sound waves and picks up the echoes as they bounce off organs. A computer turns these echoes into an image on a screen.

TVUS is often the first test done if an ovarian problem is suspected. It can show whether a mass is solid (a tumor) or fluid-filled (a cyst), and it helps. It can also help the doctor decide which masses or cysts are more worrisome by letting them get a better look at the size and appearance of an ovary.

A CT scan is an x-ray test that makes detailed cross-sectional images of your body. It typically does not show small ovarian tumors well, but it can show larger tumors and whether cancer has spread to nearby structures, lymph nodes, or organs like the liver.

CT scans can be used to guide a biopsy of a suspected metastasis (area of spread). For a CT-guided needle biopsy, CT scans are repeated while a doctor moves a biopsy needle toward the mass, until the scans show that the needle is in the mass. The needle removes a small sample to be examined in the lab.

MRI scans uses strong magnets to create cross-sectional pictures of your insides. A contrast material called gadolinium may be injected into a vein before the scan to see details better.

MRI scans are not used often to look for ovarian cancer, but they are helpful to examine the brain and spinal cord where cancer could spread.

If you have been diagnosed with cancer, a PET scan may be done to see if it has spread to lymph nodes or other parts of the body. For this test, you will be given a small amount of radioactive sugar. Because cancer cells grow quickly, they absorb more of the sugar than normal cells. A special camera creates an image showing areas of radioactivity in the body.

PET scan images are not as detailed as CT or MRI scans. Typically, a PET and CT scan are done at the same time. A PET/CT scan lets the doctor compare areas of higher radioactivity on the PET scan with the more detailed pictures on the CT scan.

Laparoscopy uses a thin, lighted tube with a tiny camera at the end, inserted through a small incision (cut) in the lower abdomen. The camera sends images to a video monitor, allowing the doctor to see the ovaries and nearby organs.

This procedure helps when planning surgery or other treatments, and can help confirm the cancer’s stage (how far it has spread).

The only way to confirm whether a growth is cancer is to remove a sample and examine it in the lab. This is called a biopsy. For ovarian cancer, the biopsy is usually done by removing the tumor during surgery.

If you cannot have surgery because of advanced cancer or another serious medical condition, a biopsy might be done with laparoscopy or by inserting a needle through the skin into the tumor. This approach is not common, because there is a risk that the biopsy could spread the cancer. Ultrasound or a CT scan is usually used to guide the needle.

If you have ascites (fluid buildup in the abdomen), a fluid sample can be taken to check for cancer cells using a procedure called paracentesis. Your skin is numbed, and a needle and syringe are used to collect fluid from the abdominal cavity. Ultrasound may be used to guide the needle.

All tissue or fluid samples are sent to the lab and examined by a pathologist, a doctor who specializes in diagnosing and classifying diseases by studying cells under a microscope and using other lab tests.

Your doctor will order several blood tests to check your overall health and look for signs of cancer:

  • Blood counts to make sure you have enough red blood cells, white blood cells and platelets (cells that help stop bleeding).
  • Tests to measure your kidney and liver function as well as your general health.
  • Tests to measure level(s) of tumor marker(s), for example, the level of CA-125. This information can help support the diagnosis of ovarian cancer, monitor for treatment response, and assess for possible disease recurrence.

If your doctor suspects a germ cell tumor, your blood might be tested for the tumor markers human chorionic gonadotropin (HCG), alpha-fetoprotein (AFP), and/or lactate dehydrogenase (LDH).

If your doctor suspects an ovarian stromal tumor, your blood might be checked for an increase in a substance called inhibin and hormones such as estrogen and testosterone.

If you have an ovarian mass, a test called OVA1 can measure the levels of 5 proteins in the blood to help determine whether the mass should be considered “low risk” or “high risk” for cancer. This NOT a screening test or a tool to decide whether to have surgery. It is used when surgery is already planned, to help decide whether it should be done by a gynecologist or a gynecologic oncologist.

  • A "low risk" result means cancer is unlikely.
  • A "high risk" result means cancer is more likely and a referral to a gynecologic oncologist is recommended.

Genetic counseling and testing if you have ovarian cancer

If you have been diagnosed with an epithelial ovarian cancer, your doctor will likely recommend genetic counseling and genetic testing for certain inherited gene changes, even if you do not have a family history of cancer. The most common mutations found are in the BRCA1 and BRCA2 genes, but some ovarian cancers are linked to mutations in other genes, such as ATM, BRIP1, RAD51C/RAD51D, MSH2, MLH1, MSH6, or PMS6.

Genetic testing to look for inherited mutations can be helpful in several ways

  • If you have a gene mutation, you may be more likely to get other types of cancer as well. There may be ways lower your risk of these cancers, as well as having tests to find them early.
  • If you have a gene mutation, your family members (blood relatives) might also have it. They can decide if they want to be tested to learn more about their own cancer risk.
  • If you have a BRCA1 or BRCA2 mutation, at some point you might benefit from targeted drugs called PARP inhibitors.
  • Even if you do not have any of the gene mutations listed above, your tumor might be tested for some of these abnormal genes because it might give you more options for treatment.

Be cautious about home-based genetic tests, including those approved by the FDA. These tests have limitations. For example one approved test for BRCA1 and BRCA2 gene mutations only checks for a few mutations, even though there are more than 1,000 known BRCA mutations. This means the test could miss many mutations linked to cancer risk.

A genetic counselor or other qualified medical professional can help you understand the risks, benefits, and possible limits of what genetic testing can tell you. This can help you decide if testing is right for you, and which testing is best.

To learn more about genetic testing, see Should I Get Genetic Testing for Cancer Risk?

Tests for gene or protein changes in ovarian cancer

In some ovarian cancers, doctors might test the cancer cells for specific gene or protein changes to see if certain targeted or immunotherapy drugs might help treat the cancer. These tests can be done on a tumor sample taken during a biopsy or surgery.

BRCA genes are normally involved in DNA repair, and mutations in these genes can cause cells to grow out of control and turn into cancer. Ovarian cancers with BRCA gene mutations are more likely to respond to treatment with targeted drugs called PARP inhibitors.

In many ovarian cancers, the cells have high levels of the FR-alpha protein on their surfaces. Testing for FR-alpha levels can show if the cancer is more likely to respond to treatment with a targeted drug such as mirvetuximab soravtansine (Elahere).

Women who have clear cell, endometrioid, or mucinous ovarian cancer might have their tumor tested for high levels of gene changes called microsatellite instability (MSI) or changes in mismatch repair (MMR) genes such as MLH1, MSH2, MSH6, and PMS2.

Changes in MSI or in MMR genes (or both) are often seen in people with Lynch syndrome (HNPCC). Up to 10% of all ovarian epithelial cancers have changes in these genes.

There are 2 main reasons to test for MSI or for MMR gene changes:

  • To check for the possibility of Lynch syndrome. A diagnosis of Lynch syndrome can help determine if a person should have screenings for other types of cancer, such as endometrial or colon cancer. If a person does have Lynch syndrome, their relatives could also have it and may want to be tested for it.
  • To determine treatment options. Ovarian cancers that have certain MSI or MMR gene changes might be treated with immunotherapy drugs known as checkpoint inhibitors.

Some ovarian cancers might be tested for changes in one of the NTRK genes. Cells with these gene changes can lead to abnormal cell growth and cancer. Larotrectinib (Vitrakvi) and entrectinib (Rozlytrek) are targeted drugs that stop the proteins made by the abnormal NTRK genes. The number of ovarian cancers that have this mutation is very small, but this may be an option for some women.


Stages and outlook (prognosis) for ovarian cancer

After a cancer diagnosis, staging provides important information about the extent of cancer in the body and anticipated response to treatment.


Questions to ask if you have ovarian cancer

It is important to have honest, open discussions with your cancer care team. They want to answer all your questions, so that you can make informed treatment and life decisions. Consider asking these questions:

  • What type of ovarian cancer do I have?
  • Has my cancer spread beyond the ovaries?
  • What is the cancer’s stage (extent), and what does that mean?
  • Will I need other tests before we can decide on treatment?
  • Do I need to see any other doctors or health professionals?
  • If I’m concerned about the costs and insurance coverage for my diagnosis and treatment, who can help me?
  • Will I be able to have children after my treatment?
  • Should I think about genetic testing? What are my testing options? Should I take a home-based genetic test? What would the pros and cons of testing be?

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Developed by the American Cancer Society medical and editorial content team with medical review and contribution by the American Society of Clinical Oncology (ASCO).

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Last Revised: August 8, 2025

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