It can be overwhelming after being told that you have or may have ovarian cancer. A lot can happen quickly, and you might have lots of questions, like 'What happens next after a diagnosis?'
This support resource can help to guide you, your family, and your friends through this experience.
Information and support
If you need additional information or would like support, you can visit the ovarian cancer page or call Cancer Council on 13 11 20 to talk to an experienced healthcare professional.
For more information about melanoma, visit Cancer Council’s Understanding Ovarian Cancer booklet.
For further information about ovarian cancer and patient support, call an ovarian cancer support nurse on 1300 660 334 or visit Ovarian Cancer Australia.
If you need a translator, call TIS on 13 14 50 or visit the TIS National website.
1. Initial investigation and referral
Symptoms
Your general practitioner (GP) should do a check-up to see if they can find what is making you feel unwell. They will ask you about any symptoms you might be having such as bloating or pain in your abdomen or stomach area, not feeling hungry or not wanting to eat, feeling full quickly, not being able to hold your wee in and needing to wee often.
Initial tests you may have:
Pelvic examination
The GP will look at your abdomen and vagina to check for growths or lumps.
Rectal examination
The GP inserts a gloved finger into your bottom and checks for problems in the anus and rectum. These are the parts just inside your bottom.
Pelvic ultrasound
A gynaecological sonographer (healthcare professional with experience in this type of ultrasound) inserts a small ultrasound tool into your vagina. Soundwaves are used to create a picture of your ovaries.
Computed tomography (CT) scan
Computers and x-rays are used to make a detailed picture of your ovaries.
Blood test
A sample of blood is collected to assess your general health and test for tumour markers in your body.
Tests less frequently undertaken in primary care:
Image-guided biopsy
Computers and x-rays are used to make a detailed picture of the ovaries so that a biopsy can be taken. A biopsy is where a small sample of your ovary is removed to check under a microscope. A biopsy of the ovary should only be done after specialist review.
Gastrointestinal endoscopy
A flexible tube with a camera on it (called an ‘endoscope’) is put inside your nose or throat. The endoscope takes images of the oesophagus and stomach. Your specialist or GP will tell you what you need to do to prepare for this test.
Colonoscopy
A small camera on a tube is put into your bottom to check your large bowel. Your specialist or GP will tell you what you need to do to prepare for this test.
Referrals
If your GP has concerns, you will be referred to a specialist (gynaecological oncologist) at a public hospital or in private practice for more tests. Gynaecological oncologists are doctors who are highly trained in ovarian cancer.
You can bring a family member or friend with you to your appointments.
Timeframes
Your specialist appointment should happen within two weeks of referral. If you can’t get an appointment within this time, follow up with your GP.
Questions you might want to ask
- Can I choose whether I go to a public hospital or private practice?
- Can I choose the specialist I see?
- How much will appointments cost me?
2. Diagnosis and staging
The specialist will do more tests to see if you have melanoma. Most biopsies sent to a pathology laboratory confirming a melanoma diagnosis happen in general practice. This process of working out if you have a medical problem is called making a diagnosis.
You might have one test or a mix of tests:
Blood test
If you haven’t already had a blood test, a sample of blood will be collected to test for tumour markers in your body.
Chest x-ray
An x-ray takes a picture to see if there is anything wrong with your lungs.
Positron emission tomography-computed tomography (PET-CT) scan
A small amount of radioactive material is injected and your whole body is scanned to show where the cancer is.
Magnetic resonance imaging (MRI)
A scan where magnetic fields and radio waves are used to create a detailed picture of the body.
Fluid aspiration
Your doctor uses a needle to take fluid or liquid from your abdomen. The fluid is checked under a microscope. This is done under local anaesthetic so you don’t feel pain.
You’ll undergo a pelvic ultrasound, CT scan, or image-guided biopsy, if you haven’t already had one.
These tests will give the specialist more information about the cancer, such as where exactly it is in your body, if the cancer is growing or has spread, and what stage it is at. This is called staging, which helps to work out the best treatment for you.
Timeframes
Results should be available within two weeks from when you have the tests.
Questions you might want to ask
- What is ovarian cancer?
- What tests will I have?
- How much will tests/appointments cost?
- Where should I be treated, and do I have a choice?
- What stage is my cancer?
- What support services are available to me?
3. Treatment
There are several ways to treat ovarian cancer. Your specialist will talk to you about your treatment options.
You will be treated by a team of experts, and you may need more than one treatment type to get the best results. The team will work with you and your family or carer to plan your treatment.
You might have one treatment or a mix of treatments:
Surgery is where the cancer is cut out. It is the most common treatment for ovarian cancer.
Chemotherapy uses drugs to kill cancer cells and stop the cancer growing. It might be used before surgery, after surgery or alone.
Targeted therapy uses drugs to attack specific features of cancer cells and stop the cancer growing.
Radiation therapy uses x-rays to kill cancer cells and stop the cancer growing.
For more information, visit Cancer Treatment. Supportive care (treatment or services that support you through a cancer experience) are also available.
Timeframes
Treatment should start within two weeks (surgery or chemotherapy) or four weeks (radiation therapy) of agreeing to your treatment plan.
You can ask your GP for a referral to another specialist for a second opinion.
Risk of lymphoedema
Some treatments for cancer, commonly surgery, involving the lymph node areas such as the armpit and the groin, may increase your risk of developing lymphoedema (swelling of a body region). Your specialist should discuss this risk with you and arrange for it to be managed appropriately.
Clinical trials
You may be offered to take part in a clinical trial. Clinical trials are used to test whether new treatments are safe and work better than current treatments. Many people with cancer are now living longer, with a better quality of life, because of clinical trials.
Complementary therapies
Speak to your healthcare team about any complementary therapies (including dietary supplements like vitamins) you use or would like to use. Something as common as vitamins might not work well with your treatment.
For more information on clinical trials, visit the Australian Cancer Trials page.
Questions you might want to ask
- What treatment do you recommend?
- Where will I have to go to have treatment?
- What will treatment cost and how much of the cost will I have to pay myself?
- What activities/exercise will help me during and after treatment?
- Can I still work?
- How will the treatment affect my day-to-day life?
- Who are the people in my team and who is my main contact person?
- What side effects could I have from treatment?
- Who do I contact if I am feeling unwell or have any questions?
- Will treatment affect my ability to have a child?
4. After treatment
Recovery
Cancer treatment can cause a range of physical and emotional changes.
Follow-up care plan
Your healthcare team will work with you to make a plan for you and your GP. This plan will explain:
- who your main contact person is after treatment
- how often you should have check-ups and what tests this will include
- understanding and dealing with side effects of treatment
- how to get help quickly if you think the cancer has returned or is worse
Many people worry that the cancer will return. Your specialist and healthcare team will talk with you about your needs and can refer you to other healthcare professionals and community support services.
Other information you may get:
- signs and symptoms to look out for if the cancer returns
- late effects of treatment and the specialists you may need to see
- how to make healthy lifestyle choices to give you the best chance of recovery and staying well
For more information, visit After Cancer Treatment.
Questions you might want to ask
- Who should I contact if I am feeling unwell?
- What can I do to be as healthy as possible?
- Where can I get more help?
5. If cancer returns
Sometimes, cancer can come back after treatment. It can come back in the same place or can appear somewhere different in your body.
If cancer returns, you may be referred to the specialist or the hospital where you were first treated, or to a different specialist.
Treatment will depend on how far the cancer has spread, how fast-growing it might be, and the symptoms you are experiencing.
Questions you might want to ask
- Where is the cancer and has it spread?
- What are my treatment options?
- What are the chances that the treatment will work this time?
- Is there a clinical trial available?
- Where else can I get support?
Advance care planning
Your GP or healthcare team may talk with you, your family, and carer about your future treatment and medical needs.
Advance care directive
Sometimes known as a living will, an advance care directive is a legally binding document that you prepare to let your family and healthcare team know about the treatment and care you might want or not want in case you become too unwell to make those decisions yourself.
For more information, visit Advance Care Planning Australia.
Palliative care
Your specialist may refer you to palliative care services, but this doesn’t always mean end-of-life care. Today, people can be referred to these services much earlier if they’re living with cancer or if their cancer returns. Palliative care can help you to live as well as you can, including managing pain and symptoms. This care may be at home, in a hospital or at another location you choose.
Speak to your GP or specialist or visit Palliative Care Australia.
Making treatment decisions
You may decide not to have treatment at all, or to only have some treatment to reduce pain and discomfort. You may want to discuss your decision with your healthcare team, GP, family and carer.
For more information, visit Advanced Cancer Treatment.
Questions you might want to ask
- What can you do to reduce my symptoms?
- What extra support can I get if my family and friends care for me at home?
- Can you help me to talk to my family about what is happening?
- What support is available for my family or carer?
- Can I be referred to a community support service?
6. Questions of cost
You may have to pay for some appointments, tests, medications, accommodation, travel or parking. Speak with your GP, specialist or private health insurer (if you have one) to understand what is covered and what your out-of-pocket costs may be.
If you have concerns about costs, talk to your healthcare team or a social worker about:
- being bulk-billed or being treated in the public system
- help with accommodation during treatment
- the possible financial impact of your treatment
You can call Cancer Council on 13 11 20 to speak to a healthcare professional about financial support. For more information about costs, visit Practical and financial assistance and What will I have to pay for treatment.
7. Further support
Listen to audio in your language
Ovarian cancer support
You can speak to specially trained staff at Cancer Council on 13 11 20. They can answer your questions about the effects of cancer, explain what will happen during treatment and link you to support groups and other community resources.
If you need an interpreter, call TIS (Translating and Interpreting Service) on 13 14 50.
For support and advice for carers, call the Carers Association on 1800 242 636.
More support options
Australian Cancer Survivorship Centre
Has general and tumour-specific information, primarily focused on the post-treatment survivorship phase
• Telephone: (03) 9656 5207
• Website: www.petermac.org/cancersurvivorship
beyondblue
Information on depression, anxiety and related disorders, available treatment and support services
• Telephone: 1300 22 4636
• Website: www.beyondblue.org.au
Look Good, Feel Better
A non-medical, free community service program dedicated to teaching women how to manage the appearance-related side-effects caused by cancer treatment
• Telephone: 1800 650 960 (Monday to Thursday 9.00am to 5.00pm)
• Website: www.lgfb.org.au
Cancer Australia
Information on cancer prevention, screening, diagnosis, treatment and supportive care for Australians affected by cancer, and their families and carers
• Telephone: 1800 624 973
• Website: www.canceraustralia.gov.au
Ovarian Cancer Australia
Specific information on ovarian cancer
• Telephone: 1300 660 334
• Website: www.ovariancancer.net.au
CanTeen
Australian organisation for young people living with cancer offers support, information, and resources
• Telephone: 1800 226 833
• Website: www.canteen.org.au
Care Search: Palliative Care Knowledge network
Information for patients and carers on living with illness, practical advice on how to care, and finding services
• Telephone: (08) 7221 8233
• Website: www.caresearch.com.au
National Health Services Directory
A directory providing information on local hospital and community services
• Website: www.nhsd.com.au
Optimal care pathways have been developed for health professionals and health services. However, patients and carers may find useful information in this version to help understand the processes their treating health professionals are following.