- Cancer Information
- Managing side effects
- Fertility and cancer
- The effects of cancer treatment on women’s fertility
The effects of cancer treatment on women’s fertility
Here we provide an overview of cancer treatments and how they affect women’s fertility. The most common treatments for cancer are chemotherapy, radiation therapy, surgery and hormone therapy. Other treatments include immunotherapy and targeted therapy.
Learn more about:
- Radiation therapy
- Hormone therapy
- Other treatments
- Avoiding pregnancy during treatment
- Fertility outcomes
Chemotherapy uses drugs to kill or slow the growth of cancer cells. These are called cytotoxic drugs and they are designed to affect fast-growing cells such as cancer cells. This means they can also damage other cells that grow quickly, such as the reproductive cells.
The risk of infertility depends on several factors:
- the types of chemotherapy drugs used – damage to eggs is more common with chemotherapy drugs in the alkylating class
- the dose and duration of chemotherapy treatment – the risk increases with higher doses and longer treatment times
- your age – the number and quality of eggs start to decline naturally as a woman gets older.
Chemotherapy can cause some women’s periods to become irregular, but they often return after treatment ends. For other women, periods may stop, which will bring on menopause. After menopause, women can’t conceive children with their own eggs. For more on this, see Fertility outcomes.
Some chemotherapy drugs can also affect your heart and lungs.
If the drugs cause long-term muscle damage, this may complicate a future pregnancy and delivery. Your specialist will talk to you about what precautions to take during pregnancy.
|If you are treated with both chemotherapy and radiation therapy, the risk of infertility is higher.|
Radiation therapy (also called radiotherapy) uses x-rays to kill cancer cells or damage them so they cannot grow and multiply. It can be delivered externally by external beam radiation, or given internally.
The risk of infertility will vary depending on the area treated and the dose of the radiation therapy.
- External or internal radiation therapy to the pelvic area (for cancer of the rectum, bladder, cervix or vagina) can stop the ovaries producing hormones. This results in temporary or permanent
- Treatment to the pelvic area can increase the risk of miscarriage, premature birth and low birth
- Radiation therapy to the brain may damage the pituitary gland, which releases hormones that stimulate the ovaries to release an egg each month.
Surgery that removes part or all of the reproductive organs, such as the ovaries, fallopian tubes, uterus and cervix, can cause infertility.
Removal of the uterus and cervix (hysterectomy)
This may be used to treat gynaecological cancers, such as cancer of the cervix, ovary, uterus and endometrium (lining of the uterus), and sometimes, cancer of the vagina. After a hysterectomy, you will be unable to become pregnant and your periods will stop.
Removal of the ovaries (oophorectomy)
If both ovaries are removed (bilateral oophorectomy) and you haven’t already been through menopause, you will experience early menopause. You will no longer have periods or be able to become pregnant naturally.
Removal of the whole bladder (radical cystectomy)
If bladder cancer has spread to the abdominal area, the urethra, uterus, ovaries, fallopian tubes and a part of the vagina are often removed. If you have not yet gone through menopause, this will cause your periods to stop and you will be unable to have children naturally.
|Reducing the impact of surgery
Sometimes, it’s possible to save the reproductive organs (known as fertility-sparing surgery). This may be an option for some types of early-stage gynaecological cancers. Learn more about fertility-sparing techniques such as ovarian transposition (oophoropexy) and trachelectomy.
Hormones are naturally produced in the body; however, they can cause some types of cancers to grow. The aim of hormone therapy is to slow down the growth of the cancer.
A hormone receptor is a protein on a cell. Hormone therapy is used for women who have hormone receptors on their cancer cells. This means the growth of cancer cells is affected by the female hormones oestrogen and progesterone. Cancer cells with hormone receptors on them are said to be hormone receptor positive. There are two types of hormone receptors: oestrogen receptors and progesterone receptors.
Hormone therapy blocks the hormones that are required for fertility, so you will have to wait to try for a baby. However, it may be possible to store eggs or embryos before hormone therapy – learn more about this process.
Anti-oestrogen drugs (such as tamoxifen, goserelin and aromatase inhibitors) are used to treat oestrogen-sensitive cancers to reduce the risk of recurrence. Many anti-oestrogen drugs are taken for several years. During this time, pregnancy should be avoided, as there is a risk the drugs could harm an unborn child.
|If you are on hormone therapy and want to become pregnant, talk to your treatment team or fertility specialist about the advantages and disadvantages of stopping hormone therapy.|
Stem cell transplants, immunotherapy and targeted therapy are other ways of treating cancer.
Stem cell transplants often require high doses of chemotherapy and, possibly, radiation therapy. These are given before the transplant to destroy cancer cells in the body and weaken the immune system so that it will not attack a donor’s cells during the transplant. The risk of infertility after high-dose chemotherapy or radiation therapy is high.
The effects of immunotherapy and targeted therapy on fertility and pregnancy are not yet fully understood. Early research suggests some targeted therapy drugs can cause early menopause.
It is important to discuss your fertility options with your cancer treatment team or fertility specialist.
Some women are able to conceive after cancer treatment without medical assistance. However, about one in three women will experience one of the following issues.
Acute ovarian failure
During treatment, and for some time afterwards, the ovaries often stop producing hormones because of the damage caused by the cancer treatment. This is known as acute ovarian failure. It is often temporary, and you will have occasional or no periods, and symptoms similar to menopause. If ovarian failure continues for a number of years, it is less likely that your ovaries will work normally again.
Menopause before the age of 40 is known as early menopause or premature ovarian insufficiency (POI). This is when you stop having menstrual periods because egg numbers are very low.
The eggs may have been destroyed or damaged by treatment. If too many eggs are damaged during treatment, menopause is permanent. Early menopause could occur immediately or many years after treatment depending on your age, type of treatment and dose.
While menopause means you won’t ovulate, it is still possible to carry a baby if you have a uterus and use stored eggs or donor eggs. A small number of women with POI (5–10%) have a chance of becoming pregnant naturally, because in some rare cases, a remaining egg may mature and be fertilised by a sperm.
It feels like menopause is discussed as a treatment side effect, not as this massive impact on who you are as a person. I’m facing menopause 20 years earlier than my friends.
- a dry or tight vagina
- a loss/reduction of interest in sex (low libido)
- hot flushes and night sweats
- pain in joints
- problems falling asleep and staying asleep
- feeling more anxious or
The symptoms are usually more severe when menopause starts suddenly, because the body hasn’t had time to get used to the gradual decrease in hormone levels.
There are various ways to manage the symptoms of menopause.
Early menopause can also cause the bones to weaken (osteoporosis). Talk to your doctor about having a bone density test or taking medicines to prevent your bones weakening. Osteoporosis Australia has more information – call 1800 242 141 or visit osteoporosis.org.au.
Talk to your doctor about the benefits and risks of hormone replacement therapy (HRT). This replaces the hormones usually produced by the ovaries, and can be taken as tablets, creams or skin patches.
Taking HRT containing oestrogen may increase the risk of some diseases. Ask your doctor whether it is safe to use. Some women with a hormone-sensitive cancer may be advised not to take HRT. Vaginal moisturisers available over the counter can help with vaginal discomfort and dryness.
Non-hormonal options, such as acupuncture, can also help. Taking calcium and vitamin D tablets, and performing some weight-bearing exercises to strengthen the bones, can relieve some menopausal symptoms. Exercise can also help with mood changes and energy levels, and will help keep your bones strong. Discuss the best options for your situation with your doctor.
|Your feelings about early menopause
When cancer treatment causes early menopause, the impact on your emotions, body image and relationships can be significant.
If you are a young woman, experiencing menopause much earlier than you expected may affect your sense of identity, or make you feel older than your age or peers.
If you are an older woman, going through menopause earlier than you expected may be upsetting. But some older women say they feel relieved to not have to worry about regular periods.
You may find it difficult to start new intimate relationships after going through menopause. For more on this, see Relationships and sexuality.
It may take time to accept the changes you’re experiencing. Talking to a family member, friend or counsellor may help.
We thank the reviewers of this information: Dr Yasmin Jayasinghe, Paediatric Gynaecologist, Royal Children’s Hospital Melbourne, Co-chair Fertility Preservation Taskforce, Melbourne, and Senior Lecturer, Department of Obstetrics and Gynaecology, University of Melbourne, VIC; Dr Peter Downie, Head, Paediatric Haematology-Oncology and Director, Children’s Cancer Centre, Monash Children’s Hospital, and Director, Victorian Paediatric Integrated Cancer Service, VIC; Carmen Heathcote, 13 11 20 Consultant, Cancer Council Queensland; Aaron Lewis, Consumer; Pampa Ray, Consumer; Dr Sally Reid, Gynaecologist, Fertility SA and Advanced Gynaecological Surgery Centre, Visiting Consultant, Women’s and Children’s Hospital, and Clinical Senior Lecturer, School of Paediatrics and Reproductive Health, The University of Adelaide, SA; A/Prof Kate Stern, Head, Fertility Preservation Service, The Royal Women’s Hospital and Melbourne IVF and Head, Endocrine/Metabolic Clinic, Royal Women’s Hospital, and Co-chair, AYA cancer fertility preservation guidance working group, VIC.
Fertility and Cancer was developed as part of a research study into the experience of fertility after cancer led by Prof Jane Ussher at the Centre for Health Research, Western Sydney University. For a list of the other chief and partner investigators, see cancercouncil.com.au. We acknowledge the input of Dr Amanda Hordern and Prof Jane Ussher, who collaborated on the original draft. We thank CanTeen Australia and the American Cancer Society for permission to draw on their resources. We also thank the cancer survivors who took part in the Western Sydney University research project on fertility and cancer, and whose accounts have been quoted in this booklet.
View the Cancer Council NSW editorial policy.
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