Vaginal cancer
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What is vaginal cancer?
Cancers that start in the vagina are rare. In the UK, about 250 people are diagnosed with vaginal cancer each year.
It is more common for cancer to start in an area close by, such as the cervix or womb, and grow into the vagina. This information is not about cancer that has spread to the vagina from other areas. This information is about cancers that start in the vagina. These are called primary vaginal cancers.
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The vagina
People born with a vagina include:
- women
- trans (transgender) men
- people assigned female at birth.
Vaginal cancer does not affect men, trans women or people assigned male at birth.
The vagina is a muscular tube that extends from the opening of the womb (cervix) to the folds of skin between the legs (vulva). It allows blood from periods (menstruation) to drain out of the body. It is also the birth canal which is the passage a baby comes through during birth.
The female reproductive system
Types of vaginal cancer
There are different types of vaginal cancer. This information is only about:
- squamous cell cancer (SCC)
- adenocarcinoma of the vagina.
These vaginal cancers are treated in a similar way.
Squamous cell cancer (SCC)
The most common type of vaginal cancer is squamous cell cancer (SCC). This starts in squamous cells that line the vagina. It usually starts in the upper part of the vagina and is more common over the age of 60.
Adenocarcinoma
Adenocarcinoma is rare. It starts in the glandular cells in the vagina. These normally make liquid to lubricate the vagina. It is most common under the age of 30.
Rare types
Some other less common types of vaginal cancer include:
For more information about these, you can call or chat online with our cancer information specialists.
Symptoms of vaginal cancer
The most common symptoms of vaginal cancer are:
- vaginal bleeding after the menopause, between periods or after sex
- blood-stained vaginal discharge
- pain when peeing (passing urine), needing to pee often, or blood in your pee
- pain in the pelvic (lower tummy) area
- constipation
- feeling you need to poo, even though you have just been (tenesmus)
- swelling (fluid) in your legs.
These symptoms can be caused by many other conditions. But it is important to visit your doctor if you have any of these symptoms.
Very rarely, some people may get a fistula. This is an abnormal opening between 2 parts of the body that are not usually connected. For example, this could be between the vagina and the bladder or bowel. This can cause incontinence, which is the leaking of pee or poo.
Some people do not have any symptoms. The vaginal cancer might be found while having an examination, or screening (smear test) to check for cervical cancer.
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Causes and risk factors of vaginal cancer
Doctors do not know the exact causes of vaginal cancer. But there are risk factors that can increase your chance of developing it.
The main risk factor for vaginal cancer is HPV (human papilloma virus). This means that younger people can be affected.
Having a risk factor does not mean you will get vaginal cancer. And not having a risk factor does not mean you will not develop it.
Like other cancers, vaginal cancer is not infectious. You cannot catch it or pass it on to other people.
Age
Vaginal cancer is rare, but more likely:
- as you get older
- after the menopause.
It is uncommon, but younger people can also be affected.
HPV (human papilloma virus)
The main risk factor for vaginal cancer is infection with the human papilloma virus (HPV). People with HPV who smoke may have a higher risk. But most people who get HPV will not get vaginal cancer.
Vaginal intra-epithelial neoplasia (VaIN)
VaIN is the name for pre-cancerous changes in cells lining the vagina. It can develop if HPV remains in the vagina for a long time.
If VaIN is not treated, there is a chance it may eventually develop into vaginal cancer in some people.
Cancer or pre-cancerous changes in the cervix
People who have had cervical cancer or pre-cancerous changes in the cervix (CIN) have an increased risk of developing vaginal cancer. This is likely to be linked to HPV, which is the main cause of cervical cancer and CIN. This risk may be higher in people who smoke. But most people who have had cervical cancer or CIN will never develop vaginal cancer.
A weakened immune system
Your immune system helps protect your body from infection and illness. Other medical conditions such as HIV can affect the immune system. Some people need to take medicines to suppress the immune system.
If the immune system is not working well, it is less likely to get rid of infections like HPV.
Radiotherapy to the pelvis
People who have had radiotherapy to the pelvis may have a very slightly increased risk of vaginal cancer.
Diethylstilbestrol (DES)
Diethylstilbestrol (DES) can increase the risk of a very rare type of vaginal cancer called clear cell adenocarcinoma (CCA). Your risk is increased if your mother was prescribed the drug DES when she was pregnant with you.
DES has not been used for a long time. Doctors prescribed it to some pregnant women between 1940 and 1970. The risk is not very high, but you should have yearly check-ups to check for early signs of CCA.
Diagnosis of vaginal cancer
If you have symptoms, you will usually begin by seeing your GP, who will examine you. If they think that your symptoms could be caused by cancer, they will refer you to a specialist doctor.
They may arrange some of the following tests:
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Internal (vaginal) exam
An internal (vaginal) examination is when the doctor gently checks the inside of the vagina for any lumps or swellings.
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Taking a sample of cells from the cervix
This is the same test that is used for cervical screening. It checks for HPV and any abnormal cells in the cervix.
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Vaginoscopy
A vaginoscopy is a test similar to a colposcopy. It uses a microscope, called a colposcope, to closely examine the vagina. A sample of tissue (biopsy) is taken from any areas that look abnormal.
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Examination under anaesthetic (EUA)
An EUA is an examination of the vagina and cervix under a general anaesthetic. It allows your doctor to examine you thoroughly without it being uncomfortable.
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Transvaginal ultrasound scan
Another test you may have is called a transvaginal ultrasound scan. An ultrasound scan uses sound waves to make up a picture of inside the womb and vagina.
Further tests for vaginal cancer
If the tests show you have vaginal cancer, you will have further tests. Most of these are to find out whether the cancer has spread to the pelvis or other parts of the body. This helps your doctors plan the best treatment for you. They will explain more about the tests you need. These may include:
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Blood tests
You have blood tests to check your general health.
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CT scan
A CT scan takes a series of x-rays which builds up a detailed picture of the inside of the body.
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MRI scan
An MRI scan uses magnetism to build up a detailed picture of areas of your body.
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PET-CT scan
A PET-CT scan is a positron emission tomography scan (PET) and CT scan together. The CT scan takes a series of x-rays to build up a detailed picture, and the PET scan uses low-dose radiation to measure the activity of cells in different parts of the body.
Waiting for test results can be a difficult time, we have more information that can help.
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Staging and grading of vaginal cancer
The results of your tests help your doctors find out more about the size and position of the cancer and whether it has spread. This is called staging.
A doctor decides the grade of the cancer by how the cancer cells look under the microscope. This gives an idea of how quickly the cancer might grow or spread.
Knowing the stage and grade helps your doctors plan the best treatment for you.
A number between 1 and 4 is given to describe the stage of the cancer, depending on:
- its growth in the vagina and surrounding tissues
- whether it has spread to lymph nodes or other organs.
Your cancer doctor will tell you the stage of the cancer when they have all your test results. Knowing the stage of the cancer helps your doctors advise you on the best treatment.
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Treatment for vaginal cancer
A team of specialists will meet to discuss the best possible treatment for you. This is called a multidisciplinary team (MDT).
Your treatment will depend on:
- the stage of the cancer
- your general health
- your preferences.
Your doctor or cancer specialist or nurse will explain the different treatments and their side effects. They will also talk to you about things to consider when making treatment decisions before you agree (consent) to have treatment.
Your cancer team may also give you advice about preparing for your treatment. This is sometimes called prehabilitation. It helps to improve your fitness and diet and to get you ready mentally before treatment.
The treatment you have will depend on different factors. These include:
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Radiotherapy
Radiotherapy treats cancer using high-energy rays. This is the most common treatment for vaginal cancer.
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Chemotherapy
Chemotherapy uses anti-cancer drugs to destroy cancer cells. Chemotherapy is often given with radiotherapy (chemoradiation).
It may also be given to treat vaginal cancer that has spread to other parts of the body. Sometimes it is given before surgery, or radiotherapy but this is not common.
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Chemoradiation
Chemotherapy is often given with radiotherapy to treat vaginal cancer. This is called chemoradiation. The combination of treatments can be more effective than radiotherapy on its own. The chemotherapy drug most commonly used is cisplatin This is usually given once a week throughout radiotherapy through a drip (IV infusion).
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Surgery
Surgery is usually only used for small stage 1 cancers and for cancers that were not cured by radiotherapy.
You may have some treatments as part of a clinical trial.
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After vaginal cancer treatment
Follow-up after treatment for vaginal cancer
You will have regular check-ups during and after your treatment. Follow-up appointments are a good time to talk to your cancer doctor or specialist nurse about any concerns you have. Between your follow-up appointments, it is important to let them know as soon as possible if you have any problems or notice new symptoms. You can also call your specialist nurse if you have questions or need advice.
For some people, follow-up appointments will be every few months for the first couple of years. But they will be once or twice a year after that. If the cancer is advanced, your doctor or specialist nurse can tell you how often you will have follow-up appointments and what these might involve.
At these appointments they will ask questions about how you are and how you are recovering from any treatment. You may have an internal examination.
They will also ask if you have any symptoms. They can talk to you about symptoms to be aware of such as vaginal bleeding or discharge.
You may get anxious between appointments. This is natural. It may help to get support from family, friends or a support organisation.
Some people will have a different kind of follow-up where you are asked to contact your cancer team if you have any concerns. This may be called Patient Initiated Follow up or PIFU. If you are having this type of follow up, your doctor or specialist nurse will explain what to be aware of.
We have more information about follow-up care after treatment.
Late effects of radiotherapy
Radiotherapy for vaginal cancer can sometimes cause side effects that do not go away. Or they may develop months or years after treatment. If this happens, there are lots of ways they can be managed or treated.
Sex life
Vaginal cancer and its treatments can affect your sexual wellbeing. They can cause changes that are physical, emotional and practical. How you feel about your body (body image) may change. You may have changes to your usual roles or routines. These areas are often linked. If there is a change to one area, it can affect another.
You may not feel like having sex for a while after treatment. If you have a partner, you may both need time to get used to any changes. You can still share your feelings for each other through cuddling, massage, kissing and stroking.
After treatment, you may find that your sex life slowly improves. Some of the changes caused by treatments get better but some may be permanent. You may need time to adjust. Talk to your doctor or CNS if you have any problems or are worried about this. They can explain what to expect. There are often things that can help.
We have more about cancer and sex that includes information about coping with changes during and after treatment. We also have information about how cancer can affect how you feel about your yourself (body image).
Wellbeing and recovery
Taking good care of yourself can help speed up your recovery after vaginal cancer treatment. Even small lifestyle changes may improve your wellbeing and long term health.
Even if you already have a healthy lifestyle, you may choose to make some positive changes after treatment. We have more information on leading a healthy lifestyle after treatment.
More information and advice
We know cancer can affect you physically, emotionally and financially. We have information and advice about different ways cancer might impact you, such as help with:
Support if you're affected by vaginal cancer
It is common to have many different emotions when you are told you have cancer. These include anger, shock, guilt, anxiety and fear. These are all normal feelings. There are lots of different reactions to cancer. There is no right or wrong way to feel. You will cope with things in your own way.
Talking to family, friends or other people affected by cancer, may help. Or you may prefer to get help from people who do not know you well. You may decide you do not want to talk about how you are feeling.
It is important to know where to get support or information if you need it. People often need support even some time after vaginal cancer treatment. But sometimes it is difficult to know who to ask for help.
To find support:
- ask your GP or someone from your cancer team for advice about support in your area
- find cancer support services near you
- call the Macmillan Support Line free on 0808 808 00 00
- chat to our cancer information specialists online
- visit our Online Community vaginal cancer forum to talk to people who have been affected by vaginal cancer, share your experience, and ask questions.
The HOPE programme is a free 6 week self-management course designed to help you develop techniques and strategies when living with or after cancer. Topics include goal setting, fatigue management, and wellbeing. You can sign up for the online HOPE programme. Or to find out more about face to face programmes in your area, email ServiceOpsSupport@macmillan.org.uk
Other organisations who offer information and support
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The Eve Appeal
Tel 020 7605 0100
Email office@eveappeal.org.uk
UK national charity raising awareness and funding research into the five gynaecological cancers – ovarian, womb, cervical, vaginal and vulval.
About our information
This information has been written, revised and edited by Macmillan Cancer Support’s Cancer Information Development team. It has been reviewed by expert medical and health professionals and people living with cancer.
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References
Below is a sample of the sources used in our vaginal cancer information. If you would like more information about the sources we use, please contact us at informationproductionteam@macmillan.org.uk
Nout R.A, Calaminus G, Planchamp F, et al. ESTRO/ESGO/SIOPe Guidelines for the management of patients with vaginal cancer. International Journal of Gynecologic Cancer Published Online First: 19 June 2023. doi: 10.1136/ijgc-2023-004695. https://ijgc.bmj.com/content/early/2023/06/19/ijgc-2023-004695 (accessed January 2024).
Adams TS, Rogers LJ, Cuello MA. Cancer of the vagina: 2021 update. Int J Gynecol Obstet. 2021;155(Suppl. 1):19– 27. https://doi.org/10.1002/ijgo.13867 (accessed January 2024).
Miss Eva Myriokefalitaki
Reviewer
Consultant Gynaecological Oncology Surgeon
Date reviewed

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We use gender-inclusive language and talk to our readers as ‘you’ so that everyone feels included. Where clinically necessary we use the terms ‘men’ and ‘women’ or ‘male’ and ‘female’. For example, we do so when talking about parts of the body or mentioning statistics or research about who is affected.
You can read more about how we produce our information here.
