Medicines
How much does exemestane actually help? The numbers explained
Exemestane lowers the chance of hormone receptor positive breast cancer coming back after surgery in women past menopause. But how much it helps one woman depends on her starting risk. This page explains what the main trials showed, how to read relative and absolute benefit, and what makes the benefit larger or smaller for you.
On this page
- How much does exemestane actually help?
- The main evidence behind exemestane
- Terms that change how a benefit sounds
- The vocabulary, in plain language
- What the numbers cannot promise
- What makes the benefit larger or smaller for you
- How to protect the benefit you are taking the tablets for
- What people assume about the benefit of exemestane
- Common questions about the benefit of exemestane
The short answer
How much does exemestane actually help?
Exemestane is an aromatase inhibitor tablet for hormone receptor positive breast cancer in women who have been through menopause, or in younger women whose ovaries have been switched off. After surgery for early breast cancer, its job is to lower the chance that the cancer comes back, either in the breast area or elsewhere in the body. It does this by stopping most of the oestrogen the body still makes after menopause. Large studies have shown that hormone therapy after surgery is one of the most effective parts of treatment for this type of cancer, and that aromatase inhibitors such as exemestane lower the risk of recurrence further than tamoxifen in postmenopausal women. Combined results from many trials found that, during the years when the two treatments differed, the chance of recurrence was roughly a fifth to a third lower with an aromatase inhibitor, and deaths from breast cancer were modestly lower over the long term. Exemestane has also been shown to help when women switch to it after a few years of tamoxifen. How much this means for you depends on your own starting risk. The same relative reduction gives a large benefit to someone whose cancer had a high chance of returning, and a smaller benefit to someone whose risk was already low. Taking the tablets regularly for the full planned time is what turns these trial results into real protection.
The benefit is real and well studied
Exemestane has been tested in large trials involving many thousands of women over many years.
Your own benefit depends on your risk
Tumour size, grade, lymph nodes and other features decide how much a risk reduction is worth to you.
Taking it steadily matters
Missing many doses or stopping early reduces the protection the trials showed.
This page gives general information only. Your oncologist can explain what the figures mean for you.What the studies showed
The main evidence behind exemestane
Each of these trials asked a different question, and together they explain where exemestane is used.
Switching after tamoxifen
Women who switched to exemestane after two to three years of tamoxifen had fewer recurrences than those who stayed on tamoxifen, with a small improvement in survival.
Exemestane from the start
Taking exemestane for the whole five years worked about as well as starting with tamoxifen and switching to exemestane.
Both approaches are reasonable choices.Compared with anastrozole
A large trial found exemestane and anastrozole gave similar results in keeping cancer away, with small differences in side effects.
Before menopause, with ovarian suppression
For younger women at higher risk, exemestane with treatment that stops the ovaries lowered recurrence more than tamoxifen with ovarian suppression.
Other settings studied
- Advanced cancer after a non-steroidal aromatase inhibitor
- Combined with everolimus for hormone-resistant cancer
- Lowering breast cancer risk in high-risk women
Reading the numbers
Terms that change how a benefit sounds
Words you may hear
The vocabulary, in plain language
- Aromatase inhibitor
- A tablet that stops the body turning other hormones into oestrogen after menopause.
- Adjuvant treatment
- Treatment given after surgery to lower the chance of cancer returning.
- Recurrence
- Cancer that comes back in the breast area or elsewhere after treatment.
- Baseline risk
- Your chance of recurrence before hormone therapy is taken into account.
- Adherence
- Taking a medicine as prescribed, without missing doses or stopping early.
- Meta-analysis
- A study that pools the results of many trials to give a clearer overall answer.
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Being straight with you
What the numbers cannot promise
Trial figures describe what happened to large groups of women. They cannot say exactly what will happen to one person.
Some cancers return despite treatment
Exemestane lowers the risk of recurrence, but it does not remove it. Some women do everything recommended and still have a recurrence.
Many would have stayed well anyway
Many women whose cancer never returns would have stayed well without hormone therapy. It is not possible to know in advance who those women are.
Older trials, newer patients
Treatment has improved since many of these trials began, so today's absolute benefits may differ.
What this page cannot tell you
It cannot calculate your personal benefit. Your oncologist can use your tumour details, and sometimes online risk tools, to estimate it with you.
Your own situation
What makes the benefit larger or smaller for you
The same tablet can mean very different things to two women, because their cancers carried different risks from the start.
Features that raise the benefit
Larger tumours, cancer in the lymph nodes, higher grade and a strongly hormone-sensitive cancer with other risk features all raise the starting risk, so a reduction protects more.
Features that lower it
A very small, low-grade, node-negative cancer already has a low chance of returning. Hormone therapy still helps, but the absolute gain is smaller.
Genomic test results
Tests on the tumour can refine the estimate of recurrence risk and help decide how much extra treatment makes sense.
Getting the full benefit
How to protect the benefit you are taking the tablets for
The protection seen in trials depends on taking exemestane regularly for the planned time.
Build a daily habit
Take the tablet after the same meal each day, and use a pill box or phone reminder.
Treat side effects early
Joint pain, hot flushes and low mood are the common reasons women stop. Most can be eased, and switching to another aromatase inhibitor is sometimes possible.
Talk before stopping
If you are thinking of stopping, speak to your oncologist first. There may be a way to keep some or all of the benefit.
Commonly believed
What people assume about the benefit of exemestane
Surgery removes visible cancer, but hormone therapy targets tiny cells that may remain unseen.
A relative reduction can sound large while the absolute gain is small if your risk was low.
Trials suggest the aromatase inhibitors give broadly similar protection.
Protection from a full course of hormone therapy continues for years after the tablets end.
Questions we are asked
Common questions about the benefit of exemestane
Can my doctor give me a personal number?
Often, yes. Using details such as tumour size, grade, lymph nodes, receptor results and age, your oncologist can estimate your chance of recurrence with and without hormone therapy. These tools give an estimate, not a certainty, but they help you see what the tablets are likely to add.
Is exemestane better than tamoxifen?
For postmenopausal women, aromatase inhibitors such as exemestane lower recurrence a little more than tamoxifen overall. Tamoxifen is still a good option for some women, for example if aromatase inhibitor side effects are hard or bone health is a concern. The best choice depends on your health.
Does exemestane help me live longer?
Hormone therapy after surgery lowers deaths from breast cancer over the long term. Compared with tamoxifen, aromatase inhibitors give a modest further reduction. Survival differences take many years to appear in trials, which is why the figures are usually smaller than those for recurrence.
Is there extra benefit from taking it longer than five years?
For some women at higher risk, extending hormone therapy lowers late recurrence a little more. The extra gain is usually smaller than in the first five years, and side effects continue. Your oncologist weighs your risk, bone health and wishes before suggesting a longer course.
How much does missing doses reduce the benefit?
Occasional missed tablets are unlikely to matter much. Studies of women who regularly miss doses or stop early show a higher chance of recurrence. If you often forget or struggle with side effects, tell your team so you can find a solution together.
Does exemestane help in advanced breast cancer?
Yes. It can control hormone receptor positive advanced cancer, including after another aromatase inhibitor has stopped working. It may be combined with everolimus. In advanced cancer the aim is to control the disease for as long as possible, rather than prevent recurrence.
Can exemestane prevent breast cancer in healthy women?
A trial in postmenopausal women at high risk found exemestane lowered the chance of developing invasive breast cancer. It is not routinely used this way everywhere, and side effects matter more when you do not have cancer. A specialist can advise on risk-reducing options.
Is the benefit the same for men?
Men with hormone receptor positive breast cancer usually take tamoxifen. Aromatase inhibitors alone may not lower oestrogen enough in men, so they are generally combined with treatment that reduces male hormone production. Evidence in men is more limited than in women.
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Sources
- The Lancet — Aromatase inhibitors versus tamoxifen in early breast cancer: patient-level meta-analysis of the randomised trials
- Cancer Research UK — Exemestane (Aromasin)
- National Cancer Institute — Hormone Therapy for Breast Cancer
This page is general information, not a prescription. Do not change or stop any treatment based on what you read here. If anything is worrying you, contact your own treating team — or call our helpline and we will help you reach the right specialist.