The short answer
Combined hormonal contraception moves cancer risk in two directions at once. It substantially and durably lowers ovarian and endometrial cancer risk, and modestly raises breast and cervical cancer risk while you are using it. The absolute breast cancer increase is roughly one extra case per 7,690 users per year, and the effect fades within about ten years of stopping.
Oral contraceptive use is associated with a 30 to 50 percent lower risk of ovarian cancer, protection that increases with duration of use and can persist up to 30 years after stopping.
Endometrial cancer risk is reduced by at least 30 percent, with greater reduction for longer use, and the protection persists for many years after stopping.
Colorectal cancer risk is 15 to 20 percent lower among users.
Breast cancer risk is modestly raised: about 7 percent higher across all users, about 24 percent higher in current users, declining after stopping with no increase evident by 10 years after use ends.
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The full explanation.
There is no single verdict here
Combined hormonal contraception moves cancer risk in two directions at once. It lowers the risk of some cancers a lot, and for a long time. It raises the risk of others a little, and only for a while. Anyone telling you the pill simply causes cancer has dropped half the evidence. So has anyone telling you it simply prevents it.
What follows is both halves, with the absolute numbers where they exist.
Risks that go down
Ovarian cancer. Users have a 30 to 50 percent lower risk than non-users. The protection grows the longer you use it. It carries on for up to 30 years after stopping. This is one of the largest and most lasting protective effects known for any widely used medication.
Endometrial cancer. Risk drops by at least 30 percent. Again, longer use means a bigger drop, and the protection lasts for many years after stopping.
Colorectal cancer. Use is linked to 15 to 20 percent lower risk.
These are not small or short-lived findings. They are also the part most often left out of news coverage.
Risks that go up
Breast cancer. Across all users, risk is about 7 percent higher. Among current users it is about 24 percent higher, and that figure does not shift much with how long you have used it. Risk falls after stopping. NCI states that no increase is evident by 10 years after use has ended. A large Danish study found a roughly 20 percent increase for current and recent users. Depending on the exact formulation, that ranged from none at all up to 60 percent.
The absolute version is the one to hold onto. ACOG translates the Danish findings into one extra invasive breast cancer for every 7,690 women using hormonal contraception for a year. For women under 35 it is about one per 50,000, because baseline breast cancer risk at younger ages is very low.
Cervical cancer. Risk rises with how long you use it. It is about 10 percent higher with less than 5 years of use. It is about 60 percent higher with 5 to 9 years. With 10 or more years it is roughly doubled. Risk falls after stopping. Here is the essential context: persistent high-risk HPV infection is the necessary cause of cervical cancer. So HPV vaccination and keeping up with cervical screening do far more than any contraceptive decision.
About the Group 1 label
IARC classifies combined oestrogen-progestogen contraceptives in Group 1. It is worth knowing exactly what that means, because out of context it looks alarming.
Group 1 answers one narrow question. Is the evidence strong that this can cause cancer in people? For combined oral contraceptives, the answer is yes — based, IARC says, on raised risk of breast cancer among current and recent users only, of cervical cancer, and of liver cancer in populations at low risk of hepatitis B. That is all the label asserts. It is a statement about scientific certainty, not about how much risk anyone carries. And it makes no attempt to weigh that against the protection the same monograph records: IARC states there is convincing evidence these agents protect against cancer of the endometrium and ovary.
That is why a Group 1 classification should never be read as a recommendation for or against using something.
How to actually decide
This is a conversation with a clinician who knows your history. It is not a decision to make from a fact sheet. Nothing here is a reason to start or stop a medication on your own.
Bring the things that shift the balance. Your family history of breast and ovarian cancer. Whether you carry a known cancer predisposition variant. Your age. Whether you smoke. Your cervical screening and HPV vaccination status. And which method you are actually considering, since most of this evidence comes from combined oral contraceptives rather than from IUDs, implants or progestogen-only methods.
Bring the non-cancer side too, because it is part of the same decision. That means how well the method prevents pregnancy, clot risk, bleeding, cycle control, and endometriosis or PCOS symptoms. It also means the health risks of an unintended pregnancy, which ACOG notes are greater than the breast cancer risk described here.
ACOG's overall framing is worth ending on. Hormonal contraceptives protect against ovarian, endometrial and colon cancers. So overall cancer risk may be slightly lower in users than in non-users. That does not make the breast and cervical findings unimportant. It makes them one part of a balance you get to weigh with someone who knows your situation.
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Common questions
So does the pill cause cancer or prevent it?
Both, depending on which cancer. It substantially and durably lowers ovarian and endometrial cancer risk and modestly lowers colorectal risk, while modestly raising breast and cervical cancer risk during and shortly after use. There is no single verdict, which is exactly why this is a decision to make with a clinician who knows your history rather than from a headline. ACOG notes that overall cancer risk may be slightly lower in hormonal contraceptive users than non-users.
How worried should I be about the breast cancer finding?
The relative figures sound larger than the absolute ones. ACOG's framing is one additional invasive breast cancer for every 7,690 women using hormonal contraception for a year, and about one per 50,000 for women under 35, because baseline breast cancer risk at younger ages is very low. The risk also declines after stopping, with no increase evident by ten years after use ends.
Why is IARC's classification Group 1 if the pill also prevents cancers?
Because Group 1 answers only one narrow question: is the evidence strong that this can cause cancer in humans? For combined oral contraceptives, yes — on the basis of breast cancer in current and recent users, cervical cancer, and liver cancer in populations at low hepatitis B risk. The classification does not attempt to weigh that against the protection IARC's own monograph records against cancer of the endometrium and ovary. A Group 1 label is not a recommendation about whether to use something.
Does the cervical cancer finding mean the pill causes cervical cancer?
Persistent infection with high-risk HPV is the necessary cause of cervical cancer. Long-term oral contraceptive use is associated with higher risk among people with that infection, and the association weakens after stopping. The practical implications are HPV vaccination and keeping up with cervical screening, which are far more powerful levers than contraceptive choice.
What about IUDs, implants and progestogen-only methods?
The best-studied evidence is for combined oral contraceptives, and the figures on this page reflect that. Progestogen-only and long-acting methods have their own evidence bases which are less complete, and levonorgestrel IUDs have their own risk profile. Ask specifically about the method you are considering rather than assuming the pill data transfers.
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Written by: Cancer ExplainedSources last checked: 2026-07-30 what this meansLast updated: 2026-08-13Next planned review: 2027-07-30
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Cancer Explained does not originate medical claims. Every page restates guidance already published by the National Cancer Institute, the CDC, the USPSTF and the FDA, in plain language, with the source cited so you can check the original yourself. AI does the translating and organizing; automated checks test claims, citations, clarity and safety before anything publishes. We do not employ clinicians and do not intend to — our work is translation and navigation, not clinical judgment. Nothing here is personal medical advice, and no page can account for your particular situation.
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How this page was created
Cancer Explained does not originate medical claims. Every page restates guidance already published by the National Cancer Institute, the CDC, the USPSTF and the FDA, in plain language, with the source cited so you can check the original yourself. AI does the translating and organizing; automated checks test claims, citations, clarity and safety before anything publishes. We do not employ clinicians and do not intend to — our work is translation and navigation, not clinical judgment. Nothing here is personal medical advice, and no page can account for your particular situation.
Editorial status: Source checked — This page was written with AI assistance and checked line by line against the sources listed on it. That confirms the sources support what the page says. It is not a medical review, and it does not confirm the page is complete or right for your situation.
Human medical review: not completed. Pages here are not signed off by a clinician before they publish. That is not an oversight we are quietly working around: we restate published guidance and cite it, so the authority belongs to the source rather than to us, and every page names where its claims come from — you can verify us instead of trusting us. Where a volunteer clinician has reviewed a page, their name and credentials appear on it; where no name appears, no clinician has checked it. We are glad to have reviewers and are recruiting them, and we do not hold pages back waiting for one. Use this site to understand your situation and to ask better questions of the people treating you.
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