The short answer
Trodelvy (Sacituzumab govitecan) is a targeted therapy called an antibody-drug conjugate. It links an antibody that finds a protein (Trop-2) on cancer cells to a chemotherapy payload, delivering the chemo more directly to the cancer. It is used to help treat triple-negative breast cancer and some hormone-receptor-positive breast cancers, and is usually given as an IV infusion. Like all cancer medicines it can cause side effects; this page explains the common ones and the warning signs to report. It is educational only and not a substitute for your care team's advice.
Trodelvy is the brand name; its generic name is sacituzumab govitecan.
It is a targeted therapy called an antibody-drug conjugate — it links an antibody that finds a protein (Trop-2) on cancer cells to a chemotherapy payload, delivering the chemo more directly to the cancer.
It is used to help treat triple-negative breast cancer and some hormone-receptor-positive breast cancers.
It is usually given as an IV infusion.
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The full explanation.
An antibody carrying chemotherapy to Trop-2
This drug has two halves joined together. That design is called an antibody-drug conjugate.
The first half is an antibody that finds Trop-2, a protein sitting on the surface of many breast cancer cells. The second half is SN-38, the active form of the chemotherapy drug irinotecan. A chemical link holds them together.
The antibody docks onto the cancer cell. The link breaks. The chemotherapy is released right there, instead of everywhere at once. Some of it also leaks to nearby cells, which is part of how it works and part of why side effects still happen.
Trodelvy is the brand name; sacituzumab govitecan is the generic name.
The two problems in the boxed warning
The FDA boxed warning names low white cells and diarrhea. Both are common enough that your team plans for them from the start.
Neutropenia, a drop in infection-fighting white cells, happened in 64% of people in the trials. It reached a severe grade in 48%. It can begin in the very first cycle. Blood is checked regularly, and a growth-factor injection called G-CSF is recommended in advance for anyone at higher risk.
Diarrhea: have a plan before day one
Diarrhea occurred in 62% of people, and was severe in 10%.
That is not a side effect to manage by waiting. Ask three things before your first dose. Which anti-diarrhea medicine should I keep at home? At what point do I start taking it? And at what point do I call you instead?
The label's approach is to check first that an infection is not the cause, then start the anti-diarrhea plan your team gave you promptly — if you were not given one, that is a same-day call, not a reason to improvise from a pharmacy shelf. Dehydration is the real danger, and it has caused kidney injury. Keep drinking, and call if you cannot keep fluids down.
A gene called UGT1A1 changes your risk
Your liver clears SN-38 using an enzyme made by the UGT1A1 gene. Some people inherit two copies of a slower version, known as UGT1A1*28.
In them the chemotherapy hangs around longer. Among people with two copies of that version, severe neutropenia occurred in 57%. Anemia is also more likely.
Testing for this is available. If you have had a bad reaction to irinotecan in the past, or a family member has, say so before you start.
Which breast cancers it treats
Triple-negative breast cancer that is metastatic or cannot be removed by surgery. It is used first line on its own for people who are not candidates for a PD-1 or PD-L1 drug. It is used first line with pembrolizumab when the tumor's PD-L1 combined positive score is 10 or more. And it is used after two or more earlier treatments, at least one of them for spread disease.
Hormone-receptor-positive, HER2-negative breast cancer that is metastatic or unresectable, after hormone-based treatment and at least two more treatments for spread disease.
An earlier accelerated approval covered urothelial cancer, the cancer of the bladder and urinary tract. It was withdrawn in November 2024 and is no longer an approved use. If you find a page describing this drug for bladder cancer, it is out of date.
Days 1 and 8, then a week off
The dose is worked out from your weight and given into a vein on day 1 and day 8 of every 21-day cycle. So it is two visits, then a week with none.
You are given medicines beforehand to reduce infusion reactions and sickness. Staff watch you during the infusion and for at least half an hour afterwards.
One safety note belongs to the pharmacy as much as to you. This drug must never be swapped for, or given with, irinotecan.
When to get help sooner
- Call 911 or go to an emergency department if a rash, swelling, wheeze or dizziness comes on during an infusion or soon after it, or if you cannot stand up without the room spinning after a day of diarrhea.
- Call your cancer team the moment it happens, day or night, if your temperature hits 100.4°F (38°C) or higher, or you get chills and shivering. Low white cells start in the very first cycle with this drug, so a fever is a medical emergency and needs assessing within the hour. If you cannot reach the team quickly, go to an emergency department and tell them at once that you are on sacituzumab govitecan.
- Go to an emergency department the same day if diarrhea keeps going despite the loperamide plan you were given, you cannot keep fluids down, or you have stopped passing much urine. Severe diarrhea on this drug has caused kidney injury, and fluids into a vein may be needed. Ring your care team on the way.
- Call your care team within a day or two if stairs leave you breathless, or you look pale and feel worn out in a way that is new. Hair thinning, nausea and ordinary tiredness are rarely urgent, but tell your team anyway, because there is usually something that helps.
Sources
- https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=57a597d2-03f0-472e-b148-016d7169169d
- https://www.cancer.gov/about-cancer/treatment/drugs/sacituzumabgovitecan-hziy
- https://www.fda.gov/drugs/resources-information-approved-drugs/withdrawn-cancer-accelerated-approvals
- https://www.cdc.gov/cancer-preventing-infections/patients/fever.html
Words to know
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Common questions
What is Trodelvy?
Trodelvy (Sacituzumab govitecan) is a targeted therapy called an antibody-drug conjugate. It links an antibody that finds a protein (Trop-2) on cancer cells to a chemotherapy payload, delivering the chemo more directly to the cancer. It is used to help treat triple-negative breast cancer and some hormone-receptor-positive breast cancers.
How is Trodelvy given?
It is usually given as an IV infusion. It is given as an intravenous (IV) infusion — a slow drip into a vein — at a clinic or hospital, usually repeated on a schedule of cycles with rest periods in between. The exact schedule is set by your care team.
What are the common side effects of Trodelvy?
Commonly reported side effects include low blood counts, diarrhea, nausea, tiredness, and hair thinning. Not everyone gets them, and many can be managed. Tell your care team about anything new or worsening.
Does Trodelvy cure cancer?
That depends on the person, the cancer type, and its stage. For some people a medicine like this can control cancer for a long time or be part of a curative plan; for others the goal is to slow the cancer or ease symptoms. Your care team can explain the goal in your situation.
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Sources last checked: 2026-08-13 what this meansLast updated: 2026-08-21Next planned review: 2027-01-14
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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: Editorial review complete — This page completed Cancer Explained's editorial checks (sources, safety, plain language, duplication). It has not been reviewed by a physician or other healthcare professional.
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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