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Capecitabine (Xeloda)

Raw research findings for this medication. Mostly single studies, not curated or confirmed robust.

About Capecitabine

What it is

Capecitabine is a chemotherapy medicine taken as tablets. The body converts it, step by step and largely inside tumour tissue, into fluorouracil (5-FU), which stops cancer cells from making the DNA they need to divide. It is used for bowel cancer, breast cancer and some cancers of the stomach and pancreas. It is sold as Xeloda, among other names.

How genes come into it

DPYD makes the enzyme dihydropyrimidine dehydrogenase, which breaks down most of the fluorouracil that capecitabine turns into. A few DPYD variants (among them *2A, rs3918290, and c.2846A>T, rs67376798) make less working enzyme; people who carry one have far more of the drug active for longer, with a much higher chance of severe side effects. About 3 to 8 in 100 people of European ancestry carry one such variant. CPIC and DPWG have published guidelines on DPYD, and the US drug label discusses it. Other genes such as TYMS, CDA and MTHFR have been studied, with weaker evidence.

Published guidelines

Clinical guidelines that name a gene for Capecitabine. They sort people into groups by the gene copies they carry.

CPIC guideline: DPYD. DPYD activity score 0 to 2. Strong. 2018.

DPWG guideline: DPYD. DPYD activity score 0 to 2. 2020.

US FDA: DPYD. DPYD activity score 0 to 1.5. 2025.

US FDA: DPYD. DPYD activity score 0 to 1.5. Data that Support Therapeutic Management Recommendations.

What research found

Every published finding on gene variants and Capecitabine. Upload your DNA file to see which of these rows apply to you.

Rated evidence (70 rated variants)

PharmGKB weighs all studies of a variant and rates how strong the evidence is, from 1A (strongest) to 4.

DPYD rs67376798: Level 1A · replicated. Toxicity: Neoplasms. 28.

DPYD rs3918290: Level 1A · replicated. Toxicity: Neoplasms. 28.

DPYD rs2297595: Level 1A · replicated. Toxicity: Neoplasms. 17.

DPYD rs1801158: Level 1A · replicated. Toxicity: Neoplasms. 13.

Metabolism (5 findings)

Studies of how quickly the body processes this medication.

MTHFR rs1801133: Genotype GG is associated with increased exposure to capecitabine in people with Neoplasms as compared to genotypes AA + AG.

CDA rs2072671: Allele C is not associated with metabolism of capecitabine in people with Breast Neoplasms as compared to allele A.

CES2 rs11075646: Allele C is not associated with metabolism of capecitabine in people with Breast Neoplasms as compared to allele G.

DPYD rs1801159: Allele C is not associated with metabolism of capecitabine in people with Breast Neoplasms as compared to allele T.

Response (62 findings)

Studies of how well it worked in people carrying a variant.

AREG rs11942466: Genotypes AA + AC is associated with decreased response to capecitabine and radiotherapy in people with Rectal Neoplasms as compared to genotype CC.

CDA rs2072671: Genotypes AA + AC is associated with decreased response to capecitabine in women with Breast Neoplasms as compared to genotype CC.

CDA rs532545: Genotype CC is associated with decreased response to capecitabine in women with Breast Neoplasms as compared to genotypes CT + TT.

CYP1A1 rs1048943: Genotypes AG + GG are associated with increased response to capecitabine and docetaxel in women with Breast Neoplasms as compared to genotype AA.

Dosing (15 findings)

Studies of how much of the drug people needed or tolerated.

DPYD rs3918290: Genotype CT is associated with dose of capecitabine or fluorouracil in people with Colorectal Neoplasms as compared to genotype CC.

DPYD rs3918290: Genotype CT is associated with decreased dose of capecitabine in people with Colorectal Neoplasms as compared to genotype CC.

DPYD rs56038477: Genotype CT is associated with dose of capecitabine or fluorouracil in people with Colorectal Neoplasms as compared to genotype CC.

DPYD rs67376798: Genotype AT is associated with dose of capecitabine or fluorouracil in people with Colorectal Neoplasms as compared to genotype TT.

Side effects (2 findings)

Studies of side effects in people carrying a variant.

TYMS rs183205964: Allele C is associated with increased discontinuation of capecitabine, fluorouracil or tegafur in people with Neoplasms as compared to allele G.

DPYD rs3918290: Genotype CT is associated with decreased dose of capecitabine.

Study findings and evidence levels: PharmGKB (CC BY-SA 4.0). Guidelines: CPIC and DPWG, as bundled in PharmCAT. Most studies were done mainly in people of European ancestry.

Related Drugs

More drugs from the same category

5-FU (Antimetabolites)

Alimta (Antimetabolites)

Cytosar-U (Antimetabolites)

Not a prescribing recommendation. This page is educational information about pharmacogenomic research and clinical guidelines - it is not medical or dosing advice, and not a prediction of how any medication will work for you. Never start, stop, or change a medication or dose based on it; talk to your doctor or pharmacist, who can order clinical-grade testing if appropriate.

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Content updated September 2026.

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