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Anthracyclines (class)

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

About Anthracyclines

What it is

Anthracyclines are a class of chemotherapy medicines, first isolated from Streptomyces bacteria, that slip between DNA strands and block topoisomerase II. The class includes doxorubicin, daunorubicin, epirubicin and idarubicin, with the related mitoxantrone, used for breast cancer, leukaemias, lymphomas and sarcomas. Damage to the heart muscle limits the total amount a person can receive. This page collects studies on the class as a group.

How genes come into it

Most gene studies on the class concern heart damage, mainly in children treated for cancer: SLC28A3 (rs7853758 is linked to lower risk), RARG and UGT1A6 have the strongest findings, and CBR1 and CBR3, which form cardiotoxic breakdown products, have also been studied. A RARG variant has been proposed for screening in children, but no CPIC or DPWG guideline exists.

What research found

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

Rated evidence (30 rated variants)

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

SLC28A3 rs7853758: Level 2B · replicated. Toxicity: Cardiotoxicity. 5.

RARG rs2229774: Level 3. Toxicity: Cardiotoxicity, Neoplasms. 7.

SLC28A3 rs885004: Level 3. Toxicity: Neoplasms. 2.

CBR3 rs1056892: Level 3. Toxicity: Heart Failure, Neoplasms. 2.

Response (12 findings)

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

GSTM1 GSTM1 non-null, GSTM1 null: GSTM1 null is associated with decreased response to anthracyclines and related substances, capecitabine, cyclophosphamide, fluorouracil and taxanes in women with Breast Neoplasms as compared to GSTM1 non-null.

GSTP1 rs1695: Allele A is associated with increased response to anthracyclines and related substances in women with Breast Neoplasms as compared to allele G.

rs833058: Allele T is not associated with response to anthracyclines and related substances, bevacizumab, cyclophosphamide, docetaxel, epirubicin and taxanes in women with Breast Neoplasms as compared to allele C.

EGLN3 rs1629140: Allele A is not associated with response to anthracyclines and related substances, bevacizumab, cyclophosphamide, docetaxel, epirubicin and taxanes in women with Breast Neoplasms as compared to allele G.

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

Adriamycin (Anthracyclines)

Cerubidine (Anthracyclines)

Ellence (Anthracyclines)

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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