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drugsProductApproved1974🇪🇺🇬🇧🇯🇵🇨🇳🇦🇺

Doxorubicin

The red chemotherapy drug from a soil bacterium that is still the backbone of treatment for sarcoma, lymphoma and breast cancer, limited by cumulative heart damage.

Approved 1974. Backbone of AIM/doxorubicin-ifosfamide (sarcoma), CHOP/R-CHOP (lymphoma), ABVD/AVD (Hodgkin), AC/EC (breast), and MAP (osteosarcoma). Cumulative cardiotoxicity above ~400-450 mg/m2 limits use; dexrazoxane and liposomal formulations mitigate. Also the payload of early ADC attempts.

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Doxorubicin
PubChem
Mechanism, step by step
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1.Intercalates between DNA base pairs

Modality
Cytotoxic chemotherapy (anthracycline)
Mechanism
Topoisomerase II poisoning and DNA intercalation with free-radical generation; cardiotoxicity via topoisomerase IIβ in cardiomyocytes.
Brand / code
Adriamycin
Dosing & schedule
Route
IV
Schedule
75 mg/m2 every 3 weeks (sarcoma, single agent or with ifosfamide); 50 mg/m2 in CHOP; 25 mg/m2 days 1, 15 in ABVD
Dose modifications
Lifetime cumulative limit ~450 mg/m2 (lower with chest RT); hepatic dose reduction
Monitoring
Baseline and serial echocardiography or MUGA; counts; extravasation precautions
Medicare
Part B (clinician-administered)

Given by infusion or injection in a clinic or hospital outpatient department, so it is a Part B drug: Medicare pays 80% after the Part B deductible and the patient owes 20% coinsurance, uncapped in Original Medicare unless a Medigap policy applies. Generic.

Commercial insurance
covered on label

Multi-source generic; covered under the medical benefit without prior authorisation in most plans, as part of standard regimens.

Sources: Medicare.gov: Chemotherapy · Medicare.gov: Prescription drugs (outpatient, Part B). Not medical or financial advice; verify with your plan.

Not appraisedSearch NICE
Notes
Long-established generic: never subject to a technology appraisal; funded routinely through hospital formularies and NHS England systemic anti-cancer therapy protocols.
NHS England
Routinely funded for the appraised indication (or via managed access)

Sources: NICE search: doxorubicin. Funding decisions are indication-specific and change monthly; verify with NICE and your treating team.

Regulatory

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Approvals

RegionYearIndication
US1974Broad: sarcomas, lymphomas, leukaemias, breast, and other solid tumours

Safety

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Toxicity profile
Adverse eventAny gradeGrade 3+
Neutropenia
single-agent 75 mg/m2 (ANNOUNCE control arm)
60%
Cardiomyopathy (cumulative)
at 400 mg/m2; rises steeply above 550 mg/m2
5%
Alopecia
90%
Nausea/vomiting
60%

Events listed without rates were not read from a primary source; see the label. Blank cells mean the figure was not sourced, not that it is zero.

Cost & access

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Cost & access
CountryReimbursement
United Statesgeneric

List prices are manufacturer or Medicare figures where publicly disclosed; net prices after rebates are usually lower. Reimbursement changes; check the payer.

Trials

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Recruiting now (live from ClinicalTrials.gov)

Recruiting trials near you · live from ClinicalTrials.gov
Doxorubicin
intervention: Doxorubicin
Open on ClinicalTrials.gov →

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Key papers

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rctNew England Journal of Medicine 2024changed practice
SWOG S1826: nivolumab plus AVD chemotherapy versus brentuximab-AVD for advanced Hodgkin lymphoma in adolescents and adults

S1826 moved checkpoint blockade into first-line Hodgkin lymphoma and made N-AVD a preferred regimen for advanced disease in patients from adolescence to older age, while removing radiotherapy for most. It also showed the value of a single trial spanning paediatric and adult groups. Longer follow-up is needed for overall survival and late immune effects in young patients.

rctNew England Journal of Medicine 2022changed practice
POLARIX: swapping vincristine for the antibody-drug conjugate polatuzumab vedotin in first-line treatment of diffuse large B-cell lymphoma

POLARIX gave the first new first-line standard for DLBCL since rituximab was added to CHOP, and pola-R-CHP is now approved and widely used, especially in higher-risk or ABC-type disease. The gain is modest and survival is unchanged, so many clinicians still use R-CHOP in lower-risk or GCB-type patients. Cost and subgroup uncertainty drive ongoing debate.

rctNew England Journal of Medicine 2018changed practice
ECHELON-1: brentuximab vedotin replacing bleomycin in first-line chemotherapy for advanced Hodgkin lymphoma

ECHELON-1 made a targeted antibody-drug conjugate part of first-line Hodgkin therapy and eventually showed that this saves lives, not just relapses. It set the reference arm against which nivolumab-AVD (SWOG S1826) and BrECADD (HD21) were later compared. Neuropathy is the main price and needs proactive dose modification.

Latest papers

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Literature trend3,263 papers in the last 12 months0% vs prior 12How this is computed
Latest papers · live from Europe PMC
Open in Europe PMC

Query for this drug: (TITLE:"Doxorubicin" OR ABSTRACT:"Doxorubicin" OR TITLE:"Adriamycin" OR ABSTRACT:"Adriamycin") AND (cancer OR tumor OR tumour OR oncology OR carcinoma OR lymphoma OR leukemia OR leukaemia OR myeloma OR sarcoma OR melanoma OR glioma). Results are unfiltered search hits about Doxorubicin, not a curated reading list.

Connected

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