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March 1, 1991American Journal of Hematology35 citations

Severe and fatal anthracycline cardiotoxicity at cumulative doses below 400 mg/m2: Evidence for enhanced toxicity with multiagent chemotherapy

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RWRaymond G. Watts

Structured PICO

Does multiagent chemotherapy enhance anthracycline cardiotoxicity at cumulative doses below 400 mg/m2 in patients with extremity sarcomas?

P
Population
3 patients with extremity sarcomas
I
Intervention
Multiagent chemotherapy consisting of doxorubicin, high-dose methotrexate, bleomycin, cyclophosphamide, dactinomycin, and cisplatinum with cumulative anthracycline doses less than 400 mg/m2
O
Outcome
Severe, progressive cardiomyopathy and congestive heart failuresafety

Multiagent chemotherapy may enhance anthracycline cardiotoxicity, causing severe cardiomyopathy at cumulative doses previously considered safe (<400 mg/m2).

Abstract

Three cases of severe, progressive, and in two cases, fetal cardiomyopathy secondary to anthracycline chemotherapy are reported. All of the patients were receiving multiagent chemotherapy for extremity sarcomas consisting of doxorubicin, high-dose methotrexate, bleomycin, cyclophosphamide, dactinomycin, and cisplatinum at the onset of their congestive heart failure. Cardiomyopathy developed in each patient at cumulative anthracycline doses less than 400 mg/m2. These cases suggest that enhanced cardiotoxicity may occur when anthracyclines are used in combination with other agents such as cyclophosphamide, bleomycin, cisplatinum, and methotrexate and that cumulative anthracycline doses considered to be "safe" may need to be lowered in these circumstances.

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Cite This Study

Raymond G. Watts (1991) studied this question.

synapsesocial.com/papers/6a838534030d4352c5167764https://doi.org/10.1002/ajh.2830360314
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