Literature DB >> 455324

Adriamycin cardiotoxicity: a survey of 1273 patients.

C Praga, G Beretta, P L Vigo, G R Lenaz, C Pollini, G Bonadonna, R Canetta, R Castellani, E Villa, C G Gallagher, H von Melchner, M Hayat, P Ribaud, G De Wasch, W Mattsson, R Heinz, R Waldner, K Kolaric, R Buehner, W Ten Bokkel-Huyninck, N I Perevodchikova, L A Manziuk, H J Senn, A C Mayr.   

Abstract

Valuable information was collected on the medical history and clinical course of 1273 patients entered in clinical trials with Adriamycin (ADR) carried out in 12 European cancer centers. A coded patient form was used for the data collection carried out in each center by a qualified physician following a guideline which was discussed and accepted by all of the participants. The aim of the study was to define the incidence, characteristics, and possible co-factors of the cardiomyopathy (CMP) in patients treated with combination chemotherapy regimens including ADR. The mean total dose of ADR was 268 mg/m2 (range, 15--1251 mg/m2), and 5.1% of the patients received a total dose of greater than 550 mg/m2. A "definite" ADR-related CMP was observed in 1.7% of the cases; another 3% of the cases were reported as "possible" ADR-CMP since the role played by the drug could not be clearly defined. "Definite" ADR-CMP was fatal in eight patients (0.6%) while "possible" ADR-CMP was fatal in 13 patients (1.0%). Among the possible co-factors examined, the following ones were found to be significantly associated with the occurrence of a "definite" ADR-CMP: (a) total dose of ADR; (b) vincristine when given both before and concomitantly with ADR; (c) bleomycin when given before ADR; and (d) radiotherapy to the mediastinum when given concomitantly with ADR. Furthermore, none of 182 patients receiving ADR by slow infusion developed a "definite" ADR-CMP, while 2% of the patients treated by bolus injection did so. The occurrence of a "possible" ADR-CMP was found to be significantly associated with two pre-existing pathologic conditions (electrocardiogram [ECG] abnormalities and hypertension) but not with the treatment-related co-factors for the "definite" ADR-CMP mentioned above. Other variables examined, such as sex, age, cancer type, baseline liver function, and cyclophosphamide treatment, did not seem to influence the risk of ADR-CMP. Data on ECG changes occurring during ADR treatment were also reported and their incidence was found to be strictly related to the frequency of the ECG monitoring.

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Year:  1979        PMID: 455324

Source DB:  PubMed          Journal:  Cancer Treat Rep        ISSN: 0361-5960


  49 in total

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4.  Age and left ventricular ejection fraction identify patients with advanced breast cancer at high risk for development of epirubicin-induced heart failure.

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5.  Hemodynamic effects of chronic 4'epi-adriamycin administration.

Authors:  J Milei; J J Ale; G Garay; F Otero; A Z Comba; H O Gugliotta; R A Storino
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6.  Early mitoxantrone-induced cardiotoxicity in secondary progressive multiple sclerosis.

Authors:  F Paul; J Dörr; J Würfel; H-P Vogel; F Zipp
Journal:  BMJ Case Rep       Date:  2009-07-07

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8.  Modulation of adriamycin-induced changes in serum free fatty acids, albumin and cardiac oxidative stress.

Authors:  N Iliskovic; T Li; N Khaper; V Palace; P K Singal
Journal:  Mol Cell Biochem       Date:  1998-11       Impact factor: 3.396

9.  Anticancer Chemotherapy and it's Anaesthetic Implications (Current Concepts).

Authors:  R P Gehdoo
Journal:  Indian J Anaesth       Date:  2009-02

10.  Multiple impairments of cutaneous nociceptor function induced by cardiotoxic doses of Adriamycin in the rat.

Authors:  Krisztina Boros; Gábor Jancsó; Mária Dux; Zoltán Fekécs; Péter Bencsik; Orsolya Oszlács; Márta Katona; Péter Ferdinandy; Antal Nógrádi; Péter Sántha
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2016-06-24       Impact factor: 3.000

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