Does the Multidrug-Resistance Modulator Cyclosporin a Increase the Cardiotoxicity of High-Dose Anthracycline Chemotherapy?

Authors

  • Ernst G. Eising Clinic and Policlinic for Nuclear Medicine, West German Tumor Center, University of Essen, Germany
  • Pascal Gries Clinic and Policlinic for Nuclear Medicine, West German Tumor Center, University of Essen, Germany
  • Jochen Eggert Department of Internal Medicine (Cancer Research), West German Tumor Center, University of Essen, Germany
  • Max E. Scheulen Department of Internal Medicine (Cancer Research), West German Tumor Center, University of Essen, Germany

DOI:

https://doi.org/10.3109/02841869709001347

Abstract

Cyclosporin A has heterogeneous effects on anthracycline-related cardiotoxicity and can prevent multidrug-resistance (MDR). The aim of this study was to explore whether the coadministration of cyclosporin A is accompanied by an increase in cardiotoxicity. Forty-three patients (27 male, 16 female, age: 18–67 yrs (mean: 47.5 yrs, SD: 11.6 yrs)) received 177 radionuclide ventriculography examinations (RNV/177 at rest, 133 at stress) before and during chemotherapy with either doxorubicin (n = 23) or epirubicin (n = 20). RNV studies were applied up to 11 times in the follow-up of the patients. A maximum of 10 courses of chemotherapy was performed. In the doxorubicin group only, the age of the patients and the cumulative dose of the chemotherapeutic agent had a significant negative impact on left ventricular ejection fractions, whereas cyclosporin A had a significant positive influence (multiple analysis of regression, p < 0.05). Cyclosporin A did not cause any significant increase in cardiotoxicity in our patients.

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Published

1997-01-01

How to Cite

Eising, E. G. ., Gries, P. ., Eggert, J. ., & Scheulen, M. E. . (1997). Does the Multidrug-Resistance Modulator Cyclosporin a Increase the Cardiotoxicity of High-Dose Anthracycline Chemotherapy?. Acta Oncologica, 36(7), 735–740. https://doi.org/10.3109/02841869709001347