Bleomycin, actinomycin-D, and cisplatin treatment of ovarian germ-cell malignancies contributes to reducing adverse drug reactions.

  • Authors:
    • T Sumi
    • O Ishiko
    • H Yoshida
    • S Ogita
  • View Affiliations

  • Published online on: November 1, 2000     https://doi.org/10.3892/or.7.6.1235
  • Pages: 1235-1243
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Abstract

Sixteen ovarian germ-cell malignancy (OGCM) patients between 1983 and 1999 were randomly divided into the BEP group (n=6; bleomycin, etoposide and cisplatin) and the BAP group (n=10; bleomycin, actinomycin-D and cisplatin). The patients were evaluated for adverse drug reactions (ADRs) based on severity-grading of the National Cancer Institute Common Toxicity Criteria. The ADRs in the BAP group were milder than in the BEP group, as seen in regard to alopecia (p=0.0126), low hemoglobin (p=0.0147), and decreased neutrophil count (p=0.0197). The five-year survival rate was 87.5% in the BAP group and 83.3% in the BEP group, and the difference was not significant (p=0.5954). BAP therapy is likely to be more beneficial for OGCM patients than BEP therapy, because ADRs are reduced with no difference in outcome.

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Nov-Dec 2000
Volume 7 Issue 6

Print ISSN: 1021-335X
Online ISSN:1791-2431

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Spandidos Publications style
Sumi T, Ishiko O, Yoshida H and Ogita S: Bleomycin, actinomycin-D, and cisplatin treatment of ovarian germ-cell malignancies contributes to reducing adverse drug reactions.. Oncol Rep 7: 1235-1243, 2000
APA
Sumi, T., Ishiko, O., Yoshida, H., & Ogita, S. (2000). Bleomycin, actinomycin-D, and cisplatin treatment of ovarian germ-cell malignancies contributes to reducing adverse drug reactions.. Oncology Reports, 7, 1235-1243. https://doi.org/10.3892/or.7.6.1235
MLA
Sumi, T., Ishiko, O., Yoshida, H., Ogita, S."Bleomycin, actinomycin-D, and cisplatin treatment of ovarian germ-cell malignancies contributes to reducing adverse drug reactions.". Oncology Reports 7.6 (2000): 1235-1243.
Chicago
Sumi, T., Ishiko, O., Yoshida, H., Ogita, S."Bleomycin, actinomycin-D, and cisplatin treatment of ovarian germ-cell malignancies contributes to reducing adverse drug reactions.". Oncology Reports 7, no. 6 (2000): 1235-1243. https://doi.org/10.3892/or.7.6.1235