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Treatment of resistant non-Hodgkin's lymphomas with cisplatin, etoposide, and bleomycin. | LitMetric

Treatment of resistant non-Hodgkin's lymphomas with cisplatin, etoposide, and bleomycin.

Cancer Chemother Pharmacol

1st Division of Medical Oncology, National Tumor Institute, Naples, Italy.

Published: August 1990

AI Article Synopsis

  • A study tested a PEB chemotherapy regimen (cisplatin, etoposide, and bleomycin) on 23 patients with hard-to-treat non-Hodgkin's lymphomas, specifically those who had not responded well to previous treatments.
  • The treatment resulted in 4 complete remissions and 4 partial responses, giving an overall response rate of 35%, indicating some effectiveness, but many patients did not respond.
  • The most common side effect was vomiting, experienced by all patients, while moderate hematologic toxicity was noted but resolved after treatment cycles, suggesting some tolerance to the therapy in patients who had relapsed rather than those who were refractory.

Article Abstract

A combination of cisplatin (60 mg/m2 i.v. on day 1), etoposide (100 mg/m2 i.v. on days 1-3) and bleomycin (15 mg i.v. on days 1 and 8) (PEB regimen) was given every 4 weeks as salvage therapy in 10 refractory and 13 relapsing patients with poor-prognosis non-Hodgkin's lymphomas. All but one of these patients had previously been treated with anthracycline-containing combination chemotherapy. We observed 4 complete remissions (CRs) and 4 partial responses (PRs), whereas 3 patients showed only a minor response (MR) and 12 were considered to be induction failures. Therefore, the objective (CR + PR) response rate was 35%. The most frequent side effect was vomiting, registered in all patients despite antiemetic treatment. Hematologic toxicity was of moderate degree, and bone marrow recovery was observed after almost all cycles after a 3-week rest period. Since objective responses were achieved only in relapsing patients, the PEB regimen seemed to be effective in these cases, whereas it was useless in early refractory non-Hodgkin's lymphomas.

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Source
http://dx.doi.org/10.1007/BF02897236DOI Listing

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