Addition of verapamil and tamoxifen to the initial chemotherapy of small cell lung cancer a phase I/II study

A. Figueredo, A. Arnold, M. Goodyear, B. Findlay, A. Neville, R. Normandeau, A. Jones

Producción científica: Contribución a una revistaArtículorevisión exhaustiva

44 Citas (Scopus)

Resumen

Based on experimental observations that verapamil and tamoxifen reverse multiple drug resistance, the authors investigated the feasibility of combining both agents with the initial chemotherapy of extensive small cell lung cancer. Overall, in a consecutive series of 58 patients the most important toxicity was myelosuppression, and there was a 24% rate of severe infections. Therapeutic results included 24% complete and 34% partial response rates, median time to disease progression of 32 weeks, and median survival of 46 weeks. In three consecutive cohorts of patients the dose of either tamoxifen or verapamil were escalated by 25% and 33%, respectively. The cohort of patients receiving verapamil 360 mg/day and tamoxifen 100 mg/day (level 2) had slightly more toxicity but also more responses than the other groups. Therefore, the authors recommend that these doses be used in controlled trials to confirm the promising results of their study.

Idioma originalEnglish
Páginas (desde-hasta)1895-1902
Número de páginas8
PublicaciónCancer
Volumen65
N.º9
DOI
EstadoPublished - may. 1 1990
Publicado de forma externa

ASJC Scopus Subject Areas

  • Oncology
  • Cancer Research

PubMed: MeSH publication types

  • Journal Article

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