A phase I-II study of gemcitabine and paclitaxel in advanced non-small-cell lung cancer patients. Academic Article uri icon

Overview

abstract

  • Thirty patients with chemotherapy-naïve advanced non-small-cell lung cancer (NSCLC) were given escalating doses of paclitaxel (150, 175, 200 mg/m2) on day 1 in three consecutive cycles, together with a fixed dose of gemcitabine 1000 mg/m2 on days 1 and 8; cycles were repeated every three weeks. The dose escalation of paclitaxel was feasible in the majority of patients. Subsequently, 30 other NSCLC patients received a dose of 200 mg/m2 paclitaxel with gemcitabine 1000 mg/m2 in a phase II study. The major side effect was mild myelosuppression. A response rate of 24% was achieved in 49 fully evaluable patients. This regimen proved to be safe and easy to administer on an out-patient setting, and constitutes now one of the arms of the current EORTC randomized study for advanced NSCLC.

publication date

  • January 1, 2000

Research

keywords

  • Antineoplastic Combined Chemotherapy Protocols
  • Carcinoma, Non-Small-Cell Lung
  • Deoxycytidine
  • Lung Neoplasms
  • Paclitaxel

Identity

Scopus Document Identifier

  • 0033952737

PubMed ID

  • 10690398

Additional Document Info

volume

  • 11

issue

  • 1