AI Article Synopsis

  • A phase II study evaluated the effectiveness of induction chemotherapy (paclitaxel and carboplatin) followed by concurrent radiation therapy and additional chemotherapy in 32 patients with stage III non-small cell lung cancer.
  • The median survival time for patients was 16.9 months, with 25% surviving 5 years and 17.5% surviving 10 years, while disease progression occurred after a median of 9.5 months.
  • Toxicity levels were generally acceptable, with minimal severe side effects reported (3.1% grade 5 toxicity and 1 patient with grade 4 leucopenia).

Article Abstract

Introduction: Long-term results of a phase II study on the use of induction chemotherapy (CHT) using paclitaxel (P)-carboplatin (C) followed by a concurrent radiation therapy (RT) and weekly P and consolidation PC were reviewed.

Patients And Methods: Thirty-two patients with stage III non-small cell lung cancer started treatment with induction CHT (two cycles of P 175 mg/m, day 1 and C, area under the curve 6, day 1, given at 3-week interval), after which accelerated RT with a concomitant boost ("field-in-a-field") (1.8 Gy large fields and the boost dose 0.88 Gy) was administered in 23 fractions with 61.64 Gy and concurrent weekly P (45 mg/m). Consolidation with two cycles of PC was administered.

Results: The median follow-up for all 32 patients was 17.2 months (range, 3.8-107 months). The median survival time was 16.9 months, and the 5-year survival and 10-year survival were 25% and 17.5%, respectively. The median time for disease progression was 9.5 months, and disease-free survival was 21% at 5 and 10 years. The median time to local progression was 14.6 months, and the 5- to 10-year local progression-free survival was 35.7%. The median time to distant metastasis was 17.5 months. Toxicity was acceptable, with only one (3.1%) patient experiencing grade 5 (lung) toxicity and another patient presenting grade 4 toxicity (leucopenia).

Conclusions: The results of this single-institutional phase II study of induction CHT followed by concurrent RT-CHT and consolidation CHT in very unfavorable patient population showed acceptable results with acceptable toxicity.

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Source
http://dx.doi.org/10.1097/JTO.0b013e318200e563DOI Listing

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