Seminars in Oncology
Volume 30, Issue 1 , Pages 26-37, February 2003

Thoracic radiotherapy for limited-stage small cell lung cancer: Issues of timing, volumes, dose, and fractionation

Departments of Radiation Oncology and Medicine, University of British Columbia, British Columbia Cancer Agency, Vancouver, Canada

Abstract 

Although meta-analysis of randomized trials comparing chemotherapy alone versus chemotherapy plus thoracic irradiation demonstrated that thoracic radiotherapy reduced mortality by 14%, this analysis probably underestimates the effect of optimally delivered thoracic irradiation integrated with appropriate chemotherapy. However, there remains much debate as to the optimal timing of the radiotherapy and the radiotherapy volume, dose, and fractionation. Theoretically, early use of radiotherapy should reduce the probability of chemotherapy and radiation resistance, accelerated repopulation, and metastatic events. Deferred or sequential radiotherapy potentially allows smaller radiotherapy fields. Of the seven randomized controlled trials examining timing, only those with early chemoradiation have 5-year survival rates in excess of 20%. The “chemoradiation package” can be defined as the time from the start of chemotherapy until the completion of radiotherapy. The best median survival and long-term survival rates have been observed in trials with a chemoradiation package time of less than 6 weeks. Protocols combining chemotherapy and radiotherapy must respect radiobiologic principles concerning the time factor derived from radiotherapy fractionation studies. Semin Oncol 30:26-37. Copyright 2003, Elsevier Science (USA). All rights reserved.

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 Address reprint requests to Nevin Murray, MD, FRCPC, Clinical Professor of Medicine, University of British Columbia, British Columbia Cancer Agency, 600 W 10th Ave, Vancouver, BC, Canada V5Z 4E6.

PII: S0093-7754(03)70040-2

doi:10.1053/sonc.2003.50017

Seminars in Oncology
Volume 30, Issue 1 , Pages 26-37, February 2003