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Author Notes:

Correspondence: Mitchell Machtay, M.D., University Hospital at Case Western Reserve University, 11000 Euclid Avenue, Cleveland, OH 44106. Tel: (216) 844-2530; Fax: (216) 844-4799; E-mail: Mitchell.machtay@uhhospitals.org

There is no conflict of interest for any of the authors.

Subject:

Research Funding:

This paper is supported by RTOG U10 CA21661 and CCOP U10 CA37422 grants from the NCI.

This paper's contents are the sole responsibility of the authors and do not necessarily represent the official views of the NCI

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Oncology
  • Radiology, Nuclear Medicine & Medical Imaging
  • Radiation oncology
  • Advanced non-small-cell lung carcinoma
  • Chemoradiotherapy
  • Local-regional failure
  • Survival with respect to radiotherapy dose intensity
  • LEUKEMIA GROUP-B
  • PHASE-III TRIAL
  • HYPERFRACTIONATED RADIATION
  • CONCURRENT CHEMORADIATION
  • INDUCTION CHEMOTHERAPY
  • CONSOLIDATION DOCETAXEL
  • THORACIC RADIOTHERAPY
  • COMPETING RISK
  • FOLLOW-UP
  • CANCER

HIGHER BIOLOGICALLY EFFECTIVE DOSE OF RADIOTHERAPY IS ASSOCIATED WITH IMPROVED OUTCOMES FOR LOCALLY ADVANCED NON-SMALL CELL LUNG CARCINOMA TREATED WITH CHEMORADIATION: AN ANALYSIS OF THE RADIATION THERAPY ONCOLOGY GROUP

Tools:

Journal Title:

International Journal of Radiation Oncology - Biology - Physics

Volume:

Volume 82, Number 1

Publisher:

, Pages 425-434

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Purpose: Patients treated with chemoradiotherapy for locally advanced non-small-cell lung carcinoma (LA-NSCLC) were analyzed for local-regional failure (LRF) and overall survival (OS) with respect to radiotherapy dose intensity. Methods and Materials: This study combined data from seven Radiation Therapy Oncology Group (RTOG) trials in which chemoradiotherapy was used for LA-NSCLC: RTOG 88-08 (chemoradiation arm only), 90-15, 91-06, 92-04, 93-09 (nonoperative arm only), 94-10, and 98-01. The radiotherapeutic biologically effective dose (BED) received by each individual patient was calculated, as was the overall treatment time-adjusted BED (tBED) using standard formulae. Heterogeneity testing was done with chi-squared statistics, and weighted pooled hazard ratio estimates were used. Cox and Fine and Gray's proportional hazard models were used for OS and LRF, respectively, to test the associations between BED and tBED adjusted for other covariates. Results: A total of 1,356 patients were analyzed for BED (1,348 for tBED). The 2-year and 5-year OS rates were 38% and 15%, respectively. The 2-year and 5-year LRF rates were 46% and 52%, respectively. The BED (and tBED) were highly significantly associated with both OS and LRF, with or without adjustment for other covariates on multivariate analysis (p < 0.0001). A 1-Gy BED increase in radiotherapy dose intensity was statistically significantly associated with approximately 4% relative improvement in survival; this is another way of expressing the finding that the pool-adjusted hazard ratio for survival as a function of BED was 0.96. Similarly, a 1-Gy tBED increase in radiotherapy dose intensity was statistically significantly associated with approximately 3% relative improvement in local-regional control; this is another way of expressing the finding that the pool-adjusted hazard ratio as a function of tBED was 0.97. Conclusions: Higher radiotherapy dose intensity is associated with improved local-regional control and survival in the setting of chemoradiotherapy.

Copyright information:

© 2012 Elsevier Inc. Printed in the USA. All rights reserved.

This is an Open Access work distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (http://creativecommons.org/licenses/by-nc-nd/4.0/).

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