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Journal of Clinical Oncology, Vol 22, No 21 (November 1), 2004: pp. 4329-4340 © 2004 American Society of Clinical Oncology. DOI: 10.1200/JCO.2004.02.165 Carboplatin/Paclitaxel or Carboplatin/Vinorelbine Followed by Accelerated Hyperfractionated Conformal Radiation Therapy: Report of a Prospective Phase I Dose Escalation Trial From the Carolina Conformal Therapy ConsortiumFrom the Departments of Radiation Oncology, Medical Oncology, and Biostatistics and Bioinformatics, Duke University Medical Center, Durham; Multidisciplinary Thoracic Oncology Program, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill; Radiation Oncology, Sibley Hospital, WADC; Wake Forest University, Winston-Salem, NC; Medical University of South Carolina, Charleston, SC Address reprint requests to Lawrence B. Marks, MD, Department of Radiation Oncology, Box 3085 Duke University Medical Center, Durham, NC 27710; e-mail: marks{at}radonc.duke.edu PURPOSE: To prospectively determine the maximum-tolerated dose of accelerated hyperfractionated conformal radiotherapy (RT; 1.6 Gy bid) for unresectable locally advanced lung cancer (IIB to IIIA/B) following induction carboplatin/paclitaxel (C/T) or carboplatin/vinorelbine (C/N). METHODS: Induction chemotherapy, C/T or C/N, was followed by escalating doses of conformally-planned RT (73.6 to 86.4 Gy in 6.4-Gy increments). Concurrent boost methods delivered 1.6 and 1.25 Gy bid to the gross and clinical target volumes, respectively.
RESULTS: Between November 1997 and February 2002, 44 patients were enrolled (median age, 59 years; 59% male; stage III, 98%; median tumor size, 4 cm). Thirty-nine patients completed induction chemotherapy: 19 had a partial response, seven progressed, 15 had no response, and three were not assessable. Chemotherapy-associated toxicities were similar in the two chemotherapy groups. The incidence of grade CONCLUSION: High-dose conformal twice-daily radiation therapy to approximately 80 Gy appears tolerable in well-selected patients with unresectable lung cancer following either C/T or C/N. Dose-limiting toxicities are mainly pulmonary and esophageal. Presented at the 2001 meeting of the American Society for Therapeutic Radiology and Oncology, San Francisco, CA, November 4-8, 2001. Authors' disclosures of potential conflicts of interest are found at the end of this article.
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Copyright © 2004 by the American Society of Clinical Oncology, Online ISSN: 1527-7755. Print ISSN: 0732-183X
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