George Shenouda1, Qiang Zhang2, K Kian Ang3, Mitchell Machtay4, Matthew B Parliament5, Diane Hershock6, Mohan Suntharalingam7, Alexander Lin6, Marvin Rotman8, Abdenour Nabid9, Susan Hong10, Sarwat Shehata11, Anthony J Cmelak12, Khalil Sultanem13, Quynh-Thu Le14. 1. McGill University, Montreal, Quebec, Canada. Electronic address: George.shenouda@muhc.mcgill.ca. 2. NRG Oncology Statistics and Data Management Center. 3. University of Texas MD Anderson Cancer Center, Houston, Texas. 4. University Hospitals of Cleveland, Cleveland, Ohio. 5. Cross Cancer Institute, Edmonton, Alberta, Canada. 6. University of Pennsylvania Medical Center, Philadelphia, Pennsylvania. 7. University of Maryland Medical System, Baltimore, Maryland. 8. Brooklyn Minority-based Community Clinical Oncology Program, State University of New York Downstate Medical Center, Brooklyn, New York. 9. Centre Hospitalier Universitaire de Sherbrooke, Sherbrooke (Québec), Québec, Canada. 10. Akron City Hospital, Akron, Ohio. 11. Northeastern Ontario Regional Cancer Centre, Sudbury, Ontario, Canada. 12. Vanderbilt University Medical Center, Nashville, Tennessee. 13. McGill University, Montreal, Quebec, Canada. 14. Stanford University Medical Center, Stanford, California.
Abstract
PURPOSE: This paper reports long-term results of RTOG 9903, to determine whether the addition of erythropoietin (EPO) would improve the outcomes of radiation therapy (RT) in mildly to moderately anemic patients with head and neck squamous cell carcinoma (HNSCCa). METHODS AND MATERIALS: The trial included HNSCCa patients treated with definitive RT. Patients with stage III or IV disease receivedconcomitant chemoradiation therapy or accelerated fractionation. Pretreatment hemoglobin levels were required to be between 9.0 and 13.5 g/dL (12.5 g/dL for females). EPO, 40,000 U, was administered weekly starting 7 to 10 days before RT was initiated in the RT + EPO arm. RESULTS:A total of 141 of 148 enrolled patients were evaluable. The baseline median hemoglobin level was 12.1 g/dL. In the RT + EPO arm, the mean hemoglobin level at 4 weeks increased by 1.66 g/dL, whereas it decreased by 0.24 g/dL in the RT arm. With a median follow-up of 7.95 years (range: 1.66-10.08 years) for surviving patients and 3.33 years for all patients (range: 0.03-10.08 years), the 5-year estimate of local-regional failure was 46.2% versus 39.4% (P=.42), local-regional progression-free survival was 31.5% versus 37.6% (P=.20), and overall survival was 36.9% versus 38.2% (P=.54) for the RT + EPO and RT arms, respectively. Late toxicity was not different between the 2 arms. CONCLUSIONS: This long-term analysis confirmed that despite the ability of EPO to raise hemoglobin levels in anemic patients with HNSCCa, it did not improve outcomes when added to RT. The possibility of a detrimental effect of EPO could not be ruled out.
RCT Entities:
PURPOSE: This paper reports long-term results of RTOG 9903, to determine whether the addition of erythropoietin (EPO) would improve the outcomes of radiation therapy (RT) in mildly to moderately anemicpatients with head and neck squamous cell carcinoma (HNSCCa). METHODS AND MATERIALS: The trial included HNSCCa patients treated with definitive RT. Patients with stage III or IV disease received concomitant chemoradiation therapy or accelerated fractionation. Pretreatment hemoglobin levels were required to be between 9.0 and 13.5 g/dL (12.5 g/dL for females). EPO, 40,000 U, was administered weekly starting 7 to 10 days before RT was initiated in the RT + EPO arm. RESULTS: A total of 141 of 148 enrolled patients were evaluable. The baseline median hemoglobin level was 12.1 g/dL. In the RT + EPO arm, the mean hemoglobin level at 4 weeks increased by 1.66 g/dL, whereas it decreased by 0.24 g/dL in the RT arm. With a median follow-up of 7.95 years (range: 1.66-10.08 years) for surviving patients and 3.33 years for all patients (range: 0.03-10.08 years), the 5-year estimate of local-regional failure was 46.2% versus 39.4% (P=.42), local-regional progression-free survival was 31.5% versus 37.6% (P=.20), and overall survival was 36.9% versus 38.2% (P=.54) for the RT + EPO and RT arms, respectively. Late toxicity was not different between the 2 arms. CONCLUSIONS: This long-term analysis confirmed that despite the ability of EPO to raise hemoglobin levels in anemicpatients with HNSCCa, it did not improve outcomes when added to RT. The possibility of a detrimental effect of EPO could not be ruled out.
Authors: Mitchell Machtay; Thomas F Pajak; Mohan Suntharalingam; George Shenouda; Diane Hershock; Diana C Stripp; Anthony J Cmelak; Alan Schulsinger; Karen K Fu Journal: Int J Radiat Oncol Biol Phys Date: 2007-08-23 Impact factor: 7.038
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Authors: Carole Fakhry; Qiang Zhang; Phuc Felix Nguyen-Tân; David I Rosenthal; Randal S Weber; Louise Lambert; Andy M Trotti; William L Barrett; Wade L Thorstad; Christopher U Jones; Sue S Yom; Stuart J Wong; John A Ridge; Shyam S D Rao; James A Bonner; Eric Vigneault; David Raben; Mahesh R Kudrimoti; Jonathan Harris; Quynh-Thu Le; Maura L Gillison Journal: J Clin Oncol Date: 2017-08-04 Impact factor: 44.544