TY - JOUR
T1 - Comparison of acute toxicities in two primary chemoradiation regimens in the treatment of advanced head and neck squamous cell carcinoma
AU - Fan, Katherine Y.
AU - Gogineni, Hrishikesh
AU - Zaboli, David
AU - Lake, Spencer
AU - Zahurak, Marianna L.
AU - Best, Simon R.
AU - Levine, Marshall A.
AU - Tang, Mei
AU - Zinreich, Eva S.
AU - Saunders, John R.
AU - Califano, Joseph A.
AU - Blanco, Ray G.
AU - Pai, Sara I.
AU - Messing, Barbara
AU - Ha, Patrick K.
PY - 2012/6
Y1 - 2012/6
N2 - Purpose. The optimal dosage and frequency of platinumbased chemoradiotherapy (CRT) regimen for treating advanced head and neck squamous cell carcinoma remains unresolved. This study aims to compare the toxicity and efficacy of weekly versus more dose-intensive cisplatinbased CRTs. Methods. We reviewed 155 stage III/IV head and neck squamous cell carcinoma patients with no evidence of distant metastasis treated with one of two CRT regimens from 2000 to 2010 at Greater Baltimore Medical Center. Twicedaily radiation was provided as a split course over a 45-day period. Regimen A consisted of concomitant cisplatin (30 mg/m 2/1 h) weekly for 6 cycles; regimen B consisted of concomitant cisplatin (12 mg/m2/1 h) and 5-fluorouracil (600 mg/m 2/20 h) on days 1 through 5 and days 29 through 33. Main outcome measures included acute toxicities (myelosuppression, neurotoxicity, nephrotoxicity, gastrointestinal dysfunction), unplanned hospitalizations, and disease control at 12 months. Results. Patients on regimen A were much less likely to experience ototoxicity due to their treatment (0% vs. 9.8%, P = 0.04). They were more likely to experience thrombocytopenia acutely (46% vs. 26%, P = 0.02), but the toxicity was not limiting (grade 1-2). No significant differences exist in the incidence of other toxicities or unplanned hospitalizations. At 1 year, 97% of patients on A vs. 86% of patients on regimen B were free of disease (P = 0.11). Conclusions. With concurrent radiotherapy, low-dose, single-agent, weekly cisplatin is less likely than higherdose daily cisplatin plus 5-fluorouracil provided at the beginning and end of treatment to be associated with ototoxicity. The preliminary data suggest at least equivalent efficacy, but longer follow-up is required.
AB - Purpose. The optimal dosage and frequency of platinumbased chemoradiotherapy (CRT) regimen for treating advanced head and neck squamous cell carcinoma remains unresolved. This study aims to compare the toxicity and efficacy of weekly versus more dose-intensive cisplatinbased CRTs. Methods. We reviewed 155 stage III/IV head and neck squamous cell carcinoma patients with no evidence of distant metastasis treated with one of two CRT regimens from 2000 to 2010 at Greater Baltimore Medical Center. Twicedaily radiation was provided as a split course over a 45-day period. Regimen A consisted of concomitant cisplatin (30 mg/m 2/1 h) weekly for 6 cycles; regimen B consisted of concomitant cisplatin (12 mg/m2/1 h) and 5-fluorouracil (600 mg/m 2/20 h) on days 1 through 5 and days 29 through 33. Main outcome measures included acute toxicities (myelosuppression, neurotoxicity, nephrotoxicity, gastrointestinal dysfunction), unplanned hospitalizations, and disease control at 12 months. Results. Patients on regimen A were much less likely to experience ototoxicity due to their treatment (0% vs. 9.8%, P = 0.04). They were more likely to experience thrombocytopenia acutely (46% vs. 26%, P = 0.02), but the toxicity was not limiting (grade 1-2). No significant differences exist in the incidence of other toxicities or unplanned hospitalizations. At 1 year, 97% of patients on A vs. 86% of patients on regimen B were free of disease (P = 0.11). Conclusions. With concurrent radiotherapy, low-dose, single-agent, weekly cisplatin is less likely than higherdose daily cisplatin plus 5-fluorouracil provided at the beginning and end of treatment to be associated with ototoxicity. The preliminary data suggest at least equivalent efficacy, but longer follow-up is required.
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U2 - 10.1245/s10434-012-2219-4
DO - 10.1245/s10434-012-2219-4
M3 - Article
C2 - 22290566
AN - SCOPUS:84865126485
SN - 1068-9265
VL - 19
SP - 1980
EP - 1987
JO - Annals of Surgical Oncology
JF - Annals of Surgical Oncology
IS - 6
ER -