| Literature DB >> 21775070 |
Stuart J Wong1, Kathryn Winter, Neal J Meropol, Pramila Rani Anne, Lisa Kachnic, Asif Rashid, James C Watson, Edith Mitchell, Jondavid Pollock, Robert Jeffrey Lee, Michael Haddock, Beth A Erickson, Christopher G Willett.
Abstract
PURPOSE: To evaluate the rate of pathologic complete response (pCR) and the toxicity of two neoadjuvant chemoradiotherapy (chemoRT) regimens for Stage T3-T4 rectal cancer in a randomized Phase II study. METHODS AND MATERIALS: Patients with Stage T3 or T4 rectal cancer of <12 cm from the anal verge were randomized to preoperative RT (50.4 Gy in 1.8-Gy fractions) with concurrent capecitabine (1,200 mg/m(2)/d Mondays through Friday) and irinotecan (50 mg/m(2) weekly in four doses) (Arm 1) or concurrent capecitabine (1,650 mg/m(2)/d Monday through Friday) and oxaliplatin (50 mg/m(2) weekly in five doses) (Arm 2). Surgery was performed 4-8 weeks after chemoRT, and adjuvant chemotherapy 4-6 weeks after surgery. The primary endpoint was the pCR rate, requiring 48 evaluable patients per arm.Entities:
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Year: 2011 PMID: 21775070 PMCID: PMC3208721 DOI: 10.1016/j.ijrobp.2011.05.027
Source DB: PubMed Journal: Int J Radiat Oncol Biol Phys ISSN: 0360-3016 Impact factor: 7.038