Radiation Therapy Oncology Group 0247: a randomized Phase II study of neoadjuvant capecitabine and irinotecan or capecitabine and oxaliplatin with concurrent radiotherapy for patients with locally advanced rectal cancer

Stuart J Wong, 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, Stuart J Wong, 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.

Results: A total of 146 patients were enrolled. The protocol chemotherapy was modified because of excessive gastrointestinal toxicity after treatment of 35 patients; 96 were assessed for the primary endpoint-the final regimen described above. The patient characteristics were similar for both arms. After chemoRT, the rate of tumor downstaging was 52% and 60% and the rate of nodal downstaging (excluding N0 patients) was 46% and 40%, for Arms 1 and 2, respectively. The pCR rate for Arm 1 was 10% and for Arm 2 was 21%. For Arm 1 and 2, the preoperative chemoRT rate of Grade 3-4 hematologic toxicity was 9% and 4% and the rate of Grade 3-4 nonhematologic toxicity was 26% and 27%, respectively.

Conclusions: Preoperative chemoRT with capecitabine plus oxaliplatin for distal rectal cancer has significant clinical activity (10 of 48 pCRs) and acceptable toxicity. This regimen is currently being evaluated in a Phase III randomized trial (National Surgical Adjuvant Breast and Bowel Project R04).

Conflict of interest statement

Conflict of Interest Notification: Do not exist.

Copyright © 2012 Elsevier Inc. All rights reserved.

Figures

Figure 1
Figure 1
Schema for Radiation Therapy Oncology Group 0247 phase II study.
Figure 2
Figure 2
CONSORT patient flow diagram.

Source: PubMed

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