Phase II, Randomized Study of Concomitant Chemoradiotherapy Followed by Surgery and Adjuvant Capecitabine Plus Oxaliplatin (CAPOX) Compared With Induction CAPOX Followed by Concomitant Chemoradiotherapy and Surgery in Magnetic Resonance Imaging–Defined, Locally Advanced Rectal Cancer: Grupo Cáncer de Recto 3 Study

Author:

Fernández-Martos Carlos1,Pericay Carles1,Aparicio Jorge1,Salud Antonieta1,Safont MariaJose1,Massuti Bertomeu1,Vera Ruth1,Escudero Pilar1,Maurel Joan1,Marcuello Eugenio1,Mengual Jose Luis1,Saigi Eugenio1,Estevan Rafael1,Mira Moises1,Polo Sonia1,Hernandez Ana1,Gallen Manuel1,Arias Fernando1,Serra Javier1,Alonso Vicente1

Affiliation:

1. From the Fundacion Instituto Valenciano de Oncología; Hospital General Univeristario; and Hospital Universitario La Fe, Valencia; Corporación Sanitaria Parc Taulí, Sabadell; Hospital Arnau de Vilanova, Lerida; Hospital General, Alicante; Hospital de Navarra, Pamplona; Hospital Clinico Lozano Blesa, Zaragoza; Hospital Clinic; Hospital del Mar Barcelona; and Hospital Santa Creu y Sant Pau, Barcelona; and Clinica Quiron; and Hospital Miguel Servet, Zaragoza, Spain.

Abstract

Purpose The optimal therapeutic sequence of the adjuvant chemotherapy component of preoperative chemoradiotherapy (CRT) for patients with locally advanced rectal cancer is controversial. Induction chemotherapy before preoperative CRT may be associated with better efficacy and compliance. Patients and Methods A total of 108 patients with locally advanced rectal cancer were randomly assigned to arm A—preoperative CRT with capecitabine, oxaliplatin, and concurrent radiation followed by surgery and four cycles of postoperative adjuvant capecitabine and oxaliplatin (CAPOX)—or arm B—induction CAPOX followed by CRT and surgery. The primary end point was pathologic complete response rate (pCR). Results On an intention-to-treat basis, the pCR for arms A and B were 13.5% (95% CI, 5.6% to 25.8%) and 14.3% (95% CI, 6.4% to 26.2%), respectively. There were no statistically significant differences in other end points, including downstaging, tumor regression, and R0 resection. Overall, chemotherapy treatment exposure was higher in arm B than in arm A for both oxaliplatin (P < .0001) and capecitabine (P < .0001). During CRT, grades 3 to 4 adverse events were similar in both arms but were significantly higher in arm A during postoperative adjuvant CT than with induction CT in arm B. There were three deaths in each arm during the treatment period. Conclusion Compared with postoperative adjuvant CAPOX, induction CAPOX before CRT had similar pCR and complete resection rates. It did achieve more favorable compliance and toxicity profiles. On the basis of these findings, a phase III study to definitively test the induction strategy is warranted.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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