Oxaliplatin (3 months v 6 months) With 6 Months of Fluoropyrimidine as Adjuvant Therapy in Patients With Stage II/III Colon Cancer: KCSG CO09-07

Author:

Kim Seung Tae1ORCID,Kim Sun Young23ORCID,Lee Jeeyun1ORCID,Yun Seong Hyeon1ORCID,Kim Hee Cheol1,Lee Woo Yong1,Kim Tae Won2ORCID,Hong Yong Sang2ORCID,Lim Seok-Byung2ORCID,Baek Ji Yeon3ORCID,Oh Jae Hwan3,Ahn Joong Bae4,Shin Sang Joon4,Han Sae-Won5ORCID,Kim Seong Geun6ORCID,Kang Seok Yun7,Sym Sun Jin8ORCID,Zang Dae Young9,Kim Yeul Hong10,Choi In Sil11,Kang Jung Hun12,Kim Min-Ji13ORCID,Park Young Suk1ORCID

Affiliation:

1. Sungkyunkwan University School of Medicine, Samsung Medical Centre, Seoul, South Korea

2. Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea

3. Center for Colorectal Cancer, Research Institute and Hospital, National Cancer Center, Goyang, Korea

4. Yonsei University College of Medicine, Seoul, Korea

5. Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea

6. Good Gangan Hospital Cancer Center, Pusan, South Korea

7. Ajou University School of Medicine, Suwon, South Korea

8. Gachon University Gil Hospital, Incheon, Korea

9. Hallym University Medical Center, Hallym University, Anyang, Korea, South Korea

10. Korea University Anam Hospital, Korea University College of Medicine, Seoul, Korea

11. Seoul Metropolitan Government Seoul National University Boramae Medical Center, Seoul, Korea

12. Gyeongsang National University, Jinju, Korea

13. Statistics and Data Center, Research Institute for Future Medicine, Samsung Medical Center, Seoul, South Korea

Abstract

PURPOSE The combination of oxaliplatin and fluoropyrimidine for 6 months is one of the standard options for adjuvant therapy for high-risk stage II and III colorectal cancers (CRCs). The optimal duration of oxaliplatin to diminish neurotoxicity without compromising efficacy needs to be clarified. PATIENTS AND METHODS This open-label, randomized, phase III, noninferiority trial randomly assigned patients with high-risk stage II and III CRC to 3 and 6 months of oxaliplatin with 6 months of fluoropyrimidine groups (3- and 6-month arms, respectively). The primary end point was disease-free survival (DFS), and the noninferiority margin was a hazard ratio (HR) of 1.25. RESULTS In total, 1,788 patients were randomly assigned to the 6-month (n = 895) and 3-month (n = 893) arms, and 83.6% in the 6-month arm and 85.7% in the 3-month arm completed the treatment. The neuropathy rates with any grade were higher in the 6-month arm than in the 3-month arm (69.5% v 58.3%; P < .0001). The 3-year DFS rates were 83.7% and 84.7% in the 6-month and 3-month arms, respectively, with an HR of 0.953 (95% CI, 0.769 to 1.180; test for noninferiority, P = .0065) within the noninferiority margin. Among patients with stage III CRC treated by capecitabine plus oxaliplatin, the 3-year DFS of the 3-month arm was noninferior as compared with that of the 6-month arm with an HR of 0.713 (95% CI, 0.530 to 0.959; P = .0009). However, among patients with high-risk stage II and stage III CRC treated by infusional fluorouracil, leucovorin, and oxaliplatin, the noninferiority of the 3-month arm compared with the 6-month arm was not proven. CONCLUSION This study suggests that adding 3 months of oxaliplatin to 6 months of capecitabine could be considered an alternative adjuvant treatment for stage III CRC (ClinicalTrials.gov identifier: NCT01092481 ).

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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