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

被引:13
|
作者
Kim, Seung Tae [1 ]
Kim, Sun Young [2 ,3 ]
Lee, Jeeyun [1 ]
Yun, Seong Hyeon [1 ]
Kim, Hee Cheol [1 ]
Lee, Woo Yong [1 ]
Kim, Tae Won [2 ]
Hong, Yong Sang [2 ]
Lim, Seok-Byung [2 ]
Baek, Ji Yeon [3 ]
Oh, Jae Hwan [3 ]
Ahn, Joong Bae [4 ]
Shin, Sang Joon [4 ]
Han, Sae-Won [5 ]
Kim, Seong Geun [6 ]
Kang, Seok Yun [7 ]
Sym, Sun Jin [8 ]
Zang, Dae Young [9 ]
Kim, Yeul Hong [10 ]
Choi, In Sil [11 ]
Kang, Jung Hun [12 ]
Kim, Min-Ji [13 ]
Park, Young Suk [1 ]
机构
[1] Sungkyunkwan Univ, Samsung Med Ctr, Sch Med, Seoul, South Korea
[2] Univ Ulsan, Asan Med Ctr, Coll Med, Seoul, South Korea
[3] Natl Canc Ctr, Ctr Colorectal Canc, Res Inst & Hosp, Goyang, South Korea
[4] Yonsei Univ, Coll Med, Seoul, South Korea
[5] Seoul Natl Univ, Seoul Natl Univ Hosp, Coll Med, Seoul, South Korea
[6] Good Gangan Hosp Canc Ctr, Pusan, South Korea
[7] Ajou Univ, Sch Med, Suwon, South Korea
[8] Gachon Univ, Gil Hosp, Incheon, South Korea
[9] Hallym Univ, Med Ctr, Anyang, South Korea
[10] Korea Univ, Anam Hosp, Coll Med, Seoul, South Korea
[11] Seoul Metropolitan Govt Seoul Natl Univ Boramae M, Seoul, South Korea
[12] Gyeongsang Natl Univ, Jinju, South Korea
[13] Samsung Med Ctr, Stat & Data Ctr, Res Inst Future Med, Seoul, South Korea
关键词
WEEKLY BOLUS FLUOROURACIL; PHASE-III TRIAL; COLORECTAL-CANCER; CHEMOTHERAPY; LEUCOVORIN; DURATION; SURVIVAL; EFFICACY; SAFETY;
D O I
10.1200/JCO.21.02962
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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: ). (C) 2022 by American Society of Clinical Oncology
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页码:3868 / +
页数:13
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