Grothey Axel, Sobrero Alberto F, Shields Anthony F, Yoshino Takayuki, Paul James, Taieb Julien, Souglakos John, Shi Qian, Kerr Rachel, Labianca Roberto, Meyerhardt Jeffrey A, Vernerey Dewi, Yamanaka Takeharu, Boukovinas Ioannis, Meyers Jeffrey P, Renfro Lindsay A, Niedzwiecki Donna, Watanabe Toshiaki, Torri Valter, Saunders Mark, Sargent Daniel J, Andre Thierry, Iveson Timothy
From the Divisions of Medical Oncology (A.G.) and Biomedical Statistics and Informatics (Q.S., J.P.M., L.A.R., D.J.S.), Mayo Clinic, Rochester, MN; Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS) San Martino-IST, Genoa (A.F. Sobrero), Ospedale Papa Giovanni XXIII, Bergamo (R.L.), and IRCCS Mario Negri Institute for Pharmacological Research, Milan (V.T.) - all in Italy; Karmanos Cancer Institute, Wayne State University, Detroit (A.F. Shields); National Cancer Center Hospital East, Chiba (T. Yoshino), Yokohama City University School of Medicine, Yokohama (T. Yamanaka), and the University of Tokyo, Tokyo (T.W.) - all in Japan; the Institute of Cancer Sciences, University of Glasgow, Glasgow (J.P.), the University of Oxford, Oxford (R.K.), Christie Hospital, Manchester (M.S.), and University Hospital Southampton, Southampton (T.I.) - all in the United Kingdom; Hôpital Européen Georges-Pompidou, Sorbonne Paris Cite/Paris Descartes University (J.T.), and Saint-Antoine Hospital and Sorbonne Universités, Pierre and Marie Curie University-Paris 6 (T.A.), Paris, and Methodology and Quality of Life Unit, INSERM Unité 1098, Besançon (D.V.) - all in France; the Department of Medical Oncology, University Hospital of Heraklion, Faculty of Medicine, University of Crete, Heraklion (J.S.), and Bioclinic Thessaloniki, Thessaloniki (I.B.) - both in Greece; Dana-Farber Cancer Institute, Boston (J.A.M.); and Duke Cancer Institute, Durham, NC (D.N.).
N Engl J Med. 2018 Mar 29;378(13):1177-1188. doi: 10.1056/NEJMoa1713709.
Since 2004, a regimen of 6 months of treatment with oxaliplatin plus a fluoropyrimidine has been standard adjuvant therapy in patients with stage III colon cancer. However, since oxaliplatin is associated with cumulative neurotoxicity, a shorter duration of therapy could spare toxic effects and health expenditures.
We performed a prospective, preplanned, pooled analysis of six randomized, phase 3 trials that were conducted concurrently to evaluate the noninferiority of adjuvant therapy with either FOLFOX (fluorouracil, leucovorin, and oxaliplatin) or CAPOX (capecitabine and oxaliplatin) administered for 3 months, as compared with 6 months. The primary end point was the rate of disease-free survival at 3 years. Noninferiority of 3 months versus 6 months of therapy could be claimed if the upper limit of the two-sided 95% confidence interval of the hazard ratio did not exceed 1.12.
After 3263 events of disease recurrence or death had been reported in 12,834 patients, the noninferiority of 3 months of treatment versus 6 months was not confirmed in the overall study population (hazard ratio, 1.07; 95% confidence interval [CI], 1.00 to 1.15). Noninferiority of the shorter regimen was seen for CAPOX (hazard ratio, 0.95; 95% CI, 0.85 to 1.06) but not for FOLFOX (hazard ratio, 1.16; 95% CI, 1.06 to 1.26). In an exploratory analysis of the combined regimens, among the patients with T1, T2, or T3 and N1 cancers, 3 months of therapy was noninferior to 6 months, with a 3-year rate of disease-free survival of 83.1% and 83.3%, respectively (hazard ratio, 1.01; 95% CI, 0.90 to 1.12). Among patients with cancers that were classified as T4, N2, or both, the disease-free survival rate for a 6-month duration of therapy was superior to that for a 3-month duration (64.4% vs. 62.7%) for the combined treatments (hazard ratio, 1.12; 95% CI, 1.03 to 1.23; P=0.01 for superiority).
Among patients with stage III colon cancer receiving adjuvant therapy with FOLFOX or CAPOX, noninferiority of 3 months of therapy, as compared with 6 months, was not confirmed in the overall population. However, in patients treated with CAPOX, 3 months of therapy was as effective as 6 months, particularly in the lower-risk subgroup. (Funded by the National Cancer Institute and others.).
自2004年以来,奥沙利铂联合氟嘧啶进行6个月治疗一直是III期结肠癌患者的标准辅助治疗方案。然而,由于奥沙利铂会导致累积神经毒性,缩短治疗疗程可以避免毒性作用并节省医疗费用。
我们对六项同时进行的随机3期试验进行了前瞻性、预先计划的汇总分析,以评估与6个月治疗相比,给予FOLFOX(氟尿嘧啶、亚叶酸钙和奥沙利铂)或CAPOX(卡培他滨和奥沙利铂)3个月辅助治疗的非劣效性。主要终点是3年无病生存率。如果风险比的双侧95%置信区间上限不超过1.12,则可认为3个月治疗与6个月治疗具有非劣效性。
在12834例患者中报告了3263例疾病复发或死亡事件后,在总体研究人群中未证实3个月治疗与6个月治疗具有非劣效性(风险比,1.07;95%置信区间[CI],1.00至1.15)。对于CAPOX方案,较短疗程具有非劣效性(风险比,0.95;95%CI,0.85至1.06),但FOLFOX方案则不然(风险比,1.16;95%CI,1.06至1.26)。在联合方案的探索性分析中,在T1、T2或T3且N1期癌症患者中,3个月治疗与6个月治疗效果相当,3年无病生存率分别为83.1%和83.3%(风险比,1.01;95%CI,0.90至1.12)。在T4、N2期或两者皆有的癌症患者中,联合治疗6个月疗程的无病生存率优于3个月疗程(64.4%对62.7%)(风险比,1.12;95%CI,1.03至1.23;优越性检验P=0.01)。
在接受FOLFOX或CAPOX辅助治疗的III期结肠癌患者中,总体人群中未证实3个月治疗与6个月治疗具有非劣效性。然而,在接受CAPOX治疗的患者中,3个月治疗与6个月治疗效果相当,尤其是在低风险亚组中。(由美国国立癌症研究所等资助。)