Chibaudel Benoist, Raeisi Morteza, Cohen Romain, Yothers Greg, Goldberg Richard M, Bachet Jean-Baptiste, Wolmark Norman, Yoshino Takayuki, Schmoll Hans-Joachim, Kerr Rachel, Lonardi Sara, George Thomas J, Shacham-Shmueli Einat, Shi Qian, André Thierry, de Gramont Aimery
Department of Medical Oncology, Franco-British Hospital, Fondation Cognacq-Jay, Cancérologie Paris Ouest, Levallois-Perret, France.
Statistical Unit, ARCAD Foundation, Paris, France.
J Clin Oncol. 2024 Dec 10;42(35):4187-4195. doi: 10.1200/JCO.24.00394. Epub 2024 Sep 4.
The adjuvant treatment for stage III colon cancer (CC) is chemotherapy combining fluoropyrimidine (FP) and oxaliplatin (OX). FP regimen plus OX (FPOX) may benefit in high-risk stage II CC. We performed a pooled analysis of pivotal MOSAIC and C-07 studies evaluating FPOX for the treatment of high-risk stage II CC according to prognostic factors, number of high-risk factors, and current clinicopathologic risk classification on the basis of T stage, tumor perforation, and number of lymph nodes examined.
One thousand five hundred and ninety-five patients with stage II CC receiving FP or FPOX were pooled. The overall survival (OS) benefit of OX was analyzed using Kaplan-Meier curves and unadjusted Cox models stratified by study. Three thousand and fifty-nine patients with stage III CC were used only for interaction tests between the allocated chemotherapy and stage.
In the pooled analysis of stage II patients, independent prognostic factors in multivariable analysis were sex, age, perforation/obstruction, and tumor sidedness. There was a significant interaction in OS between stage and allocated chemotherapy with hazard ratios (HRs) of 1.03 for stage II (95% CI, 0.82 to 1.29; = .813) and 0.82 for stage III (95% CI, 0.73 to 0.92; = .001; = .073). There was no benefit from the addition of OX to FP for any of the prognostic factors. The number of high-risk factors tested was not predictive of OX benefit. According to the currently agreed clinicopathologic risk classification, no OS benefit of OX was observed, as HR was 0.86 (95% CI, 0.63 to 1.18; = .349).
No OS benefit of adjuvant OX was found in high-risk stage II CC, regardless of the definition used to characterize tumors as having a high risk for recurrence. Hence, our analysis suggests that OX should not be the standard of care for adjuvant chemotherapy for stage II CC, even in high-risk patients.
III期结肠癌(CC)的辅助治疗是氟嘧啶(FP)与奥沙利铂(OX)联合化疗。FP方案加OX(FPOX)可能对高危II期CC有益。我们根据预后因素、高危因素数量以及基于T分期、肿瘤穿孔和检查的淋巴结数量的当前临床病理风险分类,对评估FPOX治疗高危II期CC的关键MOSAIC和C-07研究进行了汇总分析。
汇总了1595例接受FP或FPOX治疗的II期CC患者。使用Kaplan-Meier曲线和按研究分层的未调整Cox模型分析OX的总生存(OS)获益情况。3059例III期CC患者仅用于分配的化疗与分期之间的交互检验。
在II期患者的汇总分析中,多变量分析中的独立预后因素为性别、年龄、穿孔/梗阻和肿瘤部位。分期与分配的化疗在OS方面存在显著交互作用,II期的风险比(HR)为1.03(95%CI,0.82至1.29;P = 0.813),III期为0.82(95%CI,0.73至0.92;P = 0.001;交互P = 0.073)。对于任何预后因素,在FP基础上加用OX均无获益。所检测的高危因素数量不能预测OX的获益情况。根据目前公认的临床病理风险分类,未观察到OX对OS有获益,HR为0.86(95%CI,0.63至1.18;P = 0.349)。
在高危II期CC中,无论用于将肿瘤表征为具有高复发风险的定义如何,均未发现辅助性OX有OS获益。因此,我们的分析表明,即使在高危患者中,OX也不应作为II期CC辅助化疗的标准治疗方案。