Assessment of the Addition of Oxaliplatin to Fluoropyrimidine-Based Adjuvant Chemotherapy in Patients With High-Risk Stage II Colon Cancer: An ACCENT Pooled Analysis.

IF 42.1 1区 医学 Q1 ONCOLOGY Journal of Clinical Oncology Pub Date : 2024-09-04 DOI:10.1200/JCO.24.00394
Benoist Chibaudel, Morteza Raeisi, Romain Cohen, Greg Yothers, Richard M Goldberg, Jean-Baptiste Bachet, Norman Wolmark, Takayuki Yoshino, Hans-Joachim Schmoll, Rachel Kerr, Sara Lonardi, Thomas J George, Einat Shacham-Shmueli, Qian Shi, Thierry André, Aimery de Gramont
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Abstract

Purpose: 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.

Patients and methods: 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.

Results: 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; P = .813) and 0.82 for stage III (95% CI, 0.73 to 0.92; P = .001; Pint = .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; P = .349).

Conclusion: 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.

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高风险 II 期结肠癌患者在氟嘧啶辅助化疗基础上加用奥沙利铂的评估:ACCENT 汇总分析
目的:III期结肠癌(CC)的辅助治疗是氟嘧啶(FP)和奥沙利铂(OX)联合化疗。FP方案加OX(FPOX)可能对高风险的II期CC有益。我们对评估FPOX治疗高危II期CC的关键性MOSAIC和C-07研究进行了汇总分析,根据预后因素、高危因素数量以及当前临床病理学风险分类(基于T分期、肿瘤穿孔和检查淋巴结数量)进行了分析:对接受 FP 或 FPOX 治疗的 1595 例 II 期 CC 患者进行了汇总。采用Kaplan-Meier曲线和未经调整的Cox模型分析了OX的总生存率(OS)。359例III期CC患者仅用于所分配化疗与分期之间的交互检验:在对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/梗阻和肿瘤侧位。分期与所分配化疗的OS之间存在明显的交互作用,II期患者的危险比(HRs)为1.03(95% CI,0.82至1.29;P = .813),III期患者的危险比(HRs)为0.82(95% CI,0.73至0.92;P = .001;Pint = .073)。就任何预后因素而言,在 FP 的基础上加用 OX 均无益处。检测的高危因素数量并不能预测 OX 的益处。根据目前商定的临床病理学风险分类,OX对OS没有益处,HR为0.86(95% CI,0.63至1.18;P = .349):结论:在高风险II期CC中,无论采用哪种定义来描述肿瘤的高复发风险,都未发现OX辅助治疗对OS有益处。因此,我们的分析表明,OX不应作为II期CC辅助化疗的标准治疗方案,即使是高危患者也是如此。
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来源期刊
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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