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

被引:5
作者
Chibaudel, Benoist [1 ]
Raeisi, Morteza [2 ]
Cohen, Romain [3 ,4 ]
Yothers, Greg [5 ]
Goldberg, Richard M. [6 ]
Bachet, Jean-Baptiste [7 ]
Wolmark, Norman [8 ]
Yoshino, Takayuki [9 ]
Schmoll, Hans-Joachim [10 ]
Kerr, Rachel [11 ]
Lonardi, Sara [12 ]
George, Thomas J. [13 ]
Shacham-Shmueli, Einat [14 ]
Shi, Qian [15 ]
Andre, Thierry [3 ,4 ,16 ]
de Gramont, Aimery [16 ,17 ]
机构
[1] Franco British Hosp, Franco British Hosp, Dept Med Oncol, Cancerol Paris Ouest, Levallois Perret, France
[2] ARCAD Fdn, Stat Unit, Paris, France
[3] Sorbonne Univ, Paris, France
[4] St Antoine Hosp, Dept Med Oncol, Paris, France
[5] Univ Pittsburgh, Dept Biostat, Pittsburgh, PA USA
[6] West Virginia Univ, Dept Med, Canc Inst, Morgantown, WV USA
[7] Sorbonne Univ, Pitie Salpetriere Hosp, AP HP, Hepatogastroenterol & Digest Oncol Dept, Paris, France
[8] NSABP Fdn, Pittsburgh, PA USA
[9] Natl Canc Ctr Hosp East, Dept Gastroenterol & Gastrointestinal Oncol, Kashiwa, Japan
[10] Martin Luther Univ Halle Wittenberg, Div Clin Res Oncol, Halle An Der Saale, Germany
[11] UCL, London, England
[12] Veneto Inst Oncol IOV IRCCS, Med Oncol, Padua, Italy
[13] Univ Florida, Div Hematol & Oncol, Gainesville, FL USA
[14] Mayo Clin, Dept Quantitat Hlth Sci, Rochester, MN USA
[15] Mayo Clin, Dept Quantitat Hlth Sci, Amiens, MN, France
[16] CRPV, Paris, France
[17] Franco British Hosp, Dept Med Oncol, Levallois Perret, France
关键词
END-POINT; FLUOROURACIL; DURATION; LEUCOVORIN; SURVIVAL; THERAPY; GUIDELINES; ACID;
D O I
10.1200/JCO.24.00394
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PURPOSEThe 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 METHODSOne 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.RESULTSIn 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).CONCLUSIONNo 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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页数:16
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