Calle Profesor Beltran Báguena no 9.,Valencia, Spain 46009.
J Clin Oncol. 2010 Feb 10;28(5):859-65. doi: 10.1200/JCO.2009.25.8541. Epub 2010 Jan 11.
PURPOSE The optimal therapeutic sequence of the adjuvant chemotherapy component of preoperative chemoradiotherapy (CRT) for patients with locally advanced rectal cancer is controversial. Induction chemotherapy before preoperative CRT may be associated with better efficacy and compliance. PATIENTS AND METHODS A total of 108 patients with locally advanced rectal cancer were randomly assigned to arm A-preoperative CRT with capecitabine, oxaliplatin, and concurrent radiation followed by surgery and four cycles of postoperative adjuvant capecitabine and oxaliplatin (CAPOX)-or arm B-induction CAPOX followed by CRT and surgery. The primary end point was pathologic complete response rate (pCR). Results On an intention-to-treat basis, the pCR for arms A and B were 13.5% (95% CI, 5.6% to 25.8%) and 14.3% (95% CI, 6.4% to 26.2%), respectively. There were no statistically significant differences in other end points, including downstaging, tumor regression, and R0 resection. Overall, chemotherapy treatment exposure was higher in arm B than in arm A for both oxaliplatin (P < .0001) and capecitabine (P < .0001). During CRT, grades 3 to 4 adverse events were similar in both arms but were significantly higher in arm A during postoperative adjuvant CT than with induction CT in arm B. There were three deaths in each arm during the treatment period. CONCLUSION Compared with postoperative adjuvant CAPOX, induction CAPOX before CRT had similar pCR and complete resection rates. It did achieve more favorable compliance and toxicity profiles. On the basis of these findings, a phase III study to definitively test the induction strategy is warranted.
目的 术前放化疗(CRT)辅助化疗部分的最佳治疗顺序在局部进展期直肠癌患者中仍存在争议。术前 CRT 前进行诱导化疗可能与更好的疗效和依从性相关。 患者和方法 共 108 例局部进展期直肠癌患者被随机分配至 A 组(术前 CRT 采用卡培他滨、奥沙利铂和同期放疗,随后手术和术后辅助卡培他滨和奥沙利铂(CAPOX)4 个周期)或 B 组(诱导 CAPOX 后 CRT 和手术)。主要终点为病理完全缓解率(pCR)。 结果 意向治疗分析中,A 组和 B 组的 pCR 分别为 13.5%(95%CI,5.6%至 25.8%)和 14.3%(95%CI,6.4%至 26.2%)。其他终点,包括降期、肿瘤退缩和 R0 切除,两组之间无统计学差异。总体而言,B 组奥沙利铂(P<0.0001)和卡培他滨(P<0.0001)的化疗暴露均高于 A 组。在 CRT 期间,两组 3 级和 4 级不良事件相似,但 A 组在术后辅助 CT 期间显著高于 B 组在诱导 CT 期间。在治疗期间,每组各有 3 例死亡。 结论 与术后辅助 CAPOX 相比,术前 CRT 前诱导 CAPOX 具有相似的 pCR 和完全切除率。它确实实现了更有利的依从性和毒性特征。基于这些发现,有必要进行 III 期研究来明确验证诱导策略。
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