首页> 美国卫生研究院文献>Gastroenterology Research and Practice >Does the Addition of Cetuximab to Radiochemotherapy Improve Outcome of Patients with Locally Advanced Rectal Cancer? Long-Term Results from Phase II Trials
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Does the Addition of Cetuximab to Radiochemotherapy Improve Outcome of Patients with Locally Advanced Rectal Cancer? Long-Term Results from Phase II Trials

机译:西妥昔单抗在放化疗中的应用是否会改善局部晚期直肠癌患者的治疗效果?第二阶段试验的长期结果

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摘要

Purpose. The addition of cetuximab to radiochemotherapy (RCT) failed to improve complete response rates in locally advanced rectal cancer (LARC). We report the long-term results in patients treated within two sequential clinical trials. Methods. Patients receiving neoadjuvant RCT using capecitabine and irinotecan (CapIri) within a phase I/II trial or CapIri + cetuximab within a phase II trial were evaluated for analysis of disease-free survival (DFS) and overall survival (OS). KRAS exon 2 mutational status had been analyzed in patients receiving cetuximab. Results. 37 patients from the CapIri trial and 49 patients from the CapIri-cetuximab treatment group were evaluable. Median follow-up time was 75.2 months. The 5-year DFS rate was 82% (CapIri) and 79% (CapIri-cetuximab) (P = 0.62). The median OS was 127.4 months. 5-year OS was 73% for both groups (CapIri and CapIri-cetuximab) (P = 0.61). No significant difference in DFS (P = 0.86) or OS (P = 0.39) was noticed between patients receiving CapIri and those receiving CapIri-cetuximab with KRAS wild-type tumors. Conclusions. As the addition of cetuximab did not improve neither DFS nor OS it should not play a role in the perioperative treatment of patients with LARC, not even of patients with (K)RAS WT tumors.
机译:目的。将西妥昔单抗加入放化疗(RCT)无法提高局部晚期直肠癌(LARC)的完全缓解率。我们报告了在两个连续临床试验中治疗的患者的长期结果。方法。在I / II期试验中使用卡培他滨和伊立替康(CapIri)或在II期试验中使用CapIri +西妥昔单抗接受新辅助RCT的患者进行了无病生存期(DFS)和总体生存期(OS)分析。已对接受西妥昔单抗的患者的KRAS外显子2突变状态进行了分析。结果。来自CapIri试验的37名患者和来自CapIri-西妥昔单抗治疗组的49名患者是可评估的。中位随访时间为75.2个月。 5年DFS率为82%(CapIri)和79%(CapIri-西妥昔单抗)(P = 0.62)。中位操作系统为127.4个月。两组(CapIri和CapIri-西妥昔单抗)的5年OS为73%(P = 0.61)。在接受CapIri的患者和接受CapIri-头孢西昔单抗治疗的KRAS野生型患者之间,DFS(P = 0.86)或OS(P = 0.39)没有显着差异。结论。由于西妥昔单抗的添加不能改善DFS和OS,因此不应在LARC患者的围手术期治疗中发挥作用,甚至(K)RAS WT肿瘤患者也不应如此。

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