III. Medizinische Klinik, Universitätsmedizin Mannheim, Universität Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167 Mannheim, Germany.
Chirurgische Klinik, Universitätsmedizin Mannheim, Universität Heidelberg, Theodor-Kutzer-Ufer 1-3, 68167 Mannheim, Germany.
Gastroenterol Res Pract. 2015;2015:273489. doi: 10.1155/2015/273489. Epub 2015 Mar 15.
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.
西妥昔单抗联合放化疗(RCT)未能提高局部晚期直肠癌(LARC)的完全缓解率。我们报告了在两项连续临床试验中治疗的患者的长期结果。
在 I/II 期试验中接受卡培他滨和伊立替康(CapIri)新辅助 RCT 的患者或在 II 期试验中接受 CapIri + 西妥昔单抗治疗的患者,评估无病生存率(DFS)和总生存率(OS)的分析。接受西妥昔单抗治疗的患者分析了 KRAS 外显子 2 突变状态。
CapIri 试验的 37 例患者和 CapIri-西妥昔单抗治疗组的 49 例患者可评估。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 OS 为 127.4 个月。两组 5 年 OS 分别为 73%(CapIri 和 CapIri-西妥昔单抗)(P=0.61)。接受 CapIri 和接受 CapIri-西妥昔单抗且 KRAS 野生型肿瘤的患者之间在 DFS(P=0.86)或 OS(P=0.39)方面没有显着差异。
由于添加西妥昔单抗既没有提高 DFS 也没有提高 OS,因此它不应在 LARC 患者的围手术期治疗中发挥作用,甚至不应在(K)RAS WT 肿瘤患者中发挥作用。