Sato Yasuyoshi, Matsusaka Satoshi, Suenaga Mitsukuni, Shinozaki Eiji, Mizunuma Nobuyuki
Department of Gastroenterology, Cancer Institute Hospital, Japanese Foundation for Cancer Research, Tokyo, Japan.
Onco Targets Ther. 2015 Nov 11;8:3329-36. doi: 10.2147/OTT.S89241. eCollection 2015.
Cetuximab and bevacizumab reportedly improve the survival of patients with metastatic colorectal cancer (mCRC), but their most effective sequence of administration is unknown. The aim of this study was to compare the survival of patients with mCRC treated with cetuximab after bevacizumab failure with that of patients with mCRC without previous bevacizumab therapy.
In total, 190 of 323 patients with mCRC treated with cetuximab from March 2006 to July 2013 were enrolled in our hospital for this retrospective study. Forty-seven patients were treated with cetuximab-based second-line therapy, 21 of whom had received prior bevacizumab; 143 patients were treated with cetuximab-based third-line therapy, 109 of whom had received prior bevacizumab. The Kaplan-Meier method with a log-rank test and Cox regression analysis were performed to evaluate the overall survival and progression-free survival (PFS) of each group of patients.
The median follow-up time was 11.8 months in patients who received second-line cetuximab-based chemotherapy and 13.7 months in those who received third-line cetuximab-based chemotherapy. Univariate analysis revealed that the median PFS was significantly longer in patients without prior bevacizumab therapy than in patients with prior bevacizumab therapy (second line, P=0.048; third line, P=0.0022). Multivariate analysis adjusted for baseline characteristics showed that third-line cetuximab-based chemotherapy with or without prior bevacizumab was significantly associated with PFS (P=0.014). Neither the presence nor the absence of prior bevacizumab administration was associated with overall survival.
Cetuximab could be more effective without prior bevacizumab. Prior bevacizumab use may decrease the efficacy of cetuximab.
据报道,西妥昔单抗和贝伐单抗可提高转移性结直肠癌(mCRC)患者的生存率,但其最有效的给药顺序尚不清楚。本研究的目的是比较贝伐单抗治疗失败后接受西妥昔单抗治疗的mCRC患者与未接受过贝伐单抗治疗的mCRC患者的生存率。
2006年3月至2013年7月期间,共有323例接受西妥昔单抗治疗的mCRC患者中的190例被纳入我院进行这项回顾性研究。47例患者接受了以西妥昔单抗为基础的二线治疗,其中21例曾接受过贝伐单抗治疗;143例患者接受了以西妥昔单抗为基础的三线治疗,其中109例曾接受过贝伐单抗治疗。采用Kaplan-Meier法结合对数秩检验和Cox回归分析来评估每组患者的总生存期和无进展生存期(PFS)。
接受以西妥昔单抗为基础的二线化疗的患者中位随访时间为11.8个月。接受以西妥昔单抗为基础的三线化疗的患者中位随访时间为13.7个月。单因素分析显示,未接受过贝伐单抗治疗的患者的中位PFS显著长于接受过贝伐单抗治疗的患者(二线治疗,P = 0.048;三线治疗,P = 0.0022)。对基线特征进行校正的多因素分析显示,接受或未接受过贝伐单抗治疗的以西妥昔单抗为基础三线化疗与PFS显著相关(P = 0.014)。既往是否使用贝伐单抗均与总生存期无关。
未使用过贝伐单抗时,西妥昔单抗可能更有效。既往使用贝伐单抗可能会降低西妥昔单抗的疗效。