British Columbia Cancer Agency and University of British Columbia, Vancouver, BC, Canada.
Clin Colorectal Cancer. 2011 Jun;10(2):97-101. doi: 10.1016/j.clcc.2011.03.004. Epub 2011 Apr 22.
As of 2006, bevacizumab was available for the treatment of metastatic colorectal cancer (mCRC) in British Columbia (BC). This study compares survival between referred patients diagnosed with mCRC in 2003/2004 (pre-bevacizumab era) and 2006 (bevacizumab era).
The BC cancer agency (BCCA) is a cancer network treating approximately 60% of patients with mCRC in BC. For this study, all patients in the BCCA diagnosed with mCRC in 2003/2004 and 2006 were included. The primary objective was to compare overall survival (OS) between the 2 cohorts.
One thousand four hundred seventeen patients were included: 969 from 2003/2004, and 448 from 2006. Between 2003/2004 and 2006, the proportion of patients treated with systemic therapy for mCRC increased (61.1% to 67.6%; P = .02). The only significant difference in treatment between the cohorts was in the proportion of patients who received bevacizumab (5.9% to 30.6%; P < .001). Median OS significantly differed between the 2 cohorts (13.8 to 17.3 months; P < .001). Median OS for patients who received systemic therapy increased (18.6-23.6 months; P = .001). Median OS for patients who did not receive systemic therapy was unchanged (6.1-5.9 months; P = .65).
In this population-based study, median OS for mCRC significantly increased between 2003/2004 and 2006. An increase in the proportion of patients treated with systemic therapy, and the addition of bevacizumab to chemotherapy, seem to have contributed to this improvement in survival.
截至 2006 年,贝伐单抗可用于治疗不列颠哥伦比亚省(BC)的转移性结直肠癌(mCRC)。本研究比较了 2003/2004 年(贝伐单抗前时代)和 2006 年(贝伐单抗时代)诊断为 mCRC 的转诊患者的生存情况。
BC 癌症机构(BCCA)是一个治疗 BC 中约 60%mCRC 患者的癌症网络。在这项研究中,BCCA 中所有 2003/2004 年和 2006 年诊断为 mCRC 的患者均被纳入研究。主要目的是比较两组患者的总生存(OS)。
共纳入 1417 例患者:2003/2004 年组 969 例,2006 年组 448 例。2003/2004 年至 2006 年间,mCRC 系统治疗患者比例增加(61.1%至 67.6%;P=0.02)。两组间唯一显著的治疗差异是接受贝伐单抗治疗的患者比例(5.9%至 30.6%;P<0.001)。两组间中位 OS 显著不同(13.8 至 17.3 个月;P<0.001)。接受系统治疗的患者中位 OS 延长(18.6-23.6 个月;P=0.001)。未接受系统治疗的患者中位 OS 保持不变(6.1-5.9 个月;P=0.65)。
在这项基于人群的研究中,2003/2004 年至 2006 年间 mCRC 的中位 OS 显著延长。接受系统治疗的患者比例增加,以及化疗中加入贝伐单抗,似乎对生存的改善有所贡献。