Department of Medical Oncology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Department of Research, Netherlands Comprehensive Cancer Organisation, Utrecht, The Netherlands.
Acta Oncol. 2020 Apr;59(4):395-403. doi: 10.1080/0284186X.2020.1722320. Epub 2020 Feb 12.
Population-based data on the implementation of guidelines for cancer patients in daily practice are scarce, while practice variation may influence patient outcomes. Therefore, we evaluated treatment patterns and associated variables in the systemic treatment of metastatic colorectal cancer (mCRC) in the Netherlands. We selected a random sample of adult mCRC patients diagnosed from 2008 to 2015 from the National Cancer Registry in 20 (4 academic, 8 teaching and 8 regional) Dutch hospitals. We examined the influence of patient, demographic and tumour characteristics on the odds of being treated with systemic therapy according to the current guideline and assessed its association with survival. Our study population consisted of 2222 mCRC patients of whom 1307 patients received systemic therapy for mCRC. Practice variation was most obvious in the use of bevacizumab and anti-EGFR therapy in patients with wild-type tumours. Administration rates did not differ between hospital types but fluctuated between individual hospitals for bevacizumab (8-92%; < .0001) and anti-EGFR therapy (10-75%; = .05). Bevacizumab administration was inversely correlated to higher age (OR:0.2; 95%CI: 0.1-0.3) comorbidity (OR:0.6; 95%CI: 0.5-0.8) and the presence of metachronous metastases (OR:0.5; 95%CI: 0.3-0.7), but patient characteristics did not differ between hospitals with low or high bevacizumab administration rates. The hazard ratios for exposure to bevacizumab and anti-EGFR therapy were 0.8 (95%CI: 0.7-0.9) and 0.6 (95%CI: 0.5-0.8), respectively. We identified significant inter-hospital variation in targeted therapy administration for mCRC patients, which may affect outcome. Age and comorbidity were inversely correlated with non-administration of bevacizumab but did not explain inter-hospital practice variation. Our data suggest that practice variation is based on individual strategy of hospitals rather than guideline recommendations or patient-driven decisions. Individual hospital strategies are an additional factor that may explain the observed differences between real-life data and results obtained from clinical trials.
人群为基础的数据表明,癌症患者在日常实践中实施指南的情况很少,而实践差异可能会影响患者的预后。因此,我们评估了荷兰转移性结直肠癌(mCRC)患者系统治疗中的治疗模式和相关变量。我们从国家癌症登记处选择了 2008 年至 2015 年在 20 家荷兰医院(4 家学术医院、8 家教学医院和 8 家区域医院)诊断的成年 mCRC 患者的随机样本。我们检查了患者、人口统计学和肿瘤特征对根据当前指南接受系统治疗的可能性的影响,并评估了其与生存的相关性。我们的研究人群包括 2222 名 mCRC 患者,其中 1307 名患者接受了 mCRC 的系统治疗。在野生型肿瘤患者中,贝伐单抗和抗 EGFR 治疗的使用差异最大。不同医院类型之间的治疗率没有差异,但贝伐单抗(8-92%;<0.0001)和抗 EGFR 治疗(10-75%;=0.05)在个别医院之间波动。贝伐单抗的使用率与较高的年龄(OR:0.2;95%CI:0.1-0.3)、合并症(OR:0.6;95%CI:0.5-0.8)和同时性转移(OR:0.5;95%CI:0.3-0.7)呈负相关,但在贝伐单抗使用率低或高的医院之间,患者特征没有差异。贝伐单抗和抗 EGFR 治疗的暴露风险比分别为 0.8(95%CI:0.7-0.9)和 0.6(95%CI:0.5-0.8)。我们发现 mCRC 患者靶向治疗管理存在显著的医院间差异,这可能会影响预后。年龄和合并症与贝伐单抗的非应用呈负相关,但不能解释医院间的实践差异。我们的数据表明,实践差异是基于医院的个体策略,而不是指南建议或患者驱动的决策。医院的个体策略是一个额外的因素,可能解释了实际数据与临床试验结果之间的差异。