NYU Grossman School of Medicine, New York, NY.
VA-New York Harbor Health Care System, New York, NY.
JCO Precis Oncol. 2021 Apr 13;5. doi: 10.1200/PO.20.00359. eCollection 2021.
Advances in precision oncology, including testing to predict response to epidermal growth factor receptor monoclonal antibodies (EGFR mAbs) in colorectal cancer (CRC), can extend patients' lives. We evaluated uptake and clinical use of molecular testing, guideline recommended since 2010, in the Veterans Affairs Healthcare System (VA).
We conducted a retrospective cohort study of patients with stage IV CRC diagnosed in the VA 2006-2015. We gathered clinical, demographic, molecular, and treatment data from the VA Corporate Data Warehouse and 29 commercial laboratories. We performed multivariable analyses of associations between patient characteristics, testing, and EGFR mAb treatment.
Among 5,943 patients diagnosed with stage IV CRC, only 1,053 (17.7%) had testing. Testing rates increased from 2.3% in 2006 to 28.4% in 2013. In multivariable regression, older patients (odds ratio, 0.17; 95% CI, 0.09 to 0.32 for ≥ age 85 < 45 years) and those treated in the Northeast and South regions were less likely, and those treated at high-volume CRC centers were more likely to have testing (odds ratio, 2.32; 95% CI, 1.48 to 3.63). Rates of potentially guideline discordant care were high: 64.3% (321/499) of wild-type (WT) went untreated with EGFR mAb and 8.8% (401/4,570) with no testing received EGFR mAb. Among -WT patients, survival was better for patients who received EGFR mAb treatment (29.6 18.8 months; < .001).
We found underuse of testing in advanced CRC, especially among older patients and those treated at lower-volume CRC centers. We found high rates of potentially guideline discordant underuse of EGFR mAb in patients with -WT tumors. Efforts to understand barriers to precision oncology are needed to maximize patient benefit.
精准肿瘤学的进步,包括预测结直肠癌(CRC)对表皮生长因子受体单克隆抗体(EGFR mAbs)反应的测试,可以延长患者的生命。我们评估了自 2010 年以来推荐的分子测试在退伍军人事务部医疗保健系统(VA)中的采用和临床应用。
我们对 2006 年至 2015 年在 VA 诊断为 IV 期 CRC 的患者进行了回顾性队列研究。我们从 VA 公司数据仓库和 29 家商业实验室收集了临床、人口统计学、分子和治疗数据。我们对患者特征、测试和 EGFR mAb 治疗之间的关联进行了多变量分析。
在 5943 名诊断为 IV 期 CRC 的患者中,仅有 1053 名(17.7%)接受了测试。测试率从 2006 年的 2.3%增加到 2013 年的 28.4%。在多变量回归中,年龄较大的患者(优势比,0.17;95%CI,0.09 至 0.32,年龄≥85 岁<45 岁)和治疗于东北地区和南部地区的患者不太可能进行测试,而在高容量 CRC 中心治疗的患者更有可能进行测试(优势比,2.32;95%CI,1.48 至 3.63)。潜在指南不一致的治疗率很高:64.3%(321/499)的野生型(WT)患者未接受 EGFR mAb 治疗,8.8%(401/4570)未进行测试的患者接受了 EGFR mAb 治疗。在-WT 患者中,接受 EGFR mAb 治疗的患者的生存时间更好(29.6 18.8 个月;<0.001)。
我们发现在晚期 CRC 中,尤其是在年龄较大的患者和治疗于低容量 CRC 中心的患者中,对测试的使用不足。我们发现,在-WT 肿瘤患者中,EGFR mAb 的潜在指南不一致的使用率低,存在很高的比例。需要努力了解精准肿瘤学的障碍,以最大限度地提高患者的获益。