Division of Surgical Oncology, The Ohio State University, Wexner Medical Center, James Cancer Center and Solove Research Institute, Columbus, OH.
Department of Surgical Oncology, University of Texas, MD Anderson Cancer Center, Houston, TX.
J Am Coll Surg. 2019 Jul;229(1):69-77.e2. doi: 10.1016/j.jamcollsurg.2019.03.011. Epub 2019 Mar 22.
The role of neoadjuvant chemotherapy in the management of colorectal liver metastases remains controversial. We sought to investigate whether neoadjuvant systemic chemotherapy contributes to clinically significant increases in postoperative morbidity and mortality using a population-based cohort.
The American College of Surgeons NSQIP Targeted Hepatectomy Participant Use Files were queried from 2014 to 2016 to identify patients with colorectal liver metastases who underwent liver resection. Patients were stratified by receipt of neoadjuvant chemotherapy using propensity score matching. Univariate and multivariable analyses were used to characterize the effect of neoadjuvant chemotherapy on perioperative morbidity and mortality.
After propensity score matching, 1,416 (50%) patients received neoadjuvant chemotherapy before hepatectomy and 1,416 (50%) underwent liver resection without neoadjuvant chemotherapy. There were no differences in age (60 vs 61 years), maximum tumor size (≤5 cm: 79% vs 80%, >5 cm: 21% vs 20%), resection type (partial hepatectomy: 69% vs 70%), simultaneous colectomy (9% vs 9%), or use of preoperative portal vein embolization (5% vs 5%) in those undergoing neoadjuvant chemotherapy compared with those who did not (all, p > 0.05). Overall 30-day postoperative morbidity (34% vs 33%), including rates of biliary fistula (6% vs 5%), post-hepatectomy liver failure (5% vs 5%), and mortality rates (0.8% vs 0.7%), were similar among patients who received neoadjuvant chemotherapy vs those who did not (all, p > 0.05). On multivariable analysis, receipt of neoadjuvant chemotherapy was not associated with increased morbidity (odds ratio 1.07; 95% CI 0.90 to 1.27; p = 0.43) or mortality (odds ratio 1.09; 95% CI 0.44 to 2.72; p = 0.85).
In this propensity-matched population-based cohort study, the use of neoadjuvant systemic chemotherapy was not associated with higher rates of complications, biliary fistula, post-hepatectomy liver failure, or mortality among patients with colorectal liver metastases undergoing liver resection.
新辅助化疗在结直肠癌肝转移治疗中的作用仍存在争议。我们旨在通过一项基于人群的队列研究,调查新辅助全身化疗是否会导致术后发病率和死亡率的临床显著增加。
从 2014 年至 2016 年,查询美国外科医师学院 NSQIP 靶向肝切除术参与者使用文件,以确定接受肝切除术的结直肠癌肝转移患者。使用倾向评分匹配对接受新辅助化疗的患者进行分层。采用单变量和多变量分析来描述新辅助化疗对围手术期发病率和死亡率的影响。
在进行倾向评分匹配后,1416(50%)例患者在肝切除术前接受新辅助化疗,1416(50%)例患者未接受新辅助化疗而行肝切除术。两组患者的年龄(60 岁比 61 岁)、最大肿瘤大小(≤5cm:79%比 80%,>5cm:21%比 20%)、切除类型(部分肝切除术:69%比 70%)、同期结肠切除术(9%比 9%)或术前门静脉栓塞术的应用(5%比 5%)差异无统计学意义(均,p>0.05)。新辅助化疗组与未接受新辅助化疗组患者的总体 30 天术后发病率(34%比 33%)相似,包括胆瘘(6%比 5%)、肝切除术后肝功能衰竭(5%比 5%)和死亡率(0.8%比 0.7%)差异无统计学意义(均,p>0.05)。多变量分析显示,接受新辅助化疗与发病率增加无关(比值比 1.07;95%置信区间 0.90 至 1.27;p=0.43)或死亡率增加无关(比值比 1.09;95%置信区间 0.44 至 2.72;p=0.85)。
在这项基于倾向评分匹配的基于人群的队列研究中,结直肠癌肝转移患者接受新辅助全身化疗与肝切除术后并发症、胆瘘、肝切除术后肝功能衰竭或死亡率的增加无关。