Division of Thoracic and Upper Gastrointestinal Surgery, Montreal General Hospital - McGill University Health Centre, Montreal, Quebec, Canada.
Department of Surgery & Cancer, Imperial College London, UK.
Ann Surg. 2022 Nov 1;276(5):799-805. doi: 10.1097/SLA.0000000000005619. Epub 2022 Jul 21.
To compare overall (OS) and recurrence-free survival (RFS) in esophageal adenocarcinoma patients with a pathologically complete response (pCR) following neoadjuvant chemotherapy (nCT) or neoadjuvant chemoradiotherapy (nCRT).
In the absence of survival differences in several prior studies comparing nCT with nCRT, the higher rate of pCR after nCRT has been suggested as reason to prefer this modality over nCT.
An international cohort study included data from 8 high-volume centers. Inclusion criteria was patients with esophageal adenocarcinoma, between 2008 and 2018, who had a pCR after nCT or nCRT. Univariate analysis was used to compare demographic factors, and Kaplan-Meier survival analysis used to compare 5-year OS and RFS between groups.
In all, 465 patients with pCR following neoadjuvant treatment were included; 132 received nCT and 333 received nCRT. There was no statistically significant difference in 5-year OS between groups (78.8% (nCT) vs 65.5% (nCRT), P =0.099), with a similar result demonstrated in multivariate analysis (HR=1.19, 95% CI 0.77-1.84). 5-year RFS was significantly reduced in patients with a pCR following neoadjuvant chemoradiotherapy (75.3% (nCRT) vs 87.1% (nCT), P =0.026). Multivariate analysis confirmed nCRT was associated with a poorer 5-year RFS (HR=1.70, 95% CI 1.22-2.99). nCRT associated with a significantly greater prevalence of 5-year distant recurrence (odds ratio=2.50, 95% CI 1.25-4.99).
The results of this international cohort study show that the prognosis of pCR following different neoadjuvant regimes differs, bringing into question the validity of this measure as an oncological surrogate when comparing neoadjuvant treatment schemes for esophageal adenocarcinoma.
比较接受新辅助化疗(nCT)或新辅助放化疗(nCRT)后病理完全缓解(pCR)的食管腺癌患者的总生存期(OS)和无复发生存期(RFS)。
在几项比较 nCT 与 nCRT 的研究中,并未观察到生存差异,而 nCRT 后 pCR 发生率更高,这被认为是 nCRT 优于 nCT 的原因。
一项国际队列研究纳入了 8 个大容量中心的数据。纳入标准为 2008 年至 2018 年间接受 nCT 或 nCRT 治疗后出现 pCR 的食管腺癌患者。采用单因素分析比较人口统计学因素,采用 Kaplan-Meier 生存分析比较两组的 5 年 OS 和 RFS。
共纳入 465 例新辅助治疗后出现 pCR 的患者;其中 132 例接受 nCT,333 例接受 nCRT。两组 5 年 OS 无统计学差异(nCT 为 78.8%,nCRT 为 65.5%,P=0.099),多因素分析也得出相似结果(HR=1.19,95%CI 0.77-1.84)。新辅助放化疗后 pCR 患者的 5 年 RFS 显著降低(nCRT 为 75.3%,nCT 为 87.1%,P=0.026)。多因素分析证实 nCRT 与较差的 5 年 RFS 相关(HR=1.70,95%CI 1.22-2.99)。nCRT 与 5 年远处复发的高发生率显著相关(比值比=2.50,95%CI 1.25-4.99)。
本国际队列研究结果表明,不同新辅助治疗方案后 pCR 的预后不同,这使得 pCR 作为比较食管腺癌新辅助治疗方案的肿瘤学替代指标的有效性受到质疑。