Association of Adjuvant Chemotherapy in Patients With Resected Pancreatic Adenocarcinoma After Multiagent Neoadjuvant Chemotherapy

医学 内科学 危险系数 比例危险模型 胰腺癌 化疗 病态的 回顾性队列研究 肿瘤科 队列 腺癌 阶段(地层学) 新辅助治疗 癌症 外科 乳腺癌 置信区间 古生物学 生物
作者
Toshitaka Sugawara,Salvador Rodriguez Franco,Samantha N. Sherman,Michael J. Kirsch,Kathryn Colborn,Jun Ishida,Samuele Grandi,Mohammed Al-Musawi,Ana Gleisner,Richard D. Schulick,Marco Del Chiaro
出处
期刊:JAMA Oncology [American Medical Association]
卷期号:9 (3): 316-316 被引量:26
标识
DOI:10.1001/jamaoncol.2022.5808
摘要

The total number of patients with pancreatic ductal adenocarcinoma (PDAC) who receive neoadjuvant chemotherapy (NAC) is increasing. However, the added role of adjuvant chemotherapy (AC) in these patients remains unknown.To evaluate the association of AC with overall survival (OS) in patients with PDAC who received multiagent NAC followed by curative-intent surgery.This retrospective, matched-cohort study used data from the National Cancer Database and included patients with PDAC diagnosed between 2010 and 2018. The study included patients at least 18 years of age who received multiagent NAC followed by surgical resection and had available records of the pathological findings. Patients were excluded if they had clinical or pathological stage IV disease or died within 90 days of their operation.All included patients received NAC and underwent resection for primary PDAC. Some patients received adjuvant chemotherapy.The main outcome was the OS of patients who received AC (AC group) vs those who did not (non-AC group). Interactions between pathological findings and AC were investigated in separate multivariable Cox regression models.In total, 1132 patients (mean [SD] age, 63.5 [9.4] years; 577 [50.1%] male; 970 [85.7%] White) were included, 640 patients in the non-AC group and 492 patients in the AC group. After being matched by propensity score according to demographic and pathological characteristics, 444 patients remained in each group. The multivariable Cox regression model adjusted for all covariates revealed an association between AC and improved survival (hazard ratio, 0.71; 95% CI, 0.59-0.85; P < .001). Subgroup interaction analysis revealed that AC was significantly associated with better OS (26.6 vs 21.2 months; P = .002), but the benefit varied by age, pathological T category, and tumor differentiation. Of note, AC was associated with better survival in patients with any pathological N category and positive margin status.In this cohort study, AC following multiagent NAC and resection in patients with PDAC was associated with significant survival benefit compared with that in patients who did not receive AC. These findings suggest that patients with aggressive tumors may benefit from AC to achieve prolonged survival, even after multiagent NAC and curative-intent resection.
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