Pathological response guides adjuvant 5-fluorouracil, leucovorin, oxaliplatin, and docetaxel (FLOT) chemotherapy in surgically resected gastro-oesophageal cancer (SPACE-FLOT): international cohort study

医学 多西紫杉醇 奥沙利铂 内科学 化疗 肿瘤科 氟尿嘧啶 胃肠病学 佐剂 新辅助治疗 四分位间距 队列 癌症 外科 结直肠癌 乳腺癌
作者
David S. Liu,Margaret M Lee,Katheryn Hall,David I. Watson,Lorenzo Ferri,Jimmy Bok Yan So,Claire L. Donohoe,Michael Michael,Niall C. Tebbutt,Darren Wong,Cuong Duong,Tim Bright,Ahmad Aly,Sonia Gill,Chao Cheng,Su Kah Goh,Matthew Read,James Tan,Sean R. Stevens,Enoch Wong
出处
期刊:British Journal of Surgery [Oxford University Press]
卷期号:112 (4) 被引量:4
标识
DOI:10.1093/bjs/znaf056
摘要

Abstract Background Many patients with locally advanced gastro-oesophageal cancers are unable to complete adjuvant 5-fluorouracil, leucovorin, oxaliplatin, and docetaxel (FLOT) chemotherapy, raising questions about its therapeutic utility. The aim of this study was to examine whether pathological response to neoadjuvant FLOT can guide its adjuvant use. Methods Patients with non-metastatic gastro-oesophageal adenocarcinoma who received neoadjuvant FLOT and underwent surgery from 1 January 2017 to 1 January 2022 from 43 hospitals across 12 countries were analysed. Pathological response was assessed using tumour regression grading systems, trichotomized into minimal responders (MR; worst category), complete responders (CR; pCR), and partial responders (PR; between MR and CR). Survival outcomes of patients who did and did not receive adjuvant FLOT were compared using Kaplan–Meier, Cox regression, propensity score matched, and sensitivity analysis. Results A total of 1887 patients (459 MR, 221 CR, and 1207 PR) were evaluated. The median follow-up was 25.5 (interquartile range 15.0–39.1) months. In the MR group, there was no difference in disease-free survival (DFS; HR 1.03 (95% c.i. 0.78 to 1.36), P = 0.836) between those who did and did not receive adjuvant FLOT. Whilst there was a difference in non-adjusted OS, this became statistically non-significant after adjusting for baseline characteristics (HR 0.96 (95% c.i. 0.70 to 1.30), P = 0.801). In the CR group, there was no difference in DFS (HR 0.88 (95% c.i. 0.41 to 1.85), P = 0.724) or OS (HR 0.69 (95% c.i. 0.31 to 1.54), P = 0.343) between those who did and did not receive adjuvant FLOT. In the PR group, adjuvant FLOT conferred a significant DFS (HR 0.68 (95% c.i. 0.55 to 0.86), P < 0.001) and OS (HR 0.55 (95% c.i. 0.44 to 0.69), P < 0.001) benefit. Conclusion Pathological response to neoadjuvant FLOT may guide the use of adjuvant FLOT, enabling personalized approaches to treatment.
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