Sutton Thomas L, Patel Ranish K, Elsheikh Mohamed, Kerch Cymon, Grossberg Aaron, Qureshi Alia P, Hunter John G, Nabavizadeh Nima, Wood Stephanie G
Department of Surgery, Oregon Heath & Science University (OHSU), Portland, OR, USA.
Department of Radiation Medicine, OHSU, Portland, OR, USA.
Ann Surg Oncol. 2025 Sep 16. doi: 10.1245/s10434-025-18304-7.
Following publication of the Chemoradiotherapy for Esophageal Cancer Followed by Surgery Study (CROSS) trial, neoadjuvant chemoradiation has become standard of care for most esophageal cancer (EC). Patients most commonly receive either 41.4 Gy (per CROSS) or 50-50.4 Gy, but little post-CROSS era data have been reported.
The National Cancer Database (NCDB) was queried for patients with EC receiving neoadjuvant chemoradiation followed by resection from 2012-2020 (n = 10,810). Patients were grouped by neoadjuvant radiation dose (41.4 Gy or 50-50.4 Gy). Overall survival (OS) was evaluated with Cox proportional hazards modeling following propensity-score matching on the basis of relevant clinicopathologic characteristics.
A total of 10,810 patients were identified, with 1450 (13.4%) receiving 41.4 Gy of radiation and 9360 (86.6%) receiving 50-50.4 Gy. At a median follow-up of 61.6 months, median OS was 59.9 months in patients receiving 41.4 Gy and 45.5 months (P < 0.001) for patients receiving 50-50.4 Gy. Following stratification by posttreatment stage, 41.4 Gy dosing remained associated with improved OS compared with 50-50.4 Gy, but was most pronounced for patients with pCR (median OS 110.0 versus 82.4 months, P < 0.001) and Tis/Stage I residual disease (median OS 92.8 versus 67.2 months, P = 0.02). Propensity matching yielded 1448 patients per group. On multivariable analysis, receipt of 41.4 Gy was independently associated with improved OS (HR 0.82, P < 0.001).
Lower neoadjuvant radiation dosage is associated with improved OS in resected EC. Until prospective trials are completed, higher radiation doses should be reserved for definitive treatment in patients ineligible for surgery, due to potential harms.
随着食管癌同步放化疗后手术研究(CROSS)试验的发表,新辅助放化疗已成为大多数食管癌(EC)的标准治疗方法。患者最常接受41.4 Gy(根据CROSS试验)或50 - 50.4 Gy的放疗,但CROSS试验后时代的数据报道较少。
查询国家癌症数据库(NCDB)中2012 - 2020年接受新辅助放化疗后进行手术切除的EC患者(n = 10810)。患者按新辅助放疗剂量(41.4 Gy或50 - 50.4 Gy)分组。在根据相关临床病理特征进行倾向评分匹配后,采用Cox比例风险模型评估总生存期(OS)。
共识别出10810例患者,其中1450例(13.4%)接受41.4 Gy放疗,9360例(86.6%)接受50 - 50.4 Gy放疗。中位随访61.6个月时,接受41.4 Gy放疗的患者中位OS为59.9个月,接受50 - 50.4 Gy放疗的患者中位OS为45.5个月(P < 0.001)。按治疗后分期分层后,与50 - 50.4 Gy相比,41.4 Gy剂量放疗仍与OS改善相关,但在达到病理完全缓解(pCR)的患者中最为明显(中位OS 110.0个月对82.4个月,P < 0.001)以及Tis/Ⅰ期残留疾病患者(中位OS 92.8个月对67.2个月,P = 0.02)。倾向匹配后每组有1448例患者。多变量分析显示,接受41.4 Gy放疗与OS改善独立相关(风险比0.82,P < 0.001)。
在接受手术切除的EC患者中,较低的新辅助放疗剂量与OS改善相关。在完成前瞻性试验之前,由于潜在危害,较高的放疗剂量应保留用于无法进行手术的患者的确定性治疗。