食管鳞状细胞癌病理完全反应后进行新辅助治疗和食管切除术后复发的风险因素。

R. Hirohata, Y. Hamai, M. Emi, Y. Ibuki, T. Kurokawa, Manato Ohsawa, Nao Kitasaki, Morihito Okada
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引用次数: 0

摘要

背景经过新辅助治疗(NAT)获得病理完全反应(pCR)的患者的预后优于未获得病理完全反应的患者。目前,在获得 pCR 后还没有进行免疫检查点抑制剂辅助治疗的指征。然而,据报道,pCR 后的复发风险为 10%-20%,预后较差。因此,我们研究了 pCR 患者的术前复发风险因素。方法 我们分析了 56 例食管鳞状细胞癌患者,他们在新辅助化放疗(NACRT)或新辅助化疗(NAC)后接受了食管切除术,并经组织学诊断为 pCR。比较了复发和未复发患者的术前因素,以确定风险因素。结果48例获得pCR的患者接受了NACRT,8例接受了NAC。10名复发患者(17.9%)接受了NACRT。在复发组中,cN2病变更常见,NAT前血红蛋白(Hb)更低。此外,在复发病例中,NAT前原发肿瘤大小径的横截面积(CSA)明显更高(P = 0.041)。包括 cTNM 分期、NAT 前 Hb 和 NAT 前 CSA 在内的多变量分析发现,NAT 前 CSA 高是复发的唯一风险因素(几率比 11.6,95% 置信区间 1.3-104.1,p = 0.028)。对无复发生存期和总生存期的 Cox 回归分析发现,只有 NAT 前高 CSA 才是预后因素。NAT前原发肿瘤的高CSA是复发的一个风险因素,需要密切监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Risk factors for recurrence of esophageal squamous cell carcinoma after pathological complete response to neoadjuvant therapy followed by esophagectomy.
BACKGROUND Prognosis of patients who achieve pathological complete response (pCR) with neoadjuvant therapy (NAT) is better than that of non-pCR patients. Currently, there is no indication for adjuvant immune checkpoint inhibitor therapy after achieving pCR. However, recurrence risk after pCR is reportedly 10%-20% with a poor prognosis. Therefore, we investigated the preoperative risk factors for recurrence in patients with pCR. METHODS We analyzed 56 patients with esophageal squamous cell carcinoma who underwent esophagectomy after neoadjuvant chemoradiotherapy (NACRT) or neoadjuvant chemotherapy (NAC) and were histologically diagnosed with pCR. Preoperative factors were compared between patients with and without recurrence to identify the risk factors. RESULTS Forty-eight patients who achieved pCR received NACRT and 8 received NAC. Ten patients who experienced recurrence (17.9%) had undergone NACRT. The cN2 lesions were more frequent, and pre-NAT blood hemoglobin (Hb) was lower in the recurrence group. In addition, the pre-NAT cross-sectional area (CSA) product of the major and minor diameters of the primary tumor before NAT was significantly higher in recurrent cases (p = 0.041). Multivariate analysis, including the cTNM stage, pre-NAT Hb, and pre-NAT CSA, identified high pre-NAT CSA as the only risk factor for recurrence (odds ratio 11.6, 95% confidence interval 1.3-104.1, and p = 0.028). Cox regression analysis of recurrence-free and overall survival identified only high pre-NAT CSA as a prognostic factor. CONCLUSIONS The recurrence risk is relatively high even in patients who achieve pCR after NAT. High pre-NAT CSA of the primary tumor is a risk factor for recurrence necessitating close surveillance.
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