Department of Gastroenterology and Endoscopy, National Cancer Center Hospital East, Chiba, Japan.
Endoscopy Division, National Cancer Center Hospital, Tokyo, Japan.
Dig Endosc. 2020 Mar;32(3):337-345. doi: 10.1111/den.13483. Epub 2019 Aug 1.
Neoadjuvant chemotherapy (nCT) followed by surgery is one of the standard treatments for resectable esophageal squamous cell carcinoma (ESCC). According to the Response Evaluation Criteria in Solid Tumors, endoscopic evaluation of a primary lesion is not recommended during nCT because of reduced objectivity. This study aimed to develop and validate endoscopic evaluation criteria for nCT.
This study retrospectively investigated patients with T2/3 ESCC who underwent nCT followed by radical esophagectomy across two institutions (test and validation sets). We retrospectively estimated the therapeutic effect by classifying patients according to degree of tumor shrinkage (evaluated with endoscopy) as follows: marked reduction (MR), half reduction (HR), insufficient reduction (IR), and progressive disease (PD). Three endoscopists evaluated patients in the test set. Another three endoscopists evaluated patients in the validation set. We analyzed recurrence-free survival (RFS) 3 years after surgery.
Of 129 patients in the test set, 44 had MR, 35 had HR, 44 had IR, and six had PD. The 3-year RFS rates were 55% (overall), 79% (MR), 54% (HR), 35% (IR), and 33% (PD). Of 91 patients in the validation set, 22 had MR, 49 had HR, 18 had IR, and two had PD. The 3-year RFS rates were 54% (overall), 77% (MR), 55% (HR), 22% (IR), and 50% (PD).
Our endoscopic criteria for nCT predicted prognosis; however, future studies are needed to further investigate our criteria before general application in the clinical setting.
新辅助化疗(nCT)后手术是可切除食管鳞癌(ESCC)的标准治疗方法之一。根据实体瘤反应评估标准,由于客观性降低,不建议在 nCT 期间对原发性病变进行内镜评估。本研究旨在开发和验证 nCT 的内镜评估标准。
本研究回顾性调查了在两个机构(测试和验证集)接受 nCT 后行根治性食管切除术的 T2/3 ESCC 患者。我们通过根据肿瘤缩小程度(内镜评估)对患者进行分类来回顾性估计治疗效果,具体分类为:明显缩小(MR)、减半缩小(HR)、缩小不足(IR)和进展性疾病(PD)。三名内镜医生在测试集中评估患者。另外三名内镜医生在验证集中评估患者。我们分析了手术后 3 年的无复发生存率(RFS)。
在测试集中的 129 名患者中,44 名患者有 MR,35 名患者有 HR,44 名患者有 IR,6 名患者有 PD。3 年 RFS 率分别为 55%(总体)、79%(MR)、54%(HR)、35%(IR)和 33%(PD)。在验证集中的 91 名患者中,22 名患者有 MR,49 名患者有 HR,18 名患者有 IR,2 名患者有 PD。3 年 RFS 率分别为 54%(总体)、77%(MR)、55%(HR)、22%(IR)和 50%(PD)。
我们的 nCT 内镜标准可预测预后;然而,在临床应用之前,还需要进一步研究我们的标准。