Local recurrence risk of esophageal squamous cell carcinoma due to intralesional damage during endoscopic submucosal dissection

被引:0
作者
Minamide, Tatsunori [1 ,3 ]
Kawata, Noboru [1 ]
Maeda, Yuki [1 ]
Yoshida, Masao [1 ]
Yamamoto, Yoichi [1 ]
Ashizawa, Hiroshi [1 ]
Takada, Kazunori [1 ]
Kishida, Yoshihiro [1 ]
Ito, Sayo [1 ]
Imai, Kenichiro [1 ]
Hotta, Kinichi [1 ]
Sato, Junya [1 ]
Ishiwatari, Hirotoshi [1 ]
Matsubayashi, Hiroyuki [1 ]
Sugino, Takashi [2 ]
Ono, Hiroyuki [1 ]
机构
[1] Shizuoka Canc Ctr, Div Endoscopy, Shizuoka, Japan
[2] Shizuoka Canc Ctr, Div Pathol, Shizuoka, Japan
[3] Shizuoka Canc Ctr, Div Endoscopy, 1007 Shimonagakubo,Nagaizumi Cho, Shizuoka 4118777, Japan
关键词
Endoscopic submucosal dissection; Esophageal squamous cell carcinoma; Pathology; Recurrence; Residual tumor; MUCOSAL RESECTION; CANCER;
D O I
10.1111/jgh.16307
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and AimIt is unclear whether additional treatment should be considered given the recurrence risk after endoscopic submucosal dissection (ESD) for esophageal squamous cell carcinoma (ESCC) when the vertical margin is positive or unclear (VM1/VMX) due to intralesional damage. This study aimed to elucidate the local recurrence risk of ESCC caused by intralesional damage during ESD. MethodsAmong consecutive patients with pT1a ESCCs initially treated by ESD at our institution between January 2006 and December 2018, ESCCs diagnosed as VM1/VMX were retrospectively reviewed. Exclusion criteria were piecemeal resection and any additional treatment after ESD. Intralesional damage included the following three types: a macroscopic hole inside the lesion, an incision from the lateral margin of the specimen into the lesion, and crushing injury or burn effect into the deepest area of the lesion without an obvious hole. The local recurrence rate after ESD was primarily analyzed. ResultsOf 1174 pT1a ESCCs initially treated using ESD, 22 lesions were histopathologically diagnosed as VM1/VMX due to intralesional damage (1.9%; 95% confidence interval [CI], 1.2-2.8%). At a median follow-up period of 60.0 (interquartile range, 15.0-84.0) months, no local recurrence was observed (0.0%; 95% CI, 0.0-13.3%) among 21 lesions finally evaluated. ConclusionsThe impact of intralesional damage during ESD for ESCC on local recurrence might be negligible. Follow-up without additional treatment may be acceptable even if intralesional damage occurs and results in VM1/VMX after ESD for pT1a ESCCs.
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收藏
页码:1802 / 1807
页数:6
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