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

It 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 th...

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Veröffentlicht in:Journal of gastroenterology and hepatology 2023-10, Vol.38 (10), p.1802-1807
Hauptverfasser: Minamide, Tatsunori, Kawata, Noboru, Maeda, Yuki, Yoshida, Masao, Yamamoto, Yoichi, Ashizawa, Hiroshi, Takada, Kazunori, Kishida, Yoshihiro, Ito, Sayo, Imai, Kenichiro, Hotta, Kinichi, Sato, Junya, Ishiwatari, Hirotoshi, Matsubayashi, Hiroyuki, Sugino, Takashi, Ono, Hiroyuki
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container_end_page 1807
container_issue 10
container_start_page 1802
container_title Journal of gastroenterology and hepatology
container_volume 38
creator Minamide, Tatsunori
Kawata, Noboru
Maeda, Yuki
Yoshida, Masao
Yamamoto, Yoichi
Ashizawa, Hiroshi
Takada, Kazunori
Kishida, Yoshihiro
Ito, Sayo
Imai, Kenichiro
Hotta, Kinichi
Sato, Junya
Ishiwatari, Hirotoshi
Matsubayashi, Hiroyuki
Sugino, Takashi
Ono, Hiroyuki
description It 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. Among 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. Of 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. The 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.
doi_str_mv 10.1111/jgh.16307
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This study aimed to elucidate the local recurrence risk of ESCC caused by intralesional damage during ESD. Among 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. Of 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. The impact of intralesional damage during ESD for ESCC on local recurrence might be negligible. 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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. The impact of intralesional damage during ESD for ESCC on local recurrence might be negligible. 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subjects Endoscopy
Esophageal cancer
Esophageal carcinoma
Lesions
Squamous cell carcinoma
title Local recurrence risk of esophageal squamous cell carcinoma due to intralesional damage during endoscopic submucosal dissection
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