Impact of preoperative tumor rupture timing on gastrointestinal stromal tumor prognosis: a retrospective multicentric cohort study

Abstract Background A gastrointestinal stromal tumor rupture entails a high risk of recurrence even after curative surgery. However, the definition of rupture is unclear, and the question of whether patients with a minor rupture should be treated with adjuvant imatinib remains controversial. Methods...

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Veröffentlicht in:Japanese journal of clinical oncology 2022-03, Vol.52 (3), p.237-243
Hauptverfasser: Chiguchi, Gaku, Cho, Haruhiko, Sato, Shinsuke, Takahashi, Tsuyoshi, Nabeshima, Kazuhito, Maruyama, Tsunehiko, Kataoka, Mikinori, Katayanagi, Sou, Kikuchi, Hirotoshi
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container_title Japanese journal of clinical oncology
container_volume 52
creator Chiguchi, Gaku
Cho, Haruhiko
Sato, Shinsuke
Takahashi, Tsuyoshi
Nabeshima, Kazuhito
Maruyama, Tsunehiko
Kataoka, Mikinori
Katayanagi, Sou
Kikuchi, Hirotoshi
description Abstract Background A gastrointestinal stromal tumor rupture entails a high risk of recurrence even after curative surgery. However, the definition of rupture is unclear, and the question of whether patients with a minor rupture should be treated with adjuvant imatinib remains controversial. Methods The present, retrospective, multicentric study enrolled 57 patients with gastrointestinal stromal tumor with a minor/major tumor rupture, of whom 46 were finally found to be eligible for analysis. Tumor ruptures were subclassified by their degree, timing and cause. Multivariate analysis was performed to identify the risk factors of all types of recurrence as well as of peritoneal recurrence only. Results The study cohort included minor (n = 24), intraoperative (n = 19) and iatrogenic (n = 20) ruptures besides the typical types (major, preoperative and spontaneous). All intraoperative ruptures were iatrogenic. In total, 27 patients (58.7%) had a recurrence in the peritoneum (n = 17) and/or the liver (n = 13) during a median follow-up period of 5.8 years, but no recurrence was observed in patients with tumor rupture as a single, high-risk factor. Multivariate analysis found the timing of tumor rupture to be an independent risk factor of poor recurrence-free survival (hazard ratio: 2.37; 95% confidence interval: 1.02–5.49; P = 0.045). Conclusions Preoperative tumor rupture in patients with a ruptured gastrointestinal stromal tumor was associated with poor recurrence-free survival. Our results suggested that a distinction should be made between preoperative and intraoperative tumor ruptures when considering the indications for adjuvant imatinib therapy for gastrointestinal stromal tumor patients with tumor rupture as a single, high-risk factor of recurrence. Preoperative and intraoperative tumor ruptures should be distinguished when considering the indications for adjuvant imatinib therapy for gastrointestinal stromal tumor patients with tumor rupture as a single, high-risk factor of recurrence.
doi_str_mv 10.1093/jjco/hyab200
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However, the definition of rupture is unclear, and the question of whether patients with a minor rupture should be treated with adjuvant imatinib remains controversial. Methods The present, retrospective, multicentric study enrolled 57 patients with gastrointestinal stromal tumor with a minor/major tumor rupture, of whom 46 were finally found to be eligible for analysis. Tumor ruptures were subclassified by their degree, timing and cause. Multivariate analysis was performed to identify the risk factors of all types of recurrence as well as of peritoneal recurrence only. Results The study cohort included minor (n = 24), intraoperative (n = 19) and iatrogenic (n = 20) ruptures besides the typical types (major, preoperative and spontaneous). All intraoperative ruptures were iatrogenic. In total, 27 patients (58.7%) had a recurrence in the peritoneum (n = 17) and/or the liver (n = 13) during a median follow-up period of 5.8 years, but no recurrence was observed in patients with tumor rupture as a single, high-risk factor. Multivariate analysis found the timing of tumor rupture to be an independent risk factor of poor recurrence-free survival (hazard ratio: 2.37; 95% confidence interval: 1.02–5.49; P = 0.045). Conclusions Preoperative tumor rupture in patients with a ruptured gastrointestinal stromal tumor was associated with poor recurrence-free survival. Our results suggested that a distinction should be made between preoperative and intraoperative tumor ruptures when considering the indications for adjuvant imatinib therapy for gastrointestinal stromal tumor patients with tumor rupture as a single, high-risk factor of recurrence. Preoperative and intraoperative tumor ruptures should be distinguished when considering the indications for adjuvant imatinib therapy for gastrointestinal stromal tumor patients with tumor rupture as a single, high-risk factor of recurrence.</description><identifier>ISSN: 1465-3621</identifier><identifier>EISSN: 1465-3621</identifier><identifier>DOI: 10.1093/jjco/hyab200</identifier><identifier>PMID: 34933335</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Antineoplastic Agents - therapeutic use ; Cohort Studies ; Gastrointestinal Stromal Tumors - drug therapy ; Gastrointestinal Stromal Tumors - surgery ; Humans ; Imatinib Mesylate - therapeutic use ; Neoplasm Recurrence, Local - pathology ; Prognosis ; Retrospective Studies</subject><ispartof>Japanese journal of clinical oncology, 2022-03, Vol.52 (3), p.237-243</ispartof><rights>The Author(s) 2021. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2021</rights><rights>The Author(s) 2021. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c347t-bdc119d912ef8eccb6710e84863a2098e70b702bb9cde1cfc031b7d519e0e0063</citedby><cites>FETCH-LOGICAL-c347t-bdc119d912ef8eccb6710e84863a2098e70b702bb9cde1cfc031b7d519e0e0063</cites><orcidid>0000-0001-6070-8156 ; 0000-0002-6450-1272</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,1585,27928,27929</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34933335$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chiguchi, Gaku</creatorcontrib><creatorcontrib>Cho, Haruhiko</creatorcontrib><creatorcontrib>Sato, Shinsuke</creatorcontrib><creatorcontrib>Takahashi, Tsuyoshi</creatorcontrib><creatorcontrib>Nabeshima, Kazuhito</creatorcontrib><creatorcontrib>Maruyama, Tsunehiko</creatorcontrib><creatorcontrib>Kataoka, Mikinori</creatorcontrib><creatorcontrib>Katayanagi, Sou</creatorcontrib><creatorcontrib>Kikuchi, Hirotoshi</creatorcontrib><title>Impact of preoperative tumor rupture timing on gastrointestinal stromal tumor prognosis: a retrospective multicentric cohort study</title><title>Japanese journal of clinical oncology</title><addtitle>Jpn J Clin Oncol</addtitle><description>Abstract Background A gastrointestinal stromal tumor rupture entails a high risk of recurrence even after curative surgery. However, the definition of rupture is unclear, and the question of whether patients with a minor rupture should be treated with adjuvant imatinib remains controversial. Methods The present, retrospective, multicentric study enrolled 57 patients with gastrointestinal stromal tumor with a minor/major tumor rupture, of whom 46 were finally found to be eligible for analysis. Tumor ruptures were subclassified by their degree, timing and cause. Multivariate analysis was performed to identify the risk factors of all types of recurrence as well as of peritoneal recurrence only. Results The study cohort included minor (n = 24), intraoperative (n = 19) and iatrogenic (n = 20) ruptures besides the typical types (major, preoperative and spontaneous). All intraoperative ruptures were iatrogenic. In total, 27 patients (58.7%) had a recurrence in the peritoneum (n = 17) and/or the liver (n = 13) during a median follow-up period of 5.8 years, but no recurrence was observed in patients with tumor rupture as a single, high-risk factor. Multivariate analysis found the timing of tumor rupture to be an independent risk factor of poor recurrence-free survival (hazard ratio: 2.37; 95% confidence interval: 1.02–5.49; P = 0.045). Conclusions Preoperative tumor rupture in patients with a ruptured gastrointestinal stromal tumor was associated with poor recurrence-free survival. Our results suggested that a distinction should be made between preoperative and intraoperative tumor ruptures when considering the indications for adjuvant imatinib therapy for gastrointestinal stromal tumor patients with tumor rupture as a single, high-risk factor of recurrence. Preoperative and intraoperative tumor ruptures should be distinguished when considering the indications for adjuvant imatinib therapy for gastrointestinal stromal tumor patients with tumor rupture as a single, high-risk factor of recurrence.</description><subject>Antineoplastic Agents - therapeutic use</subject><subject>Cohort Studies</subject><subject>Gastrointestinal Stromal Tumors - drug therapy</subject><subject>Gastrointestinal Stromal Tumors - surgery</subject><subject>Humans</subject><subject>Imatinib Mesylate - therapeutic use</subject><subject>Neoplasm Recurrence, Local - pathology</subject><subject>Prognosis</subject><subject>Retrospective Studies</subject><issn>1465-3621</issn><issn>1465-3621</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kLtPwzAQxi0EolDYmJE3GAi14zzZUMWjUiUWmCPHubSuktj4gdSVvxyXFMTELXen-92nuw-hC0puKSnZbLMRarbe8jom5ACd0CRLI5bF9PBPPUGn1m4IIWmR5MdowpKShUhP0Oei11w4rFqsDSgNhjv5Adj5XhlsvHbehE72clhhNeAVt84oOTiwTg68w7u2D3lc0EatBmWlvcMcGwgzq0F8K_a-c1LA4IwUWKi1Mi4s-2Z7ho5a3lk43-cpent8eJ0_R8uXp8X8fhkJluQuqhtBadmUNIa2ACHqLKcEiqTIGI9JWUBO6pzEdV2KBqhoBWG0zpuUlkCAkIxN0fWoG4589-H-qpdWQNfxAZS3VZzROGd5kdKA3oyoCA9YA22ljey52VaUVDvXq53r1d71gF_ulX3dQ_ML_9gcgKsRUF7_L_UFgjKRPg</recordid><startdate>20220303</startdate><enddate>20220303</enddate><creator>Chiguchi, Gaku</creator><creator>Cho, Haruhiko</creator><creator>Sato, Shinsuke</creator><creator>Takahashi, Tsuyoshi</creator><creator>Nabeshima, Kazuhito</creator><creator>Maruyama, Tsunehiko</creator><creator>Kataoka, Mikinori</creator><creator>Katayanagi, Sou</creator><creator>Kikuchi, Hirotoshi</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-6070-8156</orcidid><orcidid>https://orcid.org/0000-0002-6450-1272</orcidid></search><sort><creationdate>20220303</creationdate><title>Impact of preoperative tumor rupture timing on gastrointestinal stromal tumor prognosis: a retrospective multicentric cohort study</title><author>Chiguchi, Gaku ; Cho, Haruhiko ; Sato, Shinsuke ; Takahashi, Tsuyoshi ; Nabeshima, Kazuhito ; Maruyama, Tsunehiko ; Kataoka, Mikinori ; Katayanagi, Sou ; Kikuchi, Hirotoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c347t-bdc119d912ef8eccb6710e84863a2098e70b702bb9cde1cfc031b7d519e0e0063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Antineoplastic Agents - therapeutic use</topic><topic>Cohort Studies</topic><topic>Gastrointestinal Stromal Tumors - drug therapy</topic><topic>Gastrointestinal Stromal Tumors - surgery</topic><topic>Humans</topic><topic>Imatinib Mesylate - therapeutic use</topic><topic>Neoplasm Recurrence, Local - pathology</topic><topic>Prognosis</topic><topic>Retrospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chiguchi, Gaku</creatorcontrib><creatorcontrib>Cho, Haruhiko</creatorcontrib><creatorcontrib>Sato, Shinsuke</creatorcontrib><creatorcontrib>Takahashi, Tsuyoshi</creatorcontrib><creatorcontrib>Nabeshima, Kazuhito</creatorcontrib><creatorcontrib>Maruyama, Tsunehiko</creatorcontrib><creatorcontrib>Kataoka, Mikinori</creatorcontrib><creatorcontrib>Katayanagi, Sou</creatorcontrib><creatorcontrib>Kikuchi, Hirotoshi</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Japanese journal of clinical oncology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chiguchi, Gaku</au><au>Cho, Haruhiko</au><au>Sato, Shinsuke</au><au>Takahashi, Tsuyoshi</au><au>Nabeshima, Kazuhito</au><au>Maruyama, Tsunehiko</au><au>Kataoka, Mikinori</au><au>Katayanagi, Sou</au><au>Kikuchi, Hirotoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of preoperative tumor rupture timing on gastrointestinal stromal tumor prognosis: a retrospective multicentric cohort study</atitle><jtitle>Japanese journal of clinical oncology</jtitle><addtitle>Jpn J Clin Oncol</addtitle><date>2022-03-03</date><risdate>2022</risdate><volume>52</volume><issue>3</issue><spage>237</spage><epage>243</epage><pages>237-243</pages><issn>1465-3621</issn><eissn>1465-3621</eissn><abstract>Abstract Background A gastrointestinal stromal tumor rupture entails a high risk of recurrence even after curative surgery. However, the definition of rupture is unclear, and the question of whether patients with a minor rupture should be treated with adjuvant imatinib remains controversial. Methods The present, retrospective, multicentric study enrolled 57 patients with gastrointestinal stromal tumor with a minor/major tumor rupture, of whom 46 were finally found to be eligible for analysis. Tumor ruptures were subclassified by their degree, timing and cause. Multivariate analysis was performed to identify the risk factors of all types of recurrence as well as of peritoneal recurrence only. Results The study cohort included minor (n = 24), intraoperative (n = 19) and iatrogenic (n = 20) ruptures besides the typical types (major, preoperative and spontaneous). All intraoperative ruptures were iatrogenic. In total, 27 patients (58.7%) had a recurrence in the peritoneum (n = 17) and/or the liver (n = 13) during a median follow-up period of 5.8 years, but no recurrence was observed in patients with tumor rupture as a single, high-risk factor. Multivariate analysis found the timing of tumor rupture to be an independent risk factor of poor recurrence-free survival (hazard ratio: 2.37; 95% confidence interval: 1.02–5.49; P = 0.045). Conclusions Preoperative tumor rupture in patients with a ruptured gastrointestinal stromal tumor was associated with poor recurrence-free survival. Our results suggested that a distinction should be made between preoperative and intraoperative tumor ruptures when considering the indications for adjuvant imatinib therapy for gastrointestinal stromal tumor patients with tumor rupture as a single, high-risk factor of recurrence. Preoperative and intraoperative tumor ruptures should be distinguished when considering the indications for adjuvant imatinib therapy for gastrointestinal stromal tumor patients with tumor rupture as a single, high-risk factor of recurrence.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>34933335</pmid><doi>10.1093/jjco/hyab200</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-6070-8156</orcidid><orcidid>https://orcid.org/0000-0002-6450-1272</orcidid></addata></record>
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subjects Antineoplastic Agents - therapeutic use
Cohort Studies
Gastrointestinal Stromal Tumors - drug therapy
Gastrointestinal Stromal Tumors - surgery
Humans
Imatinib Mesylate - therapeutic use
Neoplasm Recurrence, Local - pathology
Prognosis
Retrospective Studies
title Impact of preoperative tumor rupture timing on gastrointestinal stromal tumor prognosis: a retrospective multicentric cohort study
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