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Impact of neoadjuvant treatment on rectal gastrointestinal stromal tumors

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dc.contributor.author강정현-
dc.contributor.author민병소-
dc.contributor.author이강영-
dc.contributor.author안중배-
dc.contributor.author정진옥-
dc.contributor.author김남규-
dc.date.accessioned2022-12-22T04:16:47Z-
dc.date.available2022-12-22T04:16:47Z-
dc.date.issued2022-09-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/192089-
dc.description.abstractAlthough gastrointestinal stromal tumors (GISTs) are rare disease and rectal GISTs is only 5% of total GISTs, they have the worst prognosis. Due to narrow pelvis, tumor rupture or positive resection margin are common in the management of rectal GISTs. The impact of neoadjuvant treatment on the clinical outcomes of rectal gastrointestinal stromal tumors (GISTs) remains unclear. Thus, we conducted a retrospective study to investigate the impact of neoadjuvant imatinib on rectal GIST. The cohort comprised 33 patients; of them, 10 and 23 belonged to the neoadjuvant (i.e., those who underwent neoadjuvant imatinib treatment) and the control group (i.e., those who underwent surgery without prior imatinib treatment), respectively. Neoadjuvant group was associated with more common levator ani muscle displacement (P = 0.002), and showed significantly larger radiologic tumor size (P = 0.036) than the control group. The mean tumor size was significantly decreased after imatinib treatment (6.8 cm to 4.7cm, P = 0.006). There was no significant difference in resection margin involvement (P >0.999), and sphincter preservation rates (P = 0.627) between the two groups. No difference was observed with respect to morbidities, hospital stay, local recurrence and disease-free survival. Neoadjuvant imatinib treated group had similar propensity with control group after treatment. We thought reduced tumor sized could enhance resectability and provide more chance to preserve sphincter for rectal GIST patients. Considering large tumor size and higher rate of sphincter invasion in the neoadjuvant group, imatinib treatment could be helpful as a conversion strategy to make huge and low-lying rectal GIST operable and achieve better surgical outcomes.-
dc.description.statementOfResponsibilityopen-
dc.formatapplication/pdf-
dc.languageEnglish-
dc.publisherPublic Library of Science-
dc.relation.isPartOfPLOS ONE-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAntineoplastic Agents* / therapeutic use-
dc.subject.MESHGastrointestinal Stromal Tumors* / drug therapy-
dc.subject.MESHGastrointestinal Stromal Tumors* / surgery-
dc.subject.MESHHumans-
dc.subject.MESHImatinib Mesylate / therapeutic use-
dc.subject.MESHMargins of Excision-
dc.subject.MESHNeoadjuvant Therapy-
dc.subject.MESHRectal Neoplasms* / drug therapy-
dc.subject.MESHRectal Neoplasms* / pathology-
dc.subject.MESHRetrospective Studies-
dc.titleImpact of neoadjuvant treatment on rectal gastrointestinal stromal tumors-
dc.typeArticle-
dc.contributor.collegeCollege of Medicine (의과대학)-
dc.contributor.departmentDept. of Surgery (외과학교실)-
dc.contributor.googleauthorChinock Cheong-
dc.contributor.googleauthorJeonghyun Kang-
dc.contributor.googleauthorByung Soh Min-
dc.contributor.googleauthorNam Kyu Kim-
dc.contributor.googleauthorJoong Bae Ahn-
dc.contributor.googleauthorKang Young Lee-
dc.identifier.doi10.1371/journal.pone.0270887-
dc.contributor.localIdA00080-
dc.contributor.localIdA01402-
dc.contributor.localIdA02640-
dc.contributor.localIdA02262-
dc.relation.journalcodeJ02540-
dc.identifier.eissn1932-6203-
dc.identifier.pmid36084094-
dc.contributor.alternativeNameKang, Jeonghyun-
dc.contributor.affiliatedAuthor강정현-
dc.contributor.affiliatedAuthor민병소-
dc.contributor.affiliatedAuthor이강영-
dc.contributor.affiliatedAuthor안중배-
dc.citation.volume17-
dc.citation.number9-
dc.citation.startPagee0270887-
dc.identifier.bibliographicCitationPLOS ONE, Vol.17(9) : e0270887, 2022-09-
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Surgery (외과학교실) > 1. Journal Papers

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