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Is minimally invasive radical surgery safe for patients with cervical cancer ≤2 cm in size? (MISAFE): Gynecologic Oncology Research Investigators coLLborAtion study (GORILLA-1003)
DC Field | Value | Language |
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dc.contributor.author | Kong, TW | - |
dc.contributor.author | Kim, J | - |
dc.contributor.author | Son, JH | - |
dc.contributor.author | Lee, AJ | - |
dc.contributor.author | Yang, EJ | - |
dc.contributor.author | Shim, SH | - |
dc.contributor.author | Kim, NK | - |
dc.contributor.author | Kim, Y | - |
dc.contributor.author | Suh, DH | - |
dc.contributor.author | Hwang, DW | - |
dc.contributor.author | Park, SJ | - |
dc.contributor.author | Kim, HS | - |
dc.contributor.author | Lee, YY | - |
dc.contributor.author | Yoo, JG | - |
dc.contributor.author | Lee, SJ | - |
dc.contributor.author | Chang, SJ | - |
dc.date.accessioned | 2023-09-11T06:01:44Z | - |
dc.date.available | 2023-09-11T06:01:44Z | - |
dc.date.issued | 2023 | - |
dc.identifier.issn | 0090-8258 | - |
dc.identifier.uri | http://repository.ajou.ac.kr/handle/201003/26337 | - |
dc.description.abstract | Objective: To identify clinicopathological factors associated with disease recurrence for patients with 2018 FIGO stage IA with lymphovascular invasion to IB1 cervical cancer treated with minimally invasive surgery (MIS). Methods: A total of 722 patients with cervical cancer between January 2010 and February 2021 were identified. Clinicopathological factors related to disease recurrence were analyzed. Disease-free survival (DFS) and overall survival (OS) rates were estimated using the Kaplan-Meier method. To determine prognostic factors for DFS, a Cox proportional hazard regression model was used. Results: Of 722 patients, 49 (6.8%) experienced disease recurrence (37 pelvis, 1 para-aortic lymph node, and 11 peritoneum). Five-year DFS and OS rates were 90.7% and 98.1%, respectively. In multivariate analysis, risk factors associated with disease recurrence were residual disease in the remaining cervix (OR, 3.122; 95% CI, 1.152–8.461; p = 0.025), intracorporeal colpotomy (OR, 3.252; 95% CI, 1.507–7.017; p = 0.003), and positive resection margin (OR, 3.078; 95% CI, 1.031–9.193; p = 0.044). The non-conization group had a higher percentage of stage IB1 (77.4% vs. 64.6%; p = 0.004) and larger tumor (10 mm vs. 7 mm; p < 0.001) than the conization group. Intracorporeal colpotomy and residual disease in the remaining cervix were independent variables associated with disease recurrence in patients undergoing MIS following conization. Conclusion: During MIS, patients with cervical cancer ≤2 cm in size can be vulnerable to peritoneal recurrences. Patients diagnosed with invasive cancer through conization often have low-risk pathological features, which may affect their survival outcomes. | - |
dc.language.iso | en | - |
dc.subject.MESH | Animals | - |
dc.subject.MESH | Disease-Free Survival | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Genital Neoplasms, Female | - |
dc.subject.MESH | Gorilla gorilla | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Hysterectomy | - |
dc.subject.MESH | Minimally Invasive Surgical Procedures | - |
dc.subject.MESH | Neoplasm Recurrence, Local | - |
dc.subject.MESH | Neoplasm Staging | - |
dc.subject.MESH | Retrospective Studies | - |
dc.subject.MESH | Treatment Outcome | - |
dc.subject.MESH | Uterine Cervical Neoplasms | - |
dc.title | Is minimally invasive radical surgery safe for patients with cervical cancer ≤2 cm in size? (MISAFE): Gynecologic Oncology Research Investigators coLLborAtion study (GORILLA-1003) | - |
dc.type | Article | - |
dc.identifier.pmid | 37515926 | - |
dc.subject.keyword | Cervical cancer | - |
dc.subject.keyword | Colpotomy | - |
dc.subject.keyword | Conization | - |
dc.subject.keyword | Disease recurrence | - |
dc.subject.keyword | Minimally invasive surgery | - |
dc.contributor.affiliatedAuthor | Kong, TW | - |
dc.contributor.affiliatedAuthor | Kim, J | - |
dc.contributor.affiliatedAuthor | Son, JH | - |
dc.contributor.affiliatedAuthor | Chang, SJ | - |
dc.type.local | Journal Papers | - |
dc.identifier.doi | 10.1016/j.ygyno.2023.07.009 | - |
dc.citation.title | Gynecologic oncology | - |
dc.citation.volume | 176 | - |
dc.citation.date | 2023 | - |
dc.citation.startPage | 122 | - |
dc.citation.endPage | 129 | - |
dc.identifier.bibliographicCitation | Gynecologic oncology, 176. : 122-129, 2023 | - |
dc.embargo.liftdate | 9999-12-31 | - |
dc.embargo.terms | 9999-12-31 | - |
dc.identifier.eissn | 1095-6859 | - |
dc.relation.journalid | J000908258 | - |
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