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Safety and efficacy study of laparoscopic or robotic radical surgery using an endoscopic stapler for inhibiting tumour spillage of cervical malignant neoplasms evaluating survival (SOLUTION): a multi-centre, open-label, single-arm, phase II trial protocol

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dc.contributor.authorPark, SJ-
dc.contributor.authorKong, TW-
dc.contributor.authorKim, T-
dc.contributor.authorLee, M-
dc.contributor.authorChoi, CH-
dc.contributor.authorShim, SH-
dc.contributor.authorYim, GW-
dc.contributor.authorLee, S-
dc.contributor.authorLee, EJ-
dc.contributor.authorLim, MC-
dc.contributor.authorChang, SJ-
dc.contributor.authorLee, SJ-
dc.contributor.authorLee, SH-
dc.contributor.authorSong, T-
dc.contributor.authorLee, YY-
dc.contributor.authorKim, HS-
dc.contributor.authorNam, EJ-
dc.date.accessioned2023-02-13T06:23:06Z-
dc.date.available2023-02-13T06:23:06Z-
dc.date.issued2022-
dc.identifier.urihttp://repository.ajou.ac.kr/handle/201003/24491-
dc.description.abstractBACKGROUND: The Laparoscopic Approach to Cervical Cancer trial and Surveillance, Epidemiology, and End Results program database study demonstrated that minimally invasive radical hysterectomy was inferior to abdominal radical hysterectomy in terms of disease recurrence and survival. Among risk factors related to poor prognosis after minimally invasive surgery (MIS), tumour spillage during intracorporeal colpotomy became a significant issue. Thus, we designed this trial to evaluate the efficacy and safety of minimally invasive radical hysterectomy using an endoscopic stapler for early-stage cervical cancer. METHODS: This trial is a prospective, multi-centre, open-label, single-arm, non-inferiority phase II study. The nine organisations will participate in this trial after the approval of the institutional review board. Major eligibility criteria include women aged 20 years or older with cervical cancer stage IB1 squamous cell carcinoma, adenocarcinoma, or adenosquamous carcinoma according to the revised 2009 FIGO staging system who will undergo type B2 or C hysterectomy by MIS. The primary endpoint is the 4.5-year disease-free survival (DFS) rate between abdominal radical hysterectomy and MIS using an endoscopic stapler. For calculating the sample size, we hypothesised that the 4.5-year DFS rate after MIS using an endoscopic stapler is assumed to be the same after abdominal radical hysterectomy at 90.9%, and the non-inferiority margin was 7.2%. When we consider a three-year accrual and 4.5-year follow-up, at least 13 events must happen, requiring a total of 111 patients assuming a statistical power of 80% and the one-tailed test of 5% significance. A total of 124 patients is needed, considering a drop-out rate of 10%. DISCUSSION: We expect intracorporeal colpotomy using an endoscopic stapler may prevent tumour spillage during MIS for stage IB1 cervical cancer, showing a comparable prognosis with abdominal radical surgery. TRIAL REGISTRATION: ClinicalTrials.gov ; NCT04370496 ; registration date, May 2020.-
dc.language.isoen-
dc.subject.MESHAdult-
dc.subject.MESHClinical Trials, Phase II as Topic-
dc.subject.MESHFemale-
dc.subject.MESHHumans-
dc.subject.MESHLaparoscopy-
dc.subject.MESHMulticenter Studies as Topic-
dc.subject.MESHNeoplasm Recurrence, Local-
dc.subject.MESHNeoplasm Staging-
dc.subject.MESHProspective Studies-
dc.subject.MESHRobotic Surgical Procedures-
dc.subject.MESHUterine Cervical Neoplasms-
dc.subject.MESHYoung Adult-
dc.titleSafety and efficacy study of laparoscopic or robotic radical surgery using an endoscopic stapler for inhibiting tumour spillage of cervical malignant neoplasms evaluating survival (SOLUTION): a multi-centre, open-label, single-arm, phase II trial protocol-
dc.typeArticle-
dc.identifier.pmid35346103-
dc.identifier.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962597-
dc.subject.keywordCervical cancer-
dc.subject.keywordEndoscopic stapler-
dc.subject.keywordMinimally invasive surgery-
dc.subject.keywordRecurrence-
dc.subject.keywordSurvival-
dc.contributor.affiliatedAuthorKong, TW-
dc.contributor.affiliatedAuthorChang, SJ-
dc.type.localJournal Papers-
dc.identifier.doi10.1186/s12885-022-09429-z-
dc.citation.titleBMC cancer-
dc.citation.volume22-
dc.citation.number1-
dc.citation.date2022-
dc.citation.startPage331-
dc.citation.endPage331-
dc.identifier.bibliographicCitationBMC cancer, 22(1). : 331-331, 2022-
dc.identifier.eissn1471-2407-
dc.relation.journalidJ014712407-
Appears in Collections:
Journal Papers > School of Medicine / Graduate School of Medicine > Obstetrics & Gynecology
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