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The Prognostic Role of ß-Catenin Mutations in Desmoid-type Fibromatosis Undergoing Resection Only: A Meta-analysis of Individual Patient Data.
Timbergen, Milea J M; Colombo, Chiara; Renckens, Michel; Kim, Hee Sung; Rosmalen, Joost van; Salas, Sébastien; Mullen, John T; Colombo, Piergiuseppe; Nishida, Yoshihiro; Wiemer, Erik A C; Verhoef, Cornelis; Sleijfer, Stefan; Gronchi, Alessandro; Grünhagen, Dirk J.
Afiliación
  • Timbergen MJM; Department of Surgical Oncology, Erasmus Medical Center Cancer Institute, Rotterdam, the Netherlands.
  • Colombo C; Department of Medical Oncology, Erasmus Medical Center Cancer Institute, Rotterdam, the Netherlands.
  • Renckens M; Sarcoma Service, Department of Surgery, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
  • Kim HS; Department of Radiology and Nuclear Medicine, Erasmus Medical Center, Rotterdam, the Netherlands.
  • Rosmalen JV; Department of Pathology, College of Medicine, Chung-Ang University, Seoul, South Korea.
  • Salas S; Department of Biostatistics, Erasmus Medical Center, Rotterdam, the Netherlands.
  • Mullen JT; Aix-Marseille Univ, INSERM U910, AP-HM, Hôpital de la Timone, Department of Medical Oncology and Palliative Care, Marseille, France.
  • Colombo P; Department of Surgery, Harvard Medical School and the Massachusetts General Hospital, Boston, Massachusetts.
  • Nishida Y; Department of Pathology, Humanitas Clinical and Research Center, Milan, Italy.
  • Wiemer EAC; Department of Rehabilitation and Orthopedic Surgery, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Verhoef C; Department of Medical Oncology, Erasmus Medical Center Cancer Institute, Rotterdam, the Netherlands.
  • Sleijfer S; Department of Surgical Oncology, Erasmus Medical Center Cancer Institute, Rotterdam, the Netherlands.
  • Gronchi A; Department of Medical Oncology, Erasmus Medical Center Cancer Institute, Rotterdam, the Netherlands.
  • Grünhagen DJ; Sarcoma Service, Department of Surgery, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Ann Surg ; 273(6): 1094-1101, 2021 06 01.
Article en En | MEDLINE | ID: mdl-31804402
OBJECTIVE: This meta-analysis (PROSPERO CRD42018100653) uses individual patient data (IPD) to assess the association between recurrence and CTNNB1 mutation status in surgically treated adult desmoid-type fibromatosis (DTF) patients. SUMMARY OF BACKGROUND DATA: The majority of sporadic DTF tumors harbor a CTNNB1 (ß-catenin) mutation: T41A, S45F, and S45P or are wild-type (WT). Results are conflicting regarding the recurrence risk after surgery for these mutation types. METHODS: A systematic literature search was performed on June 6th, 2018. IPD from eligible studies was used to analyze differences in recurrence according to CTNNB1 mutation status using Cox proportional hazards analysis. Predictive factors included: sex, age, mutation type, tumor site, tumor size, resection margin status, and cohort. The PRISMA-IPD guideline was used. RESULTS: Seven studies, describing retrospective cohorts were included and the IPD of 329 patients were used of whom 154 (46.8%) had a T41A mutation, 66 (20.1%) a S45F mutation, and 24 (7.3%) a S45P mutation, whereas 85 (25.8%) patients had a WT CTNNB1. Eighty-three patients (25.2%) experienced recurrence. Multivariable analysis, adjusting for sex, age, and tumor site yielded a P-value of 0.011 for CTNNB1 mutation. Additional adjustment for tumor size yielded a P-value of 0.082 with hazard ratio's of 0.83 [95% confidence interval (CI) 0.48-1.42), 0.37 (95% CI 0.12-1.14), and 0.44 (95% CI 0.21-0.92) for T41A, S45P and WT DTF tumors compared to S45F DTF tumors. The effect modification between tumor size and mutation type suggests that tumor size is an important mediator for recurrence. CONCLUSIONS: Primary sporadic DTFs harboring a CTNNB1 S45F mutation have a higher risk of recurrence after surgery compared to T41A, S45P, and WT DTF, but this association seems to be mediated by tumor size.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibromatosis Agresiva / Beta Catenina / Mutación Tipo de estudio: Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Ann Surg Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fibromatosis Agresiva / Beta Catenina / Mutación Tipo de estudio: Prognostic_studies / Systematic_reviews Límite: Humans Idioma: En Revista: Ann Surg Año: 2021 Tipo del documento: Article País de afiliación: Países Bajos
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