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Risk of Peritoneal Carcinomatosis After Risk-Reducing Salpingo-Oophorectomy: A Systematic Review and Individual Patient Data Meta-Analysis.
Steenbeek, Miranda P; van Bommel, Majke H D; Bulten, Johan; Hulsmann, Julia A; Bogaerts, Joep; Garcia, Christine; Cun, Han T; Lu, Karen H; van Beekhuizen, Heleen J; Minig, Lucas; Gaarenstroom, Katja N; Nobbenhuis, Marielle; Krajc, Mateja; Rudaitis, Vilius; Norquist, Barbara M; Swisher, Elizabeth M; Mourits, Marian J E; Massuger, Leon F A G; Hoogerbrugge, Nicoline; Hermens, Rosella P M G; IntHout, Joanna; de Hullu, Joanne A.
Afiliação
  • Steenbeek MP; Radboud University Medical Center, Radboud Institute for Health Sciences, Department of Obstetrics and Gynaecology, Nijmegen, the Netherlands.
  • van Bommel MHD; Radboud University Medical Center, Radboud Institute for Health Sciences, Department of Obstetrics and Gynaecology, Nijmegen, the Netherlands.
  • Bulten J; Radboud University Medical Center, Department of Pathology, Nijmegen, the Netherlands.
  • Hulsmann JA; Radboud University Medical Center, Radboud Institute for Health Sciences, Department of Obstetrics and Gynaecology, Nijmegen, the Netherlands.
  • Bogaerts J; Radboud University Medical Center, Department of Pathology, Nijmegen, the Netherlands.
  • Garcia C; Kaiser Permanente Northern California, Division of Gynecologic Oncology San Francisco, San Francisco CA.
  • Cun HT; Department of Gynecologic Oncology and Reproductive Medicine, University of Texas MD Anderson Cancer Center, Houston, TX.
  • Lu KH; Department of Gynecologic Oncology and Reproductive Medicine, University of Texas MD Anderson Cancer Center, Houston, TX.
  • van Beekhuizen HJ; Erasmus MC Cancer Center, University Medical Center Rotterdam, Department of Gynecological Oncology, Rotterdam, the Netherlands.
  • Minig L; Gynecologic Oncology Unit, IMED Hospitales, Valencia, Spain.
  • Gaarenstroom KN; Leiden University Medical Center, Department of Obstetrics and Gynecology, Leiden, the Netherlands.
  • Nobbenhuis M; The Royal Marsden NHS Foundation Trust, Department of Gynaecology, London, England.
  • Krajc M; Institute of Oncology Ljubljana, Department of Clinical Genetics, Ljubljana, Slovenia.
  • Rudaitis V; Vilnius University Faculty of Medicine, Clinic of Obstetrics and Gynecology, Vilnius, Lithuania.
  • Norquist BM; University of Washington, Division of Gynecologic Oncology, Seattle, WA.
  • Swisher EM; University of Washington, Division of Gynecologic Oncology, Seattle, WA.
  • Mourits MJE; University Medical Center Groningen, University of Groningen, Department of Gynecologic Oncology, Groningen, the Netherlands.
  • Massuger LFAG; Radboud University Medical Center, Radboud Institute for Health Sciences, Department of Obstetrics and Gynaecology, Nijmegen, the Netherlands.
  • Hoogerbrugge N; Radboud University Medical Center, Department of Human Genetics, Nijmegen, the Netherlands.
  • Hermens RPMG; Radboud University Medical Center, Radboud Institute for Health Sciences, Scientific Institute for Quality of Healthcare, Nijmegen, the Netherlands.
  • IntHout J; Radboud University Medical Center, Radboud Institute for Health Sciences, Department for Health Evidence, Nijmegen, the Netherlands.
  • de Hullu JA; Radboud University Medical Center, Radboud Institute for Health Sciences, Department of Obstetrics and Gynaecology, Nijmegen, the Netherlands.
J Clin Oncol ; 40(17): 1879-1891, 2022 06 10.
Article em En | MEDLINE | ID: mdl-35302882
ABSTRACT

PURPOSE:

After risk-reducing salpingo-oophorectomy (RRSO), BRCA1/2 pathogenic variant (PV) carriers have a residual risk to develop peritoneal carcinomatosis (PC). The etiology of PC is not yet clarified, but may be related to serous tubal intraepithelial carcinoma (STIC), the postulated origin for high-grade serous cancer. In this systematic review and individual patient data meta-analysis, we investigate the risk of PC in women with and without STIC at RRSO.

METHODS:

Unpublished data from three centers were supplemented by studies identified in a systematic review of EMBASE, MEDLINE, and the Cochrane library describing women with a BRCA-PV with and without STIC at RRSO until September 2020. Primary outcome was the hazard ratio for the risk of PC between BRCA-PV carriers with and without STIC at RRSO, and the corresponding 5- and 10-year risks. Primary analysis was based on a one-stage Cox proportional-hazards regression with a frailty term for study.

RESULTS:

From 17 studies, individual patient data were available for 3,121 women, of whom 115 had a STIC at RRSO. The estimated hazard ratio to develop PC during follow-up in women with STIC was 33.9 (95% CI, 15.6 to 73.9), P < .001) compared with women without STIC. For women with STIC, the five- and ten-year risks to develop PC were 10.5% (95% CI, 6.2 to 17.2) and 27.5% (95% CI, 15.6 to 43.9), respectively, whereas the corresponding risks were 0.3% (95% CI, 0.2 to 0.6) and 0.9% (95% CI, 0.6 to 1.4) for women without STIC at RRSO.

CONCLUSION:

BRCA-PV carriers with STIC at RRSO have a strongly increased risk to develop PC which increases over time, although current data are limited by small numbers of events.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Neoplasias Peritoneais / Neoplasias da Mama / Cistadenocarcinoma Seroso / Neoplasias das Tubas Uterinas Tipo de estudo: Etiology_studies / Risk_factors_studies / Systematic_reviews Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas / Neoplasias Peritoneais / Neoplasias da Mama / Cistadenocarcinoma Seroso / Neoplasias das Tubas Uterinas Tipo de estudo: Etiology_studies / Risk_factors_studies / Systematic_reviews Limite: Female / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article