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Intraluminal tumor cells and prognostic accuracy of endometrial cancer stage criteria: A multi-institution study.
Felix, Ashley S; Sinnott, Jennifer A; Cohn, David E; Duggan, Máire A; Havrilesky, Laura J; Olawaiye, Alexander B; Mariani, Andrea; Rodriquez, Monica; Brett, Mary Anne; Dinoi, Giorgia; Meade, Caitlin E; Hall, Bobbie; Goldfeld, Ester; Elishaev, Esther; Sherman, Mark E; Suarez, Adrian A.
Afiliação
  • Felix AS; Division of Epidemiology, The Ohio State University College of Public Health, Columbus, OH, United States of America. Electronic address: Ashley.Felix@osumc.edu.
  • Sinnott JA; Department of Statistics, The Ohio State University College of Arts and Sciences, Columbus, OH, United States of America.
  • Cohn DE; Division of Gynecologic Oncology, The Ohio State University College of Medicine, Columbus, OH, United States of America.
  • Duggan MA; Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Calgary, Calgary, AB, Canada; Department of Pathology and Laboratory Medicine, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
  • Havrilesky LJ; Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, Duke University Medical Center, Duke Cancer Institute, Durham, NC, United States of America.
  • Olawaiye AB; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Magee-Women's Hospital of UPMC, Pittsburgh, PA, United States of America.
  • Mariani A; Gynecology and Obstetrics, Mayo Clinic, Rochester, MN, United States of America.
  • Rodriquez M; Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Calgary, Calgary, AB, Canada; Department of Pathology and Laboratory Medicine, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
  • Brett MA; Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, University of Calgary, Calgary, AB, Canada; Department of Pathology and Laboratory Medicine, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
  • Dinoi G; Gynecology and Obstetrics, Mayo Clinic, Rochester, MN, United States of America.
  • Meade CE; Division of Epidemiology, The Ohio State University College of Public Health, Columbus, OH, United States of America.
  • Hall B; Division of Epidemiology, The Ohio State University College of Public Health, Columbus, OH, United States of America.
  • Goldfeld E; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Magee-Women's Hospital of UPMC, Pittsburgh, PA, United States of America.
  • Elishaev E; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Magee-Women's Hospital of UPMC, Pittsburgh, PA, United States of America.
  • Sherman ME; Department of Pulmonary Medicine, Mayo Clinic, Jacksonville, FL, United States of America.
  • Suarez AA; Division of Pathology, The Ohio State University College of Medicine, Columbus, OH, United States of America.
Gynecol Oncol ; 178: 130-137, 2023 Nov.
Article em En | MEDLINE | ID: mdl-37862792
ABSTRACT

OBJECTIVE:

Endometrial cancer stage is a strong prognostic factor; however, the current stage classification does not incorporate transtubal spread as determined by intraluminal tumor cells (ILTCs). We examined relationships between ILTCs and survival outcomes according to histological subtype and stage and examined whether identification of ILTCs improves prognostic accuracy of endometrial cancer staging.

METHODS:

We conducted a retrospective cohort study of women diagnosed with endometrial cancer at five academic hospitals between 2007 and 2012. Pathologists determined ILTC presence (no vs. yes) and location (free in lumen vs. attached to epithelial surface) based on pathology review of hematoxylin and eosin-stained sections of fallopian tubes. Associations between ILTCs with time to recurrence (TTR) and overall survival (OS) were examined with Cox proportional hazards models adjusted for other prognostic factors. Model discrimination metrics were used to assess the addition of ILTCs to stage for prediction of 5-year TTR and OS.

RESULTS:

In the overall study population (N = 1303), ILTCs were not independently associated with TTR (HR = 0.95, 95% CI = 0.69-1.32) or OS (HR = 0.97, 95% CI = 0.72-1.31). Among 805 women with stage I disease, ILTCs were independently associated with worse TTR (HR = 2.31, 95% CI = 1.06-5.05) and OS (HR = 2.16, 95% CI = 1.14-4.11). Upstaging early-stage cases with ILTCs present did not increase model discrimination.

CONCLUSION:

While our data do not suggest that endometrial cancer staging guidelines should be revised to include ILTCs, associations between ILTCs and reduced survival observed among stage I cases suggest this tumor feature holds clinical relevance for subgroups of endometrial cancer patients.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias do Endométrio Limite: Female / Humans Idioma: En Revista: Gynecol Oncol Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias do Endométrio Limite: Female / Humans Idioma: En Revista: Gynecol Oncol Ano de publicação: 2023 Tipo de documento: Article