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Racial Differences in the Tumor Immune Landscape and Survival of Women with High-Grade Serous Ovarian Carcinoma.
Peres, Lauren C; Colin-Leitzinger, Christelle; Sinha, Sweta; Marks, Jeffrey R; Conejo-Garcia, Jose R; Alberg, Anthony J; Bandera, Elisa V; Berchuck, Andrew; Bondy, Melissa L; Christensen, Brock C; Cote, Michele L; Doherty, Jennifer Anne; Moorman, Patricia G; Peters, Edward S; Moran Segura, Carlos; Nguyen, Jonathan V; Schwartz, Ann G; Terry, Paul D; Wilson, Christopher M; Fridley, Brooke L; Schildkraut, Joellen M.
Afiliação
  • Peres LC; Department of Cancer Epidemiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Colin-Leitzinger C; Department of Cancer Epidemiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Sinha S; Department of Cancer Epidemiology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Marks JR; Department of Surgery, Duke University School of Medicine, Durham, North Carolina.
  • Conejo-Garcia JR; Department of Immunology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Alberg AJ; Department of Epidemiology and Biostatistics, Arnold School of Public Health, University of South Carolina, Columbia, South Carolina.
  • Bandera EV; Department of Population Science, Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey.
  • Berchuck A; Department of Gynecologic Oncology, Duke University School of Medicine, Durham, North Carolina.
  • Bondy ML; Department of Epidemiology and Population Health, Stanford University School of Medicine, Stanford, California.
  • Christensen BC; Department of Epidemiology, Geisel School of Medicine, Dartmouth College, Lebanon, New Hampshire.
  • Cote ML; Department of Community and Family Medicine, Geisel School of Medicine, Dartmouth College, Lebanon, New Hampshire.
  • Doherty JA; Department of Molecular and Systems Biology, Geisel School of Medicine, Dartmouth College, Lebanon, New Hampshire.
  • Moorman PG; Population Studies and Disparities Research Program, Barbara Ann Karmanos Cancer Institute, Detroit, Michigan.
  • Peters ES; Department of Oncology, Wayne State University School of Medicine, Detroit, Michigan.
  • Moran Segura C; Department of Population Health Sciences, University of Utah, Salt Lake City, Utah.
  • Nguyen JV; Huntsman Cancer Institute, Salt Lake City, Utah.
  • Schwartz AG; Department of Community and Family Medicine, Duke University Medical Center, Durham, North Carolina.
  • Terry PD; Department of Epidemiology, College of Public Health, University of Nebraska Medical Center, Omaha, Nebraska.
  • Wilson CM; Department of Pathology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Fridley BL; Department of Pathology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, Florida.
  • Schildkraut JM; Population Studies and Disparities Research Program, Barbara Ann Karmanos Cancer Institute, Detroit, Michigan.
Cancer Epidemiol Biomarkers Prev ; 31(5): 1006-1016, 2022 05 04.
Article em En | MEDLINE | ID: mdl-35244678
ABSTRACT

BACKGROUND:

Tumor-infiltrating lymphocytes (TIL) confer a survival benefit among patients with ovarian cancer; however, little work has been conducted in racially diverse cohorts.

METHODS:

The current study investigated racial differences in the tumor immune landscape and survival of age- and stage-matched non-Hispanic Black and non-Hispanic White women with high-grade serous ovarian carcinoma (HGSOC) enrolled in two population-based studies (n = 121 in each racial group). We measured TILs (CD3+), cytotoxic T cells (CD3+CD8+), regulatory T cells (CD3+FoxP3+), myeloid cells (CD11b+), and neutrophils (CD11b+CD15+) via multiplex immunofluorescence. Multivariable Cox proportional hazard regression was used to estimate the association between immune cell abundance and survival overall and by race.

RESULTS:

Overall, higher levels of TILs, cytotoxic T cells, myeloid cells, and neutrophils were associated with better survival in the intratumoral and peritumoral region, irrespective of tissue compartment (tumor, stroma). Improved survival was noted for T-regulatory cells in the peritumoral region and in the stroma of the intratumoral region, but no association for intratumoral T-regulatory cells. Despite similar abundance of immune cells across racial groups, associations with survival among non-Hispanic White women were consistent with the overall findings, but among non-Hispanic Black women, most associations were attenuated and not statistically significant.

CONCLUSIONS:

Our results add to the existing evidence that a robust immune infiltrate confers a survival advantage among women with HGSOC; however, non-Hispanic Black women may not experience the same survival benefit as non-Hispanic White women with HGSOC. IMPACT This study contributes to our understanding of the immunoepidemiology of HGSOC in diverse populations.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas Limite: Female / Humans / Male Idioma: En Revista: Cancer Epidemiol Biomarkers Prev Assunto da revista: BIOQUIMICA / EPIDEMIOLOGIA / NEOPLASIAS Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Ovarianas Limite: Female / Humans / Male Idioma: En Revista: Cancer Epidemiol Biomarkers Prev Assunto da revista: BIOQUIMICA / EPIDEMIOLOGIA / NEOPLASIAS Ano de publicação: 2022 Tipo de documento: Article