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CA-125 Levels Are Predictive of Survival in Low-Grade Serous Ovarian Cancer-A Multicenter Analysis.
Wohlmuth, Christoph; Djedovic, Vladimir; Kjaer, Susanne K; Jensen, Allan; Glasspool, Rosalind; Roxburgh, Patricia; DeFazio, Anna; Johnatty, Sharon E; Webb, Penelope M; Modugno, Francesmary; Lambrechts, Diether; Schildkraut, Joellen M; Berchuck, Andrew; Thomsen, Liv Cecilie Vestrheim; Bjorge, Line; Høgdall, Estrid; Høgdall, Claus K; Goode, Ellen L; Winham, Stacey J; Matsuo, Keitaro; Karlan, Beth Y; Lester, Jenny; Goodman, Marc T; Thompson, Pamela J; Pejovic, Tanja; Riggan, Marjorie J; Lajkosz, Katherine; Tone, Alicia; May, Taymaa.
Afiliação
  • Wohlmuth C; Division of Gynecologic Oncology, Princess Margaret Hospital, University Health Network, Toronto, ON M5G 2M9, Canada.
  • Djedovic V; Department of Obstetrics and Gynecology, Paracelsus Medical University, 5020 Salzburg, Austria.
  • Kjaer SK; Division of Gynecologic Oncology, Princess Margaret Hospital, University Health Network, Toronto, ON M5G 2M9, Canada.
  • Jensen A; Department of Internal Medicine, University of Ottawa, Ottawa, ON K1H 8M5, Canada.
  • Glasspool R; Department of Lifestyle, Reproduction and Cancer, Danish Cancer Society Research Center, DK-2100 Copenhagen, Denmark.
  • Roxburgh P; Department of Gynaecology, Rigshospitalet, University of Copenhagen, DK-2100 Copenhagen, Denmark.
  • DeFazio A; Department of Lifestyle, Reproduction and Cancer, Danish Cancer Society Research Center, DK-2100 Copenhagen, Denmark.
  • Johnatty SE; Beatson West of Scotland Cancer Centre, University of Glasgow, Glasgow G12 0YN, UK.
  • Webb PM; Institute of Cancer Sciences, University of Glasgow, Glasgow G61 1QH, UK.
  • Modugno F; Beatson West of Scotland Cancer Centre, University of Glasgow, Glasgow G12 0YN, UK.
  • Lambrechts D; Institute of Cancer Sciences, University of Glasgow, Glasgow G61 1QH, UK.
  • Schildkraut JM; Centre for Cancer Research, The Westmead Institute for Medical Research, Sydney, NSW 2145, Australia.
  • Berchuck A; Department of Gynaecological Oncology, Westmead Hospital, Sydney, NSW 2145, Australia.
  • Thomsen LCV; The Daffodil Centre, a Joint Venture with Cancer Council NSW, The Daffodil Centre, The University of Sydney, Sydney, NSW 2145, Australia.
  • Bjorge L; Cancer Genetics Laboratory, Research Division, Peter MacCallum Cancer Center, Melbourne, VIC 3000, Australia.
  • Høgdall E; Department of Genetics and Computational Biology, QIMR Berghofer Medical Research Institute, Brisbane, QLD 4006, Australia.
  • Høgdall CK; Population Health Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD 4006, Australia.
  • Goode EL; Women's Cancer Research Center, Magee-Womens Research Institute and Hillman Cancer Center, Pittsburgh, PA 15213, USA.
  • Winham SJ; Department of Obstetrics, Gynecology and Reproductive Sciences, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA.
  • Matsuo K; Laboratory for Translational Genetics, Department of Human Genetics, KU Leuven, 3000 Leuven, Belgium.
  • Karlan BY; VIB Center for Cancer Biology, VIB, 3000 Leuven, Belgium.
  • Lester J; Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, GA 30322, USA.
  • Goodman MT; Department of Gynecologic Oncology, Duke University Hospital, Durham, NC 27710, USA.
  • Thompson PJ; Department of Obstetrics and Gynecology, Haukeland University Hospital, 5021 Bergen, Norway.
  • Pejovic T; Centre for Cancer Biomarkers CCBIO, Department of Clinical Science, University of Bergen, 5020 Bergen, Norway.
  • Riggan MJ; Department of Obstetrics and Gynecology, Haukeland University Hospital, 5021 Bergen, Norway.
  • Lajkosz K; Centre for Cancer Biomarkers CCBIO, Department of Clinical Science, University of Bergen, 5020 Bergen, Norway.
  • Tone A; Department of Pathology, Herlev Hospital, University of Copenhagen, DK-2100 Copenhagen, Denmark.
  • May T; Department of Gynaecology, Rigshospitalet, University of Copenhagen, DK-2100 Copenhagen, Denmark.
Cancers (Basel) ; 14(8)2022 Apr 13.
Article em En | MEDLINE | ID: mdl-35454861
ABSTRACT

OBJECTIVE:

Studies on low-grade serous ovarian cancer (LGSC) are limited by a low number of cases. The aim of this study was to define the prognostic significance of age, stage, and CA-125 levels on survival in a multi-institutional cohort of women with pathologically confirmed LGSC.

METHODS:

Women with LGSC were identified from the collaborative Ovarian Cancer Association Consortium (OCAC). Cases of newly diagnosed primary LGSC were included if peri-operative CA-125 levels were available. Age at diagnosis, FIGO stage, pre- and post-treatment CA-125 levels, residual disease, adjuvant chemotherapy, disease recurrence, and vital status were collected by the participating institutions. Progression-free (PFS) and overall survival (OS) were calculated. Multivariable (MVA) Cox proportional hazard models were used and hazard ratios (HR) calculated.

RESULTS:

A total of 176 women with LGSC were included in this study; 82% had stage III/IV disease. The median PFS was 2.3 years and the median OS was 6.4 years. Age at diagnosis was not significantly associated with worse PFS (p = 0.23) or OS (p = 0.3) (HR per year 0.99; 95%CI, 0.96-1.01 and 0.98; 95%CI 0.95-1.01). FIGO stage III/IV was independently associated with PFS (HR 4.26, 95%CI 1.43-12.73) and OS (HR 1.69, 95%CI 0.56-5.05). Elevated CA-125 (≥35 U/mL) at diagnosis was not significantly associated with worse PFS (p = 0.87) or OS (p = 0.78) in MVA. Elevated CA-125 (≥35 U/mL) after completion of primary treatment was independently associated with worse PFS (HR 2.81, 95%CI 1.36-5.81) and OS (HR 6.62, 95%CI 2.45-17.92). In the MVA, residual disease was independently associated with PFS (0.022), but not OS (0.85).

CONCLUSION:

Advanced LGSC was associated with poor long-term prognosis. FIGO stage and abnormal post-treatment CA-125 level are key prognostic factors inversely associated with PFS and OS. HIGHLIGHTS 1. Through a multi-center collaborative effort, data from 176 women with low-grade serous ovarian cancer were analyzed. 2. Although low-grade serous ovarian cancer is often considered indolent, the progression-free and overall survival are poor. 3. Elevated post-treatment CA-125 levels are independently associated with poor survival.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article