CA-125 Levels Are Predictive of Survival in Low-Grade Serous Ovarian Cancer-A Multicenter Analysis.
CA-125
low-grade serous cancer
ovarian cancer
survival
Journal
Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829
Informations de publication
Date de publication:
13 Apr 2022
13 Apr 2022
Historique:
received:
16
03
2022
revised:
03
04
2022
accepted:
03
04
2022
entrez:
23
4
2022
pubmed:
24
4
2022
medline:
24
4
2022
Statut:
epublish
Résumé
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. 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. 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 ( 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. 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.
Identifiants
pubmed: 35454861
pii: cancers14081954
doi: 10.3390/cancers14081954
pmc: PMC9024456
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : NCI NIH HHS
ID : R01 CA248288
Pays : United States
Organisme : Ovarian Cancer Research Fund
ID : PPD/RPCI.07
Références
Am J Surg Pathol. 2004 Apr;28(4):496-504
pubmed: 15087669
J Gynecol Oncol. 2018 Jan;29(1):e15
pubmed: 29185273
Ann Oncol. 2016 Apr;27 Suppl 1:i45-i49
pubmed: 27141071
CA Cancer J Clin. 2019 Jan;69(1):7-34
pubmed: 30620402
Int J Gynecol Cancer. 2007 May-Jun;17(3):601-6
pubmed: 17504374
Am J Surg Pathol. 2007 Aug;31(8):1168-74
pubmed: 17667538
Am J Obstet Gynecol. 2008 Apr;198(4):459.e1-8; discussion 459.e8-9
pubmed: 18395040
Gynecol Oncol. 2007 Jun;105(3):625-9
pubmed: 17320156
Cancers (Basel). 2020 Dec 11;12(12):
pubmed: 33322519
Gynecol Oncol. 2008 Mar;108(3):510-4
pubmed: 18155273
Cancer Epidemiol. 2021 Dec;75:102045
pubmed: 34638085
Int J Cancer. 2008 Jul 15;123(2):380-388
pubmed: 18431743
N Engl J Med. 1983 Oct 13;309(15):883-7
pubmed: 6310399
Gynecol Oncol. 2007 Mar;104(3):508-15
pubmed: 17113137
Ann Oncol. 2006 Aug;17(8):1234-8
pubmed: 16766592
Gynecol Oncol. 2016 Mar;140(3):457-62
pubmed: 26807488
Sci Rep. 2021 Sep 14;11(1):18190
pubmed: 34521891
Lancet. 2022 Feb 5;399(10324):541-553
pubmed: 35123694
Obstet Gynecol. 2013 Aug;122(2 Pt 1):225-232
pubmed: 23969788
Am J Surg Pathol. 2005 Aug;29(8):1034-41
pubmed: 16006797
Int Sch Res Notices. 2014 Oct 29;2014:953509
pubmed: 27382614
Gynecol Oncol. 2009 Jul;114(1):48-52
pubmed: 19361839
Mod Pathol. 2013 Sep;26(9):1255-63
pubmed: 23558569