CA-125 Levels Are Predictive of Survival in Low-Grade Serous Ovarian Cancer-A Multicenter Analysis

被引:4
|
作者
Wohlmuth, Christoph [1 ,2 ]
Djedovic, Vladimir [1 ,3 ]
Kjaer, Susanne K. [4 ,5 ]
Jensen, Allan [4 ]
Glasspool, Rosalind [6 ,7 ]
Roxburgh, Patricia [6 ,7 ]
DeFazio, Anna [8 ,9 ,10 ,11 ]
Johnatty, Sharon E. [12 ]
Webb, Penelope M. [13 ]
Modugno, Francesmary [14 ,15 ,16 ]
Lambrechts, Diether [17 ,18 ]
Schildkraut, Joellen M. [19 ]
Berchuck, Andrew [20 ]
Thomsen, Liv Cecilie Vestrheim [21 ,22 ]
Bjorge, Line [21 ,22 ]
Hogdall, Estrid [23 ]
Hogdall, Claus K. [5 ]
Goode, Ellen L. [24 ]
Winham, Stacey J. [25 ]
Matsuo, Keitaro [26 ,27 ]
Karlan, Beth Y. [28 ]
Lester, Jenny [28 ]
Goodman, Marc T. [29 ]
Thompson, Pamela J. [30 ]
Pejovic, Tanja [31 ,32 ]
Riggan, Marjorie J. [20 ]
Lajkosz, Katherine [33 ]
Tone, Alicia [1 ]
May, Taymaa [1 ]
机构
[1] Univ Hlth Network, Princess Margaret Hosp, Div Gynecol Oncol, Toronto, ON M5G 2M9, Canada
[2] Paracelsus Med Univ, Dept Obstet & Gynecol, A-5020 Salzburg, Austria
[3] Univ Ottawa, Dept Internal Med, Ottawa, ON K1H 8M5, Canada
[4] Danish Canc Soc, Res Ctr, Dept Lifestyle Reprod & Canc, DK-2100 Copenhagen, Denmark
[5] Univ Copenhagen, Rigshosp, Dept Gynaecol, DK-2100 Copenhagen, Denmark
[6] Univ Glasgow, Beatson West Scotland Canc Ctr, Glasgow G12 0YN, Lanark, Scotland
[7] Univ Glasgow, Inst Canc Sci, Glasgow G61 1QH, Lanark, Scotland
[8] Westmead Inst Med Res, Ctr Canc Res, Sydney, NSW 2145, Australia
[9] Westmead Hosp, Dept Gynaecol Oncol, Sydney, NSW 2145, Australia
[10] Univ Sydney, Daffodil Ctr, Sydney, NSW 2145, Australia
[11] Peter MacCallum Canc Ctr, Res Div, Canc Genet Lab, Melbourne, Vic 3000, Australia
[12] QIMR Berghofer Med Res Inst, Dept Genet & Computat Biol, Brisbane, Qld 4006, Australia
[13] QIMR Berghofer Med Res Inst, Populat Hlth Dept, Brisbane, Qld 4006, Australia
[14] Magee Womens Res Inst, Womens Canc Res Ctr, Pittsburgh, PA 15213 USA
[15] Hillman Canc Ctr, Pittsburgh, PA 15213 USA
[16] Univ Pittsburgh, Sch Med, Dept Obstet Gynecol & Reprod Sci, Pittsburgh, PA 15213 USA
[17] Katholieke Univ Leuven, Dept Human Genet, Lab Translat Genet, B-3000 Leuven, Belgium
[18] VIB, VIB Ctr Canc Biol, B-3000 Leuven, Belgium
[19] Emory Univ, Rollins Sch Publ Hlth, Dept Epidemiol, Atlanta, GA 30322 USA
[20] Duke Univ Hosp, Dept Gynecol Oncol, Durham, NC 27710 USA
[21] Haukeland Hosp, Dept Obstet & Gynecol, N-5021 Bergen, Norway
[22] Univ Bergen, Ctr Canc Biomarkers CCBIO, Dept Clin Sci, N-5020 Bergen, Norway
[23] Univ Copenhagen, Herlev Hosp, Dept Pathol, DK-2100 Copenhagen, Denmark
[24] Mayo Clin, Dept Quantitat Hlth Sci, Div Epidemiol, Rochester, MN 55905 USA
[25] Mayo Clin, Div Computat Biol, Dept Quantitat Hlth Sci, Rochester, MN 55905 USA
[26] Aichi Canc Ctr, Res Inst, Div Canc Epidemiol & Prevent, Nagoya, Aichi 4648681, Japan
[27] Nagoya Univ, Grad Sch Med, Div Canc Epidemiol, Nagoya, Aichi 4668550, Japan
[28] Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USA
[29] Cedars Sinai Med Ctr, Cedars Sinai Canc, Canc Prevent & Control Program, Los Angeles, CA 90048 USA
[30] Cedars Sinai Med Ctr, Samuel Oschin Comprehens Canc Inst, Canc Prevent & Genet Program, Los Angeles, CA 90048 USA
[31] Oregon Hlth & Sci Univ, Dept Obstet & Gynecol, Portland, OR 97239 USA
[32] Oregon Hlth & Sci Univ, Knight Canc Inst, Portland, OR 97239 USA
[33] Univ Toronto, Princess Margaret Canc Ctr, Biostat, Toronto, ON M5G 2C1, Canada
基金
美国国家卫生研究院; 英国医学研究理事会; 英国惠康基金; 加拿大健康研究院;
关键词
ovarian cancer; low-grade serous cancer; CA-125; survival; CARCINOMA; CHEMOTHERAPY; EXPRESSION; NADIR;
D O I
10.3390/cancers14081954
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Low-grade serous cancer (LGSC) accounts for approximately 5% of all ovarian cancers. It is characterized by its high resistance to chemotherapy. Cytoreductive surgery, therefore, is the primary treatment modality for this disease and previous studies have shown that complete removal of all visible tumor tissue should be achieved. In this study, 176 women with LGSC were included and most of them had advanced disease stages, where the disease had already spread. CA-125 is a biomarker that has been previously studied in ovarian cancer. We have found that CA-125 level following treatment of LGSC is an important and independent prognostic factor for progression-free and overall survival. It may be a better surrogate for the true amount of residual disease following treatment compared to the gross estimation of visible residual disease during surgery. 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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页数:12
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