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Tumor autoantibodies as biomarkers for predicting ovarian cancer recurrence
被引:8
|作者:
Chatterjee, Madhumita
[6
,7
]
Dyson, Greg
[2
]
Levin, Nancy K.
[6
,7
]
Shah, Jay P.
[3
]
Morris, Robert
[4
]
Munkarah, Adnan
[4
,5
]
Tainsky, Michael A.
[1
,6
,7
]
机构:
[1] Wayne State Univ, Sch Med, Ctr Mol Med & Genet, Detroit, MI USA
[2] Wayne State Univ, Sch Med, Karmanos Canc Inst, Biostat Core,Dept Oncol, Detroit, MI USA
[3] So Calif Permanente Med Grp, Dept Obstet & Gynecol, Div Gynecol Oncol, Irvine, CA USA
[4] Wayne State Univ, Sch Med, Div Gynecol Oncol, Detroit, MI USA
[5] Henry Ford Hlth Syst, Dept Womens Hlth Serv, Div Gynecol Oncol, Detroit, MI USA
[6] Wayne State Univ, Sch Med, Dept Oncol, Detroit, MI USA
[7] Karmanos Canc Inst, Program Mol Biol & Genet, Detroit, MI USA
基金:
美国国家卫生研究院;
关键词:
Ovarian cancer;
recurrence;
humoral immune response;
tumor autoantibodies;
protein arrays;
TRANSFER-RNA-SYNTHETASE;
P53;
AUTOANTIBODIES;
SERUM CA-125;
STAGE;
POLYMYOSITIS;
CARCINOMA;
RECEPTORS;
THERAPY;
PANELS;
RISK;
D O I:
10.3233/CBM-2012-0265
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Ovarian cancer (OVCA) has a high incidence of recurrence and a high rate of mortality. We performed a pilot study to evaluate the usefulness of tumor autoantibodies to tumor associated antigens (TAA) to predict OVCA recurrence. A validation study with 56 antigens, previously identified in the initial phase of the study, along with 13 known tumor antigens on protein arrays was performed on an independent cohort of recurrent and non-recurrent OVCA patients. Statistical analyses revealed that a panel of 3 antigens predicted recurrence at a median time of 9.07 months prior to clinical recurrence in a study population, where majority of patients had CA125 values less than 35 U/ml, with an average sensitivity, specificity and accuracy of 94.7%, 86.7% and 93.3% respectively. One of the top 3 antigens has been associated with the development of polymyositis (PM) which has been shown in some cases to precede the occurrence of ovarian carcinoma. Our results indicate that these 3 antigens have potential for predicting recurrence at an early time and may have better prognostic utility than CA125 alone for early therapeutic intervention. These biomarkers could guide us to identify those patients that could benefit most from maintenance or consolidation therapy.
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页码:59 / 73
页数:15
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