Cancer antigen profiling for malignant pleural mesothelioma immunotherapy: expression and coexpression of mesothelin, cancer antigen 125, and Wilms tumor 1

被引:27
作者
Eguchi, Takashi [1 ,2 ]
Kadota, Kyuichi [1 ,3 ,4 ]
Mayor, Marissa [1 ]
Zauderer, Marjorie G. [5 ]
Rimner, Andreas [6 ]
Rusch, Valerie W. [1 ]
Travis, William D. [3 ]
Sadelain, Michel [7 ]
Adusumilli, Prasad S. [1 ,7 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Surg, Thorac Serv, 1275 York Ave, New York, NY 10021 USA
[2] Shinshu Univ, Sch Med, Dept Surg, Div Thorac Surg, Matsumoto, Nagano, Japan
[3] Mem Sloan Kettering Canc Ctr, Dept Pathol, 1275 York Ave, New York, NY 10021 USA
[4] Kagawa Univ, Fac Med, Dept Diagnost Pathol, Takamatsu, Kagawa, Japan
[5] Mem Sloan Kettering Canc Ctr, Dept Med, Div Solid Tumor Oncol, Thorac Oncol Serv, New York, NY 10021 USA
[6] Mem Sloan Kettering Canc Ctr, Dept Radiat Oncol, 1275 York Ave, New York, NY 10021 USA
[7] Mem Sloan Kettering Canc Ctr, Ctr Cell Engn, 1275 York Ave, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
mesothelin; CA125; WT1; mesothelioma; chimeric antigen receptor; EXTRAPLEURAL PNEUMONECTOMY; T-CELLS; PHASE-II; NEOADJUVANT CHEMOTHERAPY; WT1; RADIATION; OVEREXPRESSION; RESPONSES; SURVIVAL; INVASION;
D O I
10.18632/oncotarget.20845
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: To develop cancer antigen-targeted immunotherapeutic strategies for malignant pleural mesothelioma (MPM), we investigated the individual and coexpressions of the cancer-associated antigens mesothelin (MSLN), cancer antigen 125 (CA125), and Wilms tumor 1 (WT1) in both epithelioid and non-epithelioid MPM. Methods: All available hematoxylin and eosin-stained slides from patients who were diagnosed with MPM (1989-2010) were reviewed. We constructed tissue microarrays from 283 patients (epithelioid = 234; non-epithelioid = 49). Intensity and distribution for each antigen were assessed by immunohistochemistry. Results: Positive expression of MSLN, CA125, and WT1 were demonstrated in 93%, 75%, and 97% of epithelioid MPM cases, and 57%, 33%, and 98% of non-epithelioid MPM cases, respectively. Triple-and double-positive antigen coexpressions were demonstrated in 72% and 23% of epithelioid MPM cases and 29% and 33% of non-epithelioid MPM cases, respectively. Complete absence of expression for all three antigens was demonstrated in <2% of MPM cases. More than two-thirds of MPM cases had >= 50% distribution of MSLN-positive cells and, among the remaining third, half had >= 50% distribution of WT1-positive cells. CA125/MSLN coexpression was observed in more than two-thirds of epithelioid MPM cases and one-third of non-epithelioid MPM cases. Conclusion: A limited number of cancer-associated antigens can target almost all MPM tumors for immunotherapy.
引用
收藏
页码:77872 / 77882
页数:11
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