Serum B-cell maturation antigen is elevated in multiple myeloma and correlates with disease status and survival

被引:236
作者
Sanchez, Eric [1 ]
Li, Mingjie [1 ]
Kitto, Alex [1 ]
Li, Jennifer [1 ]
Wang, Cathy S. [1 ]
Kirk, Dylan T. [1 ]
Yellin, Ori [1 ]
Nichols, Cydney M. [1 ]
Dreyer, Marissa P. [1 ]
Ahles, Cameryn P. [1 ]
Robinson, Austin
Madden, Erik
Waterman, Gabriel N. [3 ]
Swift, Regina A. [4 ]
Bonavida, Benjamin [2 ]
Boccia, Ralph [5 ]
Vescio, Robert A. [6 ]
Crowley, John [7 ]
Chen, Hai-ming [1 ]
Berenson, James R. [1 ,4 ]
机构
[1] Inst Myeloma & Bone Canc Res, W Hollywood, CA 90069 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
[3] Univ So Calif, Keck Sch Med, Los Angeles, CA 90033 USA
[4] James R Berenson MD Inc, W Hollywood, CA USA
[5] Ctr Canc & Blood Disorders, Bethesda, MD USA
[6] Cedars Sinai Med Ctr, Los Angeles, CA 90048 USA
[7] Canc Res & Biostat, Seattle, WA USA
关键词
multiple myeloma; B-cell maturation antigen; serum; xenografts; in vivo; TNF RECEPTOR SUPERFAMILY; LYMPHOCYTE STIMULATOR; BAFF-R; IMMUNOGLOBULIN PRODUCTION; STAGING SYSTEM; BONE-MARROW; BCMA; APRIL; TACI; PROTEIN;
D O I
10.1111/j.1365-2141.2012.09241.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although TNFRSF17 (also designated as B-cell maturation antigen (BCMA)) is expressed on tumour cells in B-cell malignancies, it has not been found in serum. The present study found that BCMA concentrations were higher in the supernatants of cultured bone marrow mononuclear cells from multiple myeloma (MM) patients than in healthy subjects. Serum BCMA levels were measured in samples from MM patients (n = 209), monoclonal gammopathy of undetermined significance (MGUS) individuals (n = 23) and age-matched controls (n = 40). BCMA was detected in the serum of untreated MM patients (n = 50) and levels were higher than in MGUS patients (P = 0.0157) and healthy subjects (P < 0.0001). Serum BCMA levels were higher among patients with progressive disease (n = 80) compared to those with responsive disease (n = 79; P = 0.0038). Among all MM patients, overall survival was shorter among patients whose serum BCMA levels were above the median (P = 0.001). We also demonstrated that sera from mice with human MM xenografts contained human BCMA, and levels correlated with the change in tumour volume in response to melphalan or cyclophosphamide with bortezomib. These results suggest that serum BCMA levels may be a new biomarker for monitoring disease status and overall survival of MM patients.
引用
收藏
页码:727 / 738
页数:12
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