Myeloma prognostic index at diagnosis might be a prognostic marker in patients newly diagnosed with multiple myeloma

被引:24
作者
Kim, Dae Sik [1 ]
Yu, Eun Sang [1 ]
Kang, Ka-Won [1 ]
Lee, Se Ryeon [1 ]
Park, Yong [1 ]
Sung, Hwa Jung [1 ]
Choi, Chul Won [1 ]
Kim, Byung Soo [1 ]
机构
[1] Korea Univ, Sch Med, Dept Internal Med, Div Hematol & Oncol, 73 Inchon Ro, Seoul 02841, South Korea
关键词
Multiple myeloma; Prognosis; Neutrophil-lymphocyte ratio; Platelet count; C-reactive protein; INTERNATIONAL STAGING SYSTEM; LYMPHOCYTE RATIO; PLATELET; CANCER; INFLAMMATION; NEUTROPHIL; SURVIVAL; CELLS; BETA;
D O I
10.3904/kjim.2016.054
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Aims: The aims of this study were to identify the value of inflammatory markers as pretreatment prognostic factors for patients with multiple myeloma (MM) and to estimate the value of a prognostic index including these markers at diagnosis. Methods: A total of 273 newly diagnosed MM patients undergoing active treatment were analyzed in this study. The prognostic values for survival of the pretreatment inflammatory markers were investigated. A myeloma prognostic index (MPI) was derived using prognostic factors determined to be independently significant on multivariate analysis. Results: A high pretreatment neutrophil-lymphocyte ratio (NLR), low platelet count, and high C-reactive protein (CRP) level had independently unfavorable significance for overall survival (OS). The MPI was derived based on these factors. Per the MPI, 1 point each was assigned to high NLR, low platelet count, and high CRP. Risk categories were stratified into low- (score 0), intermediate- (score 1), and high-risk (score 2 or 3) groups. The MPI demonstrated independent statistical significance for OS on multivariate analysis ([intermediate: hazard ratio (HR), 1.91; 95% confidence interval (CI), 1.12 to 3.24] and [high: HR, 3.37; 95% CI, 2.00 to 5.69]; p < 0.001). Moreover, this significance could be observed regardless of age, renal function, and exposure to novel agents. In addition, the International Staging System risk group could be further significantly stratified using the MPI. Conclusions: The MPI, consisting of pretreatment inflammatory markers, NLR, platelet count, and CRP, might be effective in predicting the survival of newly diagnosed MM patients undergoing active treatment.
引用
收藏
页码:711 / 721
页数:11
相关论文
共 25 条
[1]   Inflammation and cancer: back to Virchow? [J].
Balkwill, F ;
Mantovani, A .
LANCET, 2001, 357 (9255) :539-545
[2]   Prognostic factor analyses of myeloma survival with intergroup trial S9321 (INT 0141): examining whether different variables govern different time segments of survival [J].
Barlogie, Bart ;
Bolejack, Vanessa ;
Schell, Michael ;
Crowley, John .
ANNALS OF HEMATOLOGY, 2011, 90 (04) :423-428
[3]  
BATAILLE R, 1992, BLOOD, V80, P733
[4]   C-reactive protein [J].
Black, S ;
Kushner, I ;
Samols, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (47) :48487-48490
[5]   IMWG consensus on risk stratification in multiple myeloma [J].
Chng, W. J. ;
Dispenzieri, A. ;
Chim, C-S ;
Fonseca, R. ;
Goldschmidt, H. ;
Lentzsch, S. ;
Munshi, N. ;
Palumbo, A. ;
Miguel, J. S. ;
Sonneveld, P. ;
Cavo, M. ;
Usmani, S. ;
Durie, B. G. M. ;
Avet-Loiseau, H. .
LEUKEMIA, 2014, 28 (02) :269-277
[6]   Transforming growth factor β from multiple myeloma cells inhibits proliferation and IL-2 responsiveness in T lymphocytes [J].
Cook, G ;
Campbell, JDM ;
Carr, CE ;
Boyd, KS ;
Franklin, IM .
JOURNAL OF LEUKOCYTE BIOLOGY, 1999, 66 (06) :981-988
[7]   Inflammation and cancer [J].
Coussens, LM ;
Werb, Z .
NATURE, 2002, 420 (6917) :860-867
[8]  
FRITZ E, 1986, BLOOD, V68, P514
[9]   International staging system for multiple myeloma [J].
Greipp, PR ;
San Miguel, J ;
Durie, BGM ;
Crowley, JJ ;
Barlogie, B ;
Bladé, J ;
Boccadoro, M ;
Child, JA ;
Harousseau, JL ;
Kyle, RA ;
Lahuerta, JJ ;
Ludwig, H ;
Morgan, G ;
Powles, R ;
Shimizu, K ;
Shustik, C ;
Sonneveld, P ;
Tosi, P ;
Turesson, I ;
Westin, J .
JOURNAL OF CLINICAL ONCOLOGY, 2005, 23 (15) :3412-3420
[10]   Hallmarks of Cancer: The Next Generation [J].
Hanahan, Douglas ;
Weinberg, Robert A. .
CELL, 2011, 144 (05) :646-674