Increased serum C-reactive protein levels are associated with shorter survival and development of second cancers in chronic lymphocytic leukemia

被引:21
作者
Herishanu, Yair [1 ,2 ]
Polliack, Aaron [3 ]
Shenhar-Tsarfaty, Shani [4 ,5 ]
Weinberger, Ronit [6 ]
Gelman, Ram [5 ]
Ziv-Baran, Tomer [7 ]
Zeltser, David [2 ,8 ]
Shapira, Itzhak [2 ]
Berliner, Sholomo [2 ,5 ]
Rogowski, Ori [2 ,4 ]
机构
[1] Tel Aviv Sourasky Med Ctr, Dept Hematol, 6 Weizman St, IL-64239 Tel Aviv, Israel
[2] Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel
[3] Hebrew Univ Jerusalem, Sch Med, Jerusalem, Israel
[4] Internal Med C Tel Aviv Sourasky Med Ctr, Tel Aviv, Israel
[5] Internal Med E Tel Aviv Sourasky Med Ctr, Tel Aviv, Israel
[6] Clalit Hlth Serv, Immunol Lab, Tel Aviv, Israel
[7] Tel Aviv Univ, Dept Epidemiol & Prevent Med, Sch Publ Hlth, Sackler Fac Med, Tel Aviv, Israel
[8] Internal Med D Tel Aviv Sourasky Med Ctr, Tel Aviv, Israel
关键词
CLL; CRP; overall survival; prognostic factor; second malignancy; NON-HODGKINS-LYMPHOMA; INFLAMMATION; RISK; INTERLEUKIN-6; DIAGNOSIS; DISEASE; MARKER; CRP;
D O I
10.1080/07853890.2016.1232860
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Chronic lymphocytic leukemia (CLL) is characterized by a heterogeneous clinical course, ranging from stable to more aggressive disease. Herein, we determined the prognostic significance of serum C-reactive protein (CRP) levels in patients with CLL Methods: A retrospective cohort study reviewing the records of 107 consecutive treatment naive patients with CLL and a control group comprised of apparently healthy individuals attending for periodic health examinations. Results: The median CRP level of patients with CLL was 0.19 mg/dL (0-2.9). In univariate analysis, high-CRP levels (>= 0.4 mg/dL) were significantly associated with an increased risk of mortality (HR = 3.97, 95% CI 1.64-9.62, p = .002) and development of second solid cancers (HR = 4.54, 95% CI 1.57-13.11, p = .005), compared to low-CRP values (< 0.4 mg/dL). In multivariate analysis, high-CRP retained statistical significance for all-cause mortality (HR = 2.81, 95% CI 1.04-7.57, p = .04) and the development of second solid malignancies (HR = 4.54, 95% CI 1.57-13.11, p = .005). Moreover, when compared to an apparently healthy population, CLL patients with high CRP levels had more than an eightfold risk of cancer. Conclusions: Elevated baseline CRP levels are associated with shorter survival and development of second cancers in patients with CLL. We suggest that increased CRP in patients with CLL may justify a more rigorous search for second cancers.
引用
收藏
页码:75 / 82
页数:8
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