Early-mid treatment C-reactive protein level is a prognostic factor in aggressive non-Hodgkin's lymphoma

被引:29
作者
Herishanu, Yair
Perry, Chava
Braunstein, Rony
Metser, Ur
Goor, Odelia
Rogowski, Ori
Berliner, Shlomo
Polliack, Aaron
Naparstek, Elizabeth
机构
[1] Tel Aviv Sourasky Med Ctr, Dept Hematol, IL-64239 Tel Aviv, Israel
[2] Hadassah Univ Hosp, Ctr Safety & Qual, IL-91120 Jerusalem, Israel
[3] Tel Aviv Sourasky Med Ctr, Dept Nucl Med, IL-64239 Tel Aviv, Israel
[4] Tel Aviv Sourasky Med Ctr, Dept Med D, IL-64239 Tel Aviv, Israel
[5] Hadassah Univ Hosp, Dept Hematol, IL-91120 Jerusalem, Israel
关键词
C-reactive protein; early-mid treatment; prognostic factor; aggressive non-Hodgkins lymphoma;
D O I
10.1111/j.1600-0609.2007.00894.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: In the light of an emerging role for early-mid treatment 18 F-deoxyfluoroglucose positron emission tomography (FDG-PET) as an important prognostic indicator in aggressive non-Hodgkin's lymphoma (NHL), we attempted to determine whether a simple parameter, such as the early-mid treatment CRP (C-reactive protein) level, could also be utilized as a significant prognostic factor in aggressive NHL. Patients and methods: Serum CRP levels were monitored in 55 patients with aggressive NHL. The lowest value of the early mid-term CRP levels recorded was compared with the interim PET-CT results, as well as with the clinical course and eventual outcome. Results: During chemotherapy, the lowest value of early-mid treatment CRP levels significantly predicted the results of the interim FDG-PET (P = 0.04 with an odds ratio of 1.13). Patients who did not achieve an early-mid treatment CRP level of < 5 mg/L, had a shorter time to disease progression or relapse (P = 0.001) as well as a reduced overall survival (OS) (P = 0.016). Conclusions: The early-mid treatment serum CRP level is a prognostic factor in aggressive NHL. Patients who do not achieve an early-mid treatment level of < 5 mg/L have quicker disease progression or earlier relapse and also appear to have an inferior OS.
引用
收藏
页码:150 / 154
页数:5
相关论文
共 20 条
  • [1] ARMITAGE JO, 1986, INT J CLIN ONCOL EDI, P160
  • [2] CHILD JA, 1980, CANCER-AM CANCER SOC, V45, P318, DOI 10.1002/1097-0142(19800115)45:2<318::AID-CNCR2820450220>3.0.CO
  • [3] 2-C
  • [4] INTERLEUKIN-6 GENE-EXPRESSION IN NORMAL AND NEOPLASTIC-B CELLS
    FREEMAN, GJ
    FREEDMAN, AS
    RABINOWE, SN
    SEGIL, JM
    HOROWITZ, J
    ROSEN, K
    WHITMAN, JF
    NADLER, LM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1989, 83 (05) : 1512 - 1518
  • [5] Aggressive non-Hodgkin lymphoma:: Early prediction of outcome with 67Ga scintigraphy
    Front, D
    Bar-Shalom, R
    Mor, M
    Haim, N
    Epelbaum, R
    Frenkel, A
    Gaitini, D
    Kolodny, GM
    Israel, O
    [J]. RADIOLOGY, 2000, 214 (01) : 253 - 257
  • [6] [18F]fluoro-2-deoxy-D-glucose positron emission tomography (FDG-PET) in aggressive lymphoma:: an early prognostic tool for predicting patient outcome
    Haioun, C
    Itti, E
    Rahmouni, A
    Brice, P
    Rain, JD
    Belhadj, K
    Gaulard, P
    Garderet, L
    Lepage, E
    Reyes, F
    Meignan, M
    [J]. BLOOD, 2005, 106 (04) : 1376 - 1381
  • [7] Early restaging gallium scans predict outcome in poor-prognosis patients with aggressive non-Hodgkin's lymphoma treated with high-dose CHOP chemotherapy
    Janicek, M
    Kaplan, W
    Neuberg, D
    Canellos, GP
    Shulman, LN
    Shipp, MA
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (04) : 1631 - 1637
  • [8] Jerusalem G, 2000, HAEMATOLOGICA, V85, P613
  • [9] Elevated serum interleukin-6 (IL-6) is derived from neoplastic lymphoid cells in patients with B-cell non-Hodgkin's lymphoma: Correlation with extent of IL-6 expression and serum concentration
    Kato, H
    Kinoshita, T
    Suzuki, S
    Nagasaka, T
    Murate, T
    Saito, H
    Hotta, T
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1996, 92 (04) : 1014 - 1021
  • [10] Kostakoglu L, 2002, J NUCL MED, V43, P1018