Prognostic significance of combined analysis of ZAP-70 and CD38 in chronic lymphocytic leukemia

被引:35
作者
D'Arena, Giovanni
Tarnani, Michela
Rumi, Carlo
Vaisitti, Tiziana
Aydin, Sernra
De Filippi, Rosaria
Perrone, Francesco
Pinto, Antonio
Chiusolo, Patrizia
Deaglio, Silvia
Malavasi, Fabio
Laurentl, Luca
机构
[1] Fdn G Pascale, Natl Canc Inst, Hematol Oncol Unit, I-80131 Naples, Italy
[2] Univ Cattolica Sacro Cuore, Dept Hematol, I-00168 Rome, Italy
[3] Univ Turin, Immunogenet Lab, Lymphocyte Signaling Unit, I-10124 Turin, Italy
[4] Fdn G Pascale, Natl Canc Inst, Clin Trials Unit, I-80131 Naples, Italy
关键词
D O I
10.1002/ajh.20936
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The clinical heterogeneity that characterizes chronic lymphocytic leukemia (CLL) poses critical questions concerning the identification of high risk patients. Unmutated IgV(H) genes, CD38 and ZAP-70 expression have emerged as the most useful tools in identifying aggressive CLL. The simultaneous expression of ZAP-70 and CD38 in 157 patients with CLL has been evaluated. Fifty-seven patients (36%) were positive for ZAP-70 and 46 patients (29%) were positive for CD38. Both molecules were highly correlated and predictive of the clinical course of the disease. According to the simultaneous evaluation of ZAP-70 and CD38, patients were divided into three groups. In 81 patients (52%), there was a negative concordance of both molecules (ZAP-70(-)/CD38(-)); in 27 patients (17%) there was a positive concordance (ZAP-70(+)/CD38(+)); in 49 patients (31%) there was a discordant expression (ZAP-70(+)/CD38(-) and ZAP-70(-)/CD38(+)). A comparison of the clinical and laboratory data showed in ZAP-70(+)/CD38(+) patients a significantly higher bone marrow and peripheral blood lymphocytosis, lower hemoglobin levels, more advanced clinical stage, and higher number of unmutated IgV(H) status with respect to the other two groups. Furthermore, ZAP-70(+)/CD38(+) patients displayed a much shorter treatment-free interval (median 12 months vs 42 months in discordant patients and not reached in ZAP-70(-)CD38(-) patients). These results prove that the concomitant evaluation of ZAP-70 and CD38 expression allows the separation of CLL patients in prognostic subgroups and suggest that their simultaneous assessment should become an integral component of the CLL diagnostic grid.
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页码:787 / 791
页数:5
相关论文
共 27 条
[1]   Perspectives on the use of new diagnostic tools in the treatment of chronic lymphocytic leukemia [J].
Binet, JL ;
Caligaris-Cappio, F ;
Catovsky, D ;
Cheson, B ;
Davis, T ;
Dighiero, G ;
Döhner, H ;
Hallek, M ;
Hillmen, P ;
Keating, M ;
Montserrat, E ;
Kipps, TJ ;
Rai, K .
BLOOD, 2006, 107 (03) :859-861
[2]   ZAP-70 expression as a surrogate for immunoglobulin-variable-region mutations in chronic lymphocytic leukemia [J].
Crespo, M ;
Bosch, F ;
Villamor, N ;
Bellosillo, B ;
Colomer, D ;
Rozman, M ;
Marcé, S ;
López-Guillermo, A ;
Campo, E ;
Montserrat, E .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (18) :1764-1775
[3]   CD38 expression correlates with adverse biological features and predicts poor clinical outcome in B-cell chronic lymphocytic leukemia [J].
D'Arena, G ;
Musto, P ;
Cascavilla, N ;
Dell'Olio, M ;
Di Renzo, N ;
Perla, G ;
Savino, L ;
Carotenuto, M .
LEUKEMIA & LYMPHOMA, 2001, 42 (1-2) :109-114
[4]   Ig V gene mutation status and CD38 expression as novel prognostic indicators in chronic lymphocytic leukemia [J].
Damle, RN ;
Wasil, T ;
Fais, F ;
Ghiotto, F ;
Valetto, A ;
Allen, SL ;
Buchbinder, A ;
Budman, D ;
Dittmar, K ;
Kolitz, J ;
Lichtman, SM ;
Schulman, P ;
Vinciguerra, VP ;
Rai, KR ;
Ferrarini, M ;
Chiorazzi, N .
BLOOD, 1999, 94 (06) :1840-1847
[5]   CD38 and CD100 lead a network of surface receptors relaying positive signals for B-CLL growth and survival [J].
Deaglio, S ;
Vaisitti, T ;
Bergui, L ;
Bonello, L ;
Horenstein, AL ;
Tamagnone, L ;
Boumsell, L ;
Malavasi, F .
BLOOD, 2005, 105 (08) :3042-3050
[6]   CD38 is a signaling molecule in B-cell chronic lymphocytic leukemia cells [J].
Deaglio, S ;
Capobianco, A ;
Bergui, L ;
Dürig, J ;
Morabito, F ;
Dührsen, U ;
Malavasi, F .
BLOOD, 2003, 102 (06) :2146-2155
[7]  
DEAGLIO S, 2004, BLOOD S, V104, pA959
[8]   In-tandem insight from basic science combined with clinical research: CD38 as both marker and key component of the pathogenetic network underlying chronic lymphocytic leukemia [J].
Deaglio, Silvia ;
Vaisitti, Tiziana ;
Aydin, Semra ;
Ferrero, Enza ;
Malavasi, Fabio .
BLOOD, 2006, 108 (04) :1135-1144
[9]   ζ-chain associated protein 70 and CD38 combined predict the time to first treatment in patients with chronic lymphocytic leukemia [J].
Del Giudice, I ;
Morilla, A ;
Osuji, N ;
Matutes, E ;
Morilla, R ;
Burford, A ;
Maravelaki, S ;
Owusu-Ankomah, K ;
Swansbury, J ;
A'Hern, R ;
Brito-Babapulle, V ;
Catovsky, D .
CANCER, 2005, 104 (10) :2124-2132
[10]   Clinical significance of CD38 expression in chronic lymphocytic leukemia [J].
Del Poeta, G ;
Maurillo, L ;
Venditti, A ;
Buccisano, F ;
Epiceno, AM ;
Capelli, G ;
Tamburini, A ;
Suppo, G ;
Battaglia, A ;
Del Principe, MI ;
Del Moro, B ;
Masi, M ;
Amadori, S .
BLOOD, 2001, 98 (09) :2633-2639