Relevance of the Immunoglobulin VH somatic mutation status in patients with chronic lymphocytic leukemia treated with fludarabine, cyclophosphamide, and rituximab (FCR) or related chemoimmunotherapy regimens

被引:70
|
作者
Lin, Katherine I. [2 ]
Tam, Constantine S. [3 ]
Keating, Michael J. [1 ]
Wierda, William G.
O'Brien, Susan
Lerner, Susan
Coombes, Kevin R.
Schlette, Ellen [2 ]
Ferrajoli, Alessandra
Barron, Lynn L. [2 ]
Kipps, Thomas J. [4 ]
Rassenti, Laura [4 ]
Faderl, Stefan
Kantarjian, Hagop
Abruzzo, Lynne V. [2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Leukemia Dept, Unit 428, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Hematopathol Dept, Houston, TX 77030 USA
[3] St Vincents Hosp, Dept Hematol, Melbourne, Vic, Australia
[4] Univ Calif San Diego, Moores Canc Ctr, CLL Res Consortium, La Jolla, CA 92093 USA
关键词
INITIAL THERAPY; EXPRESSION; CELLS;
D O I
10.1182/blood-2008-10-184853
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although immunoglobulin V-H mutation status (IgV(H) MS) is prognostic in patients with chronic lymphocytic leukemia (CLL) who are treated with alkylating agents or single-agent fludarabine, its significance in the era of chemoimmunotherapy is not known. We determined the IgV(H) somatic mutation status (MS) in 177 patients enrolled in a phase 2 study of fludarabine, cyclophosphamide, and rituximab (FCR) and in 127 patients treated with subsequent chemoimmunotherapy protocols. IgV(H) MS did not impact significantly on the complete remission (CR) rate of patients receiving FCR or related regimens. However, CR duration was significantly shorter in patients with CLL that used unmutated IgV(H) than those whose CLL used mutated IgV(H) (TTP 47% vs 82% at 6 years, P < .001). In a multivariate model considering all baseline characteristics, IgV(H) MS emerged as the only determinant of remission duration (hazard ratio 3.8, P < .001). Our results suggest that postremission interventions should be targeted toward patients with unmutated IgV(H) status. (Blood. 2009; 113:3168-3171)
引用
收藏
页码:3168 / 3171
页数:4
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