Multivariable Model for Time to First Treatment in Patients With Chronic Lymphocytic Leukemia

被引:114
作者
Wierda, William G. [1 ]
O'Brien, Susan [1 ]
Wang, Xuemei [1 ]
Faderl, Stefan [1 ]
Ferrajoli, Alessandra [1 ]
Do, Kim-Anh [1 ]
Garcia-Manero, Guillermo [1 ]
Cortes, Jorge [1 ]
Thomas, Deborah [1 ]
Koller, Charles A. [1 ]
Burger, Jan A. [1 ]
Lerner, Susan [1 ]
Schlette, Ellen [1 ]
Abruzzo, Lynne [1 ]
Kantarjian, Hagop M. [1 ]
Keating, Michael J. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
关键词
GENE MUTATION STATUS; PROGNOSTIC INDEX; ZAP-70; EXPRESSION; CD38; BINET STAGE; SURVIVAL; DISEASE; CANCER; COMBINATIONS; PROGRESSION;
D O I
10.1200/JCO.2010.33.9002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose The clinical course for patients with chronic lymphocytic leukemia (CLL) is diverse; some patients have indolent disease, never needing treatment, whereas others have aggressive disease requiring early treatment. We continue to use criteria for active disease to initiate therapy. Multivariable analysis was performed to identify prognostic factors independently associated with time to first treatment for patients with CLL. Patients and Methods Traditional laboratory, clinical prognostic, and newer prognostic factors such as fluorescent in situ hybridization ( FISH), IGHV mutation status, and ZAP-70 expression evaluated at first patient visit to MD Anderson Cancer Center were correlated by multivariable analysis with time to first treatment. This multivariable model was used to develop a nomogram-a weighted tool to calculate 2- and 4-year probability of treatment and estimate median time to first treatment. Results There were 930 previously untreated patients who had traditional and new prognostic factors evaluated; they did not have active CLL requiring initiation of treatment within 3 months of first visit and were observed for time to first treatment. The following were independently associated with shorter time to first treatment: three involved lymph node sites, increased size of cervical lymph nodes, presence of 17p deletion or 11q deletion by FISH, increased serum lactate dehydrogenase, and unmutated IGHV mutation status. Conclusion We developed a multivariable model that incorporates traditional and newer prognostic factors to identify patients at high risk for progression to treatment. This model may be useful to identify patients for early interventional trials. J Clin Oncol 29:4088-4095. (C) 2011 by American Society of Clinical Oncology
引用
收藏
页码:4088 / 4095
页数:8
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