Patient characteristics that predict Richter's transformation in patients with chronic lymphocytic leukemia treated with ibrutinib

被引:8
|
作者
Kittai, Adam S. [1 ]
Huang, Ying [1 ]
Beckwith, Kyle A. [1 ]
Bhat, Seema A. [1 ]
Bond, David A. [1 ]
Byrd, John C. [2 ]
Goldstein, Daniel [3 ]
Grever, Michael R. [1 ]
Miller, Cecelia [4 ]
Rogers, Kerry A. [1 ]
Yano, Max [1 ]
Woyach, Jennifer A. [1 ]
机构
[1] Ohio State Univ, Dept Internal Med, Div Hematol, 1140D Lincoln Tower,1800 Cannon Dr, Columbus, OH 43210 USA
[2] Univ Cincinnati, Dept Internal Med, Cincinnati, OH USA
[3] Ohio State Univ, Dept Internal Med, Columbus, OH 43210 USA
[4] Ohio State Univ, Dept Pathol, Columbus, OH 43210 USA
关键词
OUTCOMES; CHEMOIMMUNOTHERAPY; SURVIVAL; THERAPY; COHORT;
D O I
10.1002/ajh.26755
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Chronic lymphocytic leukemia (CLL) transformation to aggressive lymphoma, known as Richter's Transformation (RT), has a dismal prognosis. There are limited data evaluating risk of RT in patients treated with ibrutinib. We performed a retrospective analysis to determine prognostic variables associated with development of RT and overall survival (OS) at progression after treatment with ibrutinib. We identified 559 patients with CLL treated with ibrutinib from 2010-2019. After a median follow-up of 44.5 months from ibrutinib start, 179 patients progressed and were included in our analysis. After a median follow-up of 20.8 months from progression, 54 out of 179 patients developed RT. Progression on treatment (hazard ratio [HR] 4.01 [1.60-10.00], p = .003), higher LDH (HR 1.80 for 2-fold increase [1.33-2.43], p = .0001), and lymphadenopathy without lymphocytosis (HR 2.88 [1.15-7.20], p = .02) were independent prognostic variables for the development of RT at progression. Progression with lymphadenopathy without lymphocytosis continued to be an independent prognostic variable of worse OS post-progression. In a subset analysis of 50 patients who obtained a PET-CT at progression, the median SUVmax for patients who would develop RT was 15.2 (n = 30, range: 4.0-46.3) versus those patients who did not develop RT with a SUVmax of 7.7 (n = 20, range: 2.3-27.2) (p = .0030). Median OS from date of RT was 4.0 months, suggesting that prognosis for RT remains poor. A lymph node biopsy to rule out RT should be considered in patients who received ibrutinib who progress on treatment, have an elevated LDH, or progress with lymphadenopathy without lymphocytosis.
引用
收藏
页码:56 / 65
页数:10
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