Treatment outcome and prognostic factors of Korean patients with chronic lymphocytic leukemia: a multicenter retrospective study

被引:5
|
作者
Choi, Yunsuk [1 ]
Lee, Jung-Hee [2 ]
Jung, Chul Won [3 ]
Jo, Jae-Cheol [1 ]
Kim, Jin Seok [4 ]
Kim, Inho [5 ]
Park, Silvia [3 ,6 ]
Cheong, June-won [4 ]
Park, Sang-Hyuk [7 ]
Kim, Sung-Yong [8 ]
Lee, Hong-Ghi [8 ]
机构
[1] Univ Ulsan, Ulsan Univ Hosp, Dept Hematol & Oncol, Coll Med, Ulsan, South Korea
[2] Univ Ulsan, Asan Med Ctr, Dept Hematol, Coll Med, Seoul, South Korea
[3] Sungkyunkwan Univ, Samsung Med Ctr, Dept Med, Sch Med, Seoul, South Korea
[4] Yonsei Univ, Severance Hosp, Dept Internal Med, Div Hematol,Coll Med, Seoul, South Korea
[5] Seoul Natl Univ Hosp, Dept Internal Med, Seoul, South Korea
[6] Catholic Univ Korea, Coll Med, Leukemia Res Inst, Dept Hematol,Seoul St Marys Hematol Hosp, Seoul, South Korea
[7] Univ Ulsan, Ulsan Univ Hosp, Dept Lab Med, Coll Med, Ulsan, South Korea
[8] Konkuk Univ, Dept Internal Med, Div Hematol Oncol, Med Ctr, 120-1 Neungdong Ro, Seoul 05030, South Korea
来源
KOREAN JOURNAL OF INTERNAL MEDICINE | 2021年 / 36卷 / 01期
基金
新加坡国家研究基金会;
关键词
Leukemia; lymphocytic; chronic; B-cell; Treatment outcome; Prognosis; Korean; SURVIVAL; INDEX; CLL; MUTATIONS; DIAGNOSIS;
D O I
10.3904/kjim.2019.210
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Aims: Compared with Western countries, chronic lymphocytic leukemia (CLL) rarely occurs in Asia and has different clinical characteristics. Thus, we aimed to evaluate the clinical characteristics, treatment outcomes, and prognostic significance of Korean patients with CLL. Methods: We retrospectively analyzed 90 patients with CLL who had received chemotherapy at 6 centers in Korea between 2000 and 2012. Results: Compared with Western patients with CLL, Korean patients with CLL express lambda (42.0%) and atypical markers such as CD22 and FMC7 (76.7% and 40.0%, respectively) more frequently. First-line chemotherapy regimens included chlorambucil (n = 43), fludarabine and cyclophosphamide (FC) (n = 20), fludarabine (n = 13), rituximab-FC (n = 4). The remaining patients were treated with other various regimens (n = 10). The 5-year overall survival (OS) and progression-free survival (PFS) rates were 79.3% and 28.1%, respectively. Multivariate analyses showed that hyperleukocytosis (>= 100 x 103/mu L), extranodal involvement, and the Binet C stage were significant negative prognostic factors for OS (hazard ratio [HR] 4.75, p = 0.039; HR 21.6, p = 0.002; and HR 4.35, p = 0.034, respectively). Cytogenetic abnormalities including complex karyotypes (>= 3), del(11q), and del(17) had a significantly adverse impact on both OS and PFS ( p < 0.001 and p = 0.010, respectively). Conclusions: Initial hyperleukocytosis, extranodal involvement, complex karyotype, del(17) and del(11q) need to be considered in the risk stratification system for CLL.
引用
收藏
页码:194 / +
页数:12
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