Moderate anemia at diagnosis is an independent prognostic marker of the EUTOS, Sokal, and Hasford scores for survival and treatment response in chronic-phase, chronic myeloid leukemia patients with frontline imatinib

被引:7
|
作者
Ko, Po-Shen [1 ,2 ]
Yu, Yuan-Bin [2 ,3 ]
Liu, Yao-Chung [1 ,2 ]
Wu, Yi-Tsui [4 ]
Hung, Man-Hsin [2 ,5 ]
Gau, Jyh-Pyng [1 ,2 ]
Liu, Chia-Jen [1 ,2 ,6 ]
Hsiao, Liang-Tsai [1 ,2 ]
Chena, Po-Min [1 ,2 ]
Chiou, Tzeon-Jye [2 ,7 ]
Liu, Chun-Yu [2 ,5 ]
Liu, Jin-Hwang [1 ,8 ,9 ]
机构
[1] Taipei Vet Gen Hosp, Dept Med, Div Hematol & Oncol, Taipei, Taiwan
[2] Natl Yang Ming Univ, Sch Med, Taipei, Taiwan
[3] Far Eastern Mem Hosp, Dept Internal Med, Div Oncol & Hematol, Taipei, Taiwan
[4] Taipei Vet Gen Hosp, Dept Nursing, Taipei, Taiwan
[5] Taipei Vet Gen Hosp, Dept Oncol, Div Med Oncol, 201 Shih Pai Rd,Sec 2, Taipei 11217, Taiwan
[6] Natl Yang Ming Univ, Inst Publ Hlth, Taipei, Taiwan
[7] Taipei Vet Gen Hosp, Dept Med, Divs Transfus Med, Taipei, Taiwan
[8] Natl Yang Ming Univ, Inst Biopharmaceut Sci, Taipei, Taiwan
[9] Natl Yang Ming Univ, Chong Hin Loon Mem Canc & Biotherapy Res Ctr, Taipei, Taiwan
关键词
Chronic myeloid leukemia; anemia; scoring systems; prognosis; COMPLETE CYTOGENETIC RESPONSE; CHRONIC GRANULOCYTIC-LEUKEMIA; TYROSINE KINASE INHIBITORS; MOLECULAR RESPONSE; EUROPEAN TREATMENT; PREDICTS SURVIVAL; FOLLOW-UP; CML; THERAPY; DISCRIMINATION;
D O I
10.1080/03007995.2017.1356708
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: This study aimed to examine the prognostic value of anemia for the diagnosis of chronic myeloid leukemia in the chronic phase (CML-CP) receiving imatinib. Methods: One hundred and fifty-four CML-CP patients were enrolled. The influences of moderate anemia with hemoglobin (Hb)< 10 g/dl, four scoring systems, and the early molecular response at 3 months (BCR-ABL <= 10%; 3M-EMR) on the achievement of a deep molecular response (DMR, MR4.5), progression-free survival (PFS), event-free survival (EFS), and overall survival (OS) were compared. Results: Moderate anemia was identified in 44 (28.6%) patients. These patients had more aggressive baseline features and higher risks, as assessed by scoring systems, and less favorable treatment responses vs those without anemia, including 3M-EMR (50.0% vs 69.1%), a complete cytogenetic response at 6 months (20.5% vs 50.9%), and a major molecular response at 12 months (22.5% vs 45.2%), with a median follow-up of 54.0 months. Furthermore, an Hb of 10 g/dl better distinguished DMR, EFS, PFS, and OS than the EUTOS, Sokal, and Hasford scores, and better predicted the responses and survivals in combination with 3M-EMR than 3M-EMR alone. Conclusions: This finding highlights the significance of anemia in CML-CP, and suggests that patients with anemia at diagnosis should be carefully monitored and might benefit from more potent TKIs if not achieving 3M-EMR.
引用
收藏
页码:1737 / 1744
页数:8
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