Ko Po-Shen, Yu Yuan-Bin, Liu Yao-Chung, Wu Yi-Tsui, Hung Man-Hsin, Gau Jyh-Pyng, Liu Chia-Jen, Hsiao Liang-Tsai, Chen Po-Min, Chiou Tzeon-Jye, Liu Chun-Yu, Liu Jin-Hwang
a Division of Hematology and Oncology, Department of Medicine , Taipei Veterans General Hospital , Taipei , Taiwan.
b School of Medicine , National Yang-Ming University , Taipei , Taiwan.
Curr Med Res Opin. 2017 Oct;33(10):1737-1744. doi: 10.1080/03007995.2017.1356708. Epub 2017 Aug 11.
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.
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.
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.
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.
本研究旨在探讨贫血对接受伊马替尼治疗的慢性期慢性髓性白血病(CML-CP)患者的预后价值。
纳入154例CML-CP患者。比较血红蛋白(Hb)<10 g/dl的中度贫血、四种评分系统以及3个月时的早期分子反应(BCR-ABL≤10%;3M-EMR)对深度分子反应(DMR,MR4.5)、无进展生存期(PFS)、无事件生存期(EFS)和总生存期(OS)的影响。
44例(28.6%)患者存在中度贫血。与无贫血患者相比,这些患者具有更具侵袭性的基线特征和更高风险,根据评分系统评估,其治疗反应较差,包括3M-EMR(50.0%对69.1%)、6个月时的完全细胞遗传学反应(20.5%对50.9%)和12个月时的主要分子反应(22.5%对45.2%),中位随访时间为54.0个月。此外,与EUTOS、Sokal和Hasford评分相比,Hb为10 g/dl能更好地区分DMR、EFS、PFS和OS,并且与3M-EMR联合使用时比单独使用3M-EMR能更好地预测反应和生存期。
这一发现凸显了贫血在CML-CP中的重要性,并表明诊断时贫血的患者应仔细监测,如果未达到3M-EMR,可能从更强效的酪氨酸激酶抑制剂中获益。