Lekovic Danijela, Gotic Mirjana, Milic Natasa, Zivojinovic Biljana, Jovanovic Jelica, Colovic Natasa, Milosevic Violeta, Bogdanovic Andrija
a Clinic for Hematology , Clinical Center of Serbia , Belgrade , Serbia.
b Medical Faculty , University of Belgrade , Belgrade , Serbia.
Hematology. 2017 Sep;22(8):460-466. doi: 10.1080/10245332.2017.1302179. Epub 2017 Mar 22.
Until recently, imatinib was the standard first-line treatment in chronic myeloid leukemia (CML). The inclusion of nilotinib and dasatinib as first-line options in CML raised a debate on treatment selection. The aim of our study was to analyze predictive parameters for imatinib response as the first-line treatment of CML patients.
The study included 168 consecutive patients with chronic phase Philadelphia-positive CML who were diagnosed and treated with Imatinib 400 mg once daily at a single university hospital. Numerous parameters were analyzed in terms of imatinib response including comorbidities as well as occurrence of second malignancies.
After the median follow-up of 87 months in 61 patients (36.3%), the imatinib failure was verified. Cox regression analysis identified hepatomegaly (p = 0.001), leukocytosis ≥ 100 × 109/l (p = 0.001), blood blasts ≥ 1% (p = 0.002), and the presence of additional cytogenetic aberrations (p = 0.002) as predictors of Imatinib failure. Based on these findings, a new prognostic model was developed according to which imatinib failure had 17% (8/47) of patients in low risk, 34.9% (30/86) of patients in intermediate risk, and 76.7% (23/30) of patients in high-risk group (HR = 3.973, 95% CI for HR 2.237-7.053, p < 0.001).
The new score allows better selection of patients who are suitable for treatment with imatinib and may guideline the clinical decision for front-line treatment of CML.
直到最近,伊马替尼仍是慢性髓性白血病(CML)的标准一线治疗药物。尼罗替尼和达沙替尼作为CML的一线治疗选择引发了关于治疗选择的争论。我们研究的目的是分析伊马替尼作为CML患者一线治疗反应的预测参数。
该研究纳入了168例连续的费城染色体阳性慢性期CML患者,这些患者在单一大学医院接受每日一次400mg伊马替尼的诊断和治疗。就伊马替尼反应分析了众多参数,包括合并症以及第二原发性恶性肿瘤的发生情况。
在61例患者(36.3%)中位随访87个月后,证实伊马替尼治疗失败。Cox回归分析确定肝肿大(p = 0.001)、白细胞增多≥100×10⁹/L(p = 0.001)、血原始细胞≥1%(p = 0.002)以及存在其他细胞遗传学异常(p = 0.002)为伊马替尼治疗失败的预测因素。基于这些发现,开发了一种新的预后模型,根据该模型,伊马替尼治疗失败的患者中低风险组占17%(8/47),中风险组占34.9%(30/86),高风险组占76.7%(23/30)(HR = 3.973,HR的95%CI为2.237 - 7.053,p < 0.001)。
新的评分系统有助于更好地选择适合伊马替尼治疗的患者,并可能指导CML一线治疗的临床决策。