Objective: To explore the influencing covariates of severe neutrophils and/or thrombocytopenia and their effect on treatment response and outcome in patients with chronic-phase chronic myeloid leukemia (CP-CML) receiving initial second-generation tyrosine kinase inhibitors (2G-TKI) . Methods: Data from consecutive patients aged ≥18 years with newly diagnosed CP-CML who received initial 2G-TKI at Peking University People's Hospital from September 2008 to November 2021 were interrogated. Binary logistic regression models and Fine-Gray and Cox regression models were applied. Results: Data from 267 patients who received initial 2G-TKI, including nilotinib (n=239, 89.5% ) and dasatinib (n=28, 10.5% ) , were interrogated. The median age was 36 (range, 18-73) years, and 156 (58.4% ) patients were male. At a median treatment period of 1.0 (0.1-3.0) month, 43 (16.1% ) patients developed grade ≥3 neutrophils and/or thrombocytopenia and recovered within 1.0 (0.1-24.6) month. Male (OR=2.9, 95% CI 1.2-6.8; P=0.018) , age of ≥36 years (OR=3.2, 95% CI 1.4-7.2, P=0.005) , a spleen below a costal margin of ≥7 cm (OR=2.8, 95% CI 1.2-6.6, P=0.020) , and a hemoglobin (HGB) level of <100 g/L (OR=2.9, 95% CI 1.3-6.8, P=0.012) at diagnosis were significantly associated with grade ≥ 3 neutrophils and/or thrombocytopenia. Based on their regression coefficients, male, age of ≥36 years, a spleen below a costal margin of ≥7 cm, and an HGB level of <100 g/L were given 1 point to form a predictive system. All patients were divided into three risk subgroups, and the incidence of severe cytopenia significantly differed among the three groups (P < 0.001) . Grade ≥3 neutrophils and/or thrombocytopenia for >2 weeks was significantly associated with lower cumulative incidences of complete cytogenetic response (CCyR, HR=0.5, 95% CI 0.3-0.7, P<0.001) and major molecular response (MMR, HR=0.4, 95% CI 0.3-0.8, P=0.004) and was not significantly associated with failure, progression, and survival. Conclusion: Male, advanced age, a large spleen, and a low HGB level were significantly associated with severe cytopenia. The four covariates were used to establish a prediction model, in which the incidence of severe cytopenia among different risk groups was significantly different. Severe cytopenia for >2 weeks was a negative factor for responses but not for outcomes.
目的: 探索二代酪氨酸激酶抑制剂(TKI)一线治疗慢性髓性白血病慢性期(CML-CP)患者发生严重血细胞减少的相关因素及其对治疗反应和结局的影响,并建立严重血细胞减少的预测模型。 方法: 纳入2008年9月至2021年11月间在北京大学人民医院确诊并服用二代TKI作为一线治疗的成年CML-CP连续病例。采用二元Logistic模型、Fine-gray模型和Cox回归模型进行分析。 结果: 共收集267例患者,中位年龄36(18~73)岁,男性156例(58.4%),服用尼洛替尼239例(89.5%),达沙替尼28例(10.5%)。43例(16.1%)患者在一线治疗开始后1.0(0.1~3.0)个月发生≥ 3级中性粒细胞和(或)血小板减少,持续1.0(0.1~24.6)个月。男性(OR=2.9,95%CI 1.2~6.8,P=0.018)、初诊年龄≥36岁(OR=3.2,95%CI 1.4~7.2, P=0.005)、脾脏肋缘下≥ 7 cm(OR=2.8,95%CI 1.2~6.6,P=0.020)以及HGB<100 g/L(OR=2.9,95%CI 1.3~6.8,P=0.012)与发生≥ 3级中性粒细胞和(或)血小板减少显著相关。根据回归系数,男性、初诊年龄≥36岁,脾脏肋缘下≥7 cm以及HGB<100 g/L各赋1分,可将患者分为低危、中危和高危3组,各组间血细胞减少发生率差异有统计学意义(P<0.001)。持续>2周的严重血液学不良反应与较低的完全细胞遗传学反应(HR=0.5,95%CI 0.3~0.7,P<0.001)和主要分子学反应(HR=0.4,95%CI 0.3~0.8,P=0.004)获得率显著相关,与二代TKI治疗失败、疾病进展和生存期无关。 结论: 男性、初诊年龄≥36岁、脾脏肋缘下≥ 7 cm以及HGB<100 g/L与初发CML-CP患者服用二代TKI期间发生严重血细胞减少显著相关,联合四者建立的预测模型有助于识别严重血细胞减少的发生风险。严重血细胞减少持续>2周是细胞遗传学和分子学反应的不利因素。.
Keywords: Cytopenia; Leukemia, myeloid, chronic; Treatment outcome; Tyrosine kinase inhibitors.