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首页> 外文期刊>Leukemia Research: A Forum for Studies on Leukemia and Normal Hemopoiesis >Age influences initial dose and compliance to imatinib in chronic myeloid leukemia elderly patients but concomitant comorbidities appear to influence overall and event-free survival
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Age influences initial dose and compliance to imatinib in chronic myeloid leukemia elderly patients but concomitant comorbidities appear to influence overall and event-free survival

机译:年龄影响慢性粒细胞白血病老年患者的伊马替尼的初始剂量和依从性,但伴随的合并症似乎影响整体生存和无事件生存

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摘要

We applied Charlson comorbidity index (CCI) stratification on a large cohort of chronic myeloid leukemia (CML) very elderly patients (>75 years) treated with imatinib, in order to observe the impact of concomitant diseases on both compliance and outcome. One hundred and eighty-one patients were recruited by 21 Italian centers. There were 95 males and 86 females, median age 78.6 years (range 75-93.6). According to Sokal score, 106 patients were classified as intermediate risk and 55 as high risk (not available in 20 patients). According to CCI stratification, 71 patients had score 0 and 110 a score ≥ 1. Imatinib standard dose was reduced at start of therapy (200-300. mg/day) in 68 patients independently from the evaluation of baseline comorbidities, but based only on physician judgement: 43.6% of these patients had score 0 compared to 34% of patients who had score ≥ 1. Significant differences were found in terms of subsequent dose reduction (39% of patients with score 0 compared to 53% of patients with score. ≥ 1) and in terms of drug discontinuation due to toxicity (35% of patients with score 0 vs 65% of patients with score ≥ 1). We did not find significant differences as regards occurrence of hematologic side effects, probably as a consequence of the initial dose reduction: 39% of patients with score 0 experienced grade 3/4 hematologic toxicity (most commonly anemia) compared to 42% of patients with score ≥ 1. Independently from the initial dose, comorbidities again did not have an impact on development of grade 3/4 non-hematologic side effects (most commonly skin rash, muscle cramps and fluid retention): 62% of patients with score 0 compared to 52.5% of patients with score ≥ 1. Notwithstanding the reduced dose and the weight of comorbidities we did not find significant differences but only a trend in terms of efficacy: 66% of patients with score 0 achieved a CCyR compared to 54% of patients with score ≥ 1. Comorbidities appeared to have an impact on median OS (40.8 months for patients with score 0 vs 20.16 months for patients with score ≥. 1) on EFS and on non-CML death rate. Our results suggest that treatment of very elderly CML patients might be influenced by personal physician perception: evaluation at baseline of comorbidities according to CCI should improve initial decision-making in this subset of patients.
机译:我们对接受伊马替尼治疗的一大批慢性髓性白血病(CML)老年患者(> 75岁)应用了Charlson合并症指数(CCI)分层,以观察伴随疾病对依从性和预后的影响。意大利的21个中心招募了181位患者。男95例,女86例,中位年龄78.6岁(范围75-93.6)。根据Sokal评分,将106例患者分类为中等风险,将55例分类为高风险(20例患者中没有)。根据CCI分层,独立于基线合并症的评估,有68例患者在治疗开始时伊马替尼的标准剂量(200-300。mg /天)降低了0分且110分≥1。独立于基线合并症的评估,但仅基于医师判断:这些患者中有43.6%的患者得分为0,而得分≥1的患者为34%,在随后的减量方面存在显着差异(得分为0的患者为39%,得分为0的患者为53%。 ≥1)以及因毒性而停药的情况(得分为0的患者占35%,得分≥1的患者占65%)。我们没有发现血液不良反应发生方面的显着差异,这可能是初始剂量降低的结果:0级患者中有39%经历了3/4级血液学毒性(最常见的是贫血),而42%的患者得分≥1。与初始剂量无关,合并症再次对3/4级非血液学副作用(最常见的是皮疹,肌肉痉挛和体液retention留)的发生没有影响:评分为0的患者中有62%得分≥1的患者中有52.5%的患者。尽管剂量减少和合并症的重量减轻,但我们并未发现显着差异,但仅在疗效方面出现了趋势:得分为0的患者中有66%达到了CCyR,而患者的这一比例为54%得分≥1。合并症似乎对EFS和非CML死亡率的中位OS(得分0的患者为40.8个月,得分≥。1的患者为20.16个月)产生影响。我们的结果表明,非常老的CML患者的治疗可能会受到个人医生的看法的影响:根据CCI在合并症基线进行评估应改善该患者亚组的初步决策。

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