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Outcomes In Older Adults with Acute Lymphoblastic Leukemia (ALL): Results From the International MRC UKALL XII/ECOG2993 Trial

机译:结果老年患者的急性淋巴细胞白血病(aLL):结果从国际mRC UKaLL XII / ECOG2993试用

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摘要

Although the incidence rate of acute lymphoblastic leukemia (ALL) is slightly higher in older than in younger adults, response rates to induction chemotherapy and survival rates are poorer. The contribution of disease-related versus treatment-related factors remains unclear. We analysed 100 older patients (age-range 55–65) treated on the UKALLXII/ECOG2993 trial compared with 1814 younger patients (age-range 14–54). We compared baseline characteristics, induction chemotherapy course, infections, drug reductions and survival outcomes. There were more Philadelphia-positive (Ph+) patients in the older group (28% vs. 17%, p=0.02), and a trend in higher combined cytogenetic risk score (46% vs. 35%, p=0.07). The complete remission rate was worse (73% vs. 93%, p<0.0001) as was five-year overall survival (21% vs. 41%, p<0.0001) and event-free survival (EFS) (19% vs. 37%, p<0.0001). Older patients had more infections during induction (81% vs. 70%, p=0.05), and drug reductions (46% vs. 28%, p=0.0009). Among older patients, Ph+ and cytogenetic risk category as well as infection during induction predicted for worse EFS. Poorer outcomes in these patients are partly due to cytogenetic risk, but there is significant morbidity and mortality with induction chemotherapy with frequent delays and drug reductions. New approaches including better risk stratification and use of targeted therapies could improve treatment for these patients.
机译:虽然急性淋巴细胞白血病的发病率(全部)比年轻成人略高,但对诱导化疗和生存率的反应率较差。疾病相关的与治疗相关因素的贡献仍然不明确。与1814名患者(年龄范围14-54岁)分析了在UKALLXII / ECOG2993试验上治疗的100名老年患者(55-65岁)(55-65岁)。我们比较基线特征,感染,药物减少和生存结果。较旧群中的费城阳性(pH +)患者(28%对17%,P = 0.02),较高的细胞遗漏风险评分(46%vs.35%,P = 0.07)。完整的缓解率更差(73%vs.93%,P <0.0001),如五年的整体存活率(21%对41%,P <0.0001)和无事项存活率(EFS)(19%对) 37%,P <0.0001)。在诱导期间(81%对70%,P = 0.05)和药物减少(46%,P = 0.0009),年龄较大的患者有更多的感染。在更老的患者中,pH +和细胞遗传学风险类以及感染期间预测到更糟糕的EF。这些患者的较差结果部分是由于细胞遗传学风险,但具有常见延迟和药物减少的诱导化疗存在显着的发病率和死亡率。新方法包括更好的风险分层和使用靶向疗法可以改善这些患者的治疗方法。

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