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首页> 外文期刊>British Journal of Haematology >Efficacy and toxicity of a paediatric protocol in teenagers and young adults with Philadelphia chromosome negative acute lymphoblastic leukaemia: results from UKALL 2003
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Efficacy and toxicity of a paediatric protocol in teenagers and young adults with Philadelphia chromosome negative acute lymphoblastic leukaemia: results from UKALL 2003

机译:费城染色体阴性急性淋巴细胞白血病少年儿童的儿科治疗方案的功效和毒性:UKALL 2003的结果

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Despite the substantial outcome improvements achieved in paediatric acute lymphoblastic leukaemia (ALL), survival in teenage and young adult (TYA) patients has remained inferior. We report the treatment outcomes and toxicity profiles observed in TYA patients treated on the UK paediatric ALL trial, UKALL2003. UKALL2003 was a multi-centre, prospective, randomized phase III trial, investigating treatment intensification or de-escalation according to minimal residual disease (MRD) kinetics at the end of induction. Of 3126 patients recruited to UKALL2003, 229 (73%) were aged 16-24years. These patients were significantly more likely to have high risk MRD compared to 10-15year olds (479% vs. 366%, P=0004). Nonetheless, 5-year event-free survival for the TYA cohort (aged 16-24years) was 723% [95% confidence interval (CI): 662-784] overall and 926% (95% CI: 855-997) for MRD low risk patients. The risk of serious adverse events was higher in patients aged 10years compared to those aged 9 or younger (P<00001) and novel age-specific patterns of treatment-related toxicity were observed. TYA patients obtain excellent outcomes with a risk- and response-adapted paediatric chemotherapy protocol. Whilst those aged 10years and older have excess toxicity compared with younger patients, the age association is specific to individual toxicities.
机译:尽管小儿急性淋巴细胞白血病(ALL)取得了显着的疗效改善,但青少年和年轻成人(TYA)患者的存活率仍然较低。我们报告了在英国儿科ALL试验(UKALL2003)中治疗的TYA患者的治疗结果和毒性概况。 UKALL2003是一项多中心,前瞻性,随机III期试验,根据诱导结束时的最小残留疾病(MRD)动力学,研究治疗的强化或降级情况。在UKALL2003招募的3126名患者中,有229名(73%)年龄在16-24岁之间。与10-15岁的患者相比,这些患者发生高风险MRD的可能性明显更高(479%对366%,P = 0004)。尽管如此,TYA队列(16-24岁)的5年无事件生存率总体为723%[95%置信区间(CI):662-784],MRD为926%(95%CI:855-997)低危患者。与9岁或9岁以下的患者相比,10岁的患者发生严重不良事件的风险更高(P <00001),并且观察到了与治疗相关的毒性的新的年龄特异性模式。 TYA患者通过适应风险和反应的小儿化疗方案获得了出色的疗效。与那些年轻患者相比,年龄在10岁及以上的人有过度的毒性,但是年龄关联是针对个体毒性的。

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