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一项针对费城染色体阴性急性淋巴细胞白血病青少年和年轻成人的儿科方案的疗效与毒性:英国ALL 2003研究结果

Efficacy and toxicity of a paediatric protocol in teenagers and young adults with Philadelphia chromosome negative acute lymphoblastic leukaemia: results from UKALL 2003.

作者信息

Hough Rachael, Rowntree Clare, Goulden Nick, Mitchell Chris, Moorman Anthony, Wade Rachel, Vora Ajay

机构信息

University College Hospital, London, UK.

University Hospital of Wales, Cardiff, UK.

出版信息

Br J Haematol. 2016 Feb;172(3):439-51. doi: 10.1111/bjh.13847. Epub 2015 Dec 18.

Abstract

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 (7·3%) were aged 16-24 years. These patients were significantly more likely to have high risk MRD compared to 10-15 year olds (47·9% vs. 36·6%, P = 0·004). Nonetheless, 5-year event-free survival for the TYA cohort (aged 16-24 years) was 72·3% [95% confidence interval (CI): 66·2-78·4] overall and 92·6% (95% CI: 85·5-99·7) for MRD low risk patients. The risk of serious adverse events was higher in patients aged ≥10 years compared to those aged 9 or younger (P < 0·0001) 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 10 years and older have excess toxicity compared with younger patients, the age association is specific to individual toxicities.

摘要

尽管小儿急性淋巴细胞白血病(ALL)在治疗效果上有了显著改善,但青少年和青年(TYA)患者的生存率仍然较低。我们报告了在英国小儿ALL试验UKALL2003中接受治疗的TYA患者的治疗结果和毒性特征。UKALL2003是一项多中心、前瞻性、随机III期试验,根据诱导结束时的微小残留病(MRD)动力学研究治疗强化或降级。在招募到UKALL2003的3126名患者中,229名(7.3%)年龄在16 - 24岁之间。与10 - 15岁的患者相比,这些患者更有可能具有高风险MRD(47.9%对36.6%,P = 0.004)。尽管如此,TYA队列(年龄在16 - 24岁之间)的5年无事件生存率总体为72.3% [95%置信区间(CI):66.2 - 78.4],MRD低风险患者为92.6%(95% CI:85.5 - 99.7)。与9岁或以下的患者相比,≥10岁的患者发生严重不良事件的风险更高(P < 0.0001),并且观察到了与治疗相关毒性的新的年龄特异性模式。TYA患者通过风险和反应适应性儿科化疗方案可获得优异的治疗结果。虽然10岁及以上的患者与年轻患者相比毒性更高,但年龄与毒性的关联具有个体毒性特异性。

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