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我们应该如何治疗新诊断的青少年及年轻成人急性淋巴细胞白血病患者?

How should we treat the AYA patient with newly diagnosed ALL?

作者信息

Boissel Nicolas

机构信息

Adolescent & Young Adult Hematology Unit, Saint-Louis Hospital, EA-3518, Paris 7 University, 1 avenue Claude Vellefaux, 75010, Paris, France.

出版信息

Best Pract Res Clin Haematol. 2017 Sep;30(3):175-183. doi: 10.1016/j.beha.2017.07.008. Epub 2017 Aug 3.

Abstract

Adolescent and young adult (AYA) patients with acute lymphoblastic leukaemia (ALL) are recognized as a unique population with specific characteristics and needs. In adolescents aged 15-20 years old, the use of full paediatric protocols is supported by many comparative studies of paediatric and adult cooperative groups. In young adults, growing evidence suggests that paediatric-inspired approaches may also improve outcomes and lead to long-term survival rates of almost 70%. In the last decade, better knowledge of ALL oncogenic landscape, age distribution, and minimal residual disease prognostic impact have improved risk stratification. New targets have emerged mostly in the heterogeneous subgroup of Philadelphia-like ALL and will require both in-depth molecular investigations and specific evaluations in rare subgroups of ALL. The remaining gap with the excellent results reported in children has many other contributing factors that should not be underestimated including late or difficult access to care, or poor adherence to treatment.

摘要

青少年和青年(AYA)急性淋巴细胞白血病(ALL)患者被认为是具有特定特征和需求的独特群体。在15至20岁的青少年中,许多儿科和成人合作组的比较研究支持使用完整的儿科方案。在青年中,越来越多的证据表明,受儿科启发的方法也可能改善预后,并使长期生存率接近70%。在过去十年中,对ALL致癌格局、年龄分布以及微小残留病预后影响的更好了解改善了风险分层。新的靶点大多出现在费城样ALL的异质性亚组中,这将需要对ALL的罕见亚组进行深入的分子研究和特定评估。与儿童所报告的优异结果相比,仍存在差距,还有许多其他促成因素不应被低估,包括获得治疗较晚或困难,或治疗依从性差。

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