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儿童急性淋巴细胞白血病与复发

Childhood acute lymphoblastic leukaemia and relapse.

作者信息

Gaynon Paul S

机构信息

Hematology Oncology, Childrens Hospital of Los Angeles, University of Southern California, Los Angeles, CA 90027-6062, USA.

出版信息

Br J Haematol. 2005 Dec;131(5):579-87. doi: 10.1111/j.1365-2141.2005.05773.x.

Abstract

Acute lymphoblastic leukaemia (ALL) is the most common childhood cancer. Treatment has improved but relapsed ALL remains more common than new cases of many 'common' paediatric malignancies. We have salvage regimens with substantial complete remission (CR) rates and increasing access to haematopoietic stem cell transplantation, but most patients who relapse die. We need better therapies. Insights into pharmacology may guide more effective use of existing agents. Novel agents with activity against resistant lymphoblasts offer an appealing strategy. However, most candidate agents fail, despite enthusiastic investigators, intriguing mechanisms of action and 'compelling' preclinical data. A number of existing combinations provide a 40% complete response rate in second or third relapse. Yet survival in third remission is <10%. Novel agents must, most likely, be integrated into multiagent combinations that provide a higher CR rate or better quality CR's than our conventional combinations in order to contribute substantially to cure. The march from bench to bedside requires careful consideration of the intermediate steps.

摘要

急性淋巴细胞白血病(ALL)是儿童期最常见的癌症。治疗虽有改善,但复发性ALL仍比许多“常见”儿科恶性肿瘤的新发病例更为常见。我们有具有较高完全缓解(CR)率的挽救方案,并且造血干细胞移植的可及性也在增加,但大多数复发患者仍会死亡。我们需要更好的治疗方法。对药理学的深入了解可能会指导现有药物的更有效使用。对耐药淋巴细胞具有活性的新型药物提供了一种有吸引力的策略。然而,尽管有热情的研究人员、引人入胜的作用机制和“令人信服”的临床前数据,但大多数候选药物还是失败了。一些现有联合方案在第二次或第三次复发时的完全缓解率为40%。然而,第三次缓解后的生存率低于10%。新型药物很可能必须整合到多药联合方案中,这些方案要比我们的传统联合方案提供更高的CR率或更好质量的CR,以便对治愈做出实质性贡献。从实验室到临床的过程需要仔细考虑中间步骤。

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