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改善癌症患儿的治疗结果:靶向新药的研发。

Improving the outcome for children with cancer: Development of targeted new agents.

作者信息

Adamson Peter C

机构信息

Chair, Children's Oncology Group, The Children's Hospital of Philadelphia, Philadelphia, PA.

出版信息

CA Cancer J Clin. 2015 May-Jun;65(3):212-20. doi: 10.3322/caac.21273. Epub 2015 Mar 9.

Abstract

The outcome for children with cancer has improved significantly over the past 60 years, with greater than 80% of patients today becoming 5-year survivors. Despite this progress, cancer remains the leading cause of death from disease in children in the United States, and significant short-term and long-term treatment toxicities continue to impact the majority of children with cancer. The development of targeted new agents offers the prospect of potentially more effective and less toxic treatment for children. More than a decade since imatinib mesylate was introduced into the treatment of children with Philadelphia chromosome-positive acute lymphoblastic leukemia, transforming its outcome, a range of targeted agents has undergone study in pediatric cancer patients. Early lessons learned from these studies include a better understanding of the adverse event profile of these drugs in children, the challenge of developing pediatric-specific formulations, and the continued reliance on successful development for adult cancer indications on pediatric drug development. The collaborative research infrastructure for children with cancer in the United States is well positioned to advance novel treatments into clinical investigations for a spectrum of rare and ultra-rare childhood cancers. A greater investment of resources in target discovery and validation can help drive much needed development of new, more effective treatments for children with cancer.

摘要

在过去60年里,癌症患儿的治疗结果有了显著改善,如今超过80%的患者成为了5年生存者。尽管取得了这一进展,但癌症仍是美国儿童因病死亡的主要原因,严重的短期和长期治疗毒性继续影响着大多数癌症患儿。靶向新药的研发为儿童提供了潜在更有效且毒性更低的治疗前景。自甲磺酸伊马替尼被用于治疗费城染色体阳性急性淋巴细胞白血病患儿并改变其治疗结果以来,已有十多年时间,一系列靶向药物在儿科癌症患者中进行了研究。从这些研究中吸取的早期经验教训包括:更好地了解这些药物在儿童中的不良事件特征、开发儿科专用制剂的挑战,以及儿科药物开发对成人癌症适应症成功开发的持续依赖。美国针对癌症患儿的协作研究基础设施处于有利地位,能够将新型治疗方法推进到一系列罕见和超罕见儿童癌症的临床研究中。在靶点发现和验证方面投入更多资源,有助于推动为癌症患儿开发急需的新的、更有效的治疗方法。

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