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儿科肿瘤精准治疗的进展。

Progress in precision therapy in pediatric oncology.

机构信息

Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

出版信息

Curr Opin Pediatr. 2023 Feb 1;35(1):41-47. doi: 10.1097/MOP.0000000000001198. Epub 2022 Dec 13.

Abstract

PURPOSE OF REVIEW

The fields of precision medicine and cancer genomics in pediatric oncology are rapidly evolving. Novel diagnostic tools are critical in refining cancer diagnoses, stratifying patient risk, and informing treatment decisions. This review is timely and relevant as it discusses advantages and drawbacks of common molecular profiling techniques and highlights novel platforms, which may address select limitations. We discuss recent publications demonstrating utility of large-scale molecular profiling and feasibility and logistics of matching targeted therapies to patients.

RECENT FINDINGS

We describe the increased accessibility of next-generation sequencing, complementary profiling methods, and strategies to guide treatment decisions. We describe curation and sharing of large genomic datasets and novel mechanisms to obtain matched targeted therapies. Importantly, we discuss relevant publications in distinct disease domains that support indications for evidence-based precision therapy. Lastly, we introduce the incremental analyses that can be obtained via whole-genome and transcriptome sequencing.

SUMMARY

Here we highlight high-yield clinical scenarios of precision medicine approaches and identify the ongoing challenges including universally defining clinical actionability, optimizing trial design to account for molecular heterogeneity while acknowledging limitations in patient accrual, expanding access to molecularly targeted therapies, and validating new tools and technology to aid in precision medicine therapeutic approaches.

摘要

目的综述

精准医学和儿科肿瘤学癌症基因组学领域正在迅速发展。新型诊断工具对于细化癌症诊断、分层患者风险和指导治疗决策至关重要。由于该综述讨论了常见分子分析技术的优缺点,并强调了可能解决特定局限性的新型平台,因此具有及时性和相关性。我们讨论了最近的出版物,这些出版物展示了大规模分子分析的实用性以及将靶向治疗与患者匹配的可行性和后勤工作。

最近的发现

我们描述了下一代测序、互补分析方法以及指导治疗决策的策略的可及性增加。我们描述了大型基因组数据集的策展和共享以及获得匹配靶向治疗的新机制。重要的是,我们讨论了支持基于证据的精准治疗适应症的不同疾病领域的相关出版物。最后,我们介绍了通过全基因组和转录组测序可以获得的增量分析。

总结

在这里,我们强调了精准医学方法的高收益临床情况,并确定了正在面临的挑战,包括普遍定义临床可操作性、优化试验设计以考虑分子异质性,同时承认患者入组的局限性、扩大获得分子靶向治疗的机会,以及验证新工具和技术以辅助精准医学治疗方法。

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