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儿童癌症放射治疗并发症研究报告标准:来自 PENTEC 的经验教训。

Reporting Standards for Complication Studies of Radiation Therapy for Pediatric Cancer: Lessons From PENTEC.

机构信息

Department of Medical Physics, Memorial Sloan-Kettering Cancer Center, New York, New York.

Department of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, Tennessee.

出版信息

Int J Radiat Oncol Biol Phys. 2024 Jun 1;119(2):697-707. doi: 10.1016/j.ijrobp.2024.02.018.

Abstract

The major aim of Pediatric Normal Tissue Effects in the Clinic (PENTEC) was to synthesize quantitative published dose/-volume/toxicity data in pediatric radiation therapy. Such systematic reviews are often challenging because of the lack of standardization and difficulty of reporting outcomes, clinical factors, and treatment details in journal articles. This has clinical consequences: optimization of treatment plans must balance between the risks of toxicity and local failure; counseling patients and their parents requires knowledge of the excess risks encountered after a specific treatment. Studies addressing outcomes after pediatric radiation therapy are particularly challenging because: (a) survivors may live for decades after treatment, and the latency time to toxicity can be very long; (b) children's maturation can be affected by radiation, depending on the developmental status of the organs involved at time of treatment; and (c) treatment regimens frequently involve chemotherapies, possibly modifying and adding to the toxicity of radiation. Here we discuss: basic reporting strategies to account for the actuarial nature of the complications; the reporting of modeling of abnormal development; and the need for standardized, comprehensively reported data sets and multivariate models (ie, accounting for the simultaneous effects of radiation dose, age, developmental status at time of treatment, and chemotherapy dose). We encourage the use of tools that facilitate comprehensive reporting, for example, electronic supplements for journal articles. Finally, we stress the need for clinicians to be able to trust artificial intelligence models of outcome of radiation therapy, which requires transparency, rigor, reproducibility, and comprehensive reporting. Adopting the reporting methods discussed here and in the individual PENTEC articles will increase the clinical and scientific usefulness of individual reports and associated pooled analyses.

摘要

儿科正常组织器官临床效应(PENTEC)的主要目的是综合发表的定量文献资料,这些文献资料涉及儿科放射治疗中的剂量-体积-毒性数据。由于缺乏标准化和难以报告期刊文章中的结果、临床因素和治疗细节,此类系统评价往往具有挑战性。这具有临床意义:优化治疗计划必须在毒性和局部失败的风险之间取得平衡;为患者及其父母提供咨询需要了解特定治疗后所面临的额外风险。儿科放射治疗后结果的研究尤其具有挑战性,原因如下:(a)幸存者可能在治疗后数十年仍存活,且毒性的潜伏期可能非常长;(b)儿童的成熟可能受到辐射的影响,这取决于治疗时涉及的器官的发育状态;(c)治疗方案通常涉及化疗,这可能会改变和增加辐射的毒性。在这里,我们讨论了:用于解释并发症的累积性质的基本报告策略;异常发育建模的报告;以及标准化、全面报告数据集和多变量模型(即,考虑到辐射剂量、年龄、治疗时的发育状态和化疗剂量的同时影响)的需求。我们鼓励使用有助于全面报告的工具,例如期刊文章的电子补充材料。最后,我们强调临床医生需要能够信任放射治疗结果的人工智能模型,这需要透明度、严谨性、可重复性和全面报告。采用这里和个别 PENTEC 文章中讨论的报告方法将提高个别报告和相关汇总分析的临床和科学有用性。

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