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个体化治疗可提高高危实体瘤患儿的生存率:真实场景下的比较患者系列分析

Individualization of Treatment Improves the Survival of Children With High-Risk Solid Tumors: Comparative Patient Series Analysis in a Real-Life Scenario.

作者信息

Kyr Michal, Polaskova Kristyna, Kuttnerova Zuzana, Merta Tomas, Neradil Jakub, Berkovcova Jitka, Horky Ondrej, Jezova Marta, Veselska Renata, Klement Giannoula Lakka, Valik Dalibor, Sterba Jaroslav

机构信息

Department of Pediatric Oncology, University Hospital Brno and School of Medicine, Masaryk University, Brno, Czechia.

International Clinical Research Centre, St. Anne's University Hospital Brno, Brno, Czechia.

出版信息

Front Oncol. 2019 Jul 17;9:644. doi: 10.3389/fonc.2019.00644. eCollection 2019.

Abstract

The individualization of treatment is attractive, especially in children with high-risk cancer. In such a rare and very heterogeneous group of diseases, large population-based clinical randomized trials are not feasible without international collaboration. We therefore propose comparative patient series analysis in a real-life scenario. Open cohort observational study, comparative analysis. Seventy patients with high-risk solid tumors diagnosed between 2003 and 2015 and in whom the treatment was individualized either empirically or based on biomarkers were analyzed. The heterogeneity of the cohort and repeated measurements were advantageously utilized to increase effective sample size using appropriate statistical tools. We demonstrated a beneficial effect of empirically given low-dose metronomic chemotherapy (HR 0.46 for relapses, = 0.017) as well as various repurposed or targeted agents (HR 0.15 for deaths, = 0.004) in a real-life scenario. However, targeted agents given on the basis of limited biological information were not beneficial. Comparative patient series analysis provides institutional-level evidence for treatment individualization in high-risk pediatric malignancies. Our findings emphasize the need for a comprehensive, multi omics assessment of the tumor and the host as well whenever molecularly driven targeted therapies are being considered. Low-dose metronomic chemotherapy or local control of the disease may be a more rational option in situations where targeted treatment cannot be justified by robust evidence and comprehensive biological information. "Targeted drugs" may be given empirically with a realistic benefit expectation when based on robust rationale.

摘要

治疗个体化很有吸引力,尤其是在高危癌症患儿中。在这样一组罕见且非常异质性的疾病中,没有国际合作的情况下,基于大规模人群的临床随机试验是不可行的。因此,我们建议在现实场景中进行比较患者系列分析。开放队列观察性研究,比较分析。分析了2003年至2015年间诊断为高危实体瘤且治疗根据经验或基于生物标志物进行个体化的70例患者。利用队列的异质性和重复测量,使用适当的统计工具来增加有效样本量。我们在现实场景中证明了经验性给予低剂量节拍化疗(复发的风险比为0.46,P = 0.017)以及各种重新利用或靶向药物(死亡的风险比为0.15,P = 0.004)的有益效果。然而,基于有限生物学信息给予的靶向药物并无益处。比较患者系列分析为高危儿科恶性肿瘤的治疗个体化提供了机构层面的证据。我们的发现强调,每当考虑分子驱动的靶向治疗时,都需要对肿瘤和宿主进行全面的多组学评估。在没有充分证据和全面生物学信息支持靶向治疗的情况下,低剂量节拍化疗或局部控制疾病可能是更合理的选择。当基于充分的理论依据时,“靶向药物”可以根据经验给予,并抱有现实的获益期望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23de/6650566/181e56a36386/fonc-09-00644-g0001.jpg

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