Dao Long, Ragoonanan Dristhi, Yi Sofia, Swinford Rita, Petropoulos Demetrios, Mahadeo Kris M, Li Shulin
Department of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.
Division of Pediatric Nephrology, University of Texas Health Science Center Houston, Houston, TX, United States.
Front Oncol. 2020 Nov 11;10:579219. doi: 10.3389/fonc.2020.579219. eCollection 2020.
Pediatric organ failure and transplant populations face significant risks of morbidity and mortality. The risk of organ failure itself may be disproportionately higher among pediatric oncology patients, as cancer may originate within and/or metastasize to organs and adversely affect their function. Additionally, cancer directed therapies are frequently toxic to organs and may contribute to failure. Recent reports suggest that nearly half of providers find it difficult to provide prognostic information regarding organ failure due to unknown disease trajectories. Unfortunately, there is a lack of uniform methodology in detecting the early symptoms of organ failure, which may delay diagnosis, initiation of treatment and hinder prognostic planning. There remains a wide array of outstanding scientific questions regarding organ failure in pediatrics but emerging data may change the landscape of prognostication. Liquid biopsy, in which disease biomarkers are detected in bodily fluids, offers a noninvasive alternative to tissue biopsy and may improve prompt detection of organ failure and prognostication. Here, we review potential liquid biopsy biomarkers for organ failure, which may be particularly useful among pediatric oncology patients. We synthesized information from publications obtained on PubMed, Google Scholar, clinicaltrials.gov, and Web of Science and categorized our findings based on the type of biomarker used to detect organ failure. We highlight the advantages and disadvantages specific to each type of organ failure biomarker. While much work needs to be done to advance this field and validate its applicability to pediatric cancer patients facing critical care complications, herein, we highlight promising areas for future discovery.
儿科器官衰竭和移植人群面临着较高的发病和死亡风险。儿科肿瘤患者出现器官衰竭的风险可能尤其高,因为癌症可能起源于器官内部和/或转移至器官,并对其功能产生不利影响。此外,针对癌症的治疗通常对器官有毒性,可能导致器官衰竭。最近的报告表明,由于疾病发展轨迹不明,近一半的医疗服务提供者发现难以提供有关器官衰竭的预后信息。不幸的是,在检测器官衰竭的早期症状方面缺乏统一的方法,这可能会延迟诊断、治疗的开始,并阻碍预后规划。关于儿科器官衰竭仍有一系列悬而未决的科学问题,但新出现的数据可能会改变预后的局面。液体活检是在体液中检测疾病生物标志物,它为组织活检提供了一种非侵入性替代方法,可能会改善器官衰竭的早期检测和预后。在这里,我们综述了可能用于器官衰竭的液体活检生物标志物,这在儿科肿瘤患者中可能特别有用。我们综合了从PubMed、谷歌学术、clinicaltrials.gov和科学网获取的出版物中的信息,并根据用于检测器官衰竭的生物标志物类型对我们的发现进行了分类。我们强调了每种类型的器官衰竭生物标志物的优缺点。虽然要推进这一领域并验证其对面临重症监护并发症的儿科癌症患者的适用性还有很多工作要做,但在此我们突出了未来发现的有希望的领域。