提高生活质量的同时维持生存:由高级医师领导的降低儿童脑肿瘤患者放射剂量的试点可行性研究

Jennifer L. Raybin, PhD, RN, CPNP, Andrew Donson, Nicholas K. Foreman, MRCP, Rajeev Vibhakar, MD, Michael H. Handler, MD, Arthur K. Liu, MD, PhD
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摘要

目的:肿瘤科高级医师(APs)处于治疗不良反应的第一线。在脑肿瘤患儿中,颅骨照射(CSI)等治疗方法会导致神经认知损伤、内分泌病变和耳毒性。大剂量 CSI 并发化疗可使高危胚胎性肿瘤(非无性细胞性)获得良好的生存率(70%),但在多学科长期随访中,APs 通常会治疗明显的不良反应。本研究的目的是测试以全科医生为主导的方案减少放射剂量的可行性。方法:一个跨学科团队开展了这项试点研究,主要结果是 10 名患者中死亡人数少于 2 人(存活率为 80%)。次要结果是由介入治疗师主导的治疗方案的可行性和治疗的急性/晚期效应。作为肿瘤治疗研究的主要研究者,AP 发挥了先锋作用。排除标准包括年龄小于 3 岁和无增生。CSI从36Gy降至24Gy。所有其他治疗均为标准治疗。结果:存活率超过了主要结果阈值(88%);应计率(80%)和随访神经认知测试率(75%)均可接受。8 名 3 至 19 岁的儿童(男 = 8)患有不同分子亚型的肿瘤。其中一名患儿在确诊后2.5年因多器官功能衰竭死亡(无肿瘤证据)。平均生存期为 11 年,其中两人获得大学学位,一人获得研究生学位。与高剂量的 CSI 相比,急性和晚期效应均有所降低。结论:治疗癌症不良反应的介入治疗师也可以开展临床前瞻性研究,以维持生存率并提高生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Maintaining Survival While Improving Quality of Life: An Advanced Practitioner–Led Pilot Feasibility Study to Reduce Radiation Dose in Children With Brain Tumors
Purpose: Oncology advanced practitioners (APs) are on the front line in treating adverse effects. Among children with brain tumors, treatments such as craniospinal irradiation (CSI) cause neurocognitive injury, endocrinopathies, and ototoxicity. High-dose CSI with concurrent chemotherapy allows high-risk embryonal tumors (non-anaplastic) good survival (70%), but significant distressing effects are commonly treated by APs in multidisciplinary long-term follow-up. The aim of this study was to test feasibility of reducing radiation dose with an AP-led protocol. Methods: An interdisciplinary team developed this pilot study with the primary outcome of fewer than two deaths in 10 patients (80% survival). Secondary outcomes were feasibility of an AP-led treatment protocol and acute/late effects of treatment. The AP held a pioneering role as principal investigator of a tumor treatment study. Exclusion criteria included age less than 3 years and anaplasia. The CSI was reduced from 36 to 24 Gy. All other treatment was standard. Results: Survival rate exceeded the primary outcome threshold (88%); the accrual rate (80%) and follow-up neurocognitive testing rate (75%) were acceptable. Eight children ages 3 to 19 years (M = 8) with tumors of varied molecular subtyping were enrolled. The single death occurred 2.5 years from diagnosis of multiorgan failure (without evidence of tumor). The mean survival is 11 years, with two college and one graduate degrees. Acute and late effects were decreased compared with the higher-dose CSI. Conclusion: APs who treat cancer adverse effects can also conduct clinical prospective studies to maintain survival rates and improve quality-of life-outcomes.
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