基于患者报告结果的数字化健康干预远程监测乳腺癌化疗患者平台的可行性与实现

IF 2.8 Q2 ONCOLOGY
JCO Clinical Cancer Informatics Pub Date : 2025-08-01 Epub Date: 2025-08-13 DOI:10.1200/CCI-25-00018
Daniela Donadon de Oliveira Rodrigues, Bianca Sakamoto Ribeiro Paiva, Domicio Carvalho Lacerda, Sérgio Vicente Serrano, Alessandra Menezes Morelle, Carlos Barrios, Matheus Soares Rocha, Paulo Alfredo Casanova Schulze, Carlos Eduardo Paiva
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引用次数: 0

摘要

目的:乳腺癌(BC)是妇女发病和死亡的主要原因。在常规随访中,症状和治疗相关的副作用往往未被发现。数字卫生干预措施为实时监测和个性化护理提供了有前景的工具。我们旨在实施并评估基于移动健康电子患者报告结果(ePRO)平台的可行性,该平台用于远程监测接受(新)辅助化疗的BC患者。方法:这项前瞻性观察性研究纳入了在巴西巴雷托斯肿瘤医院开始化疗的BC (TNM期1至3)患者。参与者使用ThummiOnco平台进行4-6个月的远程监测,并遵循标准化协议。通过平台使用情况、患者报告的症状(根据不良事件通用术语标准)在48-72小时内的缓解情况以及医疗保健结果(包括额外咨询、剂量减少、治疗中断/停药、住院和死亡率)来评估可行性。采用描述性统计进行统计分析。结果:在2022年10月至2023年6月期间,纳入67例符合条件的患者(中位年龄51岁),其中62%接受了新辅助化疗。每位患者访问应用程序的中位数为38次,每天报告6.65次症状,依从性为94%。在48小时内,67%的患者报告的症状完全缓解,而在72小时内,治愈率为75.4%。关于分级缓解,83%的1级症状、69.5%的2级症状和54.8%的3级症状完全缓解。34例患者需要补充会诊。剂量减少10例(14.9%),治疗中断/停止35例(52.2%),住院7例(10.4%)。一名患者死于疾病进展。结论:远程监护有助于早期发现和处理症状。大多数报告都是通过该平台解决的,对医疗团队的额外要求最低。未来的研究应该评估不同人群的成本效益和可扩展性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Feasibility and Implementation of a Digital Health Intervention Electronic Patient-Reported Outcomes-Based Platform for Telemonitoring Patients With Breast Cancer Undergoing Chemotherapy.

Purpose: Breast cancer (BC) is a leading cause of morbidity and mortality among women. Symptoms and treatment-related side effects often go undetected during routine follow-ups. Digital health interventions offer promising tools for real-time monitoring and personalized care. We aimed to implement and evaluate the feasibility of a mobile health electronic Patient-Reported Outcomes (ePRO)-based platform for telemonitoring patients with BC undergoing (neo)adjuvant chemotherapy.

Methods: This prospective observational study enrolled patients with BC (TNM stages I to III) initiating chemotherapy at Barretos Cancer Hospital in Brazil. Participants were telemonitored using the ThummiOnco platform for 4-6 months, following a standardized protocol. Feasibility was assessed through platform usage, resolution of patient-reported symptoms (according to Common Terminology Criteria for Adverse Events) within 48-72 hours, and health care outcomes, including additional consultations, dose reductions, treatment interruptions/discontinuations, hospitalizations, and mortality. Statistical analysis was performed using descriptive statistics.

Results: Between October 2022 and June 2023, 67 eligible patients (median age 51 years) were included, with 62% receiving neoadjuvant chemotherapy. The median number of app accesses per patient was 38, with 6.65 daily symptom reports and 94% adherence. At 48 hours, 67% of patient-reported symptoms were fully resolved, whereas at 72 hours the resolution rate was 75.4%. Regarding resolution by grade, 83% of grade 1, 69.5% of grade 2, and 54.8% of grade 3 symptoms were fully resolved. Complementary consultations were needed for 34 patients. Dose reductions occurred in 10 (14.9%), treatment interruptions/discontinuations in 35 (52.2%), and hospitalizations in seven (10.4%). One patient died from progressive disease.

Conclusion: Telemonitoring facilitated early symptom identification and management. Most reports were resolved through the platform, with minimal additional demands on the health care team. Future studies should assess cost-effectiveness and scalability across diverse populations.

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CiteScore
6.20
自引率
4.80%
发文量
190
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