Unsupervised dynamic ePRO reporting of immunotherapy related symptoms in cancer patients.

IF 1.8 3区 医学 Q3 ONCOLOGY
Oncology Pub Date : 2025-07-10 DOI:10.1159/000546026
Anna Kristina Stauffacher, Louise von Stockar, Hans-Friedrich Witschel, Stefanie Hayoz, Ulf Petrausch, Thomas Schmid, Andreas Jakob, Gerd A Kullak-Ublick, Andreas Trojan
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引用次数: 0

Abstract

Introduction: The use of electronic patient reported outcome (ePRO) in patients has been demonstrated to improve patient care and symptom management in curative and palliative settings. We examined the electronic and dynamic reporting of wellbeing, symptoms, and cognition in unsupervised patients with solid cancers of bladder, breast and lung in neoadjuvant, adjuvant and metastatic therapy settings. Participants undergoing immune checkpoint inhibitor (ICI) treatment were provided a mobile smartphone app for standardized and structured reporting on wellbeing and symptoms according to the CTCAE Criteria, as well as cognitive test and vital parameters.

Case presentation: Data of 14 patients was available for descriptive analysis. Besides checkpoint inhibition, patients received concomitant chemotherapy with carboplatin and taxanes. Three patients were excluded for lack of app usage. The eleven patients presented here entered a total of 9624 symptom ratings and rated their wellbeing 2983 times. Patients recorded a median number of symptom entries of 453 (IQR 109-1401). 49 different symptoms were reported in total with a median of 8 per patient (IQR 4-15). Of the 24 symptoms that were frequently shared among multiple patients, all are considered clinically relevant and associated with immunotherapeutic interventions. The most commonly patient reported symptoms were fatigue (82%), diarrhea (45%), limb and muscle pain (45%), sleep problems (45%) and dyspnea (36%). Overall, symptoms severity was reported at grades between 0.1 (very mild) to 9.0 (very severe), at a mean grade of 2.6. The most severely rated unique entry was for limb and muscle pain, edema of limbs showed the highest mean rating (5.9). The median duration of app use was 195 days (IQR 108-472). The descriptive analysis showed a general trend of patients with higher grade symptoms reporting a lower grade of wellbeing but no clear association with cognitive performance.

Conclusion: Unsupervised patients showed high app usage adherence and frequency of data entries, which was comparable to previous reports on supervised patients undergoing immunotherapeutic interventions.

癌症患者免疫治疗相关症状的无监督动态ePRO报告
在患者中使用电子患者报告结果(ePRO)已被证明可以改善治疗和姑息环境中的患者护理和症状管理。我们研究了在新辅助、辅助和转移性治疗环境下,无人监督的膀胱癌、乳腺癌和肺癌实体癌患者的健康、症状和认知的电子和动态报告。接受免疫检查点抑制剂(ICI)治疗的参与者提供了一个移动智能手机应用程序,根据CTCAE标准,以及认知测试和重要参数,对健康和症状进行标准化和结构化报告。病例介绍:14例患者的资料可用于描述性分析。除了检查点抑制外,患者还接受卡铂和紫杉烷的联合化疗。3例患者因缺乏应用程序使用而被排除。这11名患者总共输入了9624个症状评分,并对他们的健康状况进行了2983次评分。患者记录的症状条目中位数为453 (IQR 109-1401)。总共报告了49种不同的症状,平均每位患者8种(IQR 4-15)。在多名患者中经常出现的24种症状中,所有症状都被认为与临床相关并与免疫治疗干预有关。最常见的患者报告症状是疲劳(82%)、腹泻(45%)、肢体和肌肉疼痛(45%)、睡眠问题(45%)和呼吸困难(36%)。总体而言,报告的症状严重程度在0.1(非常轻微)至9.0(非常严重)之间,平均等级为2.6。评分最高的是肢体和肌肉疼痛,肢体水肿的平均评分最高(5.9)。应用程序使用的中位数持续时间为195天(IQR 108-472)。描述性分析显示,总体趋势是症状较严重的患者报告的健康程度较低,但与认知表现没有明确的联系。结论:未受监督的患者显示出较高的app使用依从性和数据输入频率,这与之前对接受免疫治疗干预的受监督患者的报道相当。
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来源期刊
Oncology
Oncology 医学-肿瘤学
CiteScore
6.00
自引率
2.90%
发文量
76
审稿时长
6-12 weeks
期刊介绍: Although laboratory and clinical cancer research need to be closely linked, observations at the basic level often remain removed from medical applications. This journal works to accelerate the translation of experimental results into the clinic, and back again into the laboratory for further investigation. The fundamental purpose of this effort is to advance clinically-relevant knowledge of cancer, and improve the outcome of prevention, diagnosis and treatment of malignant disease. The journal publishes significant clinical studies from cancer programs around the world, along with important translational laboratory findings, mini-reviews (invited and submitted) and in-depth discussions of evolving and controversial topics in the oncology arena. A unique feature of the journal is a new section which focuses on rapid peer-review and subsequent publication of short reports of phase 1 and phase 2 clinical cancer trials, with a goal of insuring that high-quality clinical cancer research quickly enters the public domain, regardless of the trial’s ultimate conclusions regarding efficacy or toxicity.
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