Revisiting the OGIPRO Trial: Dynamic Electronic Patient-Reported Outcomes Compared with EQ-5D-5L in HER2-Positive Breast Cancer

重新审视 OGIPRO 试验:动态电子患者报告结局与 EQ-5D-5L 在 HER2 阳性乳腺癌中的比较

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Abstract

INTRODUCTION: Patient-reported outcomes (PROs) are increasingly valued in oncology for capturing treatment tolerability and quality of life, and they are emerging as important data sources for precision-medicine and AI-driven clinical workflows. While the EQ-5D-5L questionnaire remains a widely used standardized instrument, dynamic electronic PROs (ePROs) collected via mobile applications generate richer, higher-frequency longitudinal data. Their alignment with established PRO measures, however, is not well-understood, limiting their integration into routine care and downstream analytic applications. In the prospective OGIPRO trial (KEK-ZH 2021-D0051), patients with HER2-positive breast cancer reported well-being and symptoms via the Medidux ePRO platform alongside weekly EQ-5D-5L assessments. In this retrospective analysis, we used linear mixed-effects modeling to examine associations between: (i) dynamic ePRO well-being and the EQ-5D-5L visual analogue scale (VAS); (ii) dynamic ePRO symptom grades and EQ-5D-5L domain sums; (iii) ePRO symptom grades and EQ-5D-5L disutility using the EQ-5D-5L value set for Germany. MATERIALS AND METHODS: The analytic dataset comprised 13,699 dynamic ePRO data points (3376 well-being ratings and 10,323 symptom grades across 91 symptom types) from 53 patients, forming high-frequency longitudinal patient trajectories. Of these, 252 and 226 time-aligned observations, respectively, were used for direct comparison with EQ-5D-5L VAS and domain scores. RESULTS: Dynamic ePRO well-being showed strong agreement with EQ-5D-5L VAS (β = 1.061, 95% CI: 1.015-1.107), with low between-patient variability. In contrast, the agreement between aggregated ePRO symptom grades and EQ-5D-5L domain sums was weaker (β = 0.404, 95% CI: 0.307-0.501) and more heterogeneous across patients. The same applied to the agreement between ePRO symptom grades and EQ-5D-5L disutility (β = 0.213; 95% CI: 0.151-0.275). DISCUSSION: Dynamic ePRO well-being aligns closely with EQ-5D-5L VAS scores, supporting its use as a pragmatic substitute in clinical and research settings. Aggregated symptom grades, however, showed limited concordance with EQ-5D-5L domains, indicating the need for more granular analyses on larger datasets. CONCLUSIONS: Overall, dynamic ePRO systems provide validated, high-resolution longitudinal patient data and represent a scalable foundation for patient monitoring and data-driven decision support in oncology, including future AI-based precision-medicine applications.

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