Department of Research and Development, Netherlands Comprehensive Cancer Organisation, Utrecht, the Netherlands.
Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.
BMC Cancer. 2020 May 20;20(1):455. doi: 10.1186/s12885-020-06954-7.
Despite the embedding of bladder cancer management in European guidelines, large variation in clinical practice exists for applied diagnostics and treatments. This variation may affect patients' outcomes including complications, disease recurrence, progression, survival, and health-related quality of life (HRQL). Lack of detailed clinical data and HRQL data hampers a comprehensive evaluation of bladder cancer care. Through prospective data registration, this study aims to provide insight in bladder cancer care in the Netherlands and to identify barriers and modulators of optimal bladder cancer care.
This study is a nationwide prospective cohort study including all patients who were newly diagnosed with high-risk non-muscle invasive bladder cancer (HR-NMIBC; Tis and/or T1, N0, M0/x) or non-metastatic muscle invasive bladder cancer (MIBC; ≥T2, N0/x-3, M0/x) in the Netherlands between November 1st 2017 and October 31st 2019. Extensive data on patient- and tumor characteristics, diagnostics, treatment and follow-up up to 2 years after diagnosis will be collected prospectively from electronic health records in the participating hospitals by data managers of the Netherlands Cancer Registry (NCR). Additionally, patients will be requested to participate in a HRQL survey shortly after diagnosis and subsequently at 6, 12 and 24 months. The HRQL survey includes six standardized questionnaires, e.g. SCQ Comorbidity score, EQ-5D-5 L, EORTC-QLQ-C30, EORTC-QLQ-BLM30, EORTC-QLQ-NMIBC24 and BCI. Variation in care and deviation from the European guidelines will be assessed through descriptive analyses and multivariable multilevel analyses. Survival analyses will be used to assess the association between variation in care and relevant outcomes such as survival.
The results of this observational study will guide modifications of clinical practice and/or adaptation of guidelines and may set the agenda for new specific research questions in the management of bladder cancer.
Retrospectively registered in the Netherlands Trial Register. Trial identification number: NL8106. Registered on October 22nd 2019.
尽管膀胱癌管理已纳入欧洲指南,但在应用诊断和治疗方面仍存在较大的临床实践差异。这种差异可能会影响患者的结局,包括并发症、疾病复发、进展、生存和健康相关生活质量(HRQL)。缺乏详细的临床数据和 HRQL 数据阻碍了对膀胱癌治疗的全面评估。通过前瞻性数据登记,本研究旨在提供荷兰膀胱癌治疗的深入了解,并确定最佳膀胱癌治疗的障碍和调节剂。
本研究是一项全国性的前瞻性队列研究,纳入了 2017 年 11 月 1 日至 2019 年 10 月 31 日期间在荷兰新诊断为高危非肌肉浸润性膀胱癌(HR-NMIBC;Tis 和/或 T1、N0、M0/x)或非转移性肌肉浸润性膀胱癌(MIBC;≥T2、N0/x-3、M0/x)的所有患者。将由荷兰癌症登记处(NCR)的数据管理员从参与医院的电子健康记录中前瞻性地收集关于患者和肿瘤特征、诊断、治疗以及诊断后 2 年内随访的广泛数据。此外,患者将在诊断后不久以及 6、12 和 24 个月时被要求参加 HRQL 调查。HRQL 调查包括六个标准化问卷,例如 SCQ 合并症评分、EQ-5D-5L、EORTC-QLQ-C30、EORTC-QLQ-BLM30、EORTC-QLQ-NMIBC24 和 BCI。通过描述性分析和多变量多层次分析评估护理差异和对欧洲指南的偏离情况。生存分析将用于评估护理差异与生存等相关结局之间的关联。
这项观察性研究的结果将指导临床实践的修改和/或指南的调整,并可能为膀胱癌管理中的新具体研究问题设定议程。
在荷兰试验注册处回顾性注册。试验识别号:NL8106。于 2019 年 10 月 22 日注册。