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影像指导膀胱癌治疗路径再设计:膀胱癌路径 RCT。

Image directed redesign of bladder cancer treatment pathways: the BladderPath RCT.

机构信息

Institute of Cancer Research, London, UK.

Cancer Research Clinical Trials Unit, Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.

出版信息

Health Technol Assess. 2024 Aug;28(42):1-65. doi: 10.3310/DEHT5407.

Abstract

BACKGROUND

Transurethral resection of bladder tumour has been the mainstay of bladder cancer staging for > 60 years. Staging inaccuracies are commonplace, leading to delayed treatment of muscle-invasive bladder cancer. Multiparametric magnetic resonance imaging offers rapid, accurate and non-invasive staging of muscle-invasive bladder cancer, potentially reducing delays to radical treatment.

OBJECTIVES

To assess the feasibility and efficacy of the introducing multiparametric magnetic resonance imaging ahead of transurethral resection of bladder tumour in the staging of suspected muscle-invasive bladder cancer.

DESIGN

Open-label, multistage randomised controlled study in three parts: feasibility, intermediate and final clinical stages. The COVID pandemic prevented completion of the final stage.

SETTING

Fifteen UK hospitals.

PARTICIPANTS

Newly diagnosed bladder cancer patients of age ≥ 18 years.

INTERVENTIONS

Participants were randomised to Pathway 1 or 2 following visual assessment of the suspicion of non-muscle-invasive bladder cancer or muscle-invasive bladder cancer at the time of outpatient cystoscopy, based upon a 5-point Likert scale: Likert 1-2 tumours considered probable non-muscle-invasive bladder cancer; Likert 3-5 possible muscle-invasive bladder cancer. In Pathway 1, all participants underwent transurethral resection of bladder tumour. In Pathway 2, probable non-muscle-invasive bladder cancer participants underwent transurethral resection of bladder tumour, and possible muscle-invasive bladder cancer participants underwent initial multiparametric magnetic resonance imaging. Subsequent therapy was determined by the treating team and could include transurethral resection of bladder tumour.

MAIN OUTCOME MEASURES

Feasibility stage: proportion with possible muscle-invasive bladder cancer randomised to Pathway 2 which correctly followed the protocol. Intermediate stage: time to correct treatment for muscle-invasive bladder cancer.

RESULTS

Between 31 May 2018 and 31 December 2021, of 638 patients approached, 143 participants were randomised; 52.1% were deemed as possible muscle-invasive bladder cancer and 47.9% probable non-muscle-invasive bladder cancer. Feasibility stage: 36/39 [92% (95% confidence interval 79 to 98%)] muscle-invasive bladder cancer participants followed the correct treatment by pathway. Intermediate stage: median time to correct treatment was 98 (95% confidence interval 72 to 125) days for Pathway 1 versus 53 (95% confidence interval 20 to 89) days for Pathway 2 [hazard ratio 2.9 (95% confidence interval 1.0 to 8.1)], = 0.040. Median time to correct treatment for all participants was 37 days for Pathway 1 and 25 days for Pathway 2 [hazard ratio 1.4 (95% confidence interval 0.9 to 2.0)].

LIMITATIONS

For participants who underwent chemotherapy, radiotherapy or palliation for multiparametric magnetic resonance imaging-diagnosed stage T2 or higher disease, it was impossible to conclusively know whether these were correct treatments due to the absence of histopathologically confirmed muscle invasion, this being confirmed radiologically in these cases. All patients had histological confirmation of their cancers. Due to the COVID-19 pandemic, we were unable to realise the final stage.

CONCLUSION

The multiparametric magnetic resonance imaging-directed pathway led to a substantial 45-day reduction in time to correct treatment for muscle-invasive bladder cancer, without detriment to non-muscle-invasive bladder cancer participants. Consideration should be given to the incorporation of multiparametric magnetic resonance imaging ahead of transurethral resection of bladder tumour into the standard pathway for all patients with suspected muscle-invasive bladder cancer. The improved decision-making accelerated time to treatment, even though many patients subsequently needed transurethral resection of bladder tumour. A proportion of patients can avoid transurethral resection of bladder tumour completely, reducing costs and morbidity, given the much lower cost of magnetic resonance imaging and biopsy compared to transurethral resection of bladder tumour.

FUTURE WORK

Further work to cross-correlate with the recently developed Vesical Imaging-Reporting and Data System will improve accuracy and aid dissemination. Longer follow-up to examine the effect of the pathway on outcomes is also required. Incorporation of liquid deoxyribonucleic acid-based biomarkers may further improve the quality of decision-making and should also be investigated further.

STUDY REGISTRATION

This study is registered as ISRCTN 35296862.

FUNDING

This award was funded by the National Institute for Health and Care Research (NIHR) Health Technology Assessment programme (NIHR award ref: NIHR135775) and is published in full in ; Vol. 28, No. 42. See the NIHR Funding and Awards website for further award information.

摘要

背景

经尿道膀胱肿瘤切除术(TURBT)是膀胱癌分期的主要手段,已应用 60 余年。分期不准确的情况很常见,导致肌层浸润性膀胱癌的治疗延误。多参数磁共振成像(mpMRI)可快速、准确、无创地对肌层浸润性膀胱癌进行分期,有可能减少根治性治疗的延迟。

目的

评估在疑似肌层浸润性膀胱癌的 TURBT 术前引入 mpMRI 的可行性和疗效。

设计

在三个阶段(可行性阶段、中间阶段和最终临床阶段)进行的开放标签、多阶段随机对照研究。由于 COVID-19 大流行,最终阶段未能完成。

地点

英国 15 家医院。

参与者

年龄≥18 岁的新诊断膀胱癌患者。

干预措施

根据 5 分李克特量表(Likert 量表),对门诊膀胱镜检查时非肌层浸润性膀胱癌或肌层浸润性膀胱癌的可疑程度进行视觉评估,将患者随机分配至途径 1 或 2:Likert 1-2 肿瘤被认为是可能的非肌层浸润性膀胱癌;Likert 3-5 肿瘤可能是肌层浸润性膀胱癌。在途径 1 中,所有患者均行 TURBT。在途径 2 中,可能的非肌层浸润性膀胱癌患者行 TURBT,可能的肌层浸润性膀胱癌患者行初始 mpMRI。随后的治疗由治疗团队决定,可能包括 TURBT。

主要结局指标

可行性阶段:被随机分配至途径 2 且可能患有肌层浸润性膀胱癌的患者比例,以及该组患者是否按方案正确进行治疗。中间阶段:肌层浸润性膀胱癌患者正确治疗的时间。

结果

2018 年 5 月 31 日至 2021 年 12 月 31 日,共纳入 638 例患者,其中 143 例患者被随机分组;52.1%被认为可能患有肌层浸润性膀胱癌,47.9%被认为是可能的非肌层浸润性膀胱癌。可行性阶段:36/39 例(92%(95%置信区间 79 至 98%))肌层浸润性膀胱癌患者按正确的治疗方案进行治疗。中间阶段:途径 1 的中位正确治疗时间为 98 天(95%置信区间 72 至 125 天),途径 2 为 53 天(95%置信区间 20 至 89 天)[风险比 2.9(95%置信区间 1.0 至 8.1)],=0.040。途径 1 和途径 2 治疗的所有患者的中位时间分别为 37 天和 25 天[风险比 1.4(95%置信区间 0.9 至 2.0)]。

局限性

对于接受 mpMRI 诊断为 T2 或更高分期疾病的患者接受化疗、放疗或姑息治疗,由于缺乏组织病理学证实的肌层浸润,这些患者无法进行根治性治疗,这在这些病例中是通过放射学证实的。所有患者均经组织学证实患有癌症。由于 COVID-19 大流行,我们无法完成最终阶段。

结论

mpMRI 指导的治疗途径使肌层浸润性膀胱癌的正确治疗时间缩短了 45 天,而对非肌层浸润性膀胱癌患者没有影响。考虑将 TURBT 术前引入多参数 MRI 作为所有疑似肌层浸润性膀胱癌患者的标准治疗途径。尽管许多患者随后需要 TURBT,但这种改善的决策加速了治疗时间,即使在这种情况下,也能减少对患者的伤害。鉴于与 TURBT 相比,磁共振成像和活检的成本要低得多,因此可以避免一部分患者进行 TURBT,从而降低成本和发病率。

未来工作

进一步交叉关联最近开发的膀胱影像学报告和数据系统(Vesical Imaging-Reporting and Data System),将提高准确性并有助于推广。还需要进行更长时间的随访,以研究该途径对结果的影响。进一步研究还需要纳入液体脱氧核糖核酸(DNA)为基础的生物标志物,以进一步改善决策质量。

研究注册

本研究在英国国家健康与保健卓越研究所(NIHR)健康技术评估计划(NIHR 奖项参考:NIHR135775)下注册,并全文发表在;第 28 卷,第 42 期。有关该奖项的更多信息,请访问 NIHR 资助和奖项网站。

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