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

IF 3.5 2区 医学 Q1 HEALTH CARE SCIENCES & SERVICES
Nicholas James, Sarah Pirrie, Wenyu Liu, James Catto, Kieran Jefferson, Prashant Patel, Ana Hughes, Ann Pope, Veronica Nanton, Harriet P Mintz, Allen Knight, Jean Gallagher, Richard T Bryan
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引用次数: 0

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)], p = 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 Health Technology Assessment; Vol. 28, No. 42. See the NIHR Funding and Awards website for further award information.

以图像为导向重新设计膀胱癌治疗路径:BladderPath RCT。
背景:60 多年来,经尿道膀胱肿瘤切除术一直是膀胱癌分期的主要方法。分期不准确是普遍现象,导致肌肉浸润性膀胱癌治疗延误。多参数磁共振成像为肌层浸润性膀胱癌提供了快速、准确和无创的分期,有可能减少根治性治疗的延误:评估在经尿道膀胱肿瘤切除术前引入多参数磁共振成像对疑似肌层浸润性膀胱癌进行分期的可行性和有效性:设计:开放标签、多阶段随机对照研究,分三部分:可行性、中期和最终临床阶段。COVID大流行阻碍了最后阶段的完成:15 家英国医院:新确诊的膀胱癌患者,年龄≥ 18 岁:干预措施:在门诊膀胱镜检查时,根据5点Likert量表对非肌层浸润性膀胱癌或肌层浸润性膀胱癌的怀疑进行目测评估后,将参与者随机分配到路径1或路径2:Likert 1-2 级为可能的非肌肉浸润性膀胱癌;Likert 3-5 级为可能的肌肉浸润性膀胱癌。在路径 1 中,所有参与者都接受了经尿道膀胱肿瘤切除术。在路径 2 中,可能为非肌肉浸润性膀胱癌的参与者接受了经尿道膀胱肿瘤切除术,可能为肌肉浸润性膀胱癌的参与者接受了初步的多参数磁共振成像。随后的治疗由治疗小组决定,可能包括经尿道膀胱肿瘤切除术:可行性阶段:可能患有肌层浸润性膀胱癌并被随机分配到路径 2 且正确遵循方案的比例。中期阶段:肌肉浸润性膀胱癌的正确治疗时间:2018年5月31日至2021年12月31日期间,在接触的638名患者中,143名参与者被随机分配;52.1%被视为可能的肌层浸润性膀胱癌,47.9%被视为可能的非肌层浸润性膀胱癌。可行性阶段:36/39 名[92%(95% 置信区间为 79% 至 98%)]肌肉浸润性膀胱癌参与者按照正确的路径进行了治疗。中期阶段:路径 1 的正确治疗中位时间为 98 天(95% 置信区间为 72 到 125 天),而路径 2 为 53 天(95% 置信区间为 20 到 89 天)[危险比为 2.9(95% 置信区间为 1.0 到 8.1)],P = 0.040。所有参与者接受正确治疗的中位时间,路径 1 为 37 天,路径 2 为 25 天[危险比 1.4(95% 置信区间 0.9 至 2.0)]:对于因多参数磁共振成像诊断为 T2 期或以上疾病而接受化疗、放疗或姑息治疗的参与者,由于缺乏组织病理学证实的肌肉侵犯,因此无法最终确定这些治疗是否正确,这些病例中的肌肉侵犯是由放射学证实的。所有患者的癌症都得到了组织学证实。由于 COVID-19 大流行,我们无法实现最后阶段的治疗:结论:多参数磁共振成像引导路径使肌肉浸润性膀胱癌的正确治疗时间大幅缩短了 45 天,而对非肌肉浸润性膀胱癌患者并无损害。应考虑将经尿道膀胱肿瘤切除术前的多参数磁共振成像纳入所有疑似肌层浸润性膀胱癌患者的标准治疗路径。尽管许多患者随后需要进行经尿道膀胱肿瘤切除术,但决策的改进加快了治疗时间。与经尿道膀胱肿瘤切除术相比,磁共振成像和活检的成本要低得多,因此一部分患者可以完全避免经尿道膀胱肿瘤切除术,从而降低成本和发病率:与最近开发的膀胱成像报告和数据系统交叉关联的进一步工作将提高准确性并有助于推广。此外,还需要进行更长时间的随访,以检查该路径对治疗效果的影响。纳入基于液体脱氧核糖核酸的生物标记物可进一步提高决策质量,也应进一步研究:本研究注册号为 ISRCTN 35296862:该奖项由美国国家健康与护理研究所(NIHR)健康技术评估项目资助(NIHR奖项编号:NIHR135775),全文发表于《健康技术评估》第28卷第42期。如需了解更多奖项信息,请访问 NIHR Funding and Awards 网站。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Health technology assessment
Health technology assessment 医学-卫生保健
CiteScore
6.90
自引率
0.00%
发文量
94
审稿时长
>12 weeks
期刊介绍: Health Technology Assessment (HTA) publishes research information on the effectiveness, costs and broader impact of health technologies for those who use, manage and provide care in the NHS.
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