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. 2023 Jul 3;146(7):2717-2722.
doi: 10.1093/brain/awad063.

Towards a multi-arm multi-stage platform trial of disease modifying approaches in Parkinson's disease

Collaborators, Affiliations

Towards a multi-arm multi-stage platform trial of disease modifying approaches in Parkinson's disease

Tom Foltynie et al. Brain. .

Abstract

An increase in the efficiency of clinical trial conduct has been successfully demonstrated in the oncology field, by the use of multi-arm, multi-stage trials allowing the evaluation of multiple therapeutic candidates simultaneously, and seamless recruitment to phase 3 for those candidates passing an interim signal of efficacy. Replicating this complex innovative trial design in diseases such as Parkinson's disease is appealing, but in addition to the challenges associated with any trial assessing a single potentially disease modifying intervention in Parkinson's disease, a multi-arm platform trial must also specifically consider the heterogeneous nature of the disease, alongside the desire to potentially test multiple treatments with different mechanisms of action. In a multi-arm trial, there is a need to appropriately stratify treatment arms to ensure each are comparable with a shared placebo/standard of care arm; however, in Parkinson's disease there may be a preference to enrich an arm with a subgroup of patients that may be most likely to respond to a specific treatment approach. The solution to this conundrum lies in having clearly defined criteria for inclusion in each treatment arm as well as an analysis plan that takes account of predefined subgroups of interest, alongside evaluating the impact of each treatment on the broader population of Parkinson's disease patients. Beyond this, there must be robust processes of treatment selection, and consensus derived measures to confirm target engagement and interim assessments of efficacy, as well as consideration of the infrastructure needed to support recruitment, and the long-term funding and sustainability of the platform. This has to incorporate the diverse priorities of clinicians, triallists, regulatory authorities and above all the views of people with Parkinson's disease.

Keywords: Parkinson’s disease; complex innovative trial design; multi-arm; multi-stage; platform trial.

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Conflict of interest statement

The authors report no competing interests.

Figures

Figure 1
Figure 1
The P2P platform trial. The P2P platform trial plans to recruit people at risk of developing PD on the basis of known genetic risks and/or prodromal symptoms such as REM sleep behaviour disorder to identify treatments which prevent or delay the conversion to motor PD. The EJS ACT-PD platform plans to recruit people with established motor PD to identify treatments that will prevent or delay subsequent progression of motor and non-motor symptoms.

References

    1. James ND, Sydes MR, Clarke NW, et al. . Addition of docetaxel, zoledronic acid, or both to first-line long-term hormone therapy in prostate cancer (STAMPEDE): Survival results from an adaptive, multiarm, multistage, platform randomised controlled trial. Lancet. 2016;387:1163–1177. - PMC - PubMed
    1. RECOVERY Collaborative Group, Horby P, Lim WS, et al. . Dexamethasone in hospitalized patients with COVID-19. N Engl J Med. 2021;384:693–704. - PMC - PubMed
    1. Marek K, Siderowf A, Coffey C, et al. . Path to prevention (P2P) – developing a prodromal PD progression biomarker program [abstract]. Mov Disord. 2019;34:S64-S64. Accessed 24 June 2022. https://www.mdsabstracts.org/abstract/path-to-prevention-p2p-developing-...
    1. Fereshtehnejad S, Postuma RB. Subtypes of Parkinson's disease: What do they tell us about disease progression? Curr Neurol Neurosci Rep. 2017;17:34. - PubMed
    1. Winder-Rhodes SE, Evans JR, Ban M, et al. . Glucocerebrosidase mutations influence the natural history of Parkinson's disease in a community-based incident cohort. Brain. 2013;136:392–399. PMID: 23413260. - PubMed

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