The impact of melanoma and drug treatment in the real world

  • Research type

    Research Database

  • IRAS ID

    289653

  • Contact name

    Mark Larkin

  • Contact email

    mark.larkin@vitaccess.com

  • Research summary

    The impact of melanoma and drug treatment in the real world

  • REC name

    London - Bloomsbury Research Ethics Committee

  • REC reference

    20/LO/1304

  • Date of REC Opinion

    24 Dec 2020

  • REC opinion

    Unfavourable Opinion

  • Data collection arrangements

    Adults with any type or stage of melanoma complete validated patient-reported outcome (PRO) measures at their own convenience via their smartphone, instead of only during clinic visits. Optional features designed to help participants to manage their condition and its treatment include the ability to prospectively build an exportable record of symptoms, mood and side effects, a clinician-validated knowledge section and a community feature allowing participants the option to communicate with and search for other users.

    The data is available in real time and securely transferred from each smartphone to secure storage where they are anonymised and aggregated for analysis. The philanthropic business model encourages research via free dataset access to academic researchers and via a paid subscription for industry. Findings from the study have been presented at national and international conferences; patient-led development through regular feedback sessions and workshops allows for a patient-centric approach and ongoing study improvements.

  • Research programme

    Launched in 2017, the app was developed by the patient advocacy group Melanoma UK in collaboration with Vitaccess Ltd, a digital health scale-up, and The Royal Marsden NHS Foundation Trust. In recent years, immuno-oncology therapies have transformed melanoma treatment. However, despite improvements in clinical outcomes, there is a deficit in granular patient-reported outcome data. The Melanoma UK observational study explores the real-world impact of melanoma by collecting data from melanoma patients via a bespoke "bring your own device" app. Specifically, the registry objectives are to better understand the impact of melanoma and its treatment on patients, and to identify how treatment pathways are changing in light of these new immunotherapies over time. The Melanoma UK observational study allows for recruitment of a broader range of patients than is possible in clinical trials. The output is data that can be used by health researchers to build a granular, real-time understanding of the impact of disease and treatment on participants’ everyday lives.

  • Research database title

    The impact of melanoma and drug treatment in the real world

  • Establishment organisation

    Vitaccess Ltd

  • Establishment organisation address

    2nd Floor Nucleus House

    2 Lower Mortlake Road

    Richmond

    TW9 2JA