ArticleBMJ open2025
Personalising anal cancer radiotherapy dose (PLATO): protocol for a multicentre integrated platform trial.
Article in BMJ open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- [Update on anal dysplasia and anal cancer].Dermatologie (Heidelberg, Germany) · 2026Review
- Rewriting the future of anal cancer care: From disparities to data-driven decisions.ESMO gastrointestinal oncology · 2026Article
- Optimising chemoradiotherapy in anal cancer.ESMO gastrointestinal oncology · 2026Review
- Outcomes after (chemo)radiotherapy for anal cancer - A nationwide cohort study.Clinical and translational radiation oncology · 2026Article
- Sarcopenia and cancer outcomes: thresholds need to account for age-related changes in muscle mass.British journal of cancer · 2026Article
- Inguinal CTV contouring in anal cancer: comparative validation of inguinal lymph nodes contouring guidelines and implications for consensus.Clinical and translational radiation oncology · 2026Article
- Chemoradiotherapy for anal canal cancers: Does the choice of boost technique matter?Journal of contemporary brachytherapy · 2026Article
- A Systematic Review Defining Early Anal Squamous Cell Carcinoma and Identifying Treatment.Cancers · 2025Review
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Authors and funding
19 authors.
Funding
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Abstract
introductionThe incidence of anal carcinoma is increasing, with the current gold standard treatment being chemoradiotherapy. There is currently a wide range in the radiotherapy dose used internationally which may lead to overtreatment of early-stage disease and potential undertreatment of locally advanced disease.PLATO is an integrated umbrella trial protocol which consists of three trials focused on assessing risk-adapted use of adjuvant low-dose chemoradiotherapy in anal margin tumours (ACT3), reduced-dose chemoradiotherapy in early anal carcinoma (ACT4) and dose-escalated chemoradiotherapy in locally advanced anal carcinoma (ACT5), given with standard concurrent chemotherapy. METHODS AND ANALYSIS: The primary endpoints of PLATO are locoregional failure (LRF)-free rate for ACT3 and ACT4 and LRF-free survival for ACT5. Secondary objectives include acute and late toxicities, colostomy-free survival and patient-reported outcome measures. ACT3 will recruit 90 participants: participants with removed anal tumours with margins ≤1 mm will receive lower dose chemoradiotherapy, while participants with anal tumours with margins >1 mm will be observed. ACT4 will recruit 162 participants, randomised on a 1:2 basis to receive either standard-dose intensity modulated radiotherapy (IMRT) in combination with chemotherapy or reduced-dose IMRT in combination with chemotherapy. ACT5 will recruit 459 participants, randomised on a 1:1:1 basis to receive either standard-dose IMRT in combination with chemotherapy, or one of two increased-dose experimental arms of IMRT with synchronous integrated boost in combination with chemotherapy. ETHICS AND DISSEMINATION: This study has been approved by Yorkshire & The Humber - Bradford Leeds Research Ethics Committee (ref: 16/YH/0157, IRAS: 204585), July 2016. Results will be disseminated via national and international conferences, peer-reviewed journal articles and social media. A plain English report will be shared with the study participants, patients' organisations and media. TRIAL REGISTRATION NUMBER: ISRCTN88455282.
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