Evidence map›Paper›PMID 42766600›Full record

Trial reportPloS one2026

Health-related quality of life with adjuvant immune checkpoint inhibition in renal cell carcinoma: A qualitative study of UK participants in the phase III RAMPART trial.

Sophie Merrick, Annabelle South, Elena Frangou, Hannah L Rush, Grisma Patel, Jemima Thompson, Hannah Plant, Lisa Pickering, Ruth E Langley, Duncan C Gilbert and 3 more

Abstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Sophie MerrickUCL Innovative Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, United Kingdom.ORCID https://orcid.org/0000-0001-8080-1948
Annabelle SouthUCL Innovative Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, United Kingdom.ORCID https://orcid.org/0000-0001-8912-2001
Elena FrangouUCL Innovative Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, United Kingdom.ORCID https://orcid.org/0000-0002-5978-292X
Hannah L RushUCL Innovative Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, United Kingdom.
Grisma PatelUCL Innovative Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, United Kingdom.
Jemima ThompsonUCL Innovative Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, United Kingdom.ORCID https://orcid.org/0000-0002-1853-3599
Hannah PlantUCL Innovative Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, United Kingdom.
Lisa PickeringThe Royal Marsden Hospital NHS Foundation Trust, London, United Kingdom.ORCID https://orcid.org/0000-0002-7579-340X
Ruth E LangleyUCL Innovative Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, United Kingdom.
Duncan C GilbertUCL Innovative Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, United Kingdom.
Thomas PowlesSt Bartholomew's Hospital, London, United Kingdom.
James LarkinThe Royal Marsden Hospital NHS Foundation Trust, London, United Kingdom.ORCID https://orcid.org/0000-0001-5569-9523
Angela MeadeUCL Innovative Clinical Trials Unit, Institute of Clinical Trials and Methodology, UCL, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionRAMPART is an international phase III trial evaluating adjuvant immune checkpoint inhibitors (ICIs) after nephrectomy for renal cell carcinoma. ICIs have a distinct toxicity profile that can significantly impact health-related quality of life (HRQoL); however existing HRQoL questionnaires were developed in a pre-ICI era and may not fully capture the patient experience. To address this, we embedded a qualitative interview sub-study within RAMPART among UK participants to explore the impact of ICIs on HRQoL in depth.

methodsEligible participants were enrolled in RAMPART at UK sites and randomised to Arm B (durvalumab q4w for 1 year) or C (durvalumab q4w for 1 year plus tremelimumab at day 1 and week 4). Participants were purposively selected to ensure representation across baseline characteristics, treatment tolerance, toxicity development, and recurrence status. Interviews were conducted online, via telephone and in person, with transcripts analysed using the framework method.

resultsOf 220 eligible participants, 71 were invited; with recruitment closing early due to a high response rate. 37 expressed interest, and 23 were interviewed. Two themes were generated based on participant insights: Living in a Changed Body and Mind and It Depends on Your Life: How Context Shapes the Impact of Immune Related Adverse Events (irAEs). The findings suggest that participants often placed greater importance on the duration and chronicity of irAEs than their severity when describing impacts on HRQoL. Persistent toxicities, including fatigue, arthralgia, and diarrhoea, disrupted daily functioning, while cognitive changes and emotional strain were common. Employment, financial security, and caregiving responsibilities influenced the impact of irAEs, whereas supportive relationships and structured follow-up mitigated their burden.

conclusionsChronic irAEs can negatively affect HRQoL, mental health, and the ability to work. Clinical trials evaluating ICIs should report toxicity grade, duration, and resolution to better inform patient decision-making. Development of ICI-specific HRQoL tools that capture the impact of persistent irAEs is needed, alongside clear care pathways for management of chronic irAEs.

Indexed as

Carcinoma, Renal CellImmune Checkpoint InhibitorsKidney NeoplasmsQuality of LifeAdultAgedFemaleHumansMaleMiddle AgedQualitative ResearchUnited KingdomImmune Checkpoint Inhibitors

Identifiers

PMID42766600
PMCPMC13592578

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.