REFINE-lung will test whether reduced pembrolizumab dose frequency after 6 months of standard treatment is safe and effective. Patients treated with 1st line pembrolizumab who are progression free and otherwise planning to continue therapy at 6 months will be initially randomised to control 6 weekly versus interventional 12 weekly therapy. If an interim analysis shows that the 12 weekly treatment is no less effective, subsequent patients will also be randomised to 9, 15 and 18 weekly treatment frequency arms. Patients who progress on a reduced frequency arm will be offered re-escalation to standard 6 weekly therapy.
Immunotherapy with pembrolizumab targeting the T cell inhibitory PD-1 receptor has significantly improved outcomes in advanced non-small cell lung cancer (NSCLC). Approximately 3600 new patients are treated in the 1st line setting per year in England alone and up to 25% remain on 6 weekly pembrolizumab for 2 years. However, pharmacological and clinical trial data suggest current frequent dosing for 2 years result in overtreatment. Indeed, pembrolizumab remains bound to its target receptor for up to 100 days following a single dose and studies in multiple tumour types have found no relationship between dose and patient outcome. Moreover, anti-PD1 treated patients who respond but discontinue therapy either as planned after 2 years, or earlier because of toxicity, can either remain in remission and/or be sensitive to re-challenge with pembrolizumab. REFINE-lung will test whether reduced pembrolizumab dose frequency (9, 12, 15, 18 weeks) after 6 months of standard treatment is safe and effective. This UK study represents a unique opportunity to determine whether pembrolizumab dose frequency can be safely reduced in NSCLC, resulting in significant cost benefits to the NHS and globally, in addition to enhanced patient QoL associated with fewer hospital attendances and reduced toxicity.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
1,750
Pembrolizumab to be given at 400mg intravenous over 5 different frequencies
Royal Bournemouth Hospital
Bournemouth, United Kingdom
RECRUITINGRoyal Sussex County Hospital
Brighton, United Kingdom
RECRUITINGBristol Haematology and Oncology Centre
Bristol, United Kingdom
RECRUITINGQueen's Hospital
Burton-on-Trent, United Kingdom
Overall survival at 2 years
Survival at 2 years, defined as from commencing pembrolizumab (18 months after randomisation) to death due to any cause or study termination
Time frame: 18 months from randomisation
Overall survival from study entry
Survival, defined as from commencing pembrolizumab (18 months after randomisation) to death due to any cause or study termination
Time frame: 2 years
Progression free survival
Progression free survival as assessed by RECIST v1.1, defined as time from study entry to first evidence of disease progression or death due to any cause
Time frame: 2 years
Overall response rate
Overall response rate (ORR) as assessed by RECIST v1.1, defined as complete response (CR) or partial response (PR)
Time frame: 2 years
Duration of response
Duration of response (DoR) as assessed by RECIST v1.1, defined as time from study entry to change in response from CR or PR to stable disease (SD) or progressive disease (PD)
Time frame: 2 years
Incidence of adverse events
Safety and tolerability as assessed by adverse events according to the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0
Time frame: 2 years
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Cambridge University Hospitals NHS Foundation Trust
Cambridge, United Kingdom
NOT_YET_RECRUITINGEast Kent Hospitals University NHS Foundation Trust
Canterbury, United Kingdom
RECRUITINGVelindre Cancer Centre
Cardiff, United Kingdom
RECRUITINGColchester Hospital
Colchester, United Kingdom
RECRUITINGRoyal Derby Hospital
Derby, United Kingdom
RECRUITINGNHS Lothian
Edinburgh, United Kingdom
RECRUITING...and 27 more locations