Atezolizumab plus stereotactic ablative radiotherapy for medically inoperable patients with early-stage non-small cell lung cancer: a multi-institutional phase I trial.
Arta M MonjazebMegan E DalyGuilluame LuxardiEmanual MaverakisAlexander A MerleevAlina I MarusinaAlexander D BorowskyAmin MirhadiStephen L ShiaoLaurel BeckettShuai ChenDavid EasthamTianhong LiLogan V VickHeather M McGeeFrances LaraLeslie GarciaLeigh Anne MorrisRobert J CanterJonathan W RiessKurt A SchalperWilliam J MurphyKaren KellyPublished in: Nature communications (2023)
Stereotactic ablative radiotherapy (SABR) is a standard-of-care for medically-inoperable-early-stage non-small cell lung cancer (NSCLC). One third of patients progress and chemotherapy is rarely used in this population. We questioned if addition of the immune-checkpoint-inhibitor (ICI) atezolizumab to standard-of-care SABR can improve outcomes. We initiated a multi-institutional single-arm phase I study (NCT02599454) enrolling twenty patients with the primary endpoint of maximum tolerated dose (MTD); secondary endpoints of safety and efficacy; and exploratory mechanistic correlatives. Treatment is well tolerated and full dose atezolizumab (1200 mg) is the MTD. Efficacy signals include early responses (after 2 cycles of ICI, before initiation of SABR) in 17% of patients. Biomarkers of functional adaptive immunity, including T cell activation in the tumor and response to ex-vivo stimulation by circulating T cells, are highly predictive of benefit. These results require validation and are being tested in a phase III randomized trial.
Keyphrases
- early stage
- end stage renal disease
- phase iii
- locally advanced
- healthcare
- chronic kidney disease
- ejection fraction
- newly diagnosed
- clinical trial
- small cell lung cancer
- prognostic factors
- palliative care
- peritoneal dialysis
- radiation therapy
- open label
- squamous cell carcinoma
- randomized controlled trial
- patient reported outcomes
- quality improvement
- type diabetes
- phase ii
- brain metastases
- radiation induced
- insulin resistance
- double blind
- patient reported
- replacement therapy