About this trial
This study includes patients with advanced non-small cell lung cancer (NSCLC) - either unresectable stage III or stage IV adenocarcinoma without actionable driver mutations - who are treated with pembrolizumab in combination with platinum-based doublet chemotherapy, irrespective of PD-L1 expression levels.
The primary objective is to assess treatment response through integration of serial T-cell receptor (TCR) repertoire sequencing (Rep-seq), capturing longitudinal changes in T-cell clonality and diversity. These immune dynamics will be correlated with radiographic response assessed by RECIST 1.1, with the aim of improving the accuracy of response classification, including differentiation between progression, pseudo-progression, and hyperprogression.
Additionally, circulating tumor DNA (ctDNA) levels will be measured longitudinally (pre-treatment and during treatment) to evaluate their potential as a complementary biomarker of disease burden and treatment efficacy in the context of chemo-immunotherapy.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Histologically confirmed diagnosis of NSCLC adenocarcinoma stage IV or unresectable stage III.
Have measurable disease based on RECIST 1.1.
Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1.
Adequate organ function.
Disqualifiers
Aberration in one or more of molecular drivers.
Has received prior systemic anti-cancer therapy prior to allocation.
Known active CNS metastases and/or carcinomatous meningitis.
Known additional malignancy.
Trial design
Single group
Treatments tested in this trial
Pembrolizumab (KEYTRUDA®)
DrugIV Pembrolizumab 200 mg combined with pemetrexed and platinum (investigator's choice of cisplatin or carboplatin) every 3 weeks
Treatment groups
Trial outcomes
Primary outcomes
Change in T-cell Receptor (TCR) Repertoire Clonality and Diversity Relative to Disease Response Assessed by RECIST v1.1
TCR sequencing will be performed on peripheral blood samples to assess clonality and diversity metrics. Changes in these metrics will be analyzed relative to clinical disease response evaluated according to RECIST version 1.1 criteria.
Sponsors and contacts
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Rabin Medical Center
Lead sponsor
MSD Pharmaceuticals LLC
Collaborator
This trial is not recruiting at the moment. You can still explore other options: