A Study Evaluating Sotorasib Platinum Doublet Combination Versus Pembrolizumab Platinum Doublet Combination as a Front-Line Therapy in Participants With Stage IV or Advanced Stage IIIB/C Nonsquamous Non-Small Cell Lung Cancers (CodeBreaK 202)
Study Details
Study Description
Brief Summary
The primary objective of this study is to compare progression-free survival (PFS) in participants who receive sotorasib with platinum doublet chemotherapy versus participants who receive pembrolizumab with platinum doublet chemotherapy.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 3 |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Sotorasib combined with carboplatin and pemetrexed Sotorasib administered in combination with carboplatin and pemetrexed. |
Drug: Sotorasib
Oral administration
Other Names:
|
| Active Comparator: Pembrolizumab combined with carboplatin and pemetrexed Pembrolizumab administered in combination with carboplatin and pemetrexed. |
Drug: Pembrolizumab
Intravenous administration
|
Outcome Measures
Primary Outcome Measures
- Progression-free Survival (PFS) [From Baseline up to end of study (EOS) (approximately 5.5 years)]
PFS is defined as the time from randomization until the first documentation of radiologic disease progression or death due to any cause, whichever occurs first. Progression will be based on Response Evaluation Criteria in Solid Tumors (RECIST) v1.1, per Blinded Independent Central Review (BICR).
Secondary Outcome Measures
- Objective Response Rate (ORR) [From Baseline up to EOS (approximately 5.5 years)]
Objective response is defined as the best overall response of complete response (CR) or partial response (PR), based on RECIST v1.1, per BICR.
- Overall Survival (OS) [From Baseline up to EOS (approximately 5.5 years)]
OS is defined as the time from randomization until death due to any cause.
- Change in Quality-of-Life Questionnaire Core 30 (QLQ-C30) Dyspnea Domain Score [From Baseline to Week 12]
- Change in Quality-of-Life Questionnaire Lung Cancer 13 (QLQ-LC13) Symptoms of Dyspnea Subscale [From Baseline to Week 12]
- Change in QLQ-LC13 Symptoms of Cough Subscale [From Baseline to Week 12]
- Change in QLQ-LC13 Symptoms of Chest Pain Subscale [From Baseline to Week 12]
- Change in Physical Function as Measured by QLQ-C30 [From Baseline to Week 12]
- Change in Global Health Status as Measured by QLQ-C30 [From Baseline to Week 12]
- Progression-free Survival 2 (PFS2) [From Baseline up to EOS (approximately 5.5 years)]
PFS2 is defined as the time from randomization to progression per investigator after initiation of new anticancer therapy or treatment beyond progression (ie, second progression) or death from any cause, whichever occurs first.
- Change in QLQ-LC13 Subscale Scores [From Baseline up to EOS (approximately 5.5 years)]
- Change in QLQ-C30 Subscale Scores [From Baseline up to EOS (approximately 5.5 years)]
- Time to Deterioration in QLC-LC13 Subscale Scores [From Baseline to Week 12]
- Time to Deterioration in QLC-C30 Subscale Scores [From Baseline to Week 12]
- Change in Summary Scores and Visual Analogue Scale (VAS) Scores [From Baseline up to EOS (approximately 5.5 years)]
Measured by EuroQol-5 Dimension (EQ-5D-5L).
- Duration of Response [From Baseline up to EOS (approximately 5.5 years)]
Duration of response is defined as the time from the first documentation of objective response until the first documentation of disease progression per BICR or death due to any cause, whichever occurs first.
- Time to Response [From Baseline up to EOS (approximately 5.5 years)]
Defined as the time from randomization to first evidence of PR or CR per BICR.
- Disease Control [From Baseline up to EOS (approximately 5.5 years)]
Defined as CR plus PR plus stable disease based on RECIST v1.1 per BICR.
- PFS [From Baseline up to EOS (approximately 5.5 years)]
Based on investigator tumor assessments per RECIST v1.1.
- Objective Response [From Baseline up to EOS (approximately 5.5 years)]
Based on investigator tumor assessments per RECIST v1.1.
- Number of Participants With Treatment-Emergent Adverse Events [From Baseline up to EOS (approximately 5.5 years)]
- Number of Participants With Clinically Significant Changes in Vital Signs [From Baseline up to EOS (approximately 5.5 years)]
- Number of Participants With Clinically Significant Changes in Clinical Laboratory Tests [From Baseline up to EOS (approximately 5.5 years)]
- Maximum Plasma Concentration (Cmax) of Sotorasib [Pre-dose Day 1 up to Day 64]
- Minimum Plasma Concentration (Cmin) of Sotorasib [Pre-dose Day 1 up to Day 64]
- Area Under The Curve (AUC) of Sotorasib [Pre-dose Day 1 up to Day 64]
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Histologically or cytologically confirmed diagnosis of nonsquamous stage IV or advanced Stage IIIB or IIIC NSCLC with KRAS p. G12C mutation and negative for PD-L1 expression by central testing or local laboratory testing confirmed through central testing
-
No history of systemic anticancer therapy in metastatic/non-curable settings
-
Eastern Cooperative Oncology Group (ECOG) ≤ 1
Exclusion Criteria:
-
Mixed histology NSCLC with either small-cell or large-cell neuroendocrine cell component or predominant squamous cell histology
-
Participants with tumors known to harbor molecular alterations for which targeted therapy is locally approved
-
Symptomatic (treated or untreated) brain metastases
-
Gastrointestinal (GI) tract disease causing the inability to take oral medication
-
Myocardial infarction within 6 months of randomization, unstable arrhythmias, or unstable angina
-
Prior therapy with a KRAS G12C inhibitor
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Amgen
Investigators
- Study Director: MD, Amgen
Study Documents (Full-Text)
None provided.More Information
Additional Information:
Publications
None provided.- 20190341
- 2022-501863-41