本研究的第2階段部分評估MRTX849單藥治療和與pembrolizumab合併治療在伴有KRAS G12C突變和任何PD-L1 TPS的晚期NSCLC患者羣組中的有效性和安全性,這些患者是一線治療的候選者。 研究的第3階段部分比較了adagrasib聯合pembrolizumab與pembrolizumab在不可切除、局部晚期或轉移性鱗狀或
適應症:Advanced Non-Small Cell Lung Cancer、Metastatic Non-Small Cell Lung Cancer
收案條件
納入條件
- Phase 2: Histologically confirmed diagnosis of unresectable or metastatic NSCLC with KRAS G12C mutation and any PD-L1 TPS
- Phase 3: Histologically confirmed diagnosis of unresectable or metastatic squamous or nonsquamous NSCLC with KRAS G12C mutation and PD-L1 TPS\>=50%
- Phase 3: Presence of measurable disease per RECIST1.1
- Phase 3: CNS Inclusion - Based on screening brain imaging, patients must have one of the following:
- No evidence of brain metastases
- Untreated brain metastases not needing immediate local therapy
- Previously treated brain metastases not needing immediate local therapy
排除條件
- Phase 2 and Phase 3: Prior systemic treatment for locally advanced or metastatic NSCLC including chemotherapy, immune checkpoint inhibitor therapy, or a therapy targeting KRAS G12C mutation (e.g., AMG 510).
- Phase 2: Active brain metastases
- Phase 3: Patients with known central nervous system (CNS) lesions must not have any of the following:
- Any untreated brain lesions \> 2.0 cm in size
- Any brainstem lesions
- Ongoing use of systemic corticosteroids for control of symptoms of brain lesions at a total daily dose of \> 10 mg of prednisone (or equivalent) prior to randomization.
- Have poorly controlled (\> 1/week) generalized or complex partial seizures, or manifest neurologic progression due to brain lesions notwithstanding CNS-directed therapy
- Phase 3: Radiation to the lung \> 30 Gy within 6 months prior to the first dose of study treatment
收案條件維持 ClinicalTrials.gov 原始英文登錄資料,實際收案資格以研究團隊的正式評估與受試者同意書為準。資料來源:ClinicalTrials.gov,每兩週自動更新,最後同步:2026年10月8日。