Pembrolizumab, Lenvatinib and Chemotherapy After TKIs in NSCLC

• Status: Not yet recruiting
• Trial end date: 2024-12-01
• Target enrollment: 0
• Participant gender: All

Summary

Adding chemotherapy or anti-VEGF to immunotherapy is an emerging strategy to enhance the efficacy of immunotherapy in many cancers. This phase 2 study aims to explore the preliminary efficacy of combination pembrolizumab with lenvatinib and chemotherapy in NSCLC patients with sensitizing EGFR, ALK, or ROS1 genetic aberration refractory to standard targeted therapy.

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Dr Joanne CHIU
• Treatments: Carboplatin; Lenvatinib; Pembrolizumab; Pemetrexed

Criteria

Main Inclusion Criteria:

• Histologically proven NSCLC

• Unresectable or metastatic NSCLC, including squamous cell carcinoma, harboring sensitizing EGFR, ALK, or ROS1 genetic aberrations who have received standard of care targeted therapy and have progressed on treatment. Patients with known T790M mutation should have received osimertinib and failed.

• Measurable disease per RECIST 1.1

• ECOG performance status ≤ 1

• Adequate organ function

• Adequately controlled blood pressure

Main Exclusion Criteria:

• Prior exposure to immunotherapy or chemotherapy

• Active untreated brain metastasis and/or carcinomatous meningitis

• Active, known or suspected autoimmune disease

• History of (noninfectious) pneumonitis that required systemic steroids or current pneumonitis/interstitial lung disease

• Condition requiring systemic treatment with either corticosteroids (> 10 mg daily prednisone equivalent) or other immunosuppressive medications

• Baseline proteinuria ≥ 1 g/24 hrs

• Electrolyte abnormalities that have not been corrected

• Significant cardiovascular impairment

• Gastrointestinal pathology that might affect the absorption of lenvatinib

• Preexisting grade ≥ 3 gastrointestinal or non gastrointestinal fistula

• Bleeding or thrombotic disorders or subjects at risk for severe hemorrhage

• Radiographic evidence of intratumoral caviations, encasement, or invasion of a major blood vessel

• Known history of tuberculosis

• Active, acute, or chronic clinically significant infections requiring therapy, including hepatitis B, hepatitis C, and HIV

• ECG with long QTc interval ≥ 470 ms