Clinical trial · Interventional
Pembrolizumab, Lenvatinib and Chemotherapy After TKIs in NSCLC
A Phase 2 Open-label Single-arm Study to Evaluate the Combination of Pembrolizumab, Lenvatinib and Chemotherapy in Non-small Cell Lung Cancer (NSCLC) Harbouring Targetable Mutation and Failed Standard Tyrosine Kinase Inhibitors
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (6)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| ALK Gene Rearrangement Positive | — | UNRESOLVED | — |
| EGFR Activating Mutation | — | UNRESOLVED | — |
| EGF-R Positive Non-Small Cell Lung Cancer | — | UNRESOLVED | — |
| Nsclc | Lung Non-Small Cell Carcinoma | ALIAS | 0.90 |
| ROS1 Gene Rearrangement | — | UNRESOLVED | — |
| ROS1 Positive NSCLC - Reactive Oxygen Species 1 Positive Non-Small Cell Lung Cancer | — | UNRESOLVED | — |
Interventions
Interventions (4)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Carboplatin | Drug | Carboplatin | ALIAS |
| Lenvatinib | Drug | Lenvatinib | ALIAS |
| Pembrolizumab | Drug | Pembrolizumab | ALIAS |
| Pemetrexed | Drug | Pemetrexed | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Treatment
- interventionNames
- Drug: Pembrolizumab
- Drug: Lenvatinib
- Drug: Pemetrexed
- Drug: Carboplatin
Primary outcomes (1)
- measure
- Overall response rate
- timeFrame
- 24 months
- description
- Proportion of patients who have a confirmed CR or PR per RECIST 1.1
Secondary outcomes (3)
- measure
- Progression-free survival
- timeFrame
- 24 months
- description
- Time from randomization to the first documented disease progression per RECIST 1.1 or death due to any cause, whichever occurs first
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
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
References
Publications (1)
- DERIVEDChan HW, Tse CCL, Li YC, Leung R, Kwok GW, Wong JSL, Li KH, Tsang JWY, Li CW, Lo JWY, Tang V, Hui R, Yau T, Ho JCM, Chiu JWY. A phase 2, open-label, single-arm study evaluating the combination of pembrolizumab, lenvatinib, carboplatin and pemetrexed in patients with metastatic non-small cell lung cancer harbouring targetable genomic alterations who progressed on standard tyrosine kinase inhibitors. Invest New Drugs. 2025 Dec;43(6):1191-1200. doi: 10.1007/s10637-025-01589-6. Epub 2025 Nov 10. PMID 41212380