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Recruiting Phase 2 NCT06305715

NCT06305715 Radiation Prior to TKI to Delay Progression in Advanced Driver-Mutated Non-small Cell Lung Cancers (RadiaNCe Lung X)

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Clinical Trial Summary
NCT ID NCT06305715
Status Recruiting
Phase Phase 2
Sponsor Medical College of Wisconsin
Condition Non Small Cell Lung Cancer
Study Type INTERVENTIONAL
Enrollment 34 participants
Start Date 2024-09-18
Primary Completion 2027-06-15

Trial Parameters

Condition Non Small Cell Lung Cancer
Sponsor Medical College of Wisconsin
Study Type INTERVENTIONAL
Phase Phase 2
Enrollment 34
Sex ALL
Min Age 18 Years
Max Age N/A
Start Date 2024-09-18
Completion 2027-06-15
Interventions
Radiation TherapyTargeted TKI therapy

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Brief Summary

This prospective, two-part, single-arm, phase II trial is designed to evaluate whether the use of definitive radiation to the primary lung lesion prolongs progression-free survival (PFS) in treatment-naïve, metastatic, driver-mutated non-small cell lung cancers (NSCLC) patients who are subsequently placed on a tyrosine kinase inhibitor (TKI).

Eligibility Criteria

Inclusion Criteria Part 1 1. Age ≥18 years. 2. Patient must have a pathologically-confirmed diagnosis of non-small cell lung cancer (NSCLC). 3. An identifiable primary lung lesion must be present based on the consensus opinion of the medical oncology and radiation oncology investigators. 4. Patient did not previously receive radiation therapy to the primary lung lesion. Previous or concurrent palliative radiation to symptomatic metastatic lesions and definitive radiation to central nervous system metastases are allowable. 5. Patient must have advanced disease, either stage IV or stage IIIB/C that is not amenable to definitive multi-modality therapy. 6. Patient must not have received prior targeted therapy for NSCLC. A subject may receive up to 2 cycles of standard cytotoxic chemotherapy for NSCLC prior to trial enrollment. For example, a cycle of carboplatin and pemetrexed is given once every 3 weeks. 7. Patient must have measurable disease as defined by RECIST v1.1. 8. Patient must ha

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