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RecruitingNCT05430009

Liver SBRT in Combination With Immune Checkpoint Inhibition in Patients With Metastatic Non-small Cell Lung Cancer

Phase I Trial of Feasibility and Safety of Liver SBRT in Combination With Immune Checkpoint Inhibition in Patients With Metastatic Non-small Cell Lung Cancer

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
12 (estimated)
Sponsor
VA Ann Arbor Healthcare System · Federal
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Determine the feasibility of liver stereotactic body radiation therapy (SBRT) given in combination with systemic therapy (immune checkpoint inhibitors) in adult patients with metastatic NSCLC with liver metastases.

Conditions

Interventions

TypeNameDescription
RADIATIONLiver SBRT24-45 Gy delivered in 3-5 fractions to 1-4 lesions.
DRUGPembrolizumab200 mg every 3 weeks or 400 mg every 6 weeks

Timeline

Start date
2022-06-17
Primary completion
2025-12-15
Completion
2026-06-15
First posted
2022-06-24
Last updated
2022-08-01

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05430009. Inclusion in this directory is not an endorsement.

Liver SBRT in Combination With Immune Checkpoint Inhibition in Patients With Metastatic Non-small Cell Lung Cancer (NCT05430009) · Clinical Trials Directory