Response of Bony Metastasis to Tyrosine Kinase Inhibitors in Non-Small Cell Lung Cancers With Actionable Driver Mutations.
Start Date
4/28/2020
Completion Date
4/28/2028
Summary
The purpose of this study is to assess percentage reduction in the of urine NTX and serum CTX , in patients with NSCLC and bone metastases 1) with actionable driver oncogene on standard of care (SOC) TKI at 3 months post treatment and 2) without actionable mutations on standard of care therapy (chemotherapy/immunotherapy) treated with zoledronic acid or denosumab at the same time period.
Detailed Description
This is an observational study involving two arms of NSCLC with metastatic bony disease at the time of enrollment in the study. One group will have an actionable driver oncogene and initiate treatment in any line with a TKI as standard of care and concurrent to participation to this study; expected to have an objective response rate in ≥40% who have not previously seen anti-bone resorptive therapy. The other group will not have actionable mutations and initiate treatment with chemotherapy/immunotherapy along with new onset therapy with IV zoledronic acid 4mg Q4 weeks or subcutaneous denosumab 120 mg Q12 weeks for bone disease, which is standard of care and would be concurrent to participation in this study. Baseline and on-treatment imaging and serum total alkaline phosphatase will be performed per SOC. Additional non-SOC bone turnover markers including , urine N-telopeptide (NTX) and serum C-terminal telopeptide (CTX), will be checked at baseline and then at 1, 3, 6, and 12 months.
Eligibility Criteria
Age Range: 18 years to 100 years
Interventions
Tyrosine Kinase Inhibitor
Zoledronic Acid 4 MG/100 ML Intravenous Solution [ZOMETA]
Denosumab 120 MG/1.7 ML Subcutaneous Solution [XGEVA]
Conditions
Locations
University of Colorado Hospital
Aurora, Colorado 80045
United States
Lone Tree Medical Center
Lone Tree, Colorado 80124
United States