This is an open-label, prospective single arm Phase II trial that investigates the role of ablative stereotactic body radiation therapy (SBRT) in oncogene driven metastatic non-small cell lung cancer (mNSCLC) patients with oligoprogressive disease (OPD) on targeted therapy (TKI) followed by circulating tumor DNA (ctDNA) analysis for tailoring targeted therapies.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
60
SBRT/high-dose radiotherapy Standard of care targeted therapy
SBRT/high-dose radiotherapy Second-line targeted therapy
Radiation Medicine Program, Princess Margaret Cancer Centre, University Health Network
Toronto, Ontario, Canada
Progression-free-survival
Progression-free-survival 1 (PFS1) will be determined from the first day of SBRT to oligoprogressive sites to the day of diagnosis of radiological progression in the subsequent imaging (irrespective of change in systemic therapy in group B, essentially second-line) or death
Time frame: 1 year
Subsequent progression-free-survival
Subsequent PFS will be calculated from the date of first radiological progression after SBRT to second radiological progression or change to 3rd line systemic therapy or death or loss to follow-up, whichever comes first.
Time frame: 1 year
Acute and Late Toxicities
For SBRT combined with TKI (using CTCAE Version 5.0)
Time frame: 1 year
Reported Adverse Events
PRO-CTCAE Questionnaire
Time frame: 1 year
Quality of Life Outcome
QLQ-LC1 Questionnaire
Time frame: 1 year
Quality of Life Outcome
EORTC-QLQ-C30 Questionnaire
Time frame: 1 year
Cost-effectiveness
EQ-5D-5L Questionnaire
Time frame: 1 year
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