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.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
46
200 mg Q3W
8 mg daily
500 mg/m2 Q3W
AUC5 Q3W
Queen Mary Hospital
Hong Kong, Hong Kong
RECRUITINGOverall response rate
Proportion of patients who have a confirmed CR or PR per RECIST 1.1
Time frame: 24 months
Progression-free survival
Time from randomization to the first documented disease progression per RECIST 1.1 or death due to any cause, whichever occurs first
Time frame: 24 months
Overall survival
Time from randomization to death from any cause or last follow-up date
Time frame: 36 months
The incidence, severity as graded by NCI CTCAE v5.0, seriousness and relationship to study medication of adverse events (AEs)
Safety and tolerability
Time frame: 24 months
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