Observe the efficacy and safety of sunvozertinib in the real world in the treatment of EGFRm aNSCLC patients with previous EGFR-TKI treatment
Locally advanced or metastatic NSCLC with EGFR-sensitive mutations who have been previously treated with EGFR-TKIs and PD for last therapy can be involved in this study. Investigators will assess patients whether to be suitable for sunvozertinib treatment. And this study will evaluate the safety and efficacy.
Study Type
OBSERVATIONAL
Enrollment
55
sunvozertinb, a EGFR-TKI, 300mg QD oral
Qiming Wang
Zhengzhou, Henan, China
Objective Response Rate (ORR)
assess the proportion of subjects who have a complete response (CR) or a partial response (PR)\]
Time frame: Time from first dose to last dose, up to 24 month
Progression-free survival (PFS)
To assess anti-tumor activity of Sunvozertinib according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 by investigator
Time frame: Time from first dose to first documented disease progression assessed by investigator or death due to any cause up to 24 month
Overall survival (OS)
To assess anti-tumor activity of Sunvozertinib according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 by investigator
Time frame: Time Frame: Time from first dose to the death of the subject due to any cause assessed up to 36 months.
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