Efficacy and Safety of the Combination of Anlotinib and JS001 in EGFR-TKI Resistant T790M-Negative NSCLC

Baodong Qin

Status: Unknown

Conditions: Anlotinib; NSCLC Stage IV; EGFR T790M-negative; JS001

Study type: Observational

Funder types: Other

Identifiers

NCT04116918

AJERTNN

Details and patient eligibility

About

This study is designed to evaluate the efficacy and safety of the combination of Anlotinb and JS001 in EGFR-TKI resistant T790M-negative NSCLC patients.

Full description

All EGFR mutation NSCLC patients with EGFR-TKIs eventually develop acquired resistance and in 40%-50% of these the resistance mechanism is based on the EGFR T790M mutation who could receive Osimertinib. Several alternative mechanisms of escape from EGFR-TKIs have been detected in NSCLC patients without the T790M, such as Met application, BRAF mutation, PIK3CA mutation, etc, who could receive the combination of EGFR-TKI with comparable target drug. Given the lack of targeted therapy for the majority of T790M-negative patients, platinum-doublet chemotherapy remains the standard of care with low effectiveness. In the present study, we aimed to evaluate the efficacy and safety of the combination of Anlotinb and JS001 in EGFR-TKI resistant T790M-negative NSCLC patients.

Enrollment: 100 estimated patients

Sex: All

Ages: 18 months to 75 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult patients >=18 years of age
• Inoperable locally advanced, recurrent, and/or metastatic NSCLC patients with EGFR sensitive mutation
• EGFR-TKI resistent
• EGFR T790M negative
• Expected survival ≥ 3 month;
• ECOG / PS score: 0-2;
• the main organ function to meet the following criteria: HB ≥ 90g / L, ANC ≥ 1.5 × 109 / L, PLT ≥ 80 × 109 / L,BIL <1.5 times the upper limit of normal (ULN); Liver ALT and AST <2.5 × ULN and if liver metastases, ALT and AST <5 × ULN; Serum Cr ≤ 1 × ULN, endogenous creatinine clearance ≥50ml/min

Exclusion criteria

• EGFR-T790M positive
• with druggable gene alteration;
• Patient can not comply with research program requirements or follow-up;