Toripalimab in Combination With Chemotherapy and Antiangiogenic Agents in Patients With Non-Small Cell Lung Cancer After Failure of Immunotherapy (PD-1/L1 Inhibitors)

Tianjin Medical University

Status and phase

Not yet enrolling

Phase 2

Conditions

Non Small Cell Lung Cancer Recurrent

Treatments

Drug: Toripalimab, Anlotinib and Chemotherapy

Study type

Interventional

Funder types

Other

Identifiers

NCT05842018

JS001-NSCLC-CO396

Details and patient eligibility

About

This is a phase II, single arm, open-label, single-center study to evaluate the efficacy and safety of Toripalimab combined with Chemotherapy and Antiangiogenic Agents in patients with Non-Small Cell Lung Cancer After Failure of Immunotherapy (PD-1/L1 inhibitors)

Enrollment

30 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients voluntarily participate in this study, signed and dated informed consent with good compliance and follow-up;
Diagnosed as locally advanced and / or metastatic non-small cell lung adenocarcinoma (NSCLC) by cytology or histology;
First-line PD-1/PD-L1 inhibitors treatment failure;
Provide detectable specimens (tissue or blood) for genotyping before enrollment, and the patients should be with negative EGFR and ALK gene test results;
Had at least one measurable lesion according to RECIST 1.1 criteria
Anticipated overall survival more than 3 months;
ECOG (Eastern Cooperative Oncology Group) scale 0-2;
Normal organ function and bone marrow function;
Resistant to first-line immune checkpoint inhibitor therapy and discontinued for more than 4 weeks;
Women of childbearing age must have taken reliable contraceptive measures and performed a pregnancy test (serum or urine) within 7 days prior to enrollment, and the results were negative, and were willing to use appropriate methods during the trial and 4 weeks after the last administration of the test drug.

Exclusion criteria

Patients with small cell lung cancer (including small cell carcinoma and non-small cell carcinoma mixed lung cancer) ;
Patients who have previously permanently discontinued immunotherapy due to immune-related serious adverse reactions;
Patients who previously treated with antiangiogenic agents;
A history of other malignancies within 5 years prior to inclusion, except for cervical carcinoma in situ, basal or squamous cell skin cancer, localized prostate cancer treated with radical surgery, and ductal carcinoma in situ treated with radical surgery;
Active, known or suspected autoimmune disease;
Active or chronic hepatitis C or/and hepatitis B infection;
History of interstitial lung disease.