The Combination of Apatinib and Camerlizumab for Advanced Lung Cancer Patients With Muti-line Therapy

Lung Cancer Clinical Trial

Official title:

The Combination of Apatinib and Camerlizumab for Advanced Lung Cancer Patients

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04782622
• Other study ID #: ApatPEM
• Status: Recruiting
• Start date: March 1, 2021
• Est. completion date: March 1, 2023

Study information

• Verified date: March 2021
• Source: The Affiliated Hospital of Qingdao University
• Contact: Xiaochun Zhang
• Phone: +8653282913271
• Email: zhangxiaochun9670[@]126.com
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

The combination of Apatinib and Camrelizumab for progressed NSCLC patients with muti-line therapy : a phaseⅠB clinical study.

Brief Summary: Immunotherapy has made a major progress in Lung cancer.However, challenges such as primary and acquired resistance, small fraction of benefit population and lack of predictive and prognostic biomarkers even exist. The overall objective response rate is lower than 20% in second line-treatment and the progression-free survival (PFS) is also similar to or poorer than that of conventional second-line chemotherapy. Apatinib is a novel, orally administered, multitarget receptor tyrosine kinase inhibitor that inhibits VEGFR, PDGFR, FGFR, c-Kit, and other kinases. It functions by inhibiting tumor angiogenesis and proliferative signaling pathways. We would observe and analyze the effectiveness and safety of apatinib combined with Camrelizumab for advanced NSCLC after muti-line therapy to explore the synergistic effect of anti-angiogenic agents and immunotherapy.

Description:

Enrolled patients received apatinib plus Camrelizumab treatment (apatinib, 250mg, qd; Camrelizumab, 5mg/kg, iv, d1, 21day as a cycle.)

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: March 1, 2023
• Est. primary completion date: January 1, 2022
• Gender: All
• Age group: 18 Years to 90 Years

Eligibility

Inclusion Criteria:

Clinical diagnosis of Lung cancer Ability to comply with protocol Aged = 18 years Histologically documented NSCLC that is currently locally advanced or metastatic NSCLC Disease progression during or following at least one line treatment. Measurable disease, as defined by RECIST v1.1 ECOG performance status of 0 or 1 Life expectancy = 12 weeks Adequate hematologic and end organ function, defined by the following laboratory results obtained within 14 days prior to the first study treatment: ANC = 1.5 × 109/L (without granulocyte colony-stimulating factor support within 2 weeks of laboratory test used to determine eligibility) WBC counts > 2.5 × 109/L and < 15 × 109/L Lymphocyte count = 0.5 × 109/L Serum albumin = 2.5 g/dL Platelet count = 100 × 109/L (without transfusion within 2 weeks of laboratory test used to determine eligibility) Hemoglobin = 9.0 g/dL Patients may be transfused or receive erythropoietic treatment to meet this criterion.

Liver function tests meeting one of the following criteria:

AST or ALT = 2.5 × upper limit of normal (ULN), with alkaline phosphatase

= 2.5 × ULN or AST and ALT = 1.5 × ULN in conjunction with alkaline phosphatase > 2.5 × ULN Serum bilirubin = 1.5 × ULN Patients with known Gilbert's disease who have serum bilirubin level = 3 × ULN may be enrolled. INR and aPTT = 1.5 × ULN This applies only to patients who are not receiving therapeutic anticoagulation; patients receiving therapeutic anticoagulation should be on a stable dose for at least 1 week prior to randomization. Creatinine clearance = 30 mL/min Cockcroft-Gault, Chronic Kidney Disease Epidemiology Collaboration, or Modification of Diet in Renal Disease formulas may be used for creatinine clearance calculation. Note that 24-hour urine collection is not required but is allowed.

Exclusion Criteria:

Active or untreated CNS metastases as determined by computed tomography (CT) or magnetic resonance imaging (MRI) evaluation during screening and prior radiographic assessments Leptomeningeal disease Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedures Uncontrolled hypertension Perior used anti-angiogenic agents or immune checkpoint inhibitors.

Related Conditions & MeSH terms

• Lung Cancer
• Lung Neoplasms

Intervention

Drug:
• Apatinib+Camrelizumab
Apatinib 250mg po qd+Camrelizumab 200mg ivdrip q14d

Locations

Country	Name	City	State
China	Xiaochun Zhang	Qingdao	None Selected

Sponsors (1)

Lead Sponsor	Collaborator
The Affiliated Hospital of Qingdao University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Objective response rate	Objective response rate	03.01.2021 to 03.01.2022
Primary	Progression free survival	progression free survival	03.01.2021 to 03.01.2022