Status:
COMPLETED
Safety and Tolerability Evaluation of Sintilimab in Combination With Radiation in Stage IV NSCLC Patients
Lead Sponsor:
Sichuan University
Collaborating Sponsors:
Innovent Biologics (Suzhou) Co. Ltd.
Conditions:
Stage IV NSCLC
Eligibility:
All Genders
18-70 years
Phase:
PHASE1
Brief Summary
This pilot phase I trial aims to investigate the safety and tolerability of anti-programmed cell death-1 (PD-1) monoclonal antibody Sintilimab (also called IBI308) in combination with concurrent stere...
Detailed Description
This exploratory phase I study will be conducted in two steps: Step A: A low dose radiotherapy (LDRT) dose escalation, 6 patients per cohort (a total of 18 patients) will be enrolled to determine the...
Eligibility Criteria
Inclusion
- Patients with histologically or cytologically confirmed stage IV NSCLC.
- Enough tumor tissue samples.
- No previous radiation, chemotherapy, immunotherapy. Patients who have received neoadjuvant or adjuvant chemotherapy 12 months before enrollment is permitted.
- At least three measurable disease according to RECIST 1.1 that meet SBRT and LDRT radiation requirement as protocol defined
- PD-L1 expression positive (TPS \>1%)
- Be ≥18 years of age on day of signing informed consent and ≤75 years old.
- ECOG 0-1.
- Patients must have normal organ and marrow function as defined below: Total bilirubin \</= 1.5 mg/dL. Aminotransferase (AST) Serum Glutamic Oxaloacetic Transaminase (SGOT)/ Alanine Aminotransferase (ALT) Serum Glutamic-Pyruvic Transaminase (SGPT) \<2.5 X institutional upper limit of normal (patients with liver involvement will be allowed \</= 5.0 X institutional upper normal limit) \*WBC \>/= 3500/uL, ANC \>/= 1500/uL \*Platelets \>/= 90K \*Hemoglobin \>/= 9g/dL \*Creatinine \</= 1.5 x ULN.
- Be willing and able to provide written informed consent/assent for the trial.
- Patients should be able to tolerate a course of radiotherapy as assessed by the investigator.
- No contradiction to radiation per radio-oncologists' judgments
- Life expectancy of \> 6 months.
Exclusion
- EGFR/ALK/ROS-1 mutation or mutation status unknown.
- Has evidence of interstitial lung disease or active, non-infectious pneumonitis.
- Subjects with coronary bypass operation.
- Subjects with insufficient heart function, liver function and kidney function.
- Subjects with severe uncontrollable psychotic symptoms.
- Treatment with systemic corticosteroids or other systemic immunosuppressive medications (including but not limited to prednisone, dexamethasone, cyclophosphamide, azathioprine, methotrexate, thalidomide, anti-tumor necrosis factor agents) within 4 weeks prior to enrollment or anticipated requirement for systemic immunosuppressive medications during the trial.
- Subjects with active, known or suspected autoimmune disease such as interstitial pneumonia, uveitis, Crohn's disease, autoimmune thyroiditis. Subjects with cured childhood asthma, type I diabetes mellitus only requiring hormone replacement.
- Known history of allogeneic organ or allogeneic hemopoietic stem cell transplantation.
- Known hypersensitivity or allergy to monoclonal antibody.
- Subjects with a history of interstitial lung disease.
- Uncontrolled concomitant disease, including but not limited to :
- 1)Active or poorly controlled severe infection 2)Human Immunodeficiency Virus (HIV) infection (HIV antibody positive) 3)Known acute or chronic active hepatitis B (HBV DNA positive) infection or acute or chronic active hepatitis C (HCV antibody positive and HCV RNA positive) infection 4)Active tuberculosis 5)Symptomatic congestive heart failure (New York Heart Association grade III-IV) or symptomatic, poorly controlled arrhythmia 6)Uncontrolled hypertension (SBP ≥ 160mmHg or DBP ≥ 100mmHg) 7)Prior arterial thromboembolism event, including myocardial infarction, unstable angina, stroke and transient ischemic attack, within 6 months of enrollment 8)Concomitant disease needs anticoagulant therapy 9)Uncontrolled hypercalcemia（Ca2+\>1.5mmol/L or Ca \>12mg/dl or corrected Serum Calcium \>ULN），or Symptomatic hypercalcemia during diphosphonate therapy
- 12\. Other primary malignancy, with the exception of: (radical Non-melanoma skin cancer or cured cervical in-situ carcinoma;).
- 13\. Subjects with other diseases or abnormal Lab test results which might increase the risk of enrollment and treatment or Interfere with the interpretation of study results could be excluded according to the judgments of investigator.
- 14\. Pregnant or lactating women.
Key Trial Info
Start Date :
January 18 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 8 2022
Estimated Enrollment :
29 Patients enrolled
Trial Details
Trial ID
NCT03812549
Start Date
January 18 2019
End Date
July 8 2022
Last Update
March 4 2025
Active Locations (1)
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1
West China Hospital, Sichuan University
Chengdu, Sichuan, China, 610041