Clinical trial

Efficacy and Safety of Tislelizumab Combined Treatment in Refractory Natural Killer/T-cell Lymphoma

Name
XHLSG-NK-1903
Description
Natural killer/T-cell lymphoma (NKTCL) patients with relapsed/refractory disease had very poor outcome. Anti-PD-1 antibody showed promising results in response, but but the complete remission rate of was low. Some anti-PD-1 antibody based regimen showed higher and deeper response in NKTCL patients.
Trial arms
Trial start
2021-09-17
Estimated PCD
2022-12-30
Trial end
2023-12-30
Status
Completed
Treatment
tislelizumab, azacytidine, lenalidomide
tislelizumab, 200mg, iv, day 1, every 21 days. azacytidine, 75mg/m2, ih, days 1-7, every 21 days. lenalidomide, 25mg, po, days 1-14, every 21 days.
Arms:
TALE regimen
Other names:
Tileilizhu Dankang
tislelizumab, etoposide, pegaspargase
tislelizumab, 200mg, iv, day 1, every 21 days. etoposide, 100mg, iv, days 1-3, every 21 days. pegaspargase, 2000U/m2, day 1, every 21 days
Arms:
TEPA regimen
Other names:
Tileilizhu Dankang
Size
62
Primary endpoint
Overall response rate
Week 12 +/-7 days
Eligibility criteria
Inclusion Criteria: 1. Patients with biopsy histopathology, immunohistochemistry and EBER test meet ing the WHO 2016 diagnostic criteria for NK/T cell lymphoma. 2. With progressive disease after asparaginase-based combined chemotherapy 3. Have experienced multiple courses of PD-1/PD-L1 treatment with non-responsive or progressive disease. 4. PET/CT or CT/MRI with at least one measurable lesion or objectively evaluable lesion. 5. General ECOG score 0-3 points. 6. The laboratory examination within 1 week before enrollment meets the following conditions: Blood routine: Hb\>80g/L, PLT\>50×109/L. Liver function: ALT, AST, TBIL ≤ 2 times the upper limit of normal. Renal function: Cr is normal. Blood coagulation test: plasma fibrinogen ≥1.0g/L. Heart function: LVEF≥50%, ECG did not indicate any acute myocardial infarction, arrhythmia, or atrioventricular block of degree I or more. 7. Signed informed consent form. 8. Voluntarily comply with research protocols, follow-up plans, laboratory and auxiliary examinations. Exclusion Criteria: 1. Patients with a history of pancreatitis (only patients who are planning to undergo PD1 combined with pegaspargase are excluded). 2. Severe infections require ICU treatment. 3. Combined HCV or HIV infection. Patients with HBV infection who receive antiviral treatment at the same time will not be excluded. 4. There are serious complications such as fulminant DIC. 5. Impairment of important organ functions: such as respiratory failure, chronic congestive heart failure with NYHA grade ≥2, decompensated liver or kidney insufficiency, hypertension and diabetes that cannot be controlled despite active treatment, nearly 6 years old There were cardio-cerebrovascular thrombotic or hemorrhagic events within months. 6. Pregnant and lactating women. 7. Have a history of autoimmune diseases, have disease activity in the past 6 months, and are still receiving oral immunosuppressive therapy within the past three months, and the daily dose of oral prednisone is greater than 10 mg.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['NA'], 'designInfo': {'allocation': 'NON_RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 62, 'type': 'ACTUAL'}}
Updated at
2024-03-04

1 organization

1 product

2 indications