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Completed

NCT Number: NCT05058755

Tislelizumab Combined Treatment in Refractory Extranodal NK/T-cell Lymphoma

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.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Xinhua Hospital,Shanghai Jiao Tong University School of Medicine

Shanghai, Shanghai Municipality, 200092, China

About this study

About 20-30% of early-stage patients and 40-60% of late-stage NKTCL patients will experience disease relapse and refractory disease, and the median survival time of relapsed patients is about 6 months. PD-1 antibody is an effective drug for the treatment of patients with relapsed/refractory NKTCL, but the response rate and complete remission rate of monotherapy are low. How to improve the prognosis of patients is an important way to try combination therapy. In this study, we aim to explore the effectiveness and safety of a novel anti-PD-1 antibody, tislelizumab, in combination with different drugs (tislelizumab plus azacytidine and lenalidomide, or tislelizumab plus etoposide and pegaspargase) to treat refractory NK/T.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with biopsy histopathology, immunohistochemistry and EBER test meet ing the WHO 2016 diagnostic criteria for NK/T cell lymphoma.
  • With progressive disease after asparaginase-based combined chemotherapy
  • Have experienced multiple courses of PD-1/PD-L1 treatment with non-responsive or progressive disease.
  • PET/CT or CT/MRI with at least one measurable lesion or objectively evaluable lesion.
  • General ECOG score 0-3 points.
  • 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.

  • Signed informed consent form.
  • Voluntarily comply with research protocols, follow-up plans, laboratory and auxiliary examinations.

Exclusion criteria

  • Patients with a history of pancreatitis (only patients who are planning to undergo PD1 combined with pegaspargase are excluded).
  • Severe infections require ICU treatment.
  • Combined HCV or HIV infection. Patients with HBV infection who receive antiviral treatment at the same time will not be excluded.
  • There are serious complications such as fulminant DIC.
  • 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.
  • Pregnant and lactating women.
  • 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.

Treatment and study plan

tislelizumab, azacytidine, lenalidomide

Drug

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.

Other names: Tileilizhu Dankang

tislelizumab, etoposide, pegaspargase

Drug

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

Other names: Tileilizhu Dankang

Primary outcomes

  1. Overall response rate

    Time frame: Week 12 +/-7 days

    The overall response rate will be assessed on Week 12

Secondary outcomes

  1. Complete response rate

    Time frame: Week 12 +/-7 days

    The complete response rate will be assessed on Week 12

  2. Progression free survival

    Time frame: 1-year

    Progression free survival is the time from entry onto the treatment until lymphoma progression or death of any reason.

  3. Overall survival

    Time frame: 1-year

    Overall survival is defined as the time from entry onto the treatment until death of any reason

  4. Treatment-Related Adverse Events as Assessed by CTCAE v5.0

    Time frame: Treatment-Related Adverse Events will be assessed and graded by NCI CTCAE v5.0.

    From day 1 of each course of chemotherapy to the 3 months after the last dose of therapy

Sponsors and collaborators

Lead sponsor

Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

Other

Registry information

Official study title

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

Important dates

Study start
2021
Primary completion
2022
Study completion
2023
First posted
Sep 28, 2021
Registry last updated
Mar 4, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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