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NCT Number: NCT05182957

Clinical Study on Anti-PD-1 Plus Lenalidomide and Azacitidine in Relapsed/Refractory Peripheral T-cell Lymphoma

Aim of this study will evaluate the Efficacy and Safety of Anti-PD-1 monoclonal antibody Combined Lenalidomide and Azacitidine in Relapsed/Refractory Peripheral T-cell Lymphoma Patients.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

The First Affiliated Hospital of Soochow University

Suzhou, Jiangsu, 215000, China

Location status: Recruiting

Location contact

Caixia Li, M.D

CONTACT

[email protected]

+86 512 67781856

About this study

Peripheral T-cell lymphomas (PTCLs) are malignancies of immunologically mature T-cells that arise in peripheral lymphoid tissues. Compared with B-cell lymphoma, the treatment methods of PTCL are more limited, the first-line therapy is usually CHOP-like therapy, but the efficacy is poor, 5-year overall survival rate (OS) is only 30%-40%. Anti-PD-1 monoclonal antibody, Lenalidomide and Azacitidine can all have tumor-killing effects, and the three have complementary theoretical basis in the mechanism of action. This study will evaluate the efficacy and safety of Anti-PD-1 monoclonal antibody Combined Lenalidomide and Azacitidine in Relapsed/Refractory Peripheral T-cell Lymphoma patients.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Pathological immunohistochemistry or flow cytometry confirmed that R/R PTCL with measurable (diameter greater than 1.5cm) lesions meets any of the following conditions: 1> After 4 courses of standard first-line therapy or 2 courses of more than two-line therapy, the lesions were reduced by <50%; 2> PTCL with disease progression after first-line or induction therapy; 3> After hematopoietic stem cell transplantation, new lesions appear or the size of previously affected lesions increased by more than 50%.
  • Age ≥ 18 years.
  • ECOG≤2分.
  • The main organ functions need to meet the following conditions:Hemogram needs to meet HB ≥70*1012/L,PLT≥50*109/L,NE≥1*109/L;LVEF≥50%;CR≤132umol/l or CCr≥60 ml/min;ALT and AST≤2 times normal range;Lung function≤Level 1;dyspnea(CTCAE v5.0),and blood oxygen saturation without oxygen absorption> 91%.
  • Subjects of child-bearing or child-fathering potential must be willing to practice birth control from the time of enrollment on this study until the follow-up one year period of the study.
  • Estimated survival time ≥3 months.
  • Voluntary signing of informed consent.

Exclusion criteria

  • Accepted major surgery within 4 weeks before treatment.
  • Prior malignancy (other than Relapsed/Refractory Peripheral T-cell Lymphoma), except for cured malignant tumors with no active lesions for 3 years;Adequate treatment of inactive lesions in non-melanoma skin cancer,malignant tonsilloma or carcinoma in situ;
  • Patients who have previously received failed allogeneic hematopoietic stem cell transplantation.
  • Have stroke or intracranial hemorrhage within 3 months.
  • Evidence of complications or medical conditions, including but not limited, that may interfere the conduct of the study or place the patient at serious risk:significant cardiovascular disease(class 3 or 4 cardiac disease as defined by the New York Heart Association Functional Classification、myocardial infarction within 6 months of screening、uncontrolled or symptomatic arrhythmias) and/or significant lung disease.
  • HIV infection and/or active hepatitis B or active hepatitis C.
  • Uncontrolled systemic infection.
  • Pregnant or breasting-feeding women.
  • According to the researchers' judgment, any life-threatening disease, medical condition or organ system dysfunction which can endanger the patient's safety and Interfer with the absorption or metabolism of anti-PD-1 monoclonal antibody plus Lenalidomide and Azacitidine,may put the results of a study at unnecessary risk.

Treatment and study plan

Anti-PD-1 monoclonal antibody

Drug

Anti-PD-1 monoclonal antibody, 200mg i.v d1 (/21d)

Other names: Anti-PD-1 antibody

Lenalidomide

Drug

Lenalidomide 25mg qd po d1-d10 (/21d)

Other names: Immunomodulator

Azacitidine

Drug

Azacitidine 75mg/m2 i.v d1-d7 (/21d)

Other names: 5-Ladakamycin

Primary outcomes

  1. Overall Response Rate (ORR) at 6 cycles

    Time frame: From date of first dose until completion of 6 treatment cycles, assessed up to approximately 20 weeks.

    The percentage of participants achieving a best overall response of confirmed Complete Response (CR) or Partial Response (PR) after treatment by Anti-PD-1 antibody plus Lenalidomide and Azacitidine.

Secondary outcomes

  1. Complete Response Rate at 6 cycles

    Time frame: From date of first dose until completion of 6 treatment cycles, assessed up to approximately 20 weeks.

    The percentage of patients who achieved complete response after treatment by Anti-PD-1 antibody plus Lenalidomide and Azacitidine

  2. 3-year progression-free survival (PFS) rate

    Time frame: up to 3 years

    3-year PFS rate is defined as the percentage of participants who are alive and free from disease progression at 3 years from the first dose of treatment. Participants who are alive and progression-free or lost to follow-up before 3 years will be censored at the date of last adequate tumor assessment.

  3. 3-year Overall Survival(OS) Rate

    Time frame: up to 3 years

    3-year OS rate is defined as the percentage of participants who are alive at 3 years from the first Anti-PD-1 antibody plus Lenalidomide and Azacitidine. Participants who are alive or lost to follow-up before 3 years will be censored at the date of last known follow-up.

  4. Adverse events profile

    Time frame: Measured from start of treatment until 28 days after last dose

    Number of participants with adverse events. Frequencies of toxicities based on the NCI Common Terminology Criteria for Adverse Events (CTCAE), version 5.0 will be tabulated

Study contacts

Contact information is provided by the study sponsor or research team.

Caixia Li, M.D

CONTACT

[email protected]

+86 512 67781856

Sponsors and collaborators

Lead sponsor

The First Affiliated Hospital of Soochow University

Other

Registry information

Official study title

Clinical Study on the Efficacy and Safety of Anti-PD-1 Monoclonal Antibody Combined Lenalidomide and Azacitidine in Relapsed/Refractory Peripheral T-cell Lymphoma

Important dates

Study start
2020
Primary completion
2023
Study completion
2026
First posted
Jan 10, 2022
Registry last updated
May 1, 2026

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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