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Azacitidine Plus PD-1 Therapy for R/R Hodgkin Lymphoma

NCT06190067 — Phase 2, Recruiting, 40 participants, Navy General Hospital, Beijing

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Azacitidine Plus PD-1 Therapy for Relapsed/Refractory Hodgkin Lymphoma

RegistryNCT06190067
StatusRecruiting
PhasePhase 2
Study typeInterventional; na, single group, masking: none, treatment
Enrollment40 (Estimated)
SponsorNavy General Hospital, Beijing (Other)
ConditionsRelapsed Classic Hodgkin Lymphoma, Refractory Classic Hodgkin Lymphoma
InterventionsAzacitidine Plus PD-1 therapy (Drug)
Datesstart 2023-10-30, primary completion 2026-12-01 (estimated), completion 2028-12-01 (estimated), first posted 2024-01-05, last updated 2024-01-30
Locations1 site in China

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-Summary

The goal of this phase 2 trial is to test the safety and efficacy of azacitidine when given together with PD-1 therapy in treating patients with relapsed/refractory classic Hodgkin lymphoma.

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+Detailed description

The investigators will evaluate response rate, progression free survival (PFS), overall survival (OS), and toxicity of azacytidine combined with PD-1 therapy in classic relapsed/refractory Hodgkin lymphoma.

+Arms and interventions

ArmTypeInterventionsDescription
Azacitidine Plus PD-1 therapyExperimentalDrug: Azacitidine Plus PD-1 therapyPatients were treated by Azacitidine plus PD-1 therapy
  • Azacitidine Plus PD-1 therapy (Drug), also known as Azacitidine Plus PD-1 antibody: Patients were treated by Azacytidine(75 mg/m2 subcutaneous injection qd on days 1-7) plus PD-1 therapy(200mg iv qd d8)

+Outcome measures

Primary outcomes

  • Overall Response Rate (ORR) [1 year]: ORR was defined as the proportion of patients who achieved CR or PR as their best response

Secondary outcomes

  • Overall Survival (OS) [through study completion, an average of 2 year]: OS was defined as time from diagnosis to death from any cause or the last follow-up
  • Progression Free Survival (PFS) [18 months]: PFS using local assessment of progressive disease according to Lugano Response Criteria (2014)

+Eligibility

Sex: All, ages: 18 Years to any

Inclusion Criteria:

* Pathologically confirmed Hodgkin Lymphoma according World Health Organization (WHO) classification.
* Patient is ≥ 18 years of age at the time of signing the informed consent form (ICF).
* Patient must understand and voluntarily sign an ICF prior to any study-specific assessments/procedures being conducted.
* Patient is willing and able to adhere to the study visit schedule and other protocol requirements.
* Relapsed (after partial or complete response) or refractory AITL after at least one line of systemic therapy (there is no mandatory resting period after the previous treatment as long as the biochemistry and hematology labs meet the inclusion criteria as below).
* Meet the following lab criteria: Absolute Neutrophil Count (ANC) ≥ 1,5 x 10\^9/L (≥ 1 x 10\^9/L if bone marrow (BM) involvement by lymphoma); Platelet ≥ 75 x 10\^9/L (≥ 50 x 10\^9/L if BM involvement by lymphoma); Hemoglobin ≥ 8 g/dL.
* Anticipated life expectancy at least 3 months.

Exclusion Criteria:

* Active or uncontrolled infections requiring systemic treatment within 14 days before enrollment.
* Any instability of systemic disease, including but not limited to severe cardiac, liver, kidney, or metabolic disease need therapy.
* Pregnant or lactating women.

+Locations (1)

FacilityCityCountryStatus
Navy General HospitalBeijing, Beijing MunicipalityChinaRecruiting

+Investigators

My Notes