PD-1 Inhibitor Combined With Decitabine Followed by ASCT as Second-line Therapy for Relapsed or Refractory Classic Hodgkin's Lymphoma

  • STATUS
    Recruiting
  • End date
    Jan 22, 2025
  • participants needed
    47
  • sponsor
    Institute of Hematology & Blood Diseases Hospital
Updated on 22 December 2021
platelet count
lymphoma
pd-1 inhibitor

Summary

Young patients with relapsed or refractory classic Hodgkin's lymphoma will be treated with PD-1 inhibitor combined with decitabine as second-line salvage treatment for four cycles. If PR or CR was obtained after salvage treatment, patients will receive GBM conditioning regimen followed by ASCT as consolidation therapy. High-risk R/R cHL patients will be treated with PD-1 inhibitor after ASCT for 1 year. The purpose of current study is to determine the clinical efficacy and safety of PD-1 inhibitor combined with decitabine followed by ASCT as second-line treatment in patients with relapsed or refractory classic Hodgkin's lymphoma.

Details
Condition Hodgkin Lymphoma, Adult, Relapse, Refractory Hodgkin Lymphoma
Treatment PD-1 Inhibitor
Clinical Study IdentifierNCT05137886
SponsorInstitute of Hematology & Blood Diseases Hospital
Last Modified on22 December 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Subjects must have histological confirmation of relapsed or refractory classic Hodgkin lymphoma (HL)
18 to 65 years of age
Subjects with lymphoma must have at least one measureable lesion >1 cm as defined by lymphoma response criteria
Proper functioning of the major organs: 1) The absolute value of neutrophils (≥1×10^9/L); 2) platelet count (≥75×10^9/L); 3) Serum creatinine <1.5 times Upper Limit Normal (ULN) ; 4) Serum total bilirubin < 1.5 times ULN; 5) Aspartate Aminotransferase (AST), Alanine Aminotransferase (ALT) ≤3 times ULN; 6) Serum creatinine (Cr) ≤2 ULN, or glomerular filtration rate ≥40ml/min; 7) Thyrotropin (TSH) or free thyroxine (FT4) or free triiodothyronine (FT3) were all within the normal range (±10%)
Eastern Cooperative Oncology Group (ECOG) Performance status 0-2
LVEF value measured by echocardiography ≥50%
Life expectancy > 3 months

Exclusion Criteria

Patients with central nervous system involvement by lymphoma
Patients with active autoimmune diseases requiring systematic treatment in the past two years (hormone replacement therapy is not considered systematic treatment, such as type I diabetes mellitus, hypothyroidism requiring only thyroxine replacement therapy, adrenocortical dysfunction or pituitary dysfunction requiring only physiological doses of glucocorticoid replacement therapy); Patients with autoimmune diseases who do not require systematic treatment within two years can be enrolled
Known systemic vasculitides, primary or secondary immunodeficiency(such as HIV infection or severe inflammatory disease)
Pregnant or breastfeeding women
Major surgery within 4 weeks before enrollment
Impaired cardiac function:Ejection fraction <50% on MUGA scan. QTc interval > 450msecs on baseline ECG. Myocardial infarction within 6 months prior to starting study; other clinically significant heart disease (e.g. unstable angina, congestive heart failure or uncontrolled hypertension, uncontrolled arrhythmias)
Other concurrent severe and/or uncontrolled medical conditions: Patients with another primary malignant disease, except those that do not currently require treatment; acute or chronic liver, pancreatic or severe renal disease; another severe and/or life-threatening medical disease
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