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Recruiting NCT05595447

Treatment Strategy for Relapsed/Refractory Hodgkin Lymphoma

Phase II / Phase III Interventional Hodgkin Lymphoma Refractory Hodgkin Lymphoma Relapsed Hodgkin's Disease, Adult

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Brentuximab Vedotin 50 MG [Adcetris].
Who it may be relevant to
Registry conditions: Hodgkin Lymphoma, Refractory Hodgkin Lymphoma, Relapsed Hodgkin's Disease, Adult. Basic parameters: 15 years — 90 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Mexico
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Rescue With Brentuximab Plus PD-1 Blockade Followed by Autotransplantation and Consolidation With Brentuximab Plus PD-1 Blockade in Patients With Relapsed/Refractory Hodgkin Lymphoma: Exploratory Single-arm Analysis

Overview

The choice of the best second-line therapy in patients with high LH R/R risk, it is a niche of knowledge not covered at the moment, especially the role of Brentuximab (BV) plus PD-1 blockade and auto-HSCT. What is the progression-free survival and rate of metabolic responses complete in patients with high-risk R/R HL with the treatment strategy: BV+ PD-1 blockade consolidation with Auto-HSCT and maintenance with BV + PD-blockade 1?

Detailed description

Patientes with Refractory/relapsed Hodgkin Lymphoma (HL R/R) with multiple failed therapies represent a therapeutic dilemma. The goal of next-line treatment is long-term disease control with manageable adverse reactions. Given the limited therapeutic options for patients with HL R/R, better therapies should be sought, more effective, with better tolerability, less toxicity, with increased overall survival (OS) of the patients, with the aim of improving outcomes in terms of disease-free survival progression (PFS) of the current standard treatment. Since currently only 50% of the patients with high-risk R/R HL treated with the standard regimen achieve healing. The high effectiveness and low toxicity of immunotherapy with prolonged remission or stabilization of the disease make it a new treatment option promising for HL R/R. Based on the above, a treatment strategy is proposed to rescue base with Brentuximab plus PD-1 blockade followed by autotransplantation and consolidation with Brentuximab plus PD-1 blockade in patients with Hodgkin lymphoma High-Risk Relapse/Refractory Compared to Reported OS and PFS Rates in the literature obtained with standard treatment.

Interventions

  • Drug Brentuximab Vedotin 50 MG [Adcetris]
    Brentuximab plus blocked PD-1 plus ASCT plus maintenance Brentuximab plus blocked PD-1

Primary outcome measures

  • Progression free survival [Time frame: 24 months]
Secondary outcome measures (2)
  • complete remission [Time frame: 24 months]
  • overall survival [Time frame: 24 months]

Eligibility criteria

Inclusion criteria

  • Relapsed/refractory Hodgkin lymphoma to ABVD with definition of high risk.
  • Age ≥ 18 years and ≤ 90 years.
  • Adequate liver function, defined as:
  • Total serum bilirubin ≤ 1.5 x upper limit of normal (ULN)
  • Serum aspartate aminotransferase (AST) ≤ 3.0 x ULN
  • Serum alanine aminotransferase (ALT) ≤ 3.0 x ULN
  • Adequate renal functions, defined as:
  • Serum creatinine ≤ 1.5x ULN or glomerular filtration rate \> 50ml/min.
  • ECOG performance status ≤ 3
  • Women of reproductive potential should have a serum pregnancy test or negative urine.
  • Prior signature of the informed consent.

Exclusion criteria

  • Voluntary withdrawal from the study.
  • Develop grade 3 or 4 toxicity according to the INH scale.
  • Loss of follow-up

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

Mexico · 1 center
  • Hospital Regional Alta Especialidad Bajio — León

Publications

  • Barrera Chavez ID, Viloria Alvarez JC, Zendejas Sanchez V, Rodriguez Esquivel A, Alvarez Salinas A, Amador Medina LF. Efficacy of Brentuximab-Vedotin Combined with PD-1 Inhibitors in Relapsed/Refractory Hodgkin Lymphoma with ASCT Consolidation and Maintenance Therapy: A Phase 2 Clinical Trial. Indian J Hematol Blood Transfus. 2026 Jan;42(1):93-99. doi: 10.1007/s12288-025-01986-0. Epub 2025 Feb 17. PMID 41522540

Identifiers

NCT: NCT05595447 · CI/HRAEB/038/2022

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗