drugset / Trial / NCT06563245

Summary

Generally, pediatric patients tolerate acute toxicities but are vulnerable to late effects. Thus, increasing chemotherapy intensity to achieve more rapid complete early response to limit radiation therapy is worth testing. In this CCCG-HL-2024 study, Brentuximab vedotin (Bv) was used to replace VCR and bleomycin in the ABVE-PC regimen in the previous CCCG-HD-2018 study, respectively, to form a Bv-AEPC regimen for the treatment of newly diagnosed classic Hodgkin lymphoma (cHL) in children, adolescents and young adults. On the premise of maintaining a 4-year event free survival (EFS)\>90% in the low-, intermediate-and high-risk groups, increase the early assessment complete response rate (the overall early complete response rate increased by 20%, that is, from 54.0% to 74.0%) to further reduce the proportion of children receiving radiotherapy to benefit them.

Timeline

Start
2024-09-25
Primary completion
2029-11-15
Completion
2039-11-15

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Bedamustine Unknown 180 mg/m2
Subject Brentuximab Vedotin Monoclonal antibody 1.8 mg/kg
Subject Cyclophosphamide Other / unclassified 600 mg/m2
Subject Dacarbazine Small molecule 250 mg/m2
Subject Doxorubicin Other / unclassified 25 mg/m2
Subject Etoposide Small molecule 125 mg/m2
Subject Prednisone Other / unclassified 20 mg/m2 Oral
Subject Tislelizumab Monoclonal antibody 3 mg/kg