Volume 23 Issue 5
May  2025
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LIU Lin, XIE Zhibin, WANG Meng. Clinical observation of first-line treatment with Brentuximab Vedotin combined with chemotherapy in advanced classical Hodgkin lymphoma[J]. Chinese Journal of General Practice, 2025, 23(5): 780-784. doi: 10.16766/j.cnki.issn.1674-4152.004000
Citation: LIU Lin, XIE Zhibin, WANG Meng. Clinical observation of first-line treatment with Brentuximab Vedotin combined with chemotherapy in advanced classical Hodgkin lymphoma[J]. Chinese Journal of General Practice, 2025, 23(5): 780-784. doi: 10.16766/j.cnki.issn.1674-4152.004000

Clinical observation of first-line treatment with Brentuximab Vedotin combined with chemotherapy in advanced classical Hodgkin lymphoma

doi: 10.16766/j.cnki.issn.1674-4152.004000
Funds:

 2023AH052011

 2022byzd048

 2022byzd053

  • Received Date: 2024-10-28
    Available Online: 2025-08-14
  •   Objective  To evaluate the effect of Brentuximab Vedotin (BV) combined with doxorubicin (A), vindesine (V), and dacarbazine (D) (BV-AVD-regimen) as first-line treatment for advanced classical Hodgkin lymphoma (cHL).  Methods  Clinical data of 10 patients with advanced cHL admitted to the Department of Haematology, the First Affiliated Hospital of Bengbu Medical University, from August 2021 to January 2023 with first-line application of the BV-AVD regimen were retrospectively analyzed. Data reviewed included general characteristics [gender, age, pathological type, primary site, stage, international prognostic score (IPS), and immunohistochemistry], treatment response, follow-up outcomes, and adverse reactions.  Results  Among the 10 patients, 6 were male and 4 were female, with a mean age of (44.7±13.3) years. Pathologically, 6 cases were classified as nodular sclerosis type and 4 as mixed cellularity type. Eight patients initially presented with superficial lymphadenopathy, while abdominal pain and retrosternal pain were reported in one case each. Seven patients were diagnosed with stage Ⅳ disease, and 5 had an international prognostic score (IPS) of ≥4. B symptoms were observed in 5 cases at diagnosis. Immunohistochemical analysis revealed EBER positivity in 5 patients and CD163 positivity in 3. After 2 cycles of treatment, the objective response rate (ORR) was 100%, with a complete response (CR) rate of 80%. Among the 9 evaluable patients after 6 cycles, both the ORR and CR rates were 89%. The median overall survival (OS) and progression-free survival (PFS) were not reached during follow-up. Patients with CD163 positivity had significantly shorter OS and PFS compared to CD163-negative patients (P=0.007 and P=0.001, respectively). The most common adverse events included fatigue (8 cases), nausea (8 cases), neutropenia (7 cases), febrile neutropenia (6 cases), and peripheral neuropathy (6 cases). Grade 3 adverse events occurred in only 2 patients.  Conclusion  The short-term follow-up indicates that fist-line BV-AVD treatment is effective in patients with advanced cHL, with manageable adverse effects.

     

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