Sufficient-dose Brentuximab vedotin improves prognosis in patients with classic Hodgkin lymphoma: a single-center real-world study in China - Report - MDSpire
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Sufficient-dose Brentuximab vedotin improves prognosis in patients with classic Hodgkin lymphoma: a single-center real-world study in China
Clinical Report: Optimized Dosing of Brentuximab Vedotin Enhances Outcomes
Overview
This study evaluates the efficacy and safety of brentuximab vedotin (BV) in combination with an A-AVD-like regimen compared to an ABVD-like regimen in Chinese patients with classic Hodgkin lymphoma (cHL).
Background
Classic Hodgkin lymphoma (cHL) is a highly curable malignancy, yet some patients experience poor outcomes with standard regimens like ABVD. The incorporation of targeted therapies such as brentuximab vedotin (BV) aims to enhance treatment efficacy while mitigating associated toxicities.
Data Highlights
Regimen
2-Year PFS Rate
Peripheral Neuropathy Rate
ABVD
71.1%
5.2%
A-AVD
76.7%
47.1%
Key Findings
The A-AVD group had a higher proportion of elderly patients (≥60 years) compared to the ABVD group (25.5% vs. 9.4%, p = 0.002).
First-evaluation complete response rates were similar between ABVD and A-AVD (CR: 69.3% vs. 72.5%, p = 0.549).
Overall progression-free survival (PFS) and overall survival (OS) showed no significant differences between the two regimens (PFS p=0.489; OS p = 0.230).
In patients with Ann Arbor stage III-IV, a sufficient dose of BV (≥1.15 mg/kg) significantly improved PFS compared to a reduced dose (<1.15 mg/kg) (2-year PFS 91.7% vs. 58.7%; p=0.036).
The A-AVD group exhibited a higher rate of peripheral neuropathy (47.1% vs. 5.2%, p < 0.001).
Incidences of grade 3–4 neutropenia were comparable between the two groups (17.7% in ABVD vs. 19.6% in A-AVD, p = 0.751).
Clinical Implications
Clinicians should be aware of the increased risk of peripheral neuropathy with the A-AVD regimen.
Conclusion
This study presents findings on the dosing of brentuximab vedotin in patients with classic Hodgkin lymphoma.