Abstract
Background: Brentuximab-vedotin (BV) monotherapy has shown high efficacy in heavily pre-treated patients with relapsed or refractory Hodgkin lymphoma (HL) after high-dose chemotherapy or autologous stem cell transplantation (ASCT). We retrospectively analyzed the outcomes of treatment with BV of HL patients and examined the predictive ability of PET-CT for response in this setting. Patients and methods: Records of 49 HL patients (median age, 39 years, 55% male) treated with BV for relapse (71.4%) or consolidation (28.6%) post-ASCT were analyzed. Patients who did not reach complete response (CR) on PET/CT after 4 cycles (non-responders) discontinued BV and received the next treatment line. Overall survival (OS) and progression-free survival (PFS) were compared between responders and non-responders. Results: After a median follow-up of 19.1 months, all consolidation patients were alive and none progressed. Median OS in 23 relapsed patients that did not achieve CR after 4 cycles and continued to the next treatment was 55.0 months, while all those in CR (n = 24) were alive (P = .0120). No statistically significant differences in OS were observed between responders and non-responders with relapsed HL (P = .1072). Median PFS evaluated after 4 BV cycles was significantly longer in responders compared to non-responders (47.9 vs. 1.5 months, P < .0001). Neuropathy and neutropenia were the main toxicities observed. Conclusions: HL patients treated with BV for relapse or consolidation who achieved CR by PET-CT after 4 cycles showed improved PFS and OS compared to non-responders. Non-responders treated for relapsed HL who proceeded to the next treatment line demonstrated comparable OS to responders.
| Original language | English |
|---|---|
| Pages (from-to) | e929-e937 |
| Journal | Clinical Lymphoma, Myeloma and Leukemia |
| Volume | 21 |
| Issue number | 12 |
| DOIs | |
| State | Published - Dec 2021 |
Bibliographical note
Publisher Copyright:© 2021 Elsevier Ltd
Funding
A.A. received research grants from Janssen and Bristol-Myers Squibb, consulting fees from Takeda, Gilead and Roche, honoraria from Takeda, and participated in advisory boards for Takeda, Gilead, Roche and Novartis. M.K. received research grants from Janssen and Bristol-Myers Squibb and received consulting fees from Takeda. All other authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
| Funders |
|---|
| Novartis |
| Roche |
| Gilead Sciences |
| Takeda Pharmaceutical Company |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Imaging
- Overall survival
- Progression free survival
- antibody-drug conjugate
- consolidation
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