Publication: Sequencing novel agents in the treatment of classical Hodgkin lymphoma
dc.contributor.coauthor | Ozbalak, Murat | |
dc.contributor.department | School of Medicine | |
dc.contributor.kuauthor | Ferhanoğlu, Ahmet Burhan | |
dc.contributor.schoolcollegeinstitute | SCHOOL OF MEDICINE | |
dc.date.accessioned | 2025-01-19T10:30:57Z | |
dc.date.issued | 2023 | |
dc.description.abstract | IntroductionClassical Hodgkin lymphoma (cHL) is a curable disease, with durable remission achieved in about 80% of patients following first-line treatment. Three new drugs were introduced to the daily use in cHL: brentuximab vedotin (BV), nivolumab, and pembrolizumab. All three drugs were initially approved for the treatment of relapsed/refractory cHL (RRHL) and with their promising outcomes, they are now incorporated in different stages of the treatment.Areas coveredWe performed a literature search using PubMed on all cHL studies investigating BV and CPIs within the past 10 years. We analyzed literature to presume the sequencing of these novel agents.Expert opinionAddition of BV or nivolumab to AVD backbone in the frontline setting showed promising activity in advanced stage cHL. BV and CPIs combined with chemotherapy in the second-line treatment of cHL are evaluated in phase 2 studies and comparable results are reported. The results of BrECADD, with good efficacy and toxicity profile, should be followed. Pembrolizumab was shown to be more effective in RRHL compared to BV in patients who have relapsed post-ASCT or ineligible for ASCT. BV is used in post-ASCT maintenance in high-risk cases, although its role will be questioned as it is increasingly used in the frontline treatment. | |
dc.description.indexedby | WOS | |
dc.description.indexedby | Scopus | |
dc.description.indexedby | PubMed | |
dc.description.issue | 12 | |
dc.description.publisherscope | International | |
dc.description.sponsoredbyTubitakEu | N/A | |
dc.description.volume | 16 | |
dc.identifier.doi | 10.1080/17474086.2023.2276212 | |
dc.identifier.eissn | 1747-4094 | |
dc.identifier.issn | 1747-4086 | |
dc.identifier.quartile | Q2 | |
dc.identifier.scopus | 2-s2.0-85176916714 | |
dc.identifier.uri | https://doi.org/10.1080/17474086.2023.2276212 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14288/26157 | |
dc.identifier.wos | 1102961700001 | |
dc.keywords | Classical Hodgkin lymphoma | |
dc.keywords | Brentuximab vedotin | |
dc.keywords | Checkpoint inhibitor | |
dc.keywords | Nivolumab | |
dc.keywords | Pembrolizumab | |
dc.keywords | Anti-PD1 antibody | |
dc.language.iso | eng | |
dc.publisher | Taylor & Francis Ltd | |
dc.relation.ispartof | Expert Review of Hematology | |
dc.subject | Hematology | |
dc.title | Sequencing novel agents in the treatment of classical Hodgkin lymphoma | |
dc.type | Review | |
dspace.entity.type | Publication | |
local.contributor.kuauthor | Ferhanoğlu, Ahmet Burhan | |
local.publication.orgunit1 | SCHOOL OF MEDICINE | |
local.publication.orgunit2 | School of Medicine | |
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