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http://hdl.handle.net/11452/27113
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DC Field | Value | Language |
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dc.contributor.author | Salihoğlu, Ayşe | - |
dc.contributor.author | Elverdi, Tuğrul | - |
dc.contributor.author | Karadoğan, İhsan | - |
dc.contributor.author | Paydaş, Semra | - |
dc.contributor.author | Özdemir, Evren | - |
dc.contributor.author | Erdem, Gökhan | - |
dc.contributor.author | Karadurmuş, Nuri | - |
dc.contributor.author | Akyol, Gülşah | - |
dc.contributor.author | Kaynar, L. | - |
dc.contributor.author | Yeğin, Zeynep Arzu | - |
dc.contributor.author | Şucak, Gülsan Türköz | - |
dc.contributor.author | Topçuoğlu, Pervin | - |
dc.contributor.author | Özcan, Muhit | - |
dc.contributor.author | Birtaş, Elif | - |
dc.contributor.author | Göker, Hakan | - |
dc.contributor.author | Başlar, Zafer | - |
dc.contributor.author | Ferhanoğlu, Burhan | - |
dc.date.accessioned | 2022-06-13T12:51:36Z | - |
dc.date.available | 2022-06-13T12:51:36Z | - |
dc.date.issued | 2015-03 | - |
dc.identifier.citation | Salihoğlu, A. vd. (2015). "Brentuximab vedotin for relapsed or refractory Hodgkin lymphoma: Experience in Turkey". Annals of Hematology, 94(3), 415-420. | en_US |
dc.identifier.issn | 0939-5555 | - |
dc.identifier.uri | https://doi.org/10.1007/s00277-014-2215-9 | - |
dc.identifier.uri | https://link.springer.com/article/10.1007/s00277-014-2215-9 | - |
dc.identifier.uri | http://hdl.handle.net/11452/27113 | - |
dc.description.abstract | Current treatment modalities can cure up to 70-80 % of patients with classical Hodgkin lymphoma. Approximately, 20-30 % of patients require further treatment options. Brentuximab vedotin has been approved for the treatment of relapsed and refractory Hodgkin lymphoma. In the present study, we report the experience with brentuximab vedotin as single agent in 58 patients with relapsed or refractory Hodgkin lymphoma. The objective response rate was 63.5 % with 13 complete responders (26.5 %) among 49 patients evaluated at the early phase of treatment (2-5 cycles). Upon treatment prolongation (a parts per thousand yen6 cycles), 37 patients achieved a final objective response rate of 32.4 % with 21.6 % of complete and 10.8 % of partial response. Overall survival at 12 months was 70.6 %, and progression-free survival at 12 months was 32.8 %. Median overall survival could not be reached and median progression-free survival was 7 months. While the median duration of response was 9 months in the whole cohort, it was 11.5 months in the complete responders. Complete response rates in patients treated with > 3 chemotherapy regimens before brentuximab vedotin were significantly lower (p = 0.016). Fourteen patients were subsequently transplanted. In conclusion, brentuximab vedotin provided a bridge to transplantation in approximately one quarter of the patients. The declining response rates during the course of treatment suggest that transplantation should be implemented early during brentuximab vedotin treatment. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Springer | en_US |
dc.rights | info:eu-repo/semantics/openAccess | en_US |
dc.rights | Atıf Gayri Ticari Türetilemez 4.0 Uluslararası | tr_TR |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/ | * |
dc.subject | Brentuximab vedotin | en_US |
dc.subject | Hodgkin Lymphoma | en_US |
dc.subject | Refractory | en_US |
dc.subject | Relapsed | en_US |
dc.subject | Transplantation | en_US |
dc.subject | Malignancies | en_US |
dc.subject | Intensity | en_US |
dc.subject | Hematology | en_US |
dc.subject.mesh | Adolescent | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Drug resistance, neoplasm | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Hodgkin disease | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Immunoconjugates | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle aged | en_US |
dc.subject.mesh | Recurrence | en_US |
dc.subject.mesh | Retrospective studies | en_US |
dc.subject.mesh | Treatment outcome | en_US |
dc.subject.mesh | Turkey | en_US |
dc.subject.mesh | Young adult | en_US |
dc.title | Brentuximab vedotin for relapsed or refractory Hodgkin lymphoma: Experience in Turkey | en_US |
dc.type | Article | en_US |
dc.identifier.wos | 000349225200007 | tr_TR |
dc.identifier.scopus | 2-s2.0-84925461571 | tr_TR |
dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi | tr_TR |
dc.contributor.department | Uludağ Üniversitesi/Tıp Fakültesi/İç Hastalıkları Anabilim Dalı/Hematoloji Bilim Dalı. | tr_TR |
dc.identifier.startpage | 415 | tr_TR |
dc.identifier.endpage | 420 | tr_TR |
dc.identifier.volume | 94 | tr_TR |
dc.identifier.issue | 3 | tr_TR |
dc.relation.journal | Annals of Hematology | en_US |
dc.contributor.buuauthor | Özkocaman, Vildan | - |
dc.contributor.researcherid | AAH-1854-2021 | tr_TR |
dc.relation.collaboration | Yurt içi | tr_TR |
dc.relation.collaboration | Sanayi | tr_TR |
dc.identifier.pubmed | 25231929 | tr_TR |
dc.subject.wos | Hematology | en_US |
dc.indexed.wos | SCIE | en_US |
dc.indexed.scopus | Scopus | en_US |
dc.indexed.pubmed | PubMed | en_US |
dc.wos.quartile | Q2 | en_US |
dc.contributor.scopusid | 6603145040 | tr_TR |
dc.subject.scopus | Brentuximab Vedotin; Hodgkin's Disease; Refractory Materials | en_US |
dc.subject.emtree | Brentuximab vedotin | en_US |
dc.subject.emtree | Antibody conjugate | en_US |
dc.subject.emtree | cAC10-vcMMAE | en_US |
dc.subject.emtree | Adolescent | en_US |
dc.subject.emtree | Adult | en_US |
dc.subject.emtree | Alopecia | en_US |
dc.subject.emtree | Article | en_US |
dc.subject.emtree | Cancer regression | en_US |
dc.subject.emtree | Constipation | en_US |
dc.subject.emtree | Cytopenia | en_US |
dc.subject.emtree | Drug dose reduction | en_US |
dc.subject.emtree | Drug efficacy | en_US |
dc.subject.emtree | Drug safety | en_US |
dc.subject.emtree | Fatigue | en_US |
dc.subject.emtree | Female | en_US |
dc.subject.emtree | Fever | en_US |
dc.subject.emtree | Follow up | en_US |
dc.subject.emtree | Hodgkin disease | en_US |
dc.subject.emtree | Human | en_US |
dc.subject.emtree | Limb pain | en_US |
dc.subject.emtree | Major clinical study | en_US |
dc.subject.emtree | Male | en_US |
dc.subject.emtree | Multiple cycle treatment | en_US |
dc.subject.emtree | Muscle spasm | en_US |
dc.subject.emtree | Myalgia | en_US |
dc.subject.emtree | Nausea | en_US |
dc.subject.emtree | Neuropathy | en_US |
dc.subject.emtree | Neurotoxicity | en_US |
dc.subject.emtree | Neutropenia | en_US |
dc.subject.emtree | Ophthalmoplegia | en_US |
dc.subject.emtree | Outcome assessment | en_US |
dc.subject.emtree | Overall survival | en_US |
dc.subject.emtree | Peripheral neuropathy | en_US |
dc.subject.emtree | Priority journal | en_US |
dc.subject.emtree | Progression free survival | en_US |
dc.subject.emtree | Pruritus | en_US |
dc.subject.emtree | Retrospective study | en_US |
dc.subject.emtree | Survival time | en_US |
dc.subject.emtree | Tonic seizure | en_US |
dc.subject.emtree | Treatment duration | en_US |
dc.subject.emtree | Treatment response | en_US |
dc.subject.emtree | Turkey (republic) | en_US |
dc.subject.emtree | Vomiting | en_US |
dc.subject.emtree | Clinical trial | en_US |
dc.subject.emtree | Drug effects | en_US |
dc.subject.emtree | Drug resistance | en_US |
dc.subject.emtree | Hodgkin disease | en_US |
dc.subject.emtree | Middle aged | en_US |
dc.subject.emtree | Multicenter study | en_US |
dc.subject.emtree | Pathology | en_US |
dc.subject.emtree | Recurrent disease | en_US |
dc.subject.emtree | Treatment outcome | en_US |
dc.subject.emtree | Turkey | en_US |
dc.subject.emtree | Young adult | en_US |
Appears in Collections: | Scopus Web of Science |
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