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Ofatumumab with iphosphamide, etoposide and cytarabine for patients with transplantation‐ineligible relapsed and refractory diffuse large B‐cell lymphoma
The efficacy of salvage treatment of diffuse large B‐cell lymphoma (DLBCL) patients who relapse or progress (rrDLBCL) after initial therapy is limited. Efficacy and safety of ofatumumab with iphosphamide, etoposide and cytarabine (O‐IVAC) was evaluated in a single‐arm study. Dosing was modified for...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322457/ https://www.ncbi.nlm.nih.gov/pubmed/35362096 http://dx.doi.org/10.1111/bjh.18166 |
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author | Paszkiewicz‐Kozik, Ewa Michalski, Wojciech Taszner, Michał Mordak‐Domagała, Monika Romejko‐Jarosińska, Joanna Knopińska‐Posłuszny, Wanda Najda, Jacek Borawska, Anna Chełstowska, Monika Świerkowska, Monika Dąbrowska‐Iwanicka, Anna Malenda, Agata Druzd‐Sitek, Agnieszka Konecki, Robert Kumiega, Beata Osowiecki, Michał Ostrowska, Beata Szpila, Tomasz Szymański, Marcin Targoński, Łukasz Domańska‐Czyż, Katarzyna Popławska, Lidia Giebel, Sebastian Lange, Andrzej Pluta, Andrzej Zaucha, Jan Maciej Rymkiewicz, Grzegorz Walewski, Jan |
author_facet | Paszkiewicz‐Kozik, Ewa Michalski, Wojciech Taszner, Michał Mordak‐Domagała, Monika Romejko‐Jarosińska, Joanna Knopińska‐Posłuszny, Wanda Najda, Jacek Borawska, Anna Chełstowska, Monika Świerkowska, Monika Dąbrowska‐Iwanicka, Anna Malenda, Agata Druzd‐Sitek, Agnieszka Konecki, Robert Kumiega, Beata Osowiecki, Michał Ostrowska, Beata Szpila, Tomasz Szymański, Marcin Targoński, Łukasz Domańska‐Czyż, Katarzyna Popławska, Lidia Giebel, Sebastian Lange, Andrzej Pluta, Andrzej Zaucha, Jan Maciej Rymkiewicz, Grzegorz Walewski, Jan |
author_sort | Paszkiewicz‐Kozik, Ewa |
collection | PubMed |
description | The efficacy of salvage treatment of diffuse large B‐cell lymphoma (DLBCL) patients who relapse or progress (rrDLBCL) after initial therapy is limited. Efficacy and safety of ofatumumab with iphosphamide, etoposide and cytarabine (O‐IVAC) was evaluated in a single‐arm study. Dosing was modified for elderly patients. Patients received up to six cycles of treatment. The primary end‐point was the overall response rate (ORR). Patients were evaluated every two cycles and then six and 12 months after treatment. Other end‐points included progression‐free survival (PFS), event‐free survival (EFS), overall survival (OS) and safety. Seventy‐seven patients received salvage treatment with O‐IVAC. The average age was 56.8 years; 39% had an Eastern Cooperative Oncology Group (ECOG) performance status of at least 3; 78% had disease of Ann Arbor stage 3 or 4; 58% received one or more prior salvage therapies. The ORR for O‐IVAC was 54.5%. The median duration of study follow‐up was 70 months. The median PFS and EFS were 16.3 months each. The median OS was 22.7 months. Age, ECOG performance status and the number of prior therapy lines were independent predictors of survival. Treatment‐related mortality was 15.5%. O‐IVAC showed a high response rate in a difficult‐to‐treat population and is an attractive treatment to bridge to potentially curative therapies. |
format | Online Article Text |
id | pubmed-9322457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93224572022-07-30 Ofatumumab with iphosphamide, etoposide and cytarabine for patients with transplantation‐ineligible relapsed and refractory diffuse large B‐cell lymphoma Paszkiewicz‐Kozik, Ewa Michalski, Wojciech Taszner, Michał Mordak‐Domagała, Monika Romejko‐Jarosińska, Joanna Knopińska‐Posłuszny, Wanda Najda, Jacek Borawska, Anna Chełstowska, Monika Świerkowska, Monika Dąbrowska‐Iwanicka, Anna Malenda, Agata Druzd‐Sitek, Agnieszka Konecki, Robert Kumiega, Beata Osowiecki, Michał Ostrowska, Beata Szpila, Tomasz Szymański, Marcin Targoński, Łukasz Domańska‐Czyż, Katarzyna Popławska, Lidia Giebel, Sebastian Lange, Andrzej Pluta, Andrzej Zaucha, Jan Maciej Rymkiewicz, Grzegorz Walewski, Jan Br J Haematol Haematological Malignancy‐clinical The efficacy of salvage treatment of diffuse large B‐cell lymphoma (DLBCL) patients who relapse or progress (rrDLBCL) after initial therapy is limited. Efficacy and safety of ofatumumab with iphosphamide, etoposide and cytarabine (O‐IVAC) was evaluated in a single‐arm study. Dosing was modified for elderly patients. Patients received up to six cycles of treatment. The primary end‐point was the overall response rate (ORR). Patients were evaluated every two cycles and then six and 12 months after treatment. Other end‐points included progression‐free survival (PFS), event‐free survival (EFS), overall survival (OS) and safety. Seventy‐seven patients received salvage treatment with O‐IVAC. The average age was 56.8 years; 39% had an Eastern Cooperative Oncology Group (ECOG) performance status of at least 3; 78% had disease of Ann Arbor stage 3 or 4; 58% received one or more prior salvage therapies. The ORR for O‐IVAC was 54.5%. The median duration of study follow‐up was 70 months. The median PFS and EFS were 16.3 months each. The median OS was 22.7 months. Age, ECOG performance status and the number of prior therapy lines were independent predictors of survival. Treatment‐related mortality was 15.5%. O‐IVAC showed a high response rate in a difficult‐to‐treat population and is an attractive treatment to bridge to potentially curative therapies. John Wiley and Sons Inc. 2022-04-01 2022-07 /pmc/articles/PMC9322457/ /pubmed/35362096 http://dx.doi.org/10.1111/bjh.18166 Text en © 2022 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Haematological Malignancy‐clinical Paszkiewicz‐Kozik, Ewa Michalski, Wojciech Taszner, Michał Mordak‐Domagała, Monika Romejko‐Jarosińska, Joanna Knopińska‐Posłuszny, Wanda Najda, Jacek Borawska, Anna Chełstowska, Monika Świerkowska, Monika Dąbrowska‐Iwanicka, Anna Malenda, Agata Druzd‐Sitek, Agnieszka Konecki, Robert Kumiega, Beata Osowiecki, Michał Ostrowska, Beata Szpila, Tomasz Szymański, Marcin Targoński, Łukasz Domańska‐Czyż, Katarzyna Popławska, Lidia Giebel, Sebastian Lange, Andrzej Pluta, Andrzej Zaucha, Jan Maciej Rymkiewicz, Grzegorz Walewski, Jan Ofatumumab with iphosphamide, etoposide and cytarabine for patients with transplantation‐ineligible relapsed and refractory diffuse large B‐cell lymphoma |
title | Ofatumumab with iphosphamide, etoposide and cytarabine for patients with transplantation‐ineligible relapsed and refractory diffuse large B‐cell lymphoma |
title_full | Ofatumumab with iphosphamide, etoposide and cytarabine for patients with transplantation‐ineligible relapsed and refractory diffuse large B‐cell lymphoma |
title_fullStr | Ofatumumab with iphosphamide, etoposide and cytarabine for patients with transplantation‐ineligible relapsed and refractory diffuse large B‐cell lymphoma |
title_full_unstemmed | Ofatumumab with iphosphamide, etoposide and cytarabine for patients with transplantation‐ineligible relapsed and refractory diffuse large B‐cell lymphoma |
title_short | Ofatumumab with iphosphamide, etoposide and cytarabine for patients with transplantation‐ineligible relapsed and refractory diffuse large B‐cell lymphoma |
title_sort | ofatumumab with iphosphamide, etoposide and cytarabine for patients with transplantation‐ineligible relapsed and refractory diffuse large b‐cell lymphoma |
topic | Haematological Malignancy‐clinical |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9322457/ https://www.ncbi.nlm.nih.gov/pubmed/35362096 http://dx.doi.org/10.1111/bjh.18166 |
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