Ofatumumab with iphosphamide, etoposide and cytarabine for patients with transplantation-ineligible relapsed and refractory diffuse large B-cell lymphoma.
Aged
Antibodies, Monoclonal, Humanized
Antineoplastic Combined Chemotherapy Protocols
/ adverse effects
Cytarabine
/ adverse effects
Etoposide
/ adverse effects
Humans
Ifosfamide
Lymphoma, Large B-Cell, Diffuse
/ pathology
Lymphoma, Non-Hodgkin
/ etiology
Middle Aged
Neoplasm Recurrence, Local
/ pathology
Rituximab
Salvage Therapy
IVAC protocol
ofatumumab
refractory and relapsed diffuse large B-cell lymphoma
salvage treatment
Journal
British journal of haematology
ISSN: 1365-2141
Titre abrégé: Br J Haematol
Pays: England
ID NLM: 0372544
Informations de publication
Date de publication:
07 2022
07 2022
Historique:
revised:
14
03
2022
received:
14
01
2022
accepted:
15
03
2022
pubmed:
2
4
2022
medline:
28
6
2022
entrez:
1
4
2022
Statut:
ppublish
Résumé
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.
Identifiants
pubmed: 35362096
doi: 10.1111/bjh.18166
pmc: PMC9322457
doi:
Substances chimiques
Antibodies, Monoclonal, Humanized
0
Cytarabine
04079A1RDZ
Rituximab
4F4X42SYQ6
Etoposide
6PLQ3CP4P3
ofatumumab
M95KG522R0
Ifosfamide
UM20QQM95Y
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
73-81Informations de copyright
© 2022 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.
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