Emerging therapies for the treatment of relapsed or refractory diffuse large B cell lymphoma.


Journal

Current oncology (Toronto, Ont.)
ISSN: 1718-7729
Titre abrégé: Curr Oncol
Pays: Switzerland
ID NLM: 9502503

Informations de publication

Date de publication:
08 2019
Historique:
entrez: 25 9 2019
pubmed: 25 9 2019
medline: 15 5 2020
Statut: ppublish

Résumé

Diffuse large B cell lymphoma (dlbcl) is an aggressive non-Hodgkin lymphoma, accounting for approximately 30% of lymphoma cases in Canada. Although most patients will achieve a cure, up to 40% will experience refractory disease after initial treatment, or relapse after a period of remission. In eligible patients, salvage therapy followed by high-dose therapy and autologous stem-cell transplantation (asct) is the standard of care. However, many patients are transplant-ineligible, and more than half of those undergoing asct will subsequently relapse. For those patients, outcomes are dismal, and novel treatment approaches are a critical unmet need. In this paper, we present available data about emerging treatment approaches in the latter setting and provide a perspective about the potential use of those approaches in Canada.

Identifiants

pubmed: 31548805
doi: 10.3747/co.26.5421
pii: conc-26-253
pmc: PMC6726277
doi:

Substances chimiques

Antibodies, Monoclonal 0
Antineoplastic Agents 0
Immunoconjugates 0
Piperidines 0
Pyrazoles 0
Pyrimidines 0
ibrutinib 1X70OSD4VX
Brentuximab Vedotin 7XL5ISS668
Adenine JAC85A2161
polatuzumab vedotin KG6VO684Z6

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

253-265

Déclaration de conflit d'intérêts

CONFLICT OF INTEREST DISCLOSURES We have read and understood Current Oncology’s policy on disclosing conflicts of interest, and we declare the following interests: Medical writing support provided by Anna Christofides of impact Medicom Inc. was funded by Hoffmann–La Roche Canada Inc. SA has received honoraria for consulting purposes from Janssen, Gilead, and Hoffmann–La Roche. DM has received honoraria for consulting purposes from Hoffmann–La Roche/Genentech, AbbVie, Amgen, AstraZeneca, Celgene, Gilead, Janssen, Lundbeck, Merck, and Seattle Genetics. AP has received honoraria for consulting purposes from AstraZeneca and AbbVie. RS has received honoraria for consulting purposes from Pfizer, Boehringer Ingelheim, AstraZeneca, Hoffmann–La Roche/Genentech, Lundbeck, Eli Lilly, Bristol–Myers Squibb, Merck, AbbVie, Novartis, and Takeda. BAM is an employee of Hoffmann–La Roche Canada Inc. LHS has received honoraria for consulting purposes from Hoffmann–La Roche/Genentech, AbbVie, Amgen, Apobiologix, AstraZeneca, Acerta Pharma, Celgene, Gilead, Janssen, Kite, Karyopharm, Lundbeck, Merck, MorphoSys, Seattle Genetics, Teva, Takeda, TG Therapeutics, and Versatem Oncology. She has also received research funding from Hoffmann–La Roche/Genentech. PS has no conflicts to disclose.

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Auteurs

P Skrabek (P)

Department of Hematology and Medical Oncology, University of Manitoba, and CancerCare Manitoba, Winnipeg, MB.

S Assouline (S)

Department of Medicine, Division of Hematology, Sir Mortimer B. Davis Jewish General Hospital and McGill University, Montreal, QC.

A Christofides (A)

impactMedicom Inc., Toronto, ON.

D MacDonald (D)

The Ottawa Hospital, Ottawa, ON.

A Prica (A)

Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, and University of Toronto, Toronto, ON.

R Sangha (R)

University of Alberta and Cross Cancer Institute, Edmonton, AB.

B A Matthews (BA)

Hoffmann-La Roche, Mississauga, ON.

L H Sehn (LH)

Division of Medical Oncology, University of British Columbia, and BC Cancer, Vancouver, BC.

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Classifications MeSH