Aggressive B-cell lymphoma: chasing the target.
Antineoplastic Combined Chemotherapy Protocols
/ administration & dosage
Cyclophosphamide
/ administration & dosage
Disease Progression
Doxorubicin
/ administration & dosage
Drug Delivery Systems
/ methods
Humans
Lymphoma, B-Cell
/ diagnosis
Mutation
/ genetics
Prednisone
/ administration & dosage
Randomized Controlled Trials as Topic
/ methods
Rituximab
/ administration & dosage
Vincristine
/ administration & dosage
drugs
investigational
pharmacogenetics
Journal
Journal of investigative medicine : the official publication of the American Federation for Clinical Research
ISSN: 1708-8267
Titre abrégé: J Investig Med
Pays: England
ID NLM: 9501229
Informations de publication
Date de publication:
02 2020
02 2020
Historique:
accepted:
02
10
2019
pubmed:
2
11
2019
medline:
3
7
2021
entrez:
2
11
2019
Statut:
ppublish
Résumé
One of the first achievements of molecular biology in lymphoma science was a discovery of cell of origin (COO) classification around 20 years ago with defining activated B-cell like (ABC) and germinal center B-cell like subtypes of diffuse large B-cell lymphoma (DLBCL) with the use of gene expression profiling. These categories were considered important as seemed to present different biology, response to treatment, and prognosis. Immunochemotherapy R-CHOP21 has been a standard of care for 2 decades, and it results in long-term disease-free survival or cure of 60% of patients with DLBCL but efficacy in an individual patient depends on age and other International Prognostic Index clinical risk factors and is within a range of 30% to more than 90%. Clinical attempts to enhance activity of immunochemotherapy in high-risk DLBCL like ABC or others included adding targeted agents to the R-CHOP backbone: bortezomib, lenalidomide, ibrutinib. Unfortunately, randomized clinical trials did not confirm the expected benefit. Recently, advanced molecular techniques were used to classify B-cell lymphomas beyond COO or MYC alterations and correlated with clinical outcome as illustrated by 2 recently published influential studies from the National Institutes of Health and from Dana Farber Cancer Center, USA. Advanced molecular pathogenesis descriptions of DLBCL provide a framework for actionable classifications that should be used for designing future clinical trials and hopefully bring success to treatment of high-risk aggressive lymphoma.
Identifiants
pubmed: 31672721
pii: jim-2019-001169
doi: 10.1136/jim-2019-001169
doi:
Substances chimiques
R-CHOP protocol
0
Rituximab
4F4X42SYQ6
Vincristine
5J49Q6B70F
Doxorubicin
80168379AG
Cyclophosphamide
8N3DW7272P
Prednisone
VB0R961HZT
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
331-334Informations de copyright
© American Federation for Medical Research 2020. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: JW: Advisory role: Roche, Celgene, Takeda, Janssen-Cilag, Servier, Amgen, BMS, AbbVie, Novartis, Gilead. Research funding: Roche, GSK/Novartis, Takeda, Janssen-Cilag. Lecture honoraria: Roche, Celgene, Takeda, Janssen-Cilag, Servier, Amgen, AbbVie, Gilead. Conference travel support: Roche.