Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2016;56(2):79-88.
doi: 10.3960/jslrt.56.79.

Treatment of Diffuse Large B-Cell Lymphoma

Affiliations
Review

Treatment of Diffuse Large B-Cell Lymphoma

Kana Miyazaki. J Clin Exp Hematop. 2016.

Abstract

Diffuse large B-cell lymphoma (DLBCL) comprises a heterogeneous group with pathophysiological, genetic and clinical features. Many patients can be cured with R-CHOP therapy, which is the current standard regimen. Despite recent progress in improving patient survival, the 40% survival of DLBCL patients remains poor. Therefore, the most important issue for patients with DLBCL remains the development of a new front-line therapy. Several studies have reported that intensified chemotherapy with dose-adjusted EPOCH-R or R-ACVBP was superior to R-CHOP. Gene expression profiling has identified two distinct forms of DLBCL: activated B cell-like (ABC) and germinal center B-cell-like (GCB) types. ABC DLBCL exhibits a worse prognosis than GCB DLBCL by molecular diagnosis after R-CHOP therapy. Next-generation sequencing has identified unique oncogenic mechanisms and genetic complexity, which has provided rational therapeutic targets. There are also a number of biomarkers, including CD5, and prognostic factors. Efforts to distinguish many biomarkers will be crucial for individualized treatment in the future.

PubMed Disclaimer

Conflict of interest statement

DISCLOSURE STATEMENT: The author declares that there are no conflicts of interest regarding the present paper.

Similar articles

Cited by

References

    1. WHO Classification of Tumours, Tumours of Haematopoietic and Lymphoid Tissues. Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, et al. (eds): 4th ed, Lyon, IARC, 2008
    1. Harris NL, Jaffe ES, Stein H, Banks PM, Chan JK, et al. : A revised European-American classification of lymphoid neoplasms: a proposal from the International Lymphoma Study Group. Blood 84: 1361-1392, 1994 - PubMed
    1. A predictive model for aggressive non-Hodgkin’s lymphoma. The International Non-Hodgkin’s Lymphoma Prognostic Factors Project. N Engl J Med 329: 987-994, 1993. 10.1056/NEJM199309303291402 - DOI - PubMed
    1. Miller TP, Dahlberg S, Cassady JR, Adelstein DJ, Spier CM, et al. : Chemotherapy alone compared with chemotherapy plus radiotherapy for localized intermediate- and high-grade non-Hodgkin’s lymphoma. N Engl J Med 339: 21-26, 1998. 10.1056/NEJM199807023390104 - DOI - PubMed
    1. Bonnet C, Fillet G, Mounier N, Ganem G, Molina TJ, et al. : CHOP alone compared with CHOP plus radiotherapy for localized aggressive lymphoma in elderly patients: a study by the Groupe d’Etude des Lymphomes de l’Adulte. J Clin Oncol 25: 787-792, 2007. 10.1200/JCO.2006.07.0722 - DOI - PubMed

MeSH terms