Literature DB >> 28665232

Integrating novel drugs to chemoimmunotherapy in diffuse large B-cell lymphoma.

Annalisa Chiappella1, Elisa Santambrogio1, Alessia Castellino1, Maura Nicolosi1, Umberto Vitolo1.   

Abstract

INTRODUCTION: Diffuse Large B-cell Lymphoma (DLBCL) is the most common aggressive non-Hodgkin lymphoma (NHL), with an incidence in Europe of 3.8/100.000/year. A multi-drugs chemoimmunotherapy regimen, containing rituximab, cyclophosphamide, vincristine, doxorubicin and prednisone (R-CHOP) administrated every 21 days, is the standard therapy for DLBCL patients. The discovery of several biological features of DLBCL has encouraged the introduction of novel drugs in the treatment. Areas covered: In this article, the use of standard therapies will be reviewed and will be investigated adoption of novel drugs such as Bortezomib, Bruton's tyrosine kinase, IMiDs, Venetoclax, mTOR inhibitors and other biological agents. Expert commentary: A better knowledge of the biology of DLBCL is mandatory to tailor treatment and to ameliorate the poor prognosis of DLBCL. The addition of novel drugs to standard RCHOP should represent a modern approach in the treatment of DLBCL. Ibrutinib and lenalidomide showed important results in DLBCL and the integration of these drugs in first line treatment is under investigation. Despite encouraging results using novel drugs in the setting of relapsed/refractory DLBCL, the rate of failures still remains at 40%; for these reason, continued participation in clinical trials should be encouraged.

Entities:  

Keywords:  Diffuse large B cell lymphoma; ibrutinib; lenalidomide; novel drugs; rituximab-CHOP; tazemetostat; venetoclax

Mesh:

Year:  2017        PMID: 28665232     DOI: 10.1080/17474086.2017.1350164

Source DB:  PubMed          Journal:  Expert Rev Hematol        ISSN: 1747-4094            Impact factor:   2.929


  8 in total

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2.  Bruton's Tyrosine Kinase Inhibitors for the Treatment of Autoimmune Diseases and Cancers.

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Journal:  ACS Med Chem Lett       Date:  2017-08-24       Impact factor: 4.345

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Journal:  Blood       Date:  2020-04-16       Impact factor: 22.113

4.  Voruciclib, a clinical stage oral CDK9 inhibitor, represses MCL-1 and sensitizes high-risk Diffuse Large B-cell Lymphoma to BCL2 inhibition.

Authors:  Joyoti Dey; Thomas L Deckwerth; William S Kerwin; Joseph R Casalini; Angela J Merrell; Marc O Grenley; Connor Burns; Sally H Ditzler; Chantel P Dixon; Emily Beirne; Kate C Gillespie; Edward F Kleinman; Richard A Klinghoffer
Journal:  Sci Rep       Date:  2017-12-21       Impact factor: 4.379

5.  Indolent T-cell lymphoproliferative disease with synchronous diffuse large B-cell lymphoma: A case report.

Authors:  Linjie Guo; Zhonghui Wen; Xueying Su; Shuyuan Xiao; Yufang Wang
Journal:  Medicine (Baltimore)       Date:  2019-04       Impact factor: 1.817

6.  Patient Perspectives on Health-Related Quality of Life in Diffuse Large B-Cell Lymphoma Treated with Car T-Cell Therapy: A Qualitative Study.

Authors:  Rebecca Cheng; Kayla Scippa; Frederick L Locke; Julia Thornton Snider; Heather Jim
Journal:  Oncol Ther       Date:  2021-11-15

7.  Decreased RNA‑binding protein IGF2BP2 downregulates NT5DC2, which suppresses cell proliferation, and induces cell cycle arrest and apoptosis in diffuse large B‑cell lymphoma cells by regulating the p53 signaling pathway.

Authors:  Yuying Cui; Yu Wen; Chao Lv; Dongmei Zhao; Yu Yang; Hongbin Qiu; Chennan Wang
Journal:  Mol Med Rep       Date:  2022-07-27       Impact factor: 3.423

8.  Biological Approaches to Aggressive Cutaneous B-Cell Lymphomas.

Authors:  Giulia Tadiotto Cicogna; Martina Ferranti; Annalisa Lazzarotto; Mauro Alaibac
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  8 in total

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