Treating central nervous system lymphoma in the era of precision medicine

被引:1
作者
Garcilazo-Reyes, Ytel [1 ]
Ibanez-Julia, Maria-Jose [1 ,2 ]
Hernandez-Verdin, Isaias [3 ]
Nguyen-Them, Ludovic [1 ,2 ]
Younan, Nadia [1 ,3 ]
Houillier, Caroline [1 ,4 ]
Hoang-Xuan, Khe [1 ,3 ,4 ]
Alentorn, Agusti [1 ,3 ]
机构
[1] Grp Hosp Pitie Salpetriere, APHP, Dept Neurol 2, Paris, France
[2] CH Perpignan, Dept Neurol, Perpignan, France
[3] Sorbonne Univ, Paris, France
[4] Grp Hosp Pitie Salpetriere, Reseau Expert Natl LOC Lymphomes Oculo Cerebraux, Paris, France
关键词
Bruton's tyrosine kinase inhibitors; immune checkpoint inhibitors; immune-related therapies; primary central nervous system lymphoma; lenalidomide; mTOR inhibitors; targeted therapies; B-CELL LYMPHOMA; PRIMARY CNS LYMPHOMA; MODIFIED T-CELLS; IBRUTINIB; LENALIDOMIDE; MONOTHERAPY; IMMUNOTHERAPY; INHIBITION; EXPRESSION; IMMUNITY;
D O I
10.1080/23808993.2020.1777853
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Primary central nervous system lymphoma (PCNSL) is a rare extra-nodal non-Hodgkin lymphoma that in the vast majority of cases belongs to diffuse large B-cell lymphoma (DLBCL) histology. The standard first-line treatment is based on high-dose methotrexate (HD-MTX) regimens. However, the majority of patients will relapse, leading to a poor prognosis of the disease. Areas covered: Reviewed are the potential new therapeutic approaches in PCNSL. With the advent of tailored treatment, immunomodulators and immunotherapies are appearing as new promising therapeutic approaches for this orphan disease. This review seeks to summarize the novel approaches currently under evaluation. Expert opinion: The therapeutic management of PCNSL is rapidly evolving with the description of PCNSL molecular alterations. However, due to the rarity of this disease, phase III clinical trials using new therapeutic drugs are still lacking. In addition, the vast majority of newly diagnosed PCNSL affect elderly patients, and specific and adapted clinical trials for this fragile population are warranted. Currently, the use of targeted therapies or immune-mediated treatments is only studied in relapsed/refractory (R/R) PCNSL, but the use of these approaches as a first-line treatment (compared with HD-MTX) could also be used as new promising approaches to decrease the toxicity associated with MTX regimens.
引用
收藏
页码:275 / 281
页数:7
相关论文
共 64 条
[1]   Anti-CD19 CAR T Cells in CNS Diffuse Large-B-Cell Lymphoma [J].
Abramson, Jeremy S. ;
McGree, Brianne ;
Noyes, Sarah ;
Plummer, Sean ;
Wong, Curtis ;
Chen, Yi-Bin ;
Palmer, Edwin ;
Albertson, Tina ;
Ferry, Judith A. ;
Arrillaga-Romany, Isabel C. .
NEW ENGLAND JOURNAL OF MEDICINE, 2017, 377 (08) :783-784
[2]   Programmed Death Ligand 1 Is Expressed by Non-Hodgkin Lymphomas and Inhibits the Activity of Tumor-Associated T Cells [J].
Andorsky, David J. ;
Yamada, Reiko E. ;
Said, Jonathan ;
Pinkus, Geraldine S. ;
Betting, David J. ;
Timmerman, John M. .
CLINICAL CANCER RESEARCH, 2011, 17 (13) :4232-4244
[3]   Germinal centres and B cell lymphomagenesis [J].
Basso, Katia ;
Dalla-Favera, Riccardo .
NATURE REVIEWS IMMUNOLOGY, 2015, 15 (03) :172-184
[4]   RITUXIMAB MONOTHERAPY FOR PATIENTS WITH RECURRENT PRIMARY CNS LYMPHOMA [J].
Batchelor, T. T. ;
Grossman, S. A. ;
Mikkelsen, T. ;
Ye, X. ;
Desideri, S. ;
Lesser, G. J. .
NEUROLOGY, 2011, 76 (10) :929-930
[5]   Genome-Wide Analysis Uncovers Novel Recurrent Alterations in Primary Central Nervous System Lymphomas [J].
Braggio, Esteban ;
Van Wier, Scott ;
Ojha, Juhi ;
McPhail, Ellen ;
Asmann, Yan W. ;
Egan, Jan ;
da Silva, Jackline Ayres ;
Schiff, David ;
Lopes, M. Beatriz ;
Decker, Paul A. ;
Valdez, Riccardo ;
Tibes, Raoul ;
Eckloff, Bruce ;
Witzig, Thomas E. ;
Stewart, A. Keith ;
Fonseca, Rafael ;
O'Neill, Brian Patrick .
CLINICAL CANCER RESEARCH, 2015, 21 (17) :3986-3994
[6]   Rituximab in patients with primary CNS lymphoma (HOVON 105/ALLG NHL 24): a randomised, open-label, phase 3 intergroup study [J].
Bromberg, Jacoline E. C. ;
Issa, Samar ;
Bakunina, Katerina ;
Minnema, Monique C. ;
Seute, Tatjana ;
Durian, Marc ;
Cull, Gavin ;
Schouten, Harry C. ;
Stevens, Wendy B. C. ;
Zijlstra, Josee M. ;
Baars, Joke W. ;
Nijland, Marcel ;
Mason, Kylie D. ;
Beeker, Aart ;
van den Bent, Martini ;
Beijert, Max ;
Gonzales, Michael ;
de Jong, Daphne ;
Doorduijn, Jeanette K. .
LANCET ONCOLOGY, 2019, 20 (02) :216-228
[7]   Combined Genetic Inactivation of β2-Microglobulin and CD58 Reveals Frequent Escape from Immune Recognition in Diffuse Large B Cell Lymphoma [J].
Challa-Malladi, Madhavi ;
Lieu, Yen K. ;
Califano, Olivia ;
Holmes, Antony B. ;
Bhagat, Govind ;
Murty, Vundavalli V. ;
Dominguez-Sola, David ;
Pasqualucci, Laura ;
Dalla-Favera, Riccardo .
CANCER CELL, 2011, 20 (06) :728-740
[8]   In Silico and Functional Characterization of TBL1XR1 as a Tumor Suppressor in Large B-Cell Lymphomas [J].
Chapuy, Bjoern ;
Kamburov, Atanas ;
Coughlin, Caroline A. ;
Stewart, Chip ;
Dunford, Andrew ;
Aono, Miyuki ;
Loeber, Jens ;
Sauer, Christopher ;
Su, Arthur ;
Roemer, Margaretha G. M. ;
Rodig, Scott J. ;
Getz, Gad ;
Shipp, Margaret A. .
BLOOD, 2016, 128 (22)
[9]   Class-switch recombination: Interplay of transcription, DNA deamination and DNA repair [J].
Chaudhuri, J ;
Alt, FW .
NATURE REVIEWS IMMUNOLOGY, 2004, 4 (07) :541-552
[10]   Chronic active B-cell-receptor signalling in diffuse large B-cell lymphoma [J].
Davis, R. Eric ;
Ngo, Vu N. ;
Lenz, Georg ;
Tolar, Pavel ;
Young, Ryan M. ;
Romesser, Paul B. ;
Kohlhammer, Holger ;
Lamy, Laurence ;
Zhao, Hong ;
Yang, Yandan ;
Xu, Weihong ;
Shaffer, Arthur L. ;
Wright, George ;
Xiao, Wenming ;
Powell, John ;
Jiang, Jian-Kang ;
Thomas, Craig J. ;
Rosenwald, Andreas ;
Ott, German ;
Muller-Hermelink, Hans Konrad ;
Gascoyne, Randy D. ;
Connors, Joseph M. ;
Johnson, Nathalie A. ;
Rimsza, Lisa M. ;
Campo, Elias ;
Jaffe, Elaine S. ;
Wilson, Wyndham H. ;
Delabie, Jan ;
Smeland, Erlend B. ;
Fisher, Richard I. ;
Braziel, Rita M. ;
Tubbs, Raymond R. ;
Cook, J. R. ;
Weisenburger, Dennis D. ;
Chan, Wing C. ;
Pierce, Susan K. ;
Staudt, Louis M. .
NATURE, 2010, 463 (7277) :88-U97