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Targets and treatments in primary CNS lymphoma
被引:2
|作者:
von Roemeling, Christina
[1
]
Ferreri, Andres
[2
,3
]
Soussain, Carole
[4
,5
]
Tun, Han
[6
]
Grommes, Christian
[7
,8
]
机构:
[1] Univ Florida, Preston A Wells Jr Ctr Brain Tumor Therapy, Lillian S Wells Dept Neurosurg, Gainesville, FL USA
[2] Univ Vita Salute San Raffaele, Dept Oncohematol, Milan, Italy
[3] IRCCS San Raffaele Sci Inst, Dept Oncohematol, Lymphoma Unit, Milan, Italy
[4] Inst Curie, Serv Hematol, Site St Cloud, St Cloud, France
[5] PSL Res Univ, Inst Curie, INSERM, U932, Paris, France
[6] Dept Hematol, Mayo Clin, Jacksonville, FL USA
[7] Mem Sloan Kettering Canc Ctr, Dept Neurol, 1275 York Ave, New York, NY 10065 USA
[8] Weill Cornell Med Coll, Dept Neurol, New York, NY 10065 USA
关键词:
PCNSL;
lymphoma;
TLR;
BCR;
BTK;
IRAK4;
CENTRAL-NERVOUS-SYSTEM;
B-CELL LYMPHOMA;
PHASE-II;
IBRUTINIB;
SURVIVAL;
THERAPY;
LENALIDOMIDE;
TEMSIROLIMUS;
MANAGEMENT;
DELIVERY;
D O I:
10.1080/10428194.2024.2342560
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Primary central nervous system lymphoma (PCNSL) is a rare and highly aggressive lymphoma entirely localized in the central nervous system or vitreoretinal space. PCNSL generally initially responds to methotrexate-containing chemotherapy regimens, but progressive or relapsing disease is common, and the prognosis is poor for relapsed or refractory (R/R) patients. PCNSL is often characterized by activation of nuclear factor kappa B (NF-kappa B) due to mutations in the B-cell receptor (BCR) or toll-like receptor (TLR) pathways, as well as immune evasion. Targeted treatments that inhibit key PCNSL mechanisms and pathways are being evaluated; inhibition of Bruton's tyrosine kinase (BTK) downstream of BCR activation has demonstrated promising results in treating R/R disease. This review will summarize the evidence and potential for targeted therapeutic agents to improve treatment outcomes in PCNSL. This includes immunotherapeutic and immunomodulatory approaches and inhibitors of the key pathways driving PCNSL, such as aberrant BCR and TLR signaling.
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页码:1055 / 1067
页数:13
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