Novel agents for primary central nervous system lymphoma: evidence and perspectives

被引:26
作者
Illerhaus, Gerald [1 ]
Schorb, Elisabeth [2 ]
Kasenda, Benjamin [1 ,3 ,4 ]
机构
[1] Klinikum Stuttgart, Dept Hematol Oncol & Palliat Care, Stuttgart, Germany
[2] Univ Freiburg, Fac Med, Dept Hematol Oncol & Stem Cell Transplantat, Freiburg, Germany
[3] Univ Hosp Basel, Dept Med Oncol, Basel, Switzerland
[4] Univ Hosp Basel, Inst Clin Epidemiol & Biostat, Basel, Switzerland
关键词
STEM-CELL TRANSPLANTATION; HIGH-DOSE CHEMOTHERAPY; CNS LYMPHOMA; 1ST-LINE TREATMENT; PHASE-II; LENALIDOMIDE MONOTHERAPY; SALVAGE TREATMENT; ELDERLY-PATIENTS; TYROSINE KINASE; OPEN-LABEL;
D O I
10.1182/blood-2018-01-791558
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Primary central nervous system lymphoma (PCNSL) is a rare aggressive extranodal non-Hodgkin lymphoma. Although high remission rates can be achieved with high-dose methotrexate-based immunochemotherapy, risk of relapse and associated death is still substantial in at least a third of patients. Novel agents for treating lymphoid malignancies have substantially enriched treatment options for PCNSL. Weherein systematically review the existing clinical evidence of novel agents in treatment of PCNSL, summarize ongoing studies, and discuss perspectives. The body of evidence for novel agents is still limited to noncomparative studies, but the most promising approaches include Bruton kinase inhibition with ibrutinib and immunomodulatory treatment (eg, with lenalidomide). Targeting the mammalian target of rapamycin pathway does not seem to have a meaningful clinical benefit, and evidence of checkpoint inhibition with nivolumab is limited to anecdotal evidence. Future studies should embrace the concept of induction and maintenance therapy as well as the combination of drugs with different mechanisms of action. Selection of patients based on molecular profiling and relapse patterns should be another aspect informing future comparative trials, which are urgently needed to improve prognosis for patients with PCNSL.
引用
收藏
页码:681 / 688
页数:8
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