An experience with ibrutinib monotherapy for Richter's syndrome isolated in the central nervous system.
Central nervous system
Ibrutinib
Immunoglobulin gene
Richter’s syndrome
Journal
Journal of clinical and experimental hematopathology : JCEH
ISSN: 1880-9952
Titre abrégé: J Clin Exp Hematop
Pays: Japan
ID NLM: 101141257
Informations de publication
Date de publication:
28 Dec 2022
28 Dec 2022
Historique:
pubmed:
28
11
2022
medline:
30
12
2022
entrez:
27
11
2022
Statut:
ppublish
Résumé
Richter's syndrome (RS) of the central nervous system (CNS) is known to have an extremely poor prognosis. Ibrutinib has been reported to have some activity in patients with RS, despite its poor prognosis. Although ibrutinib crosses the blood-brain barrier, its efficacy in RS patients with CNS involvement remains unknown. Here, we report a case of RS isolated in the CNS that was confirmed to be clonally related to chronic lymphocytic leukemia (CLL) by immunoglobulin heavy chain gene analysis. Although the median survival of patients with RS clonally related to CLL was significantly shorter than that of patients with RS clonally unrelated to CLL, the patient received ibrutinib monotherapy without experiencing any significant adverse events, and the disease remained stable with ibrutinib until 6 weeks later. Following whole-brain radiation therapy (40 Gy in 20 fractions) with dexamethasone, the patient has survived for five months after diagnosis. Thus, ibrutinib may be a safe and effective therapeutic option for patients with RS and CNS involvement.
Identifiants
pubmed: 36436931
doi: 10.3960/jslrt.22017
pmc: PMC9898719
doi:
Substances chimiques
ibrutinib
1X70OSD4VX
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
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