Ibrutinib in Refractory or Relapsing Primary Central Nervous System Lymphoma: A Systematic Review.
Gaurav NepalMahika KhuranaDomenica Herrera BucheliSiddhartha BhandariUtsav JoshiRiwaj BhagatJessica Holly RehrigPrasun PudasaineeYow Ka ShingJuan Fernando OrtizRajeev OjhaBikram Prasad GajurelJonathan QuinonezSamir RuxmohanTrevine AlbertSteven LicataJoel StienPublished in: Neurology international (2022)
Primary Central Nervous System Lymphoma (PCNSL) is a rare variant of Non-Hodgkin Lymphoma (NHL) representing 1-2% of all NHL cases. PCNSL is defined as a lymphoma that occurs in the brain, spinal cord, leptomeninges, or eyes. Efforts to treat PCNSL by traditional chemotherapy and radiotherapy have generally been unsuccessful as a significant proportion of patients have frequent relapses or are refractory to treatment. The prognosis of patients with Refractory or Relapsed (R/R) PCNSL is abysmal. The optimal treatment for R/R PCNSL is poorly defined as there are only a limited number of studies in this setting. Several studies have recently shown that ibrutinib, a Bruton tyrosine kinase (BTK) inhibitor, has promising results in the treatment of R/R PCNSL. However, these are preliminary studies with a limited sample size. In this systematic review, we explored and critically appraised the evidence about the efficacy of the novel agent ibrutinib in treating R/R PCNSL.
Keyphrases
- tyrosine kinase
- systematic review
- diffuse large b cell lymphoma
- spinal cord
- multiple sclerosis
- early stage
- end stage renal disease
- acute lymphoblastic leukemia
- randomized controlled trial
- spinal cord injury
- acute myeloid leukemia
- chronic kidney disease
- locally advanced
- squamous cell carcinoma
- case control
- rectal cancer
- prognostic factors
- resting state
- subarachnoid hemorrhage
- patient reported outcomes
- disease activity