Successful treatment of hemophagocytic intravascular large B-cell lymphoma with CNS involvement with BTK inhibitor combined with rituximab and high-dose methotrexate.
Fangfei ShaoWei SuXiujie ZhaoJianping HeXiaofen WangFeng GuoHaowen XiaoPublished in: Therapeutic advances in hematology (2024)
This is a case of hemophagocytic intravascular large B-cell lymphoma (IVLBCL) with central nervous system (CNS) involvement. Although R-CHOP chemotherapy regimen has been shown significant improvement in survival rate. The prognosis and outcomes remain unsatisfactory, which is identified as outstanding challenges and need solutions. Gene and molecular profiling studies may provide new therapeutic strategies, especially the BCR/TLR/IL-1R/NF-κB signaling pathway in IVLBCL. Here, we treated the hemophagocytic IVLBCL CNS-involved patient with the Bruton tyrosine kinase inhibitor (BTKi) to block NF-κB pathway, and indicated that the second-generation BTKi zanubrutinib-based treatment was feasible and efficient.
Keyphrases
- diffuse large b cell lymphoma
- signaling pathway
- high dose
- pi k akt
- blood brain barrier
- tyrosine kinase
- lps induced
- nuclear factor
- coronary artery
- low dose
- stem cell transplantation
- epithelial mesenchymal transition
- inflammatory response
- induced apoptosis
- toll like receptor
- acute lymphoblastic leukemia
- oxidative stress
- type diabetes
- immune response
- copy number
- genome wide
- single cell
- gene expression
- locally advanced
- cell proliferation
- radiation therapy
- adipose tissue
- genome wide identification
- metabolic syndrome
- single molecule
- hodgkin lymphoma
- replacement therapy
- chronic myeloid leukemia
- endoplasmic reticulum stress
- genome wide analysis
- glycemic control