Diagnostic, Pathologic, and Therapeutic Considerations for Primary CNS Lymphoma.
Christopher R D'AngeloPublished in: JCO oncology practice (2023)
Primary CNS lymphoma (PCNSL) is a rare lymphoma representing 3% of CNS malignancies. The diagnosis is complicated by the unique risks associated with brain biopsy, and the treatment is similarly complicated by the restriction of effective therapeutics able to cross the blood-brain barrier. Currently, the majority of individuals diagnosed with this disease are immunocompetent although immune deficiency related to HIV or immunosuppressive therapy remains an important risk factor. Improvements in both frontline therapy and consolidation options, including the use of hematopoietic stem-cell transplantation, have translated to improved survival. Unfortunately, patients experiencing relapsed or refractory disease often fare poorly. Here, we review key clinical, pathologic, and therapeutic aspects of PCNSL and highlight challenging clinical scenarios that may be encountered by the treating oncologist.
Keyphrases
- diffuse large b cell lymphoma
- blood brain barrier
- end stage renal disease
- acute myeloid leukemia
- neoadjuvant chemotherapy
- ejection fraction
- chronic kidney disease
- risk factors
- hepatitis c virus
- hiv positive
- human immunodeficiency virus
- replacement therapy
- hiv infected
- acute lymphoblastic leukemia
- locally advanced
- climate change
- white matter
- small molecule
- resting state
- ultrasound guided
- cell therapy
- multiple sclerosis
- south africa
- patient reported
- mesenchymal stem cells
- bone marrow
- subarachnoid hemorrhage