Novel biomarker, phosphorylated T-LAK cell-originated protein kinase (p-TOPK) can predict outcome in primary central nervous system lymphoma
Autor: | Tomohide Hayashi, Satoshi Kuroda, Yumiko Hayakawa, Takahiro Tomita, Masaki Koh, Shoichi Nagai, Takuya Akai |
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Rok vydání: | 2018 |
Předmět: |
Male
0301 basic medicine Oncology medicine.medical_specialty Lymphoma medicine.medical_treatment Disease-Free Survival Pathology and Forensic Medicine Central Nervous System Neoplasms 03 medical and health sciences 0302 clinical medicine Internal medicine Biomarkers Tumor Humans Medicine Phosphorylation Aged Aged 80 and over Mitogen-Activated Protein Kinase Kinases Chemotherapy business.industry Hazard ratio Primary central nervous system lymphoma General Medicine Middle Aged medicine.disease Radiation therapy 030104 developmental biology 030220 oncology & carcinogenesis Biomarker (medicine) Immunohistochemistry Female Neurology (clinical) business Immunostaining |
Zdroj: | Neuropathology. 38:228-236 |
ISSN: | 0919-6544 |
Popis: | This study aimed to assess whether T-lymphokine-activated killer cell-originated protein kinase (TOPK) can be a potent novel biomarker to predict the outcome in patients with primary central nervous system lymphoma (PCNSL). This study enrolled 20 patients who were histologically diagnosed as having diffuse large B-cell type PCNSL between 2005 and 2015. Using surgical specimens, the expression of TOPK and phosphorylated TOPK (p-TOPK) was analyzed on immunohistochemistry. Clinical features such as age, sex, Karnofsky performance status (KPS), ocular involvement, deep brain structure involvement, the number of lesions, chemotherapy and radiation therapy were also collected. Impacts of TOPK/p-TOPK expression on their progression-free survival (PFS) and overall survival (OS) were examined with multivariate analysis. Median PFS/OS were 24.2 and 39.0 months, respectively. On immunostaining, the mean percentage of TOPK-positive cells was 35.5 ± 20.8%, and the mean number of p-TOPK-positive cells was 13.7 ± 15.7 cells/mm2 . The higher expression of p-TOPK was significantly related to multiple lesions (P = 0.003). Multivariate analysis demonstrated that only the higher expression of p-TOPK was an independent predictor to shorten both PFS (P = 0.029; hazard ratio (HR), 5.5; 95% confidential interval (CI), 1.2-25.3) and OS (P = 0.014; HR, 7.7; 95% CI, 1.5-41.3). These findings strongly suggest that p-TOPK may be a potent biomarker to determine the outcome of patients with PCNSL and to develop novel drugs to treat PCNSL. |
Databáze: | OpenAIRE |
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