2016 Fiscal Year Final Research Report
Genetic alterations and prognostic factors for primary central nervous system lymphoma treated with R-MPV-A combination immunochemotherapy
Project/Area Number |
26462189
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Neurosurgery
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Research Institution | Kyorin University |
Principal Investigator |
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Co-Investigator(Renkei-kenkyūsha) |
NAGANE Motoo 杏林大学, 医学部, 教授 (60327468)
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Research Collaborator |
SASAKI Nobuyoshi
LEE Jeunghun
SHIMIZU Saki
SUZUKI Kaori
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Project Period (FY) |
2014-04-01 – 2017-03-31
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Keywords | 脳腫瘍 / 中枢神経系悪性リンパ腫 / 遺伝子異常 / MGMT / MYD88 / MMSE |
Outline of Final Research Achievements |
Primary central nervous system lymphoma (PCNSL) is one of the deadly malignant brain tumors, but exhibits a high response to combination immunochemotherapy with rituximab, methotrexate, procarbazine, vincristine and cytarabine (R-MPV-A). We analyzed 32 patients with newly diagnosed PCNSL composed of diffuse large B cell lymphoma (DLBCL) for potential genetic alterations as well as prognostic factors for progression-free survival (PFS). We found MYD88 mutations in 70% of patients which is much higher than in those with systemic DLBCL, while MGMT promoter was methylated in 60% of cases. Factors associated with longer PFS are age<70 years (p=0.059), single lesion (p=0.010), methylated MGMT promoter (p=0.056), and MMSE score ≧ 24 (p=0.025), but MYD88 mutations did not affect outcome (p=0.186, rather mutated MYD88 patients tended to live longer). These results suggest that methylated MGMT and high baseline MMSE score might predict higher benefit and better outcome with R-MPV-A treatment.
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Free Research Field |
脳腫瘍
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