| Literature DB >> 27649904 |
Macarena I de la Fuente1, Aya Haggiagi2, Adrienne Moul3,4, Robert J Young5, Charif Sidani6, Arnold Markoe7, Francisco Vega3, Lisa M DeAngelis2, Izidore S Lossos4,8.
Abstract
Dural lymphoma (DL) is a rare type of primary CNS lymphoma arising from the dura mater. The optimal treatment is uncertain. A retrospective review was performed on 26 DL patients. Seventeen patients underwent resection and nine had a biopsy. Twenty three patients could be assessed for a response to treatment after surgery. Thirteen received focal radiotherapy (RT), six whole brain RT (WBRT), three chemotherapy alone and one chemotherapy followed by WBRT. Twenty two achieved complete response (CR) and one a partial response (PR). Four patients relapsed (two local and two systemic). Median follow up was 64 months, with median progression free survival (PFS) and OS not reached. Three year PFS was 89% (95% CI 0.64-0.97). All patients are alive at last follow-up, demonstrating that DL is an indolent tumor with long survival. CR is achievable with focal therapy in the majority of cases, but there is a risk for relapses and long-term follow-up is recommended.Entities:
Keywords: Dural lymphoma; focal radiotherapy; marginal zone lymphoma; primary central nervous system lymphoma
Mesh:
Year: 2016 PMID: 27649904 PMCID: PMC5576515 DOI: 10.1080/10428194.2016.1218006
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022