| Literature DB >> 27604616 |
Yusuke Koizumi1,2,3, Tomoko Uehira4, Yasunori Ota5, Yoshihiko Ogawa4, Keishiro Yajima4, Junko Tanuma6, Mihoko Yotsumoto7, Shotaro Hagiwara8, Satoshi Ikegaya9, Dai Watanabe4, Hitoshi Minamiguchi10, Keiko Hodohara10, Kenta Murotani11, Hiroshige Mikamo12, Hideho Wada13, Atsushi Ajisawa14, Takuma Shirasaka4, Hirokazu Nagai15, Yoshinori Kodama16, Tsunekazu Hishima17, Makoto Mochizuki18, Harutaka Katano19, Seiji Okada20.
Abstract
Plasmablastic lymphoma (PBL) is a rare AIDS-related malignancy with a poor prognosis. Little is known about this entity, and no standard treatment regimen has been defined. To establish an adequate treatment strategy, we investigated 24 cases of PBL arising in human immunodeficiency virus-positive individuals. Most of the patients were in the AIDS stage, with a median CD4 count of 67.5/µL. Lymph nodes (58 %), gastrointestinal tract (42 %), bone marrow (39 %), oral cavity (38 %), and CNS (18 %) were the most commonly involved sites. Histology findings for the following were positive at varying rates, as follows: CD10 (56 %); CD30 (39 %); CD38 (87 %); MUM-1 (91 %); CD138 (79 %); EBER (91 %); and LMP-1 (18 %). There was a marked increase in patients in 2011-12, and the cases found in that period appeared to be more aggressive, showing a higher rate of advanced-stage PBL. Fourteen cases were treated with CHOP, while the others were treated with more intensive regimens, including bortezomib and hematopoietic stem cell transplantation. The overall median survival time was 15 months. A CD4 count of >100/µL at diagnosis and attaining complete remission in the first-line chemotherapy were associated with better outcomes (P = 0.027 and 0.0016, respectively). Host immune status and chemosensitivity are associated with improved prognosis in PBL.Entities:
Keywords: Acquired immunodeficiency syndrome; CD4; Combination antiretroviral therapy; Epstein–Barr virus; Human immunodeficiency virus; Plasmablastic lymphoma
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Year: 2016 PMID: 27604616 DOI: 10.1007/s12185-016-2082-3
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490