| Literature DB >> 27062389 |
Stefan K Barta1, Jitesh Joshi2, Nicolas Mounier3, Xiaonan Xue2, Dan Wang2, Josep-Maria Ribera4, Jose-Tomas Navarro4, Christian Hoffmann5,6, Kieron Dunleavy7, Richard F Little7, Wyndham H Wilson7, Michele Spina8, Lionel Galicier9, Ariela Noy10, Joseph A Sparano2.
Abstract
Central nervous system (CNS) involvement is reportedly more common in acquired immunodeficiency syndrome (AIDS)-related lymphomas (ARL). We describe factors and outcomes associated with CNS involvement at baseline (CNS(B) ) and relapse (CNS(R) ) in 886 patients with newly diagnosed ARL. Of 886 patients, 800 received either intrathecal (IT) therapy for CNS(B) or IT prophylaxis. CNS(B) was found in 13%. CNS(B) was not associated with reduced overall survival (OS). There was no difference in the prevalence of CNS(B) between the pre-combination antiretroviral therapy (cART) and cART eras. 5·3% of patients experienced CNS(R) at a median of 4·2 months after diagnosis (12% if CNS(B) ; 4% if not). Median OS after CNS(R) was 1·6 months. On multivariate analysis, only CNS(B) [hazard ratio (HR) 3·68, P = 0·005] and complete response to initial therapy (HR 0·14, P < 0·0001) were significantly associated with CNS(R) . When restricted to patients without CNS(B) , IT CNS prophylaxis with 3 vs. 1 agent did not significantly impact the risk of CNS(R) . Despite IT CNS prophylaxis, 5% of patients experienced CNS(R) . Our data confirms that CNS(R) in ARL occurs early and has a poor outcome. Complete response to initial therapy was associated with a reduced frequency of CNS(R) . Although CNS(B) conferred an increased risk for CNS(R) , it did not impact OS.Entities:
Keywords: AIDS-related lymphoma; acquired immunodeficiency syndrome; central nervous system relapse; lymphoma; non-Hodgkin lymphoma
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Year: 2016 PMID: 27062389 PMCID: PMC4900917 DOI: 10.1111/bjh.13998
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998