| Literature DB >> 23829536 |
Richard T Maziarz1, Zhiwei Wang, Mei-Jie Zhang, Brian J Bolwell, Andy I Chen, Timothy S Fenske, Cesar O Freytes, Robert P Gale, John Gibson, Brandon M Hayes-Lattin, Leona Holmberg, David J Inwards, Luis M Isola, Hanna J Khoury, Victor A Lewis, Dipnarine Maharaj, Reinhold Munker, Gordon L Phillips, David A Rizzieri, Philip A Rowlings, Wael Saber, Prakash Satwani, Edmund K Waller, David G Maloney, Silvia Montoto, Ginna G Laport, Julie M Vose, Hillard M Lazarus, Parameswaran N Hari.
Abstract
Pre-existing central nervous system (CNS) involvement may influence referral for autologous haematopoietic cell transplantation (AHCT) for patients with non-Hodgkin lymphoma (NHL). The outcomes of 151 adult patients with NHL with prior secondary CNS involvement (CNS(+) ) receiving an AHCT were compared to 4688 patients without prior CNS lymphoma (CNS(-) ). There were significant baseline differences between the cohorts. CNS(+) patients were more likely to be younger, have lower performance scores, higher age-adjusted international prognostic index scores, more advanced disease stage at diagnosis, more aggressive histology, more sites of extranodal disease, and a shorter interval between diagnosis and AHCT. However, no statistically significant differences were identified between the two groups by analysis of progression-free survival (PFS) and overall survival (OS) at 5 years. A matched pair comparison of the CNS(+) group with a subset of CNS(-) patients matched on propensity score also showed no differences in outcomes. Patients with active CNS lymphoma at the time of AHCT (n = 55) had a higher relapse rate and diminished PFS and OS compared with patients whose CNS lymphoma was in remission (n = 96) at the time of AHCT. CNS(+) patients can achieve excellent long-term outcomes with AHCT. Active CNS lymphoma at transplant confers a worse prognosis.Entities:
Keywords: autologous transplantation; central nervous system involvement; non-Hodgkin lymphoma; outcomes
Mesh:
Year: 2013 PMID: 23829536 PMCID: PMC3766698 DOI: 10.1111/bjh.12451
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998