Neurological Complications Involving the Central Nervous System After Allogeneic Hematopoietic Stem Cell Transplantation During a Period of Evolution in Transplant Modalities: A Cohort Analysis

被引:15
作者
Colombo, Anna Amelia [1 ]
Marchioni, Enrico [2 ]
Diamanti, Luca [3 ]
Di Matteo, Angela Maria [4 ]
Baldanti, Fausto [4 ]
Furione, Milena [4 ]
Cazzola, Mario
Ferretti, Virginia Valeria [5 ]
Pascutto, Cristiana [6 ]
Alessandrino, Emilio Paolo [1 ]
机构
[1] Fondaz IRCCS Policlinico San Matteo, Dept Hematol Oncol Dis, Transplant Bone Marrow Unit, Pavia, Italy
[2] Ist Neurolog Nazl, IRCCS C Mondino, Pavia, Italy
[3] Univ Pavia, Monza Policlin & Pavia Mondino, Neurosci Consortium, Pavia, Italy
[4] Fondazione IRCCS Policlinico San Matteo, Dept Infect Dis, Pavia, Italy
[5] Mol Virol Unit, Fondazione IRCCS Policlinico San Matteo, Virol & Microbiol, Pavia, Italy
[6] Dept Hematol Oncol Dis Fondaz IRCCS Policlin, Pavia, Italy
关键词
BONE-MARROW-TRANSPLANTATION; NON-RELAPSE MORTALITY; LEUKEMIA; DONORS; GVHD;
D O I
10.1097/TP.0000000000001257
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background Neurological complications (NC) after hematopoietic stem cell transplantation (HSCT) are rare events. The evolution of transplant procedures has resulted in improved survival and has allowed elderly patients or those with comorbidity to receive an HSCT. The risk of NC in these patients has still not been well defined. Therefore, we carried out an observational study to estimate the occurrence and identify the risks associated with NC. Methods The study cohort included 452 adult-allogeneic HSCT recipients, transplanted from 1997 to 2012. The median follow up was 1.3 year (0-15.7). A myeloablative regimen was used in 307 patients. Two hundred patients were grafted from matched unrelated donor (MUD), of these, 129 (64.5%) received an in vivo T-cell depletion. Results Out of 452 patients, 30 (6.6%) developed NC. Infections were the most frequent causes of NC (30%). Overall survival decreased in patients developing NC (P < 0.001). Univariate survival regression on the cumulative incidence of NC identified period of transplant, linear trend between 4-year periods (1997-2012) (P < 0.001), MUD (P < 0.001), and recipient's age (P = 0.034) as significant risk factors. In multivariate analysis, period of transplant (P < 0.001) and MUD (P = 0.004) remained significant independent risk factors. Matched unrelated donor recipients showed a 3.8-fold elevated risk of developing NC. Conclusions Analysis highlights a temporal trend of incidence of NC that progressively increased over time and confirms a strong association between donor type and risk of NC. Our observations suggest that, although relatively uncommon, NC after allo-HSCT, may become more frequent due to the improved overall survival in recent years.
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收藏
页码:616 / 623
页数:8
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