| Literature DB >> 26858357 |
Yasuyuki Arai1, Tadakazu Kondo2, Hirohito Yamazaki3, Katsuto Takenaka4, Junichi Sugita5, Takeshi Kobayashi6, Yukiyasu Ozawa7, Naoyuki Uchida8, Koji Iwato9, Naoki Kobayashi10, Yoshiyuki Takahashi11, Ken Ishiyama12, Takahiro Fukuda13, Tatsuo Ichinohe14, Yoshiko Atsuta15, Takehiko Mori16, Takanori Teshima5.
Abstract
Allogeneic bone marrow transplantation is an essential therapy for acquired aplastic anemia and prognosis has recently improved. However, engraftment failure and graft-versus-host disease are potential fatal complications. Various risk factors for poor prognosis have been identified, such as patient age and human-leukocyte antigen disparity, but the relationship between donor age and prognosis is still unknown. Therefore, we performed a cohort study to compare the prognosis of unrelated bone marrow transplantation from younger and older donors using the registry database in Japan. We evaluated 427 patients (age 16-72 years) with aplastic anemia who underwent bone marrow transplantation from younger (≤39 years, n=281) or older (≥40 years, n=146) unrelated donors. Overall survival of the older donor group was significantly inferior to that of the younger donor group (adjusted hazard ratio 1.64; 95% confidence interval 1.15-2.35; P<0.01). The incidence of fatal infection was significantly higher in the older donor group (13.7% vs. 7.5%; P=0.03). Primary engraftment failure and acute graft-versus-host disease were significantly more frequent in the older donor group (9.7% vs. 5.0%; adjusted hazard ratio 1.30; P=0.01, and 27.1% vs. 19.7%; adjusted hazard ratio 1.56; P=0.03, respectively). Acute graft-versus-host disease was related to a worse prognosis in the whole cohort. This study showed the inferiority of older donors in aplastic anemia; thus, donor age should be considered when multiple donors are available. A large-scale prospective study is warranted to establish a better donor selection algorithm for bone marrow transplantation in aplastic anemia. Copyright© Ferrata Storti Foundation.Entities:
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Year: 2016 PMID: 26858357 PMCID: PMC5004375 DOI: 10.3324/haematol.2015.139469
Source DB: PubMed Journal: Haematologica ISSN: 0390-6078 Impact factor: 9.941