Jantunen E, Ruutu P, Piilonen A, Volin L, Parkkali T, Ruutu T
Department of Medicine, Helsinki University Central Hospital, Finland.
Bone Marrow Transplant. 2000 Oct;26(7):759-62. doi: 10.1038/sj.bmt.1702604.
The outcome of invasive aspergillosis (IA) has been considered poor in allogeneic BMT recipients. We analyzed retrospectively the treatment and outcome of IA diagnosed during life in a recent cohort of 20 allogeneic BMT recipients. All patients were initially treated with amphotericin B (AmB) (conventional 16, liposomal 4). Due to toxicity, conventional AmB was changed to a liposomal preparation in 10 patients. Five patients also received itraconazole and three underwent surgery. Of 19 evaluable patients, two patients achieved a complete response and a partial response was observed in five patients (response rate 37%). The median survival was 37 days after the diagnosis. Only two patients (10%) were cured. The prognosis of allogeneic BMT recipients with IA has remained poor. Although treatment responses are common, immunosuppression aggravated by GVHD and its treatment, as well as the commonly disseminated presentation of IA, seem to be major obstacles to the success of therapy. Bone Marrow Transplantation (2000) 26, 759-762.
侵袭性曲霉病(IA)在异基因骨髓移植(BMT)受者中的预后一直被认为较差。我们回顾性分析了近期20例异基因BMT受者在生存期内诊断为IA的治疗情况及预后。所有患者最初均接受两性霉素B(AmB)治疗(传统剂型16例,脂质体剂型4例)。由于毒性反应,10例患者将传统AmB换为脂质体制剂。5例患者还接受了伊曲康唑治疗,3例接受了手术。在19例可评估的患者中,2例患者获得完全缓解,5例患者观察到部分缓解(缓解率37%)。诊断后的中位生存期为37天。仅2例患者(10%)治愈。异基因BMT合并IA受者的预后仍然较差。尽管治疗反应常见,但移植物抗宿主病(GVHD)及其治疗加重的免疫抑制,以及IA常见的播散性表现,似乎是治疗成功的主要障碍。《骨髓移植》(2000年)第26卷,第759 - 762页