Department of Hematology, Oita Prefectural Hospital, 2-8-1 Bunyo, Oita City, Oita, 870-8511, Japan.
Department of Hematology, Jyoban Hospital, Tokiwa Foundation, Fukushima, Japan.
Ann Hematol. 2023 Sep;102(9):2507-2516. doi: 10.1007/s00277-023-05320-4. Epub 2023 Jun 20.
Stenotrophomonas maltophilia (S. maltophilia) is an aerobic nonfermenting Gram-negative bacillus widely distributed in the environment that has inherent multidrug resistance to beta-lactam and carbapenem antibiotics. S. maltophilia infection (SMI) is known as an important fatal complication following allogeneic hematopoietic stem cell transplantation (HSCT), but its clinical characteristics have not been well clarified. A retrospective study to identify the incidence, risk factors, and outcomes of SMI after allogeneic HSCT was performed using the database of the Japanese nationwide registry, including 29,052 patients who received allogeneic HSCT in Japan between January 2007 and December 2016. A total of 665 patients developed SMI (sepsis/septic shock, 432; pneumonia, 171; other, 62). The cumulative incidence of SMI at 100 days after HSCT was 2.2%. Among risk factors identified for SMI (age ≥ 50 years, male, performance status 2-4, cord blood transplantation [CBT], myeloablative conditioning, Hematopoietic Cell Transplant-Comorbidity Index [HCT-CI] score 1-2, HCT-CI score ≥ 3, and active infectious disease at HSCT), CBT was the strongest risk factor (hazard ratio, 2.89; 95%CI, 1.94-4.32; p < 0.001). The survival rate at day 30 after SMI was 45.7%, and SMI before neutrophil engraftment was significantly associated with poor survival (survival rate 30 days after SMI, 40.1% and 53.8% in patients with SMI before and after engraftment, respectively; p = 0.002). SMI is rare after allogeneic HSCT, but its prognosis is extremely poor. CBT was a strong risk factor for SMI, and its development prior to neutrophil engraftment was associated with poor survival.
嗜麦芽寡养单胞菌(S. maltophilia)是一种广泛分布于环境中的需氧非发酵革兰阴性杆菌,对β-内酰胺类和碳青霉烯类抗生素具有固有多重耐药性。嗜麦芽寡养单胞菌感染(SMI)是异基因造血干细胞移植(HSCT)后重要的致命并发症,但临床特征尚未得到充分阐明。本研究使用日本全国登记处的数据库进行了一项回顾性研究,以确定异基因 HSCT 后 SMI 的发生率、危险因素和结局,该数据库包括 2007 年 1 月至 2016 年 12 月期间在日本接受异基因 HSCT 的 29052 例患者。共有 665 例患者发生 SMI(败血症/感染性休克,432 例;肺炎,171 例;其他,62 例)。HSCT 后 100 天 SMI 的累积发生率为 2.2%。SMI 的危险因素(年龄≥50 岁、男性、表现状态 2-4 级、脐带血移植[CBT]、清髓性预处理、造血细胞移植合并症指数[HCT-CI]评分 1-2 分、HCT-CI 评分≥3 分和 HSCT 时存在活动性传染病)中,CBT 是最强的危险因素(危险比,2.89;95%CI,1.94-4.32;p<0.001)。SMI 后 30 天的生存率为 45.7%,中性粒细胞植入前发生 SMI 与生存率差显著相关(SMI 后 30 天的生存率分别为植入前和植入后的 40.1%和 53.8%;p=0.002)。SMI 异基因 HSCT 后很少见,但预后极差。CBT 是 SMI 的一个强烈危险因素,其在中性粒细胞植入前的发生与生存率差相关。