Gastroenterology Department, Hospital Clínic de Barcelona, IDIBAPS, CIBERehd, Barcelona, Spain.
Hematology Department, Hospital Clínic de Barcelona, Barcelona, Spain.
Gut. 2016 Sep;65(9):1456-62. doi: 10.1136/gutjnl-2015-309836. Epub 2015 Nov 19.
To evaluate the feasibility and toxicity of autologous haematopoietic stem cell transplantation (HSCT) for the treatment of refractory Crohn's disease (CD).
In this prospective study, patients with refractory CD suffering an aggressive disease course despite medical treatment, impaired quality of life and in whom surgery was not an acceptable option underwent HSCT. Toxicity and complications during the procedure and within the first year following transplantation were evaluated, along with the impact of the introduction of supportive measures on safety outcomes.
26 patients were enrolled. During mobilisation, 16 patients (62%) presented febrile neutropaenia, including one bacteraemia and two septic shocks. Neutropaenia median time after mobilisation was 5 days. 5 patients withdrew from the study after mobilisation and 21 patients entered the conditioning phase. Haematopoietic recovery median time for neutrophils (>0.5×10(9)/L) was 11 days and for platelets (>20×10(9)/L) 4 days. Twenty patients (95%) suffered febrile neutropaenia and three patients (27%) presented worsening of the perianal CD activity during conditioning. Among non-infectious complications, 6 patients (28.5%) presented antithymocyte globulin reaction, 12 patients (57%) developed mucositis and 2 patients (9.5%) had haemorrhagic complications. Changes in supportive measures over the study, particularly antibiotic prophylaxis regimes during mobilisation and conditioning, markedly diminished the incidence of severe complications. During the first 12-month follow-up, viral infections were the most commonly observed complications, and one patient died due to systemic cytomegalovirus infection.
Autologous HSCT for patients with refractory CD is feasible, but extraordinary supportive measures need to be implemented. We suggest that this procedure should only be performed in highly experienced centres.
评估自体造血干细胞移植(HSCT)治疗难治性克罗恩病(CD)的可行性和毒性。
在这项前瞻性研究中,患有难治性 CD 的患者尽管接受了药物治疗,但疾病仍呈侵袭性进展、生活质量受损且手术不可行,他们接受了 HSCT。评估了手术过程中和移植后 1 年内的毒性和并发症,以及引入支持措施对安全性结果的影响。
共纳入 26 例患者。动员期间,16 例(62%)患者出现发热性中性粒细胞减少症,包括 1 例菌血症和 2 例感染性休克。动员后中性粒细胞减少的中位时间为 5 天。5 例患者在动员后退出研究,21 例患者进入预处理阶段。中性粒细胞(>0.5×109/L)和血小板(>20×109/L)的造血恢复中位时间分别为 11 天和 4 天。20 例(95%)患者发生发热性中性粒细胞减少症,3 例(27%)患者在预处理期间肛周 CD 活动度恶化。非感染性并发症中,6 例(28.5%)患者出现抗胸腺细胞球蛋白反应,12 例(57%)患者出现黏膜炎,2 例(9.5%)患者出现出血并发症。研究期间支持措施的变化,特别是动员和预处理期间抗生素预防方案的变化,显著降低了严重并发症的发生率。在最初的 12 个月随访期间,病毒感染是最常见的并发症,1 例患者因全身巨细胞病毒感染而死亡。
自体 HSCT 治疗难治性 CD 是可行的,但需要实施特殊的支持措施。我们建议该手术仅在经验丰富的中心进行。