Department of Gastroenterology, Hepatology, Endocrinology and Infectious Diseases, Freiburg University Hospital, Freiburg, Germany.
Aliment Pharmacol Ther. 2012 Oct;36(8):725-35. doi: 10.1111/apt.12032. Epub 2012 Sep 2.
Despite advances in immunosuppressive therapy, up to 10% of patients with severe Crohn's disease (CD) remain refractory to conventional treatment. Limited evidence from pilot trials suggests that high-dose immunosuppression and autologous peripheral blood stem cell transplantation (autoPBSCT) may induce remission in these patients, but there is substantial controversy regarding the safety and efficacy of this approach.
To address this issue, a monocentre phase I/II trial of autoPBSCT was performed in patients with refractory CD in our hospital.
Here, we report on the outcome of 12 patients with refractory CD treated with autoPBSCT. Briefly, CD34(+) -selected PBSCs were harvested after mobilisation therapy with cyclophosphamide and granulocyte-colony stimulating factor. Later, immunoablative conditioning therapy with high-dose cyclophosphamide followed by autoPBSCT was applied and clinical and endoscopic responses were analysed after a mean follow-up of 3.1 years (range 0.5-10.3 years).
PBSC harvest following mobilisation chemotherapy was successful in 11/12 patients and resulted in a clinical and endoscopic improvement in 7/12 patients. Subsequent conditioning and autoPBSCT were performed in nine patients and were relatively well tolerated. Among those, five patients achieved a clinical and endoscopic remission within 6 months after autoPBSCT. However, relapses occurred in 7/9 patients during follow-up, but disease activity could be controlled by low-dose corticosteroids and conventional immunosuppressive therapy.
Immunoablation by cyclophosphamide and autologous peripheral blood stem cell transplantation is safe and effective to induce remission of refractory Crohn's disease, and should be further evaluated in randomised controlled trials.
尽管免疫抑制治疗取得了进展,但仍有高达 10%的严重克罗恩病(CD)患者对常规治疗无反应。来自试验性试验的有限证据表明,高剂量免疫抑制和自体外周血干细胞移植(autoPBSCT)可能使这些患者缓解,但这种方法的安全性和疗效存在很大争议。
为了解决这个问题,我们在我院对难治性 CD 患者进行了一项自体 PBSCT 的单中心 I/II 期试验。
在这里,我们报告了 12 例难治性 CD 患者接受 autoPBSCT 的结果。简要地说,在用环磷酰胺和粒细胞集落刺激因子动员治疗后采集 CD34+ -PBSC。随后,应用高剂量环磷酰胺进行免疫清除性预处理,然后进行自体 PBSCT,在平均 3.1 年(0.5-10.3 年)的随访后分析临床和内镜反应。
12 例患者中有 11 例动员化疗后成功采集 PBSC,7 例患者临床和内镜改善。在 9 例患者中进行了随后的预处理和自体 PBSCT,且耐受性相对较好。其中,5 例患者在自体 PBSCT 后 6 个月内达到临床和内镜缓解。然而,在随访期间,7/9 例患者出现复发,但通过低剂量皮质类固醇和常规免疫抑制治疗可控制疾病活动。
环磷酰胺和自体外周血干细胞移植的免疫清除是安全有效的,可诱导难治性克罗恩病缓解,应在随机对照试验中进一步评估。