Johnston Laura J, Brown Janice, Shizuru Judith A, Stockerl-Goldstein Keith E, Stuart Monic J, Blume Karl G, Negrin Robert S, Chao Nelson J
Stanford University, Stanford, California 94305, USA.
Biol Blood Marrow Transplant. 2005 Jan;11(1):47-55. doi: 10.1016/j.bbmt.2004.10.004.
We conducted a phase II trial in 19 chronic graft-versus-host disease (cGVHD) patients with rapamycin, calcineurin inhibitors, and prednisone with the goals of controlling cGVHD, reducing prednisone use, and defining the safety of this regimen. Rapamycin was begun as second-line (n = 9) or more than second-line (n = 10) therapy. With a median follow-up of 42 months, 16 patients were evaluable for response. Nine patients discontinued rapamycin because of poor compliance/patient request (n = 2) or an adverse event (n = 7), 3 of whom were not evaluable because of withdrawal at < or =1 month or noncompliance. The adverse events included serum creatinine > or =2.4 mg/dL (n = 4), hemolytic uremic syndrome (n = 2), and relapse of malignancy (n = 1). Fifteen of 16 evaluable patients had a clinical response. Five of the 16 discontinued the drug, and 1 died of relapsed leukemia. Of the 10 patients who continued rapamycin, 2 discontinued and 1 successfully tapered all systemic immunosuppression. Three of the 10 developed progressive cGVHD with tapering immunosuppression; all responded to resumption of prior medications. Four of the 10 patients required alternate therapy for persistent or progressive cGVHD while receiving rapamycin; prednisone was discontinued (n = 2) or tapered at the time of progressive disease (n = 2). Seventeen of 19 original patients were alive. One death was due to relapsed malignancy, and 1 was due to congestive heart failure. In this report of rapamycin as cGVHD therapy, there is evidence of rapamycin's efficacy. Given the significant toxicities described, investigation of altered administration of rapamycin and calcineurin inhibitors should be pursued in future cGVHD trials.
我们对19例慢性移植物抗宿主病(cGVHD)患者进行了一项II期试验,使用雷帕霉素、钙调神经磷酸酶抑制剂和泼尼松,目的是控制cGVHD、减少泼尼松的使用,并确定该方案的安全性。雷帕霉素作为二线(n = 9)或二线以上(n = 10)治疗开始使用。中位随访42个月时,16例患者可评估反应。9例患者因依从性差/患者要求(n = 2)或不良事件(n = 7)停用雷帕霉素,其中3例因在≤1个月时退出或不依从而无法评估。不良事件包括血清肌酐≥2.4 mg/dL(n = 4)、溶血尿毒综合征(n = 2)和恶性肿瘤复发(n = 1)。16例可评估患者中有15例有临床反应。16例中有5例停药,1例死于白血病复发。在继续使用雷帕霉素的10例患者中,2例停药,1例成功逐渐减少所有全身免疫抑制治疗。10例中有3例在免疫抑制逐渐减少时发生进行性cGVHD;所有患者对恢复先前用药均有反应。10例患者中有4例在接受雷帕霉素治疗时因持续性或进行性cGVHD需要替代治疗;泼尼松停药(n = 2)或在疾病进展时逐渐减量(n = 2)。19例原始患者中有17例存活。1例死亡归因于恶性肿瘤复发,1例归因于充血性心力衰竭。在本关于雷帕霉素作为cGVHD治疗的报告中,有证据表明雷帕霉素具有疗效。鉴于所描述的显著毒性,未来cGVHD试验应探讨改变雷帕霉素和钙调神经磷酸酶抑制剂给药方式的研究。