Yu C, Storb R, Deeg H J, Graham T C, Scheuning F G, Huss R, Seidel K, Fitzsimmons W E
Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA 98104-2092, USA.
Bone Marrow Transplant. 1996 Apr;17(4):649-53.
We previously reported an synergism between methotrexate and tacrolimus (FK506) in preventing graft-versus-host disease (GVHD) in dogs given DLA-nonidentical unrelated marrow grafts after 9.2 Gy of total body irradiation (TBI). Methotrexate was given at 0.4 mg/kg i.v. on days 1, 3, 6 and 11 and FK506 at 0.15 mg/kg/day i.m. on days 0-8 and 0.5 mg/kg/day orally on days 9-90. Half of the dogs became long-term survivors. A major toxicity was gastrointestinal, and 25% of dogs died with intussusception. The current study addresses the problem of intussusception by making changes in drug doses used. In one group of dogs, FK506 was reduced to 0.075 mg/kg i.m. on days 1-8, while methotrexate was administered per original schedule. In a second group, methotrexate was reduced to a single dose on day 7, while FK506 was either administered per the original or reduced-dose schedule. None of the 17 current dogs developed intussusception, however, all but two dogs died with GVHD (n = 12) or graft failure (n = 3). Only two dogs survived after transient GVHD. Results show that there is little room for maneuvering FK506 or methotrexate doses, and hopes of reducing gastrointestinal toxicity by dose modifications while retaining the ability to prevent GVHD were not fulfilled.
我们之前报道过,在给接受9.2 Gy全身照射(TBI)后移植DLA不匹配的无关骨髓的犬只中,甲氨蝶呤和他克莫司(FK506)在预防移植物抗宿主病(GVHD)方面存在协同作用。甲氨蝶呤在第1、3、6和11天静脉注射,剂量为0.4 mg/kg,FK506在第0 - 8天肌肉注射,剂量为0.15 mg/kg/天,在第9 - 90天口服,剂量为0.5 mg/kg/天。一半的犬只成为长期存活者。主要毒性是胃肠道毒性,25%的犬只因肠套叠死亡。当前研究通过改变用药剂量来解决肠套叠问题。在一组犬只中,FK506在第1 - 8天降至0.075 mg/kg肌肉注射,而甲氨蝶呤按原方案给药。在第二组中,甲氨蝶呤在第7天减为单次剂量,而FK506按原方案或减量方案给药。目前的17只犬中没有一只发生肠套叠,然而,除两只犬外,所有犬只因移植物抗宿主病(n = 12)或移植失败(n = 3)死亡。只有两只犬在短暂的移植物抗宿主病后存活。结果表明,调整FK506或甲氨蝶呤的剂量空间很小,通过调整剂量来降低胃肠道毒性同时保留预防移植物抗宿主病能力的希望未能实现。