Ziring David A, Wu Steven S, Mow William S, Martín Martín G, Mehra Mini, Ament Marvin E
Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Mattel Children's Hospital, David Geffen School of Medicine at the University of California Los Angeles, CA 90095-1752, USA.
J Pediatr Gastroenterol Nutr. 2007 Sep;45(3):306-11. doi: 10.1097/MPG.0b013e31805b82e4.
To evaluate tacrolimus in 3 situations: for the induction of remission in children with severe steroid-resistant ulcerative colitis (UC); for steroid sparing in children with steroid-dependent UC in whom treatment with other immunosuppressants fails; and for the maintenance of remission in children with steroid-dependent and steroid-resistant UC.
We retrospectively evaluated 18 consecutive patients (13 with pancolitis) who were treated with oral tacrolimus at our institution from May 1999 to October 2005. Nine patients had steroid-resistant UC and 9 patients were steroid-dependent. We started patients initially on tacrolimus 0.2 mg/kg divided twice daily, with a goal plasma trough level of 10 to 15 ng/mL for the first 2 weeks, and then titrated doses to achieve plasma levels between 7 and 12 ng/mL after induction.
Of the 18 patients in this study, 17 showed a positive response to tacrolimus therapy (ie, cessation of diarrhea and other symptoms) and 5 showed a prolonged response to tacrolimus. The mean time from initiation of tacrolimus therapy until response was 8.5 days. The mean duration of response was 260 days. Eleven of 18 patients required colectomy, including all of the patients with steroid-resistant UC, but only 2 of 9 who were steroid-dependent. The mean time from initiation of tacrolimus until colectomy was 392 days.
It is possible that tacrolimus may benefit selected patients with steroid-dependent UC, including those who are intolerant of 6-mercaptopurine or azathioprine. Conversely, patients with steroid-resistant UC are unlikely to sustain a prolonged clinical response to tacrolimus and seem to require colectomy eventually. Careful considerations of risk versus benefit, as well as close monitoring for adverse effects, are essential in all patients.
评估他克莫司在三种情况下的应用:诱导重症激素抵抗性溃疡性结肠炎(UC)患儿缓解;在其他免疫抑制剂治疗失败的激素依赖性UC患儿中减少激素用量;维持激素依赖性和激素抵抗性UC患儿的缓解状态。
我们回顾性评估了1999年5月至2005年10月在我院接受口服他克莫司治疗的18例连续患者(13例为全结肠炎)。9例患者为激素抵抗性UC,9例为激素依赖性UC。我们最初让患者服用他克莫司0.2mg/kg,每日分两次服用,前2周目标血药谷浓度为10至15ng/mL,诱导期后调整剂量以使血药浓度达到7至12ng/mL。
本研究的18例患者中,17例对他克莫司治疗有阳性反应(即腹泻和其他症状停止),5例对他克莫司有持久反应。从开始他克莫司治疗到出现反应的平均时间为8.5天。反应的平均持续时间为260天。18例患者中有11例需要行结肠切除术,包括所有激素抵抗性UC患者,但9例激素依赖性患者中只有2例。从开始他克莫司治疗到结肠切除术的平均时间为392天。
他克莫司可能使部分激素依赖性UC患者受益,包括那些不耐受6-巯基嘌呤或硫唑嘌呤的患者。相反,激素抵抗性UC患者不太可能对他克莫司维持长期临床反应,最终似乎需要行结肠切除术。对所有患者而言,仔细权衡风险与获益以及密切监测不良反应至关重要。