Park Mi Sung, Kim Dong Hyun, Kim Duk Hwan, Park Soo Jung, Hong Sung Pil, Kim Tae Il, Kim Won Ho, Cheon Jae Hee
Department of Internal Medicine, Yonsei University College of Medicine, 50 Yonsei-ro, Seodaemun-gu, Seoul, 120-752, Republic of Korea.
Dig Dis Sci. 2015 Jan;60(1):195-204. doi: 10.1007/s10620-014-3355-4. Epub 2014 Sep 20.
The thiopurine drugs, azathioprine (AZA), and 6-mercaptopurine (6-MP) are well-established drugs for the treatment of inflammatory bowel disease (IBD). Although leukopenia is a well-recognized side effect of AZA/6-MP treatment, its association with therapeutic effects has yet to be determined. We therefore evaluated the influences of thiopurine-induced leukopenia on the long-term prognosis of IBD.
We included 196 IBD patients [45 with ulcerative colitis (UC), 68 with Crohn's disease (CD), and 83 with intestinal Behçet's disease (BD)] who were treated with AZA/6-MP and achieved remission between January 2006 and December 2012. We retrospectively analyzed patient characteristics, AZA/6-MP maintenance dose (mg/kg), the lowest white blood cell (WBC) count during AZA/6-MP treatment, duration of remission, and the occurrence of relapse. We compared the clinical variables between leukopenic (n = 120, WBC count <4,000/μL) and nonleukopenic (n = 76, WBC count ≥ 4,000/μL) patients.
The two groups were well matched for baseline clinical characteristics. The cumulative relapse-free survival rate was higher in the leukopenic group than the nonleukopenic group by Kaplan-Meier survival analysis (log-rank test, P < 0.001). On multivariate analysis, age, duration of AZA/6-MP treatment, presence of macrocytosis, and the presence of leukopenia were negatively associated with relapse (odds ratios 0.975, 0.988, 0.563, and 0.390, respectively). On subgroup analysis, the cumulative relapse-free survival rate was significantly higher in the leukopenic group than in the nonleukopenic group for all types of IBDs, including UC, CD, and intestinal BD (log-rank test, P = 0.032, 0.047, and 0.002, respectively).
Leukopenia during thiopurine maintenance therapy was associated with prolonged remission in patients with IBD and Behcet's disease.
硫唑嘌呤(AZA)和6-巯基嘌呤(6-MP)这两种硫嘌呤类药物是治疗炎症性肠病(IBD)的常用药物。虽然白细胞减少是AZA/6-MP治疗公认的副作用,但其与治疗效果的关联尚未确定。因此,我们评估了硫嘌呤诱导的白细胞减少对IBD长期预后的影响。
我们纳入了196例在2006年1月至2012年12月期间接受AZA/6-MP治疗并实现缓解的IBD患者[45例溃疡性结肠炎(UC)、68例克罗恩病(CD)和83例肠道白塞病(BD)]。我们回顾性分析了患者特征、AZA/6-MP维持剂量(mg/kg)、AZA/6-MP治疗期间的最低白细胞(WBC)计数、缓解持续时间和复发情况。我们比较了白细胞减少组(n = 120,WBC计数<4000/μL)和非白细胞减少组(n = 76,WBC计数≥4000/μL)之间的临床变量。
两组在基线临床特征方面匹配良好。通过Kaplan-Meier生存分析,白细胞减少组的累积无复发生存率高于非白细胞减少组(对数秩检验,P < 0.001)。多因素分析显示,年龄、AZA/6-MP治疗持续时间、大细胞性贫血的存在以及白细胞减少与复发呈负相关(优势比分别为0.975、0.988、0.563和0.390)。亚组分析显示,在所有类型的IBD中,包括UC、CD和肠道BD,白细胞减少组的累积无复发生存率均显著高于非白细胞减少组(对数秩检验,P分别为0.032、0.047和0.002)。
硫嘌呤维持治疗期间的白细胞减少与IBD和白塞病患者的缓解期延长有关。