Kinney Timothy, Rawlins Matthew, Kozarek Richard, France Renée, Patterson David
Section of Gastroenterology, Virginia Mason Medical Center, Seattle, Washington 98111, USA.
Am J Gastroenterol. 2003 Mar;98(3):608-12. doi: 10.1111/j.1572-0241.2003.07286.x.
Infliximab has been proven effective for treatment of active Crohn's and fistulizing Crohn's disease. We reviewed our experience with infliximab in patients with Crohn's disease to determine if its combination with immunomodulators leads to better response and longer periods of disease quiescence.
We performed a retrospective chart review of 122 patients with Crohn's disease who received infliximab infusions. Data were collected on patient demographics, clinical response to infliximab, fistula response, prednisone dose, infusion reactions/side effects, concomitant immunomodulator therapy, and time intervals between infliximab infusions.
Of 122 patients receiving infliximab infusions, 117 completed more than 2 wk of follow-up (400 infusions), and five patients had no follow-up. Co-therapies included azathioprine (AZA) in 47 (40.2%) patients, 6-mercaptopurine (6-MP) in 11 (9.4%), methotrexate (MTX) in 23 (19.7%), prednisone in 64 (54.7%), mesalamine in 51 (43.6%), and antibiotics in 16 (13.7%). Mean follow-up was 52 wk (14-864 days). Overall response rate to infliximab was similar between patients receiving immunomodulators (AZA/6-MP 87.9%, MTX 82.6%) and patients receiving infliximab alone (75%), although there was a trend toward higher response with AZA/6-MP (p = 0.10). More frequent drug reactions/side effects occurred in the infliximab alone group (22.2%) compared with patients receiving MTX (13.0%) and AZA/6-MP (13.8%), but this was not statistically significant. Prednisone dosage was reduced from a mean of 19.5 mg to 7.5 mg per day overall (p < 0.05). Fistula response and dosing intervals were not affected by concomitant immunosuppression.
Concomitant use of immunomodulators with infliximab in patients with Crohn's disease did not improve patient response to several parameters measured, including clinical response rate, dose reduction of prednisone, fistula response, and mean intervals between infliximab infusions.
英夫利昔单抗已被证明对治疗活动性克罗恩病和瘘管性克罗恩病有效。我们回顾了我们在克罗恩病患者中使用英夫利昔单抗的经验,以确定其与免疫调节剂联合使用是否能带来更好的反应和更长时间的疾病缓解期。
我们对122例接受英夫利昔单抗输注的克罗恩病患者进行了回顾性病历审查。收集了患者的人口统计学数据、对英夫利昔单抗的临床反应、瘘管反应、泼尼松剂量、输注反应/副作用、伴随的免疫调节剂治疗以及英夫利昔单抗输注之间的时间间隔。
在122例接受英夫利昔单抗输注的患者中,117例完成了超过2周的随访(400次输注),5例患者没有随访。联合治疗包括47例(40.2%)患者使用硫唑嘌呤(AZA),11例(9.4%)患者使用6-巯基嘌呤(6-MP),23例(19.7%)患者使用甲氨蝶呤(MTX),64例(54.7%)患者使用泼尼松,51例(43.6%)患者使用美沙拉嗪,16例(13.7%)患者使用抗生素。平均随访时间为52周(14 - 864天)。接受免疫调节剂(AZA/6-MP 87.9%,MTX 82.6%)的患者与单独接受英夫利昔单抗的患者(75%)对英夫利昔单抗的总体反应率相似,尽管AZA/6-MP有更高反应的趋势(p = 0.10)。与接受MTX(13.0%)和AZA/6-MP(13.8%)的患者相比,单独使用英夫利昔单抗的组中药物反应/副作用更频繁(22.2%),但这无统计学意义。泼尼松剂量总体上从平均每天19.5毫克降至7.5毫克(p < 0.05)。瘘管反应和给药间隔不受伴随免疫抑制的影响。
在克罗恩病患者中,免疫调节剂与英夫利昔单抗联合使用并未改善患者对所测量的几个参数的反应,包括临床反应率、泼尼松剂量减少、瘘管反应以及英夫利昔单抗输注之间的平均间隔。