Combination of granulocyte–monocyte apheresis and tofacitinib: Multicentre and retrospective study

Iago Rodríguez-Lago , Fiorella Cañete , Elena Guerra-del-Río , Claudia Herrera-deGuise , Eva Iglesias , Eduardo Leo , Yamile Zabana , Manuel Barreiro-de Acosta , Daniel Ginard , José Luis Cabriada
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引用次数: 0

Abstract

Objective

Granulocyte–monocyte apheresis (GMA) has shown to be safe and effective in treating ulcerative colitis (UC), also in combination with biologics. The objective of this study is to evaluate the efficacy and safety of combining GMA after primary non-response (PNR) or loss of response (LOR) to tofacitinib (TOFA) in patients with UC.

Patients and methods

Retrospective study including all patients with refractory UC who received GMA plus TOFA. Efficacy was assessed 1 and 6 months after finishing GMA by partial Mayo score, C-reactive protein (CRP) and fecal calprotectin (FC). Descriptive statistics and non-parametric tests were used in the statistical analysis.

Results

Twelve patients were included (median 46 years [IQR, 37–58]; 67% female; 67% E3). Patients were mostly receiving TOFA 10 mg bid (75%), and 33% also concomitant steroids at baseline. Median partial Mayo score at baseline was 7 (IQR, 5–7), and it decreased to a median of 2 (IQR, 0–3) and 0 (IQR, 0–3) after 1 and 6 months (p = 0.027 and 0.020, respectively), while no differences were found in CRP and FC. Clinical remission was achieved by 6 patients both at 1 (50%) and 6 months (67%). CF values < 250 mg/kg were achieved by 2 and 4 patients at 1 and 6 months (data available in 5 and 7 patients, respectively). No patient required dose-escalation of TOFA, and one patient was able to de-escalate the drug. No patient required colectomy and all patients under steroids were able to stop them.

Conclusion

The combination of GMA and TOFA can be effective in selected cases of UC after PNR or LOR to this drug.

粒细胞-单核细胞分离术与托法替尼的联合应用:多中心回顾性研究
目的粒细胞-单核细胞分离术(GMA)已被证明在治疗溃疡性结肠炎(UC)方面安全有效,也可与生物制剂联合使用。本研究旨在评估 UC 患者对法替尼(TOFA)治疗原发性无应答(PNR)或失去应答(LOR)后联合 GMA 的疗效和安全性。通过部分梅奥评分、C反应蛋白(CRP)和粪便钙蛋白(FC)评估完成GMA治疗1个月和6个月后的疗效。统计分析采用了描述性统计和非参数检验。大多数患者(75%)都在接受 10 毫克/次的 TOFA 治疗,33% 的患者在基线时还同时服用类固醇。基线时梅奥部分评分的中位数为 7(IQR,5-7),1 个月和 6 个月后分别降至中位数 2(IQR,0-3)和 0(IQR,0-3)(p = 0.027 和 0.020),而 CRP 和 FC 则无差异。有 6 名患者在 1 个月(50%)和 6 个月(67%)后均获得临床缓解。分别有 2 名和 4 名患者在 1 个月和 6 个月时达到了 250 mg/kg 的 CF 值(分别有 5 名和 7 名患者的数据)。没有患者需要调整 TOFA 的剂量,其中一名患者能够降低药物剂量。没有患者需要进行结肠切除术,所有使用类固醇的患者都能停止使用类固醇。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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