World journal of gastroenterology · 2026
Long-term clinical outcomes with filgotinib in ulcerative colitis: 12-month results from the FILGUITO study.
СтатьяНаблюдательное исследованиеМногоцентровое исследованиеНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Caballero-Mateos Antonio M, Trigo-Salado Claudio, Suárez-Toribio Álvaro, Martín-Rodríguez María Del Mar, Rodríguez-González Francisco J, Valdés-Delgado Teresa, Pallarés-Manrique Héctor, Trapero-Martínez Ana María, Olmedo-Martín Raúl, Bailón-Gaona Cristina, Benitez Cantero José Manuel, Gros B, Sáez-Díaz Antonia, Hernández-Martínez Álvaro
Аннотация
BACKGROUND: Filgotinib, a JAK1-preferential inhibitor, has demonstrated efficacy in pivotal clinical trials for moderate-to-severe ulcerative colitis (UC), leading to regulatory approvals. While emerging real-world studies provide short-term effectiveness data, comprehensive long-term evidence-particularly beyond 6 months-remains scarce, especially in heavily biologic-experienced populations.
AIM: To evaluate the 12-month effectiveness, safety, and predictors of response to filgotinib in a real-world cohort of patients with moderate-to-severe UC treated across multiple centers in Andalusia, Spain.
METHODS: This multicenter, ambispective observational study (FILGUITO registry) included 104 adults with moderate-to-severe UC initiating filgotinib therapy. Demographic, clinical, laboratory, and endoscopic data were collected at baseline and at 8 weeks, 6 months, and 12 months. Effectiveness outcomes included clinical remission (Mayo partial score < 3 with no subscore > 1 and no rectal bleeding), clinical-biochemical remission (clinical remission plus fecal calprotectin < 250 μg/g), and steroid-free remission (clinical remission with no corticosteroid courses from week 8). Safety was assessed through adverse event monitoring.
RESULTS: The median age was 40.7 years (IQR: 29.5-51.0), with 56.7% male patients. The majority (79.8%) had prior advanced therapy exposure, with a median of 1 prior biologic (IQR: 1-3). Clinical remission rates were 60.8% at 8 weeks, 61.4% at 6 months, and 60.3% at 12 months (all P < 0.001 vs baseline). Clinical-biochemical remission reached 33.0%, 38.6%, and 31.0% at the same timepoints. Steroid-free remission was achieved in 60.0% at 6 months and 56.9% at 12 months. Median fecal calprotectin decreased significantly from 2000 μg/g at baseline (IQR: 755.8-2392.5) to 153 μg/g at 12 months (IQR: 21.3-569.0, P < 0.001). Treatment discontinuation occurred in 22.1% of patients by 12 months, primarily due to lack of response. Serious adverse events were rare (2.8%), with a favorable safety profile. Patients with only one prior biologic showed higher remission rates compared to those with multiple prior treatments.
CONCLUSION: Filgotinib demonstrates sustained clinical effectiveness and a favorable safety profile over 12 months in a real-world UC cohort with extensive prior biologic exposure. Effectiveness is optimized at earlier treatment lines, though meaningful benefit persists in heavily pre-treated populations.
AIM: To evaluate the 12-month effectiveness, safety, and predictors of response to filgotinib in a real-world cohort of patients with moderate-to-severe UC treated across multiple centers in Andalusia, Spain.
METHODS: This multicenter, ambispective observational study (FILGUITO registry) included 104 adults with moderate-to-severe UC initiating filgotinib therapy. Demographic, clinical, laboratory, and endoscopic data were collected at baseline and at 8 weeks, 6 months, and 12 months. Effectiveness outcomes included clinical remission (Mayo partial score < 3 with no subscore > 1 and no rectal bleeding), clinical-biochemical remission (clinical remission plus fecal calprotectin < 250 μg/g), and steroid-free remission (clinical remission with no corticosteroid courses from week 8). Safety was assessed through adverse event monitoring.
RESULTS: The median age was 40.7 years (IQR: 29.5-51.0), with 56.7% male patients. The majority (79.8%) had prior advanced therapy exposure, with a median of 1 prior biologic (IQR: 1-3). Clinical remission rates were 60.8% at 8 weeks, 61.4% at 6 months, and 60.3% at 12 months (all P < 0.001 vs baseline). Clinical-biochemical remission reached 33.0%, 38.6%, and 31.0% at the same timepoints. Steroid-free remission was achieved in 60.0% at 6 months and 56.9% at 12 months. Median fecal calprotectin decreased significantly from 2000 μg/g at baseline (IQR: 755.8-2392.5) to 153 μg/g at 12 months (IQR: 21.3-569.0, P < 0.001). Treatment discontinuation occurred in 22.1% of patients by 12 months, primarily due to lack of response. Serious adverse events were rare (2.8%), with a favorable safety profile. Patients with only one prior biologic showed higher remission rates compared to those with multiple prior treatments.
CONCLUSION: Filgotinib demonstrates sustained clinical effectiveness and a favorable safety profile over 12 months in a real-world UC cohort with extensive prior biologic exposure. Effectiveness is optimized at earlier treatment lines, though meaningful benefit persists in heavily pre-treated populations.