MedElevator Войти в исследования
← Поиск публикаций

DOI 10.3748/wjg.v31.i42.111282

Медицинская библиотека · World journal of gastroenterology · 2025

Value of tofacitinib extended induction therapy in patients with moderate-to-severe ulcerative colitis: A real-world 52-week follow-up study.

Tzouvala Maria, Zacharopoulou Eirini, Kalafateli Maria, Viazis Nikos, Psistakis Andreas, Theodoropoulou Angeliki, Drygiannakis Ioannis, Karmiris Konstantinos, Koutroubakis Ioannis E, Kevrekidou Polyxeni, Soufleris Kostas, Katsaros Marios, Giouleme Olga, Fousekis Fotios, Katsanos Konstantinos, Christodoulou Dimitrios, Gaki Aikaterini, Papathanasiou Evgenia, Bamias Giorgos, Zampeli Evanthia, Michopoulos Spyridon, Kyriakos Nikolaos, Veretanos Christos, Argyriou Konstantinos, Kapsoritakis Andreas, Tribonias George, Mantzaris Gerassimos J, Liatsos Christos

СтатьяМногоцентровое исследованиеНаблюдательное исследованиеПеревод в очереди

Аннотация

BACKGROUND

Tofacitinib is an oral, selective Janus kinase inhibitor that is approved for the treatment of ulcerative colitis (UC). The 8-week induction protocol involves the administration of 10 mg twice daily (bid) with the possibility of extending the induction period to 16 weeks. The maintenance dose of tofacitinib is either 5 mg or 10 mg bid.

AIM: To assess predictors for clinical remission and drug persistence in patients with UC receiving the extended induction tofacitinib protocol.

METHODS

This was a real-world multicenter retrospective study in patients with moderate-to-severe UC. Patients received physician-directed extended induction tofacitinib treatment. We collected clinical and demographic data at baseline and data regarding clinical, laboratory, and endoscopic evaluations, therapeutic modifications, and adverse events at the 52-week follow-up. Possible predictors for clinical remission at week 52 was the primary endpoint. Differences between patients receiving 5 mg bid vs 10 mg bid at week 52 and identification of predictors for treatment persistence were secondary endpoints.

RESULTS

Thirty-seven consecutive patients from 11 medical centers were included [51.4% males with median age 39 (17-64) years]. Twenty-eight patients continued treatment until week 52 (75.7%) with 67.9% receiving 10 mg tofacitinib; all had prior history of biologic use. We observed that 57.1% of patients achieved clinical remission (66.7% in the 5 mg tofacitinib group and 52.6% in the 10 mg tofacitinib group, P = 0.483). De-escalation to 5 mg tofacitinib was attempted in 17 patients with a success rate of 52.9%. Prior biologic use was significantly more frequent in patients treated with 10 mg tofacitinib. Active smoking was significantly associated with treatment discontinuation at week 52. We identified eight adverse events, and only one led to treatment discontinuation.

CONCLUSION

Our results supported the extended induction strategy with tofacitinib in selected patients with UC. Patients with prior failure of advanced therapies particularly benefitted, highlighting the importance of personalized maintenance regimens.

Для цитирования: Tzouvala Maria, Zacharopoulou Eirini, Kalafateli Maria, Viazis Nikos, Psistakis Andreas, Theodoropoulou Angeliki, Drygiannakis Ioannis, Karmiris Konstantinos, Koutroubakis Ioannis E, Kevrekidou Polyxeni, Soufleris Kostas, Katsaros Marios, Giouleme Olga, Fousekis Fotios, Katsanos Konstantinos, Christodoulou Dimitrios, Gaki Aikaterini, Papathanasiou Evgenia, Bamias Giorgos, Zampeli Evanthia, Michopoulos Spyridon, Kyriakos Nikolaos, Veretanos Christos, Argyriou Konstantinos, Kapsoritakis Andreas, Tribonias George, Mantzaris Gerassimos J, Liatsos Christos. Value of tofacitinib extended induction therapy in patients with moderate-to-severe ulcerative colitis: A real-world 52-week follow-up study.. World journal of gastroenterology. 2025. DOI: 10.3748/wjg.v31.i42.111282.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

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.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.