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Scientific reports · 2025

Prognostic impact of hand-foot skin reaction in regorafenib-treated adult-type diffuse gliomas: A multicenter Turkish Oncology Group study.

СтатьяМногоцентровое исследованиеНазвание и аннотация: Перевод в очереди
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Efil Safa Can, Bilgin Burak, Bilgetekin Irem, Helvaci Kaan, Sakalar Teoman, Nayir Erdinc, Erdem Palaz Fatma Esra, Guren Ali Kaan, Biter Sedat, Sahin Taha Koray, Bayram Ertugrul, Kertmen Neyran, Arslan Ahmet Melih, Asık Esra, Akdogan Orhun, Alan Ozkan, Fidan Evren, Yazici Ozan, Sahin Elif, Kut Engin, Mordag Cicek Ceren, Turker Sema, Kolkiran Nagihan, Gokoz Dogu Gamze, Sahbazlar Mustafa, Batu Aziz, Kilictas Bilgesah, Yilmaz Mesut, Oksuz Nejat Emre, Artac Mehmet, Akbas Sinem, Algin Efnan, Urun Yuksel, Sendur Mehmet Ali Nahit, Yalcin Bulent

Аннотация

Glioblastoma, IDH-wildtype is the most aggressive primary brain tumor in adults, and treatment options for recurrent disease are limited. Regorafenib, an oral multikinase inhibitor, has shown efficacy in glioblastoma at first recurrence, but its role in later recurrences and in other adult-type diffuse gliomas remains unclear. This multicenter retrospective study aimed to evaluate the safety and efficacy of regorafenib and to identify prognostic factors in patients with adult-type diffuse gliomas, including glioblastoma, who were treated at the second or subsequent recurrences. A total of 68 patients from 22 institutions were analyzed. The median overall survival (OS) was 3.84 months, and the median progression-free survival was 2.46 months. The objective response rate was 13%, and the disease control rate was 48%. Adverse events occurred in 80.9% of patients, most commonly fatigue, anemia, and elevated transaminases. Hand-foot skin reaction (HFSR) of any grade was observed in 36.4% of patients and was associated with significantly improved OS (HR: 0.41; p = 0.005). Regorafenib demonstrated a manageable safety profile and modest activity in this heavily pretreated population. The development of HFSR emerged as a potential prognostic marker for treatment benefit. Taken together, our findings support further exploration of regorafenib in this setting and suggest that HFSR may serve as a practical marker to guide treatment continuation.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты