Prospective validation of a biomarker-driven response prediction model to romiplostim in lower-risk myelodysplastic neoplasms - results of the EUROPE trial by EMSCO.
СтатьяНазвание 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.
Kubasch Anne Sophie, Giagounidis Aristoteles, Metzgeroth Georgia, Jonasova Anna, Herbst Regina, Diaz Jose Miguel Torregrosa, De Renzis Benoit, Götze Katharina S, Huetter-Kroenke Marie-Luise, Gourin Marie-Pierre, Slama Borhane, Dimicoli-Salazar Sophie, Cony-Makhoul Pascale, Laribi Kamel, Park Sophie, Jersemann Katja, Schipp Dorothea, Metzeler Klaus H, Tiebel Oliver, Sockel Katja, Gloaguen Silke, Mies Anna, Chermat Fatiha, Thiede Christian, Sapena Rosa, Schlenk Richard F, Fenaux Pierre, Platzbecker Uwe, Adès Lionel
Аннотация
The EUROPE phase 2 trial investigated the predictive value of biomarkers on the clinical efficacy of single agent romiplostim (ROM) treatment in patients with lower-risk myelodysplastic neoplasms (LR-MDS) and thrombocytopenia within the 'European Myelodysplastic Neoplasms Cooperative Group' (EMSCO) network. A total of 77 patients with LR-MDS and a median platelet count of 25/nl were included, all patients received ROM at a starting dose of 750 μg by SC injection weekly. Thirty-two patients (42%) achieved a hematologic improvement of platelets (HI-P) with a median duration of 340 days. Neutrophil (HI-N) and erythroid (HI-E) responses were observed in three (4%) and seven (9%) patients, respectively. We could not confirm previous reports that HI-P correlated with baseline endogenous thrombopoietin levels and platelet transfusion history, but SRSF2 mutation status and hemoglobin levels at baseline were significantly linked to HI-P. Sequential analysis of variant allelic frequency of mutations like SRSF2 did not reveal an impact of ROM on clonal evolution in both responders and non-responders. In summary, our study confirms the safety and efficacy of ROM in LR-MDS patients and may allow to better define subgroups of patients with a high likelihood of response.