Analysis of Predictive Factors for Early Response to Ruxolitinib in 320 Patients with Myelofibrosis From the Polish Adult Leukemia Group (PALG) Registry

鲁索利替尼 骨髓纤维化 医学 骨髓增生性肿瘤 内科学 白细胞增多症 血液学 体质症状 置信区间 胃肠病学 骨髓 疾病
作者
Joanna Góra-Tybor,Aleksandra Gołoś,Damian Mikulski,Grzegorz Helbig,Tomasz Sacha,Krzysztof Lewandowski,Joanna Niesiobędzka‐Krężel,Maria Bieniaszewska,Hubert Wysogląd,Olga Grzybowska‐Izydorczyk,Ilona Seferyńska,Marta Sobas,Maria Czyżewska,Agnieszka Michalska,Waldemar Sawicki,Malwina Mazur,Marek Hus,Ewa Bodzenta,Magdalena Olszewska‐Szopa,Martyna Włodarczyk
出处
期刊:Clinical Lymphoma, Myeloma & Leukemia [Elsevier BV]
卷期号:23 (1): e19-e26 被引量:2
标识
DOI:10.1016/j.clml.2022.10.002
摘要

Ruxolitinib is widely used in myelofibrosis (MF). However, some patients do not optimally respond and require more efficacious treatment. Our analysis aimed to establish predictors of ruxolitinib response.We designed a multicenter, retrospective analysis of the efficacy of ruxolitinib treatment in patients with MF in 15 Polish hematology centers. As responses to ruxolitinib occur within the first 6 months, we used this point to evaluate the efficacy of treatment. Symptoms response was defined as ≥50% reduction of the MF constitutional symptoms assessed by Myeloproliferative Neoplasm Symptom Assessment Form Total Symptom Score (MPN-SAF TSS). Spleen response was defined as ≥50% reduction of the difference between the spleen's baseline length and the upper limit norm measured by ultrasonography.320 MF patients were enrolled. At 6 months of therapy, the spleen response was detected in 140 (50%) patients, and symptoms response in 241 patients (76%). Multivariable analysis identified leukocytosis <25 G/L (OR 2.06, 95%CI: 1.12-3.88, P = .0200), and reticulin fibrosis MF 1 (OR 2.22, 95%CI: 1.11-4.46, P = .0249) contributed to better spleen response. The time interval between MF diagnosis and ruxolitinib administration shorter than 3 months, and platelets ≥150 G/L (OR 1.69, 95% CI 1.01-2.83, P = .0466) influenced symptoms response.Establishing predictive factors for ruxolitinib response is particularly important given the potential for new therapies in MF. In patients with a low likelihood of responding to ruxolitinib, using other JAK inhibitors or adding a drug with a different mechanism of action to ruxolitinib may be of clinical benefit.
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