Jung Eun Hee, Hong Junshik, Kim Sung-Yong, Park Young, Yuh Young Jin, Mun Yeung-Chul, Lee Won-Sik, Park Sung-Kyu, Bang Soo Mee
Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Department of Internal Medicine, Seoul National University College of Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Clin Lymphoma Myeloma Leuk. 2022 Oct;22(10):e931-e937. doi: 10.1016/j.clml.2022.06.008. Epub 2022 Jun 26.
INTRODUCTION/BACKGROUND: Ruxolitinib is an established treatment for myelofibrosis (MF) that has demonstrated clinical benefit by reducing spleen size and debilitating MF-related symptoms. However, despite the efficacy of ruxolitinib, anemia remains a major adverse event that causes dose modification or discontinuation in real-world practice. Additionally, dependence on red blood cell (RBC) transfusion (TF) is common during treatment; therefore, we explored the outcome of ruxolitinib therapy with a primary focus on RBC TF.
PATIENTS/METHODS: We retrospectively reviewed the medical records of 123 MF patients treated with ruxolitinib between January 2012 and April 2020 at eight academic centers in Korea.
At ruxolitinib initiation, 38 patients (30.9%) underwent ≥ 2 units of RBC TF over 8 weeks. The most common reason for permanent discontinuation was intolerant anemia (10/63, 15.9%). The most common reasons for temporary interruption were nonhematologic toxicity (26/55, 21.1%), anemia (23/55, 18.7%) and thrombocytopenia (13/55, 10.6%). Among the 123 patients in the study, 57 (46.3%), 42 (34.1%), and 40 patients (32.5%) who were receiving or stopped ruxolitinib therapy had a status of RBC TF dependence, long-term RBC TF dependence, or severe RBC TF dependence, respectively. The presence of ≥ 2 units of RBC transfusion over 8 weeks at ruxolitinib initiation was an independent risk factor for persistent RBC TF dependence.
The requirement for RBC TF is commonly encountered during treatment of MF with ruxolitinib, particularly among those with pre-existing ≥ 2 units of RBC TF over 8 weeks. For those patients, overcoming the barrier of maintenance TF is demanding.
引言/背景:芦可替尼是一种已获认可的骨髓纤维化(MF)治疗药物,已证明其通过缩小脾脏大小和缓解MF相关症状具有临床益处。然而,尽管芦可替尼有效,但贫血仍然是一个主要不良事件,在实际临床中会导致剂量调整或停药。此外,治疗期间依赖红细胞(RBC)输血(TF)很常见;因此,我们探讨了芦可替尼治疗的结果,主要关注RBC TF。
患者/方法:我们回顾性分析了2012年1月至2020年4月期间韩国8个学术中心接受芦可替尼治疗的123例MF患者的病历。
在开始使用芦可替尼时,38例患者(30.9%)在8周内接受了≥2单位的RBC TF。永久停药的最常见原因是不耐受性贫血(10/63,15.9%)。临时中断的最常见原因是非血液学毒性(26/55,21.1%)、贫血(23/55,18.7%)和血小板减少症(13/55,10.6%)。在该研究的123例患者中,分别有57例(46.3%)、42例(34.1%)和40例(32.5%)接受或停止芦可替尼治疗的患者存在RBC TF依赖、长期RBC TF依赖或严重RBC TF依赖状态。开始使用芦可替尼时8周内接受≥2单位RBC输血是持续RBC TF依赖的独立危险因素。
在用芦可替尼治疗MF期间,RBC TF需求很常见,尤其是在那些在8周内预先存在≥2单位RBC TF的患者中。对于这些患者,克服维持TF的障碍具有挑战性。