a Department of Internal Medicine , University of Michigan , Ann Arbor , MI , USA.
b Department of Biostatistics , University of Michigan , Ann Arbor , MI , USA.
Leuk Lymphoma. 2019 Apr;60(4):1036-1042. doi: 10.1080/10428194.2018.1509315. Epub 2018 Sep 20.
JAK inhibitors for myelofibrosis (MF) reduce spleen size, control constitutional symptoms, and may improve survival. We studied the clinical characteristics of 548 MF patients treated with JAK inhibitors from 2008 to 2016 to better understand predictors of splenic response. Response was defined as a 50% decrease in spleen size at early (3-4 months on therapy) and late (5-12 months) timepoints after therapy initiation. Early response positively correlated with higher doses of JAK inhibitor, baseline spleen size 5-10 cm, and hemoglobin. Early response negatively correlated with baseline spleen size >20 cm and high WBC. The strongest predictor of late response was whether a patient had a response at the earlier timepoint (OR 8.88). Our response models suggest that clinical factors can be used to predict which patients are more likely to respond to JAK inhibitors, and those who do not achieve an early response, i.e. within 3-4 months, should consider alternative treatments.
JAK 抑制剂可用于治疗骨髓纤维化(MF),能缩小脾脏、控制全身症状,并可能改善生存。我们研究了 2008 年至 2016 年间接受 JAK 抑制剂治疗的 548 例 MF 患者的临床特征,以更好地了解脾脏反应的预测因素。反应定义为治疗开始后早期(3-4 个月)和晚期(5-12 个月)脾脏大小减少 50%。早期反应与 JAK 抑制剂剂量较高、基线脾脏大小为 5-10cm 和血红蛋白水平较高呈正相关。早期反应与基线脾脏大小>20cm 和高白细胞计数呈负相关。晚期反应的最强预测因素是患者在早期是否有反应(OR 8.88)。我们的反应模型表明,临床因素可用于预测哪些患者更有可能对 JAK 抑制剂产生反应,对于那些在 3-4 个月内没有早期反应的患者,应考虑替代治疗。