通过 RED 评分评估红细胞生成异常,铁蛋白:hepcidin 比值可预测低危骨髓增生异常综合征患者对红细胞生成素的反应。
Dyserythropoiesis evaluated by the RED score and hepcidin:ferritin ratio predicts response to erythropoietin in lower-risk myelodysplastic syndromes.
机构信息
Department of Hematology, CHU Grenoble-Alpes, Grenoble
Institute for Advanced Biosciences, INSERM U1209, CNRS UMR 5309, Grenoble.
出版信息
Haematologica. 2019 Mar;104(3):497-504. doi: 10.3324/haematol.2018.203158. Epub 2018 Oct 4.
Erythropoiesis-stimulating agents are generally the first line of treatment of anemia in patients with lower-risk myelodysplastic syndrome. We prospectively investigated the predictive value of somatic mutations, and biomarkers of ineffective erythropoiesis including the flow cytometry RED score, serum growth-differentiation factor-15, and hepcidin levels. Inclusion criteria were no prior treatment with erythropoiesis-stimulating agents, low- or intermediate-1-risk myelodysplastic syndrome according to the International Prognostic Scoring System, and a hemoglobin level <10 g/dL. Patients could be red blood cell transfusion-dependent or not and were given epoetin zeta 40 000 IU/week. Serum erythropoietin level, iron parameters, hepcidin, flow cytometry Ogata and RED scores, and growth-differentiation factor-15 levels were determined at baseline, and molecular analysis by next-generation sequencing was also conducted. Erythroid response (defined according to the International Working Group 2006 criteria) was assessed at week 12. Seventy patients, with a median age of 78 years, were included in the study. There were 22 patients with refractory cytopenia with multilineage dysplasia, 19 with refractory cytopenia with unilineage dysplasia, 14 with refractory anemia with ring sideroblasts, four with refractory anemia with excess blasts-1, six with chronic myelomonocytic leukemia, two with del5q-and three with unclassifiable myelodysplastic syndrome. According to the revised International Prognostic Scoring System, 13 had very low risk, 47 had low risk, nine intermediate risk and one had high-risk disease. Twenty patients were transfusion dependent. Forty-eight percent had an erythroid response and the median duration of the response was 26 months. At baseline, non-responders had significantly higher RED scores and lower hepcidin:ferritin ratios. In multivariate analysis, only a RED score >4 (=0.05) and a hepcidin:ferritin ratio <9 (=0.02) were statistically significantly associated with worse erythroid response. The median response duration was shorter in patients with growth-differentiation factor-15 >2000 pg/mL and a hepcidin:ferritin ratio <9 (=0.0008 and =0.01, respectively). In multivariate analysis, both variables were associated with shorter response duration. Erythroid response to epoetin zeta was similar to that obtained with other erythropoiesis-stimulating agents and was correlated with higher baseline hepcidin:ferritin ratio and lower RED score. .
促红细胞生成素刺激剂通常是低危骨髓增生异常综合征患者贫血的一线治疗方法。我们前瞻性地研究了体细胞突变和无效红细胞生成的生物标志物的预测价值,包括流式细胞术 RED 评分、血清生长分化因子-15 和铁调素水平。纳入标准为无促红细胞生成素刺激剂治疗史、根据国际预后评分系统为低危或中-1 危骨髓增生异常综合征以及血红蛋白<10 g/dL。患者可以依赖或不依赖红细胞输注,并给予重组人促红细胞生成素 ζ 40 000 IU/周。在基线时测定血清促红细胞生成素水平、铁参数、铁调素、流式细胞术 Ogata 和 RED 评分以及生长分化因子-15 水平,并进行下一代测序的分子分析。根据国际工作组 2006 年的标准评估红细胞反应(定义)在第 12 周进行。70 例中位年龄为 78 岁的患者纳入研究。其中 22 例为难治性多系发育不良伴细胞减少症,19 例为难治性单系发育不良伴细胞减少症,14 例为环形铁幼粒细胞性难治性贫血,4 例为伴 1 个过多原始细胞的难治性贫血,6 例为慢性粒单核细胞白血病,2 例为 5q-缺失,3 例为未分类骨髓增生异常综合征。根据修订后的国际预后评分系统,13 例为极低危,47 例为低危,9 例为中危,1 例为高危。20 例患者依赖输血。48%的患者有红细胞反应,反应的中位持续时间为 26 个月。在基线时,无反应者的 RED 评分明显较高,铁调素:铁蛋白比值较低。多变量分析显示,仅 RED 评分>4(=0.05)和铁调素:铁蛋白比值<9(=0.02)与较差的红细胞反应显著相关。生长分化因子-15>2000 pg/mL 和铁调素:铁蛋白比值<9(=0.0008 和=0.01)的患者的中位反应持续时间更短。多变量分析显示,这两个变量均与反应持续时间较短相关。重组人促红细胞生成素 ζ 的红细胞反应与其他促红细胞生成素刺激剂相似,与较高的基线铁调素:铁蛋白比值和较低的 RED 评分相关。