Neutrophil to lymphocyte ratio (NLR) improves the risk assessment of ISS staging in newly diagnosed MM patients treated upfront with novel agents

医学 内科学 中性粒细胞与淋巴细胞比率 中性粒细胞绝对计数 血液学 无进展生存期 阶段(地层学) 队列 淋巴细胞 胃肠病学 肿瘤科 外科 总体生存率 化疗 中性粒细胞减少症 古生物学 生物
作者
Alessandra Romano,Nunziatina Laura Parrinello,Marzia L Consoli,Luigi Marchionni,Stefano Forte,Concetta Conticello,Alessandra Pompa,Alessandro Gozzetti,Giuseppe Milone,Francesco Di Raimondo,Ivan Borrello
出处
期刊:Annals of Hematology [Springer Science+Business Media]
卷期号:94 (11): 1875-1883 被引量:55
标识
DOI:10.1007/s00277-015-2462-4
摘要

Recent reports identify the ratio between absolute neutrophil count (ANC) and absolute lymphocyte count (ALC), called neutrophil to lymphocyte ratio (NLR), as a predictor of progression-free survival (PFS) and overall survival (OS) in various malignancies. We retrospectively examined the NLR in a cohort of 309 newly diagnosed multiple myeloma (MM) patients treated upfront with novel agents. NLR was calculated using data obtained from the complete blood count (CBC) at diagnosis and subsequently correlated with PFS and OS. The median NLR was 1.9 (range 0.4–15.9). Higher NLR was independent of international staging system (ISS) stage, plasma cell infiltration or cytogenetics. The 5-year PFS and OS estimates were, respectively, 18.2 and 36.4 % for patients with NLR ≥ 2 versus 25.5 and 66.6 % in patients with NLR < 2. Among younger patients (age <65 years, N = 179), NLR ≥ 2 had a negative prognostic impact on both PFS and OS, in all ISS stages. By combining ISS stage and NLR in a model limited to young patients, we found that 19 % of the patients were classified as very low risk, 70 % standard risk and 11 % very high risk. The 5-year estimates were 39.3, 19.4 and 10.9 % for PFS and 95.8, 50.9 and 23.6 % for OS for very low, standard-risk and very high-risk groups. We found NLR to be a predictor of PFS and OS in MM patients treated upfront with novel agents. NLR can be combined with ISS staging system to identify patients with dismal outcome. However, larger cohorts and prospective studies are needed to use NLR as additional parameter to personalise MM therapy in the era of novel agents.

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