Triple A Plus (AAA+) Survival Prediction Model for Essential Thrombocythemia: Analysis Involving 7308 Patients.

IF 9.9 1区 医学 Q1 HEMATOLOGY
Ayalew Tefferi, Giuseppe G Loscocco, Lior Rokach, Tamar Tadmor, Priyansh Faldu, Guy Melamed, Hilel Alapi, Maymona Abdelmagid, Rania M Abdelaziz, Muhammad Yousuf, Merry Nakhleh, Animesh Pardanani, Kebede H Begna, Mirnal M Patnaik, Natasha Szuber, Alessandra Carobbio, Tiziano Barbui, Kaaren K Reichard, Rong He, Paola Guglielmelli, Naseema Gangat, Alessandro M Vannucchi
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引用次数: 0

Abstract

Survival prediction models in essential thrombocythemia (ET) include the International Prognostic Scoring System (IPSET) and the more recently introduced triple-A (AAA) prognostic score. The latter enlists age and absolute neutrophil (ANC) and lymphocyte (ALC) counts as risk variables. In the current study, a Mayo Clinic discovery cohort of 658 patients with ET was used to identify AAA-independent risk variables. Accordingly, multivariable analysis-derived HRs (95% CI) were 15.7 (8.4-29.5) for age > 70 years (8 points); 4.2 (2.3-7.5) for age 50 to 70 years (2 points); 1.8 (1.2-2.5) for ANC ≥ 8 × 109/L (1 point); 1.4 (1.03-1.9) for ALC < 1.7 × 109/L (1 point); 1.8 (1.2-2.6) for absolute monocyte count (AMC) ≥ 0.5 × 109/L (1 point); 1.8 (1.2-2.3) for male sex (1 point); 1.8 (1.3-2.4) for arterial hypertension (1 point); and 1.6 (1.2-2.3) for arterial thrombosis (1 point). HR-weighted scoring enabled a 4-tiered risk classification: ultra-low (0-1 points; N = 94; median survival 42.7 years), low (2-4 points; N = 297; 23 years), intermediate (5 points; N = 66; 17.3 years), and high (6-14 points; N = 201; 10.8 years). Time-dependent predictive performance at 20/25 years favored AAA+ (AUC 0.92/0.91) vs. AAA (0.86/0.86) vs. IPSET (0.81/0.84). The AAA+ risk model was subsequently validated by two external cohorts from Israel (N = 5968) and Italy (N = 682). In the cohort from Israel, disease-specific mortality was assessed by comparing observed survival to an age- and sex-matched reference population, which suggested near-normal life expectancy in ultra-low risk patients. The current study highlights host-related factors as the primary determinants of longevity in ET and provides a composite risk score (AAA+) that is based on complete blood count-derived parameters and host-related factors. Predictive performance of the new model was shown to be superior to that of IPSET and AAA.

原发性血小板增多症的AAA+生存预测模型:涉及7308例患者的分析
原发性血小板增多症(ET)的生存预测模型包括国际预后评分系统(IPSET)和最近引入的AAA预后评分。后者将年龄、绝对中性粒细胞(ANC)和淋巴细胞(ALC)计数作为危险变量。在目前的研究中,梅奥诊所的658例ET患者发现队列被用来确定aaa独立的风险变量。因此,多变量分析衍生的hr (95% CI)为15.7(8.4-29.5),年龄为bb0 - 70岁(8点);50 - 70岁4.2(2.3-7.5)(2分);ANC≥8 × 109/L 1.8(1.2 ~ 2.5)(1分);ALC 9/L 1.4(1.03-1.9)(1分);绝对单核细胞计数(AMC)≥0.5 × 109/L(1分)1.8 (1.2 ~ 2.6);男性1.8分(1.2-2.3分),1分;高血压1.8分(1.3 ~ 2.4分);动脉血栓形成1.6分(1.2-2.3分),1分。hr加权评分实现了4级风险分类:超低(0-1分,N = 94,中位生存期42.7年)、低(2-4分,N = 297, 23年)、中(5分,N = 66, 17.3年)、高(6-14分,N = 201, 10.8年)。与时间相关的20/25年预测性能倾向于AAA+ (AUC 0.92/0.91)、AAA(0.86/0.86)和IPSET(0.81/0.84)。随后,来自以色列(N = 5968)和意大利(N = 682)的两个外部队列验证了AAA+风险模型。在来自以色列的队列中,通过将观察到的生存率与年龄和性别匹配的参考人群进行比较来评估疾病特异性死亡率,这表明超低风险患者的预期寿命接近正常。目前的研究强调宿主相关因素是ET患者寿命的主要决定因素,并提供了基于全血细胞计数衍生参数和宿主相关因素的复合风险评分(AAA+)。新模型的预测性能优于IPSET和AAA模型。
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来源期刊
CiteScore
15.70
自引率
3.90%
发文量
363
审稿时长
3-6 weeks
期刊介绍: The American Journal of Hematology offers extensive coverage of experimental and clinical aspects of blood diseases in humans and animal models. The journal publishes original contributions in both non-malignant and malignant hematological diseases, encompassing clinical and basic studies in areas such as hemostasis, thrombosis, immunology, blood banking, and stem cell biology. Clinical translational reports highlighting innovative therapeutic approaches for the diagnosis and treatment of hematological diseases are actively encouraged.The American Journal of Hematology features regular original laboratory and clinical research articles, brief research reports, critical reviews, images in hematology, as well as letters and correspondence.
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