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AIPSS-MF 机器学习预后评分在接受鲁索利替尼治疗的骨髓纤维化患者队列中的验证。

AIPSS-MF machine learning prognostic score validation in a cohort of myelofibrosis patients treated with ruxolitinib.

机构信息

Hematology with BMT Unit, A.O.U. "G. Rodolico-San Marco", Catania, Italy.

Department of Haematology, Guy's and St Thomas NHS Foundation Trust, London, UK.

出版信息

Cancer Rep (Hoboken). 2023 Oct;6(10):e1881. doi: 10.1002/cnr2.1881. Epub 2023 Aug 8.

DOI:10.1002/cnr2.1881
PMID:37553891
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10598243/
Abstract

BACKGROUND

In myelofibrosis (MF), new model scores are continuously proposed to improve the ability to better identify patients with the worst outcomes. In this context, the Artificial Intelligence Prognostic Scoring System for Myelofibrosis (AIPSS-MF), and the Response to Ruxolitinib after 6 months (RR6) during the ruxolitinib (RUX) treatment, could play a pivotal role in stratifying these patients.

AIMS

We aimed to validate AIPSS-MF in patients with MF who started RUX treatment, compared to the standard prognostic scores at the diagnosis and the RR6 scores after 6 months of treatment.

METHODS AND RESULTS

At diagnosis, the AIPSS-MF performs better than the widely used IPSS for primary myelofibrosis (C-index 0.636 vs. 0.596) and MYSEC-PM for secondary (C-index 0.616 vs. 0.593). During RUX treatment, we confirmed the leading role of RR6 in predicting an inadequate response by these patients to JAKi therapy compared to AIPSS-MF (0.682 vs. 0.571).

CONCLUSION

The new AIPSS-MF prognostic score confirms that it can adequately stratify this subgroup of patients already at diagnosis better than standard models, laying the foundations for new prognostic models developed tailored to the patient based on artificial intelligence.

摘要

背景

在骨髓纤维化(MF)中,不断提出新的模型评分,以提高更好地识别预后最差患者的能力。在这种情况下,人工智能骨髓纤维化预后评分系统(AIPSS-MF)和治疗 6 个月后的芦可替尼反应(RR6)在对这些患者进行分层方面可能发挥关键作用。

目的

我们旨在验证开始芦可替尼(RUX)治疗的 MF 患者的 AIPSS-MF,与诊断时的标准预后评分和治疗 6 个月后的 RR6 评分进行比较。

方法和结果

在诊断时,AIPSS-MF 比广泛使用的原发性骨髓纤维化的 IPSS(C 指数 0.636 对 0.596)和继发性骨髓纤维化的 MYSEC-PM(C 指数 0.616 对 0.593)表现更好。在 RUX 治疗期间,我们证实 RR6 在预测这些患者对 JAKi 治疗反应不足方面优于 AIPSS-MF(0.682 对 0.571)。

结论

新的 AIPSS-MF 预后评分证实,它已经可以在诊断时比标准模型更好地对这亚组患者进行充分分层,为基于人工智能为患者量身定制的新预后模型奠定了基础。

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本文引用的文献

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A Journey Through JAK Inhibitors for the Treatment of Myeloproliferative Diseases.JAK 抑制剂治疗骨髓增殖性疾病的探索之旅。
Curr Hematol Malig Rep. 2023 Oct;18(5):176-189. doi: 10.1007/s11899-023-00702-x. Epub 2023 Jul 3.
2
The pharmacotherapeutic management of patients with myelofibrosis: looking beyond JAK inhibitors.骨髓纤维化患者的药物治疗管理:超越 JAK 抑制剂。
Expert Opin Pharmacother. 2023 Sep-Dec;24(13):1449-1461. doi: 10.1080/14656566.2023.2228695. Epub 2023 Jun 26.
3
Myelofibrosis and Survival Prognostic Models: A Journey between Past and Future.
骨髓纤维化与生存预后模型:过去与未来之间的历程
J Clin Med. 2023 Mar 11;12(6):2188. doi: 10.3390/jcm12062188.
4
Ruxolitinib treatment in myelofibrosis and polycythemia vera causes suboptimal humoral immune response following standard and booster vaccination with BNT162b2 mRNA COVID-19 vaccine.芦可替尼治疗骨髓纤维化和真性红细胞增多症后,使用BNT162b2 mRNA新冠疫苗进行标准和加强接种会导致体液免疫反应欠佳。
Front Oncol. 2023 Feb 14;13:1117815. doi: 10.3389/fonc.2023.1117815. eCollection 2023.
5
Primary myelofibrosis: 2023 update on diagnosis, risk-stratification, and management.原发性骨髓纤维化:2023年诊断、风险分层及管理的最新进展
Am J Hematol. 2023 May;98(5):801-821. doi: 10.1002/ajh.26857. Epub 2023 Feb 6.
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Infection during Ruxolitinib Treatment: The Cytokines-Based Immune Response in the Setting of Immunocompromised Patients.鲁索替尼治疗期间的感染:免疫功能低下患者环境中基于细胞因子的免疫反应。
J Clin Med. 2023 Jan 11;12(2):578. doi: 10.3390/jcm12020578.
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