Identifying Patients with Polycythemia Vera at Risk of Thrombosis after Hydroxyurea Initiation: The Polycythemia Vera—Advanced Integrated Models (PV-AIM) Project

Author:

Verstovsek Srdan1,Krečak Ivan23ORCID,Heidel Florian H.4ORCID,De Stefano Valerio5ORCID,Bryan Kenneth6,Zuurman Mike W.7,Zaiac Michael7,Morelli Mara8,Smyth Aoife79,Redondo Santiago10,Bigan Erwan11,Ruhl Michael11,Meier Christoph11,Beffy Magali11,Kiladjian Jean-Jacques12

Affiliation:

1. Department of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA

2. Department of Internal Medicine, General Hospital of Sibenik-Knin County, 22000 Sibenik, Croatia

3. Faculty of Medicine, University of Rijeka, 51000 Rijeka, Croatia

4. Hematology, Oncology, Stem Cell Transplantation and Palliative Care, Internal Medicine C, University Medicine Greifswald, 17475 Greifswald, Germany

5. Sezione di Ematologia, Dipartimento di Scienze Radiologiche ed Ematologiche, Università Cattolica, Fondazione Policlinico A. Gemelli IRCCS, 00168 Roma, Italy

6. Novartis Ireland Limited, Dublin 4, Ireland, D04A9N6

7. Novartis Pharma AG, CH-4056 Basel, Switzerland

8. Novartis Farma SpA, 21040 Origgio, Italy

9. Novartis Pharmaceuticals UK Limited, London W12 7FQ, UK

10. Novartis Farmaceutica, S.A., 28033 Madrid, Spain

11. The Boston Consulting Group, Boston, MA 02210, USA

12. Centre d’Investigations Cliniques, Hôpital Saint-Louis, Université de Paris, AP-HP, INSERM, CIC1427 Paris, France

Abstract

Patients with polycythemia vera (PV) are at significant risk of thromboembolic events (TE). The PV-AIM study used the Optum® de-identified Electronic Health Record dataset and machine learning to identify markers of TE in a real-world population. Data for 82,960 patients with PV were extracted: 3852 patients were treated with hydroxyurea (HU) only, while 130 patients were treated with HU and then changed to ruxolitinib (HU-ruxolitinib). For HU-alone patients, the annualized incidence rates (IR; per 100 patients) decreased from 8.7 (before HU) to 5.6 (during HU) but increased markedly to 10.5 (continuing HU). Whereas for HU-ruxolitinib patients, the IR decreased from 10.8 (before HU) to 8.4 (during HU) and was maintained at 8.3 (after switching to ruxolitinib). To better understand markers associated with TE risk, we built a machine-learning model for HU-alone patients and validated it using an independent dataset. The model identified lymphocyte percentage (LYP), neutrophil percentage (NEP), and red cell distribution width (RDW) as key markers of TE risk, and optimal thresholds for these markers were established, from which a decision tree was derived. Using these widely used laboratory markers, the decision tree could be used to identify patients at high risk for TE, facilitate treatment decisions, and optimize patient management.

Funder

Novartis Pharma AG, Basel, Switzerland

Publisher

MDPI AG

Subject

General Biochemistry, Genetics and Molecular Biology,Medicine (miscellaneous)

Reference39 articles.

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