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Current First-Line Treatments and Low-Risk Treatment Guidelines in Polycythemia Vera (PV): A Quiz Journey

PV Guidelines Question 3


Transcript

The correct answer is first-line cytoreductive options include hydroxyurea and pegylated interferon formulations. The rationale is as follows: For patients with high-risk PV, first-line cytoreductive therapy includes either hydroxyurea or an interferon formulation used in addition to continued aspirin and therapeutic phlebotomy. High-risk patients with PV include those aged 60 years and older and/or those with prior thrombosis, whether that thrombosis be arterial or venous. The NCCN guidelines for MPNs recommend either hydroxyurea or interferon formulations for high-risk patients with PV. The choice between these agents should be individualized based on patient preference and treatment goals, such as symptom reduction and adverse event considerations. Ruxolitinib is generally used as second-line therapy rather than as standard first-line therapy in high-risk patients. 

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References

  1. Tremblay D, Kremyanskaya M, Mascarenhas J, Hoffman R. Diagnosis and treatment of polycythemia vera: a review. JAMA. 2025;333(2):153-160. doi:10.1001/jama.2024.20377 
  2. Benevolo G, Vassallo F, Urbino I, Giai V. Polycythemia vera (PV): update on emerging treatment options. Ther Clin Risk Manag. 2021;17:209-221. doi:10.2147/TCRM.S213020  
  3. Referenced with permission from the NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) for Myeloproliferative Neoplasms V.1.2026. © National Comprehensive Cancer Network, Inc. 2026. All rights reserved. Accessed March 10, 2026. To view the most recent and complete version of the guideline, go online to NCCN.org. NCCN makes no warranties of any kind whatsoever regarding their content, use or application and disclaims any responsibility for their application or use in any way.   
  4. Barbui T, Vannucchi AM, De Stefano V, et al. Ropeginterferon versus standard therapy for low-risk patients with polycythemia vera. NEJM Evid. 2023;2(6):EVIDoa2200335. doi:10.1056/EVIDoa2200335 

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