A randomized phase 3 trial of interferon-α vs hydroxyurea in polycythemia vera and essential thrombocythemia.

Journal Article (Clinical Trial, Phase III;Journal Article)

The goal of therapy for patients with essential thrombocythemia (ET) and polycythemia vera (PV) is to reduce thrombotic events by normalizing blood counts. Hydroxyurea (HU) and interferon-α (IFN-α) are the most frequently used cytoreductive options for patients with ET and PV at high risk for vascular complications. Myeloproliferative Disorders Research Consortium 112 was an investigator-initiated, phase 3 trial comparing HU to pegylated IFN-α (PEG) in treatment-naïve, high-risk patients with ET/PV. The primary endpoint was complete response (CR) rate at 12 months. A total of 168 patients were treated for a median of 81.0 weeks. CR for HU was 37% and 35% for PEG (P = .80) at 12 months. At 24 to 36 months, CR was 20% to 17% for HU and 29% to 33% for PEG. PEG led to a greater reduction in JAK2V617F at 24 months, but histopathologic responses were more frequent with HU. Thrombotic events and disease progression were infrequent in both arms, whereas grade 3/4 adverse events were more frequent with PEG (46% vs 28%). At 12 months of treatment, there was no significant difference in CR rates between HU and PEG. This study indicates that PEG and HU are both effective treatments for PV and ET. With longer treatment, PEG was more effective in normalizing blood counts and reducing driver mutation burden, whereas HU produced more histopathologic responses. Despite these differences, both agents did not differ in limiting thrombotic events and disease progression in high-risk patients with ET/PV. This trial was registered at www.clinicaltrials.gov as #NCT01259856.

Full Text

Duke Authors

Cited Authors

  • Mascarenhas, J; Kosiorek, HE; Prchal, JT; Rambaldi, A; Berenzon, D; Yacoub, A; Harrison, CN; McMullin, MF; Vannucchi, AM; Ewing, J; O'Connell, CL; Kiladjian, J-J; Mead, AJ; Winton, EF; Leibowitz, DS; De Stefano, V; Arcasoy, MO; Kessler, CM; Catchatourian, R; Rondelli, D; Silver, RT; Bacigalupo, A; Nagler, A; Kremyanskaya, M; Levine, MF; Arango Ossa, JE; McGovern, E; Sandy, L; Salama, ME; Najfeld, V; Tripodi, J; Farnoud, N; Penson, AV; Weinberg, RS; Price, L; Goldberg, JD; Barbui, T; Marchioli, R; Tognoni, G; Rampal, RK; Mesa, RA; Dueck, AC; Hoffman, R

Published Date

  • May 12, 2022

Published In

Volume / Issue

  • 139 / 19

Start / End Page

  • 2931 - 2941

PubMed ID

  • 35007321

Pubmed Central ID

  • PMC9101248

Electronic International Standard Serial Number (EISSN)

  • 1528-0020

Digital Object Identifier (DOI)

  • 10.1182/blood.2021012743


  • eng

Conference Location

  • United States