TY - JOUR
T1 - A randomized phase 3 trial of interferon-α vs hydroxyurea in polycythemia vera and essential thrombocythemia
AU - Mascarenhas, John
AU - Kosiorek, Heidi E.
AU - Prchal, Josef T.
AU - Rambaldi, Alessandro
AU - Berenzon, Dmitriy
AU - Yacoub, Abdulraheem
AU - Harrison, Claire N.
AU - McMullin, Mary Frances
AU - Vannucchi, Alessandro M.
AU - Ewing, Joanne
AU - O'Connell, Casey L.
AU - Kiladjian, Jean Jacques
AU - Mead, Adam J.
AU - Winton, Elliott F.
AU - Leibowitz, David S.
AU - De Stefano, Valerio
AU - Arcasoy, Murat O.
AU - Kessler, Craig M.
AU - Catchatourian, Rosalind
AU - Rondelli, Damiano
AU - Silver, Richard T.
AU - Bacigalupo, Andrea
AU - Nagler, Arnon
AU - Kremyanskaya, Marina
AU - Levine, Max F.
AU - Arango Ossa, Juan E.
AU - McGovern, Erin
AU - Sandy, Lonette
AU - Salama, Mohamad E.
AU - Najfeld, Vesna
AU - Tripodi, Joseph
AU - Farnoud, Noushin
AU - Penson, Alexander V.
AU - Weinberg, Rona Singer
AU - Price, Leah
AU - Goldberg, Judith D.
AU - Barbui, Tiziano
AU - Marchioli, Roberto
AU - Tognoni, Gianni
AU - Rampal, Raajit K.
AU - Mesa, Ruben A.
AU - Dueck, Amylou C.
AU - Hoffman, Ronald
N1 - Publisher Copyright:
© 2022 American Society of Hematology
PY - 2022/5/12
Y1 - 2022/5/12
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=85127134014&partnerID=8YFLogxK
U2 - 10.1182/blood.2021012743
DO - 10.1182/blood.2021012743
M3 - Article
C2 - 35007321
AN - SCOPUS:85127134014
SN - 0006-4971
VL - 139
SP - 2931
EP - 2941
JO - Blood
JF - Blood
IS - 19
ER -