» Articles » PMID: 34993148

Pegylated Interferon Alpha-2b in Patients With Polycythemia Vera and Essential Thrombocythemia in the Real World

Overview
Journal Front Oncol
Specialty Oncology
Date 2022 Jan 7
PMID 34993148
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

Several clinical trials have shown promising efficacy of pegylated interferon (Peg-IFN) in the first- and second-line polycythemia vera (PV) and essential thrombocythemia (ET). However, the efficacy and safety of Peg-IFN in the real world have rarely been reported. Hence, we conducted a prospective, single-center, single-arm, open exploratory study, which aimed to explore the hematologic response, molecular response, safety, and tolerability of patients with PV and ET treated with Peg-IFN in the real world. This study included newly diagnosed or previously treated patients with PV and ET, aged 18 years or older, admitted to the Department of Hematology of the First Affiliated Hospital of Soochow University from November 2017 to October 2019. The results revealed that complete hematological response (CHR) was achieved in 66.7% of patients with PV and 76.2% of patients with ET, and the molecular response was obtained in 38.5% of patients with PV and 50% of patients with ET after 48 weeks of Peg-IFN treatment. Peg-IFN is safe, effective and well tolerated in most patients. In the entire cohort, 4 patients (9.1%) discontinued treatment due to drug-related toxicity. In conclusion, Peg-IFN is a promising strategy in myeloproliferative neoplasms (MPNs), and Peg-IFN alone or in combination with other drugs should be further explored to reduce treatment-related toxicity and improve tolerability.

Citing Articles

Overview of dyslipidemia and metabolic syndrome in myeloproliferative neoplasms.

Gaman M, Srichawla B, Chen Y, Roy P, Dhali A, Nahian A World J Clin Oncol. 2024; 15(6):717-729.

PMID: 38946827 PMC: 11212607. DOI: 10.5306/wjco.v15.i6.717.


Interferons in the treatment of myeloproliferative neoplasms.

Vachhani P, Mascarenhas J, Bose P, Hobbs G, Yacoub A, Palmer J Ther Adv Hematol. 2024; 15:20406207241229588.

PMID: 38380373 PMC: 10878223. DOI: 10.1177/20406207241229588.


Toxicity of targeted anticancer treatments on the liver in myeloproliferative neoplasms.

Purwar S, Fatima A, Bhattacharyya H, Kutikuppala L, Cozma M, Srichawla B World J Hepatol. 2023; 15(9):1021-1032.

PMID: 37900211 PMC: 10600697. DOI: 10.4254/wjh.v15.i9.1021.

References
1.
Verger E, Soret-Dulphy J, Maslah N, Roy L, Rey J, Ghrieb Z . Ropeginterferon alpha-2b targets JAK2V617F-positive polycythemia vera cells in vitro and in vivo. Blood Cancer J. 2018; 8(10):94. PMC: 6172224. DOI: 10.1038/s41408-018-0133-0. View

2.
Harrison C, Mead A, Panchal A, Fox S, Yap C, Gbandi E . Ruxolitinib vs best available therapy for ET intolerant or resistant to hydroxycarbamide. Blood. 2017; 130(17):1889-1897. PMC: 6410531. DOI: 10.1182/blood-2017-05-785790. View

3.
Alvarez-Larran A, Pereira A, Cervantes F, Arellano-Rodrigo E, Hernandez-Boluda J, Ferrer-Marin F . Assessment and prognostic value of the European LeukemiaNet criteria for clinicohematologic response, resistance, and intolerance to hydroxyurea in polycythemia vera. Blood. 2011; 119(6):1363-9. DOI: 10.1182/blood-2011-10-387787. View

4.
Masarova L, Patel K, Newberry K, Cortes J, Borthakur G, Konopleva M . Pegylated interferon alfa-2a in patients with essential thrombocythaemia or polycythaemia vera: a post-hoc, median 83 month follow-up of an open-label, phase 2 trial. Lancet Haematol. 2017; 4(4):e165-e175. PMC: 5421384. DOI: 10.1016/S2352-3026(17)30030-3. View

5.
Tefferi A, Barbui T . Essential Thrombocythemia and Polycythemia Vera: Focus on Clinical Practice. Mayo Clin Proc. 2015; 90(9):1283-93. DOI: 10.1016/j.mayocp.2015.05.014. View