Long-term outcomes of polycythemia vera patients treated with ropeginterferon Alfa-2b
Christoph Klade,Pencho Georgiev,Dorota Krochmalczyk,Liana Gercheva-Kyuchukova,Miklos Egyed,Petr Dulíček,Árpád Illés,Halyna Pylypenko,Lylia Sivcheva,Jiri Mayer,Vera Yablokova,K. Krejcy,Victoria G. Empson,Hans Carl Hasselbalch,Robert Kralovics,Heinz Gisslinger,Jean-Jacques Kiladjian +16 more
TL;DR: Hmatologic and molecular responses and safety results after 5 years of long-term interferon alfa treatment with pegylated alfa-2b are reported.
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About: This article is published in Leukemia. The article was published on 24 Feb 2022. and is currently open access. The article focuses on the topics: Medicine & Polycythemia vera.
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Event-free survival in patients with polycythemia vera treated with ropeginterferon alfa-2b versus best available treatment
Heinz Gisslinger,Christoph Klade,Pencho Georgiev,Dorota Krochmalczyk,Liana Gercheva-Kyuchukova,Miklos Egyed,Petr Dulíček,Árpád Illés,Halyna Pylypenko,Lylia Sivcheva,Jiri Mayer,Vera Yablokova,K. Krejcy,Victoria G. Empson,Hans Carl Hasselbalch,Robert Kralovics,Jean-Jacques Kiladjian,Heinz Jean-Jacques Gisslinger Kiladjian,Heinz Gisslinger,Jean-Jacques Kiladjian +19 more
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An alternative dosing strategy for ropeginterferon alfa-2b may help improve outcomes in myeloproliferative neoplasms: An overview of previous and ongoing studies with perspectives on the future
TL;DR: Ropeginterferon alfa-2b is a novel, long-acting mono-pegylated proline-IFN-alpha-2B approved for treatment of polycythemia vera in adults, regardless of thrombotic risk level or treatment history as discussed by the authors .
References
Pegylated interferon-alfa-2a induces complete hematologic and molecular responses with low toxicity in polycythemia vera
Jean-Jacques Kiladjian,Bruno Cassinat,Sylvie Chevret,Pascal Turlure,Nathalie Cambier,Murielle Roussel,Sylvia Bellucci,Bernard Grandchamp,Christine Chomienne,Pierre Fenaux +9 more
TL;DR: Results show that pegylated IFN-alpha-2a yields high rates of hematologic and molecular response in PV with limited toxicity, and could even eliminate the JAK2 mutated clone in selected cases.
588
Ropeginterferon alfa-2b versus standard therapy for polycythaemia vera (PROUD-PV and CONTINUATION-PV): a randomised, non-inferiority, phase 3 trial and its extension study
Heinz Gisslinger,Christoph Klade,Pencho Georgiev,Dorota Krochmalczyk,Liana Gercheva-Kyuchukova,Miklos Egyed,Viktor Rossiev,Petr Dulicek,Árpád Illés,Halyna Pylypenko,Lylia Sivcheva,Jiri Mayer,Vera Yablokova,Kurt Krejcy,Barbara Grohmann-Izay,Hans Carl Hasselbalch,Robert Kralovics,Jean-Jacques Kiladjian,Franz Bauer,Nicoleta Berbec,Carlos Besses Raebel,Zita Borbényi,Horia Bumbea,Veronika Buxhofer-Ausch,Malgorzata Calbecka,Emilie Cayssials-Caylus,Mario Cazzola,Olga Cerna,Andrei Cucuianu,Delia Dima,Ernst Forjan,Emanuil Gheorghita,Richard Greil,Antonia Hatalova,Mikulas Hrubisko,János Jakucs,Polina Kaplan,S V Klymenko,Steffen Koschmieder,Mihaela Lazaroiu,Tamila Lysa,Zvenyslava Masliak,Tamás Masszi,Georgi Mihaylov,Alexander Myasnikov,Uwe Platzbecker,Mathieu Puyade,Jerome Rey,Lydia Roy,Jiri Schwarz,Aleksander Skotnicki,Irina Sokolova,Maria Soroka-Wojtaszko,Jolanta Starzak-Gwozdz,Vera Stoeva,Jose Miguel Torregrosa-Diaz,Anna Vallova,Elena Volodicheva,Krzysztof Warzocha,Ella Willenbacher,Dominik Wolf +60 more
TL;DR: The most frequently reported grade 3 and grade 4 treatment-related adverse events were increased γ-glutamyltransferase (seven [6%] of 127 patients) and increased alanine aminotransferase (four [3].
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Ropeginterferon alfa-2b, a novel IFNα-2b, induces high response rates with low toxicity in patients with polycythemia vera.
Heinz Gisslinger,Oleh Zagrijtschuk,Veronika Buxhofer-Ausch,Josef Thaler,Ernst Schloegl,Guenther Gastl,Dominik Wolf,Robert Kralovics,Robert Kralovics,Bettina Gisslinger,Karin Strecker,Alexander Egle,Thomas Melchardt,Sonja Burgstaller,Ella Willenbacher,Martin Schalling,Nicole C.C. Them,Pavla Kadlecová,Christoph Klade,Richard Greil +19 more
TL;DR: It is suggested that already low levels of ropeginterferon alfa-2b are sufficient to induce significant hematologic and molecular responses and support the development of the drug in a randomized phase 3 clinical trial.
167
Interferon-alpha for the therapy of myeloproliferative neoplasms: targeting the malignant clone
TL;DR: There is now consistent evidence showing that IFN-α is able to eliminate malignant clones harboring JAK2V617F or Calreticulin mutations, however, the molecular complexity of these diseases could hamper IFn-α efficacy, as the presence of additional non-driver mutations, like in the TET2 gene, could be associated with resistance to IFN -α.
124
Perspectives on interferon-alpha in the treatment of polycythemia vera and related myeloproliferative neoplasms: minimal residual disease and cure?
TL;DR: In patients with advanced and transforming disease towards leukemic transformation or having transformed to acute myeloid leukemia, “triple therapy” is proposed as a novel treatment modality to be tested in clinical trials combining IFN-alpha2, DNA-hypomethylator, and ruxolitinib.