KILADJIAN, Jean-Jacques, Francisca Ferrer MARIN, Haifa Kathrin AL-ALI, Alberto ALVAREZ-LARRAN, Eloise BEGGIATO, Maria BIENIASZEWSKA, Massimo BRECCIA, Veronika BUXHOFER-AUSCH, Olga CERNA, Ana-Manuela CRISAN, Catalin Doru DANAILA, De Stefano VALERIO, Konstanze DOEHNER, Victoria EMPSON, Joanna GORA-TYBOR, Martin GRIESSHAMMER, Sebastian GROSICKI, Paola GUGLIELMELLI, Valentin GARCIA-GUTIERREZ, Florian H HEIDEL, Arpad ILLES, Ciprian TOMULEASA, Chloe JAMES, Steffen KOSCHMIEDER, Maria-Theresa KRAUTH, Kurt KREJCY, Mihaela-Cornelia LAZAROIU, Jiří MAYER, Zsolt Gyoergy NAGY, Franck-Emmanuel NICOLINI, Francesca PALANDRI, Vassiliki PAPPA, Andreas Johannes REITER, Tomasz SACHA, Stefanie SCHLAGER, Stefan SCHMIDT, Evangelos TERPOS, Martin UNGER, Albert WOELFLER, Blanca Xicoy CIRICI a Christoph KLADE. ROP-ET: a prospective phase III trial investigating the efficacy and safety of ropeginterferon alfa-2b in essential thrombocythemia patients with limited treatment options. Annals of hematology. New York: Springer Verlag, 2024, roč. 103, č. 7, s. 2299-2310. ISSN 0939-5555. Dostupné z: https://dx.doi.org/10.1007/s00277-024-05665-4.
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Základní údaje
Originální název ROP-ET: a prospective phase III trial investigating the efficacy and safety of ropeginterferon alfa-2b in essential thrombocythemia patients with limited treatment options
Autoři KILADJIAN, Jean-Jacques, Francisca Ferrer MARIN, Haifa Kathrin AL-ALI, Alberto ALVAREZ-LARRAN, Eloise BEGGIATO, Maria BIENIASZEWSKA, Massimo BRECCIA, Veronika BUXHOFER-AUSCH, Olga CERNA, Ana-Manuela CRISAN, Catalin Doru DANAILA, De Stefano VALERIO, Konstanze DOEHNER, Victoria EMPSON, Joanna GORA-TYBOR, Martin GRIESSHAMMER, Sebastian GROSICKI, Paola GUGLIELMELLI, Valentin GARCIA-GUTIERREZ, Florian H HEIDEL, Arpad ILLES, Ciprian TOMULEASA, Chloe JAMES, Steffen KOSCHMIEDER, Maria-Theresa KRAUTH, Kurt KREJCY, Mihaela-Cornelia LAZAROIU, Jiří MAYER (203 Česká republika, domácí), Zsolt Gyoergy NAGY, Franck-Emmanuel NICOLINI, Francesca PALANDRI, Vassiliki PAPPA, Andreas Johannes REITER, Tomasz SACHA, Stefanie SCHLAGER, Stefan SCHMIDT, Evangelos TERPOS, Martin UNGER, Albert WOELFLER, Blanca Xicoy CIRICI a Christoph KLADE.
Vydání Annals of hematology, New York, Springer Verlag, 2024, 0939-5555.
Další údaje
Originální jazyk angličtina
Typ výsledku Článek v odborném periodiku
Obor 30205 Hematology
Stát vydavatele Spojené státy
Utajení není předmětem státního či obchodního tajemství
WWW URL
Impakt faktor Impact factor: 3.500 v roce 2022
Organizační jednotka Lékařská fakulta
Doi http://dx.doi.org/10.1007/s00277-024-05665-4
UT WoS 001182326400002
Klíčová slova anglicky Myeloproliferative neoplasms (MPNs); Essential thrombocythemia (ET); Ropeginterferon alfa-2b; ROP-ET; Phase III; Disease modification
Štítky 14110212, rivok
Změnil Změnila: Mgr. Tereza Miškechová, učo 341652. Změněno: 12. 7. 2024 08:44.
Anotace
Interferon-based therapies, such as ropeginterferon alfa-2b have emerged as promising disease-modifying agents for myeloproliferative neoplasms (MPNs), including essential thrombocythemia (ET). Current ET treatments aim to normalize hematological parameters and reduce the thrombotic risk, but they do not modify the natural history of the disease and hence, have no impact on disease progression. Ropeginterferon alfa-2b (trade name BESREMi (R)), a novel, monopegylated interferon alfa-2b with an extended administration interval, has demonstrated a robust and sustained efficacy in polycythemia vera (PV) patients. Given the similarities in disease pathophysiology and treatment goals, ropeginterferon alfa-2b holds promise as a treatment option for ET. The ROP-ET trial is a prospective, multicenter, single-arm phase III study that includes patients with ET who are intolerant or resistant to, and/or are ineligible for current therapies, such as hydroxyurea (HU), anagrelide (ANA), busulfan (BUS) and pipobroman, leaving these patients with limited treatment options. The primary endpoint is a composite response of hematologic parameters and disease-related symptoms, according to modified European LeukemiaNet (ELN) criteria. Secondary endpoints include improvements in symptoms and quality of life, molecular response and the safety profile of ropeginterferon alfa-2b. Over a 3-year period the trial assesses longer term outcomes, particularly the effects on allele burden and clinical outcomes, such as disease-related symptoms, vascular events and disease progression. No prospective clinical trial data exist for ropeginterferon alfa-2b in the planned ET study population and this study will provide new findings that may contribute to advancing the treatment landscape for ET patients with limited alternatives.
VytisknoutZobrazeno: 18. 7. 2024 11:35