Efficacy and safety of fedratinib in patients with myelofibrosis previously treated with ruxolitinib (FREEDOM2): results from a multicentre, open-label, randomised, controlled, phase 3trial


Por: Harrison, CN, Mesa, R, Talpaz, M, Al-Ali, HK, Xicoy, B, Passamonti, F, Palandri, F, Benevolo, G, Vannucchi, AM, Mediavilla, C, Iurlo, A, Kim, I, Rose, S, Brown, P, Hernandez, C, Wang, J and Kiladjian, JJ

Publicada: 1 oct 2024 Ahead of Print: 1 oct 2024
Resumen:
Background Most patients with myelofibrosis develop ruxolitinib intolerance or disease that is relapsed or refractory, and survival rates after ruxolitinib discontinuation are poor. We aimed to evaluate the safety and efficacy of fedratinib versus best available therapy (BAT) in patients with myelofibrosis previously treated with ruxolitinib. Methods FREEDOM2 was a multicentre, open-label, randomised, controlled, phase 3 trial in 86 clinics in 16 countries, in which patients aged at least 18 years with intermediate-2 or high-risk myelofibrosis that was relapsed or refractory or intolerant to ruxolitinib with Eastern Cooperative Oncology Group performance status 0-2 were stratified by spleen size by palpation, platelet count, and previous ruxolitinib treatment, and randomly assigned 2:1 by interactive response technology to receive fedratinib 400 mg per day (4 x 100 mg capsules orally once daily, open-label) or BAT. Patients received prophylactic antiemetics and thiamine supplementation, and symptomatic antidiarrhoeals as required. Primary endpoint was proportion of patients reaching spleen volume reduction (SVR) of at least 35% (SVR35) at end of cycle 6 in the intention-to-treat population. This manuscript reports the primary analysis of the trial; follow-up is ongoing. This trial is registered at clinicaltrials.gov, NCT03952039. Findings Between Sept 9, 2019 and June 24, 2022, of 316 patients screened, 201 were randomly assigned and treated (134 to fedratinib, 67 to BAT [including 52 receiving ruxolitinib]); 46 patients from the BAT group crossed over to fedratinib. Approximately half of enrolled patients were male (fedratinib 75 [56%] of 134; BAT 30 [45%] of 67) and most were White (fedratinib 106 [79%] of 134; BAT 58 [87%] of 67). At data cutoff (Dec 27, 2022), median survival follow-up was 645 weeks (IQR 379-1049). SVR35 at end of cycle 6 was seen in 48 (36%) of 134 patients receiving fedratinib versus four (6%) of 67 patients receiving BAT (30% difference; 95% CI 20-39; one-sided p-value <00001). During the first six cycles 53 (40%) of 134 patients in the fedratinib group and 8 (12%) of 67 patients in the BAT group had grade 3 or greater treatment-related adverse events, most frequently anaemia (fedratinib 12 [9%] of 134; BAT 6 [9%] of 67) and thrombocytopenia (fedratinib 16 [12%] of 134; BAT 2 [3%] of 67); one patient in the fedratinib group died from acute kidney injury suspected to be related to study drug (no treatment-related deaths in the BAT group). Gastrointestinal adverse events occurred more frequently in the fedratinib group compared with the BAT group, but were mostly grade 1-2 in severity and more frequent in early cycles, and were less frequent than in prior clinical trials. A total of 28 (21%) of 134 patients in the fedratinib group and 3 (4%) of 67 patients in the BAT group had thiamine levels below lower limit of normal per central laboratory assessment, with only one case of low thiamine in the fedratinib arm after the introduction of prophylactic thiamine supplementation. Interpretation Findings from FREEDOM2 support fedratinib as a second-line Janus kinase inhibitor option to reduce spleen size after ruxolitinib failure or intolerance in patients with myelofibrosis, and shows effective strategies for management of gastrointestinal adverse events and low thiamine concentrations through prophylaxis, monitoring, and treatment.

Filiaciones:
Harrison, CN:
 Guys & St Thomas NHS Fdn Trust, London, England

Mesa, R:
 Wake Forest Univ Sch Med, Winston Salem, NC USA

Talpaz, M:
 Univ Michigan, Canc Ctr, Ann Arbor, MI USA

Al-Ali, HK:
 Univ Klinikum Halle, Saale, Germany

:
 Univ Autonoma Barcelona, Hosp Univ Germans Trias I Pujol, Josep Carreras Leukemia Res Inst, Inst Catala Oncol, Barcelona, Spain

Passamonti, F:
 Univ Milan, Fdn IRCCS Ca Granda Osped Maggiore Policlin, Milan, Italy

Palandri, F:
 IRCCS Azienda Osped Univ Bologna, Ist Ematol Seragnoli, Bologna, Italy

Benevolo, G:
 AOU Citta Salute & Sci, Turin, Italy

Vannucchi, AM:
 Univ Firenze, AOU Careggi, Florence, Italy

Mediavilla, C:
 Hop Haut Leveque, Bordeaux, France

Iurlo, A:
 Fdn IRCCS Ca Granda Osped Maggiore Policlin, Milan, Italy

Kim, I:
 Seoul Natl Univ Hosp, Seoul, South Korea

Rose, S:
 Bristol Myers Squibb, Princeton, NJ USA

Brown, P:
 Bristol Myers Squibb, Princeton, NJ USA

Hernandez, C:
 Bristol Myers Squibb, Princeton, NJ USA

Wang, J:
 Bristol Myers Squibb, Princeton, NJ USA

Kiladjian, JJ:
 Hosp St Louis, Paris, France

 Univ Paris Cite, Paris, France
ISSN: 23523026





Lancet Haematology
Editorial
Lancet Publishing Group, THE BOULEVARD, LANGFORD LANE, KIDLINGTON, OXFORD OX5 1GB, OXON, ENGLAND, Reino Unido
Tipo de documento: Article
Volumen: 11 Número: 10
Páginas: 729-740
WOS Id: 001331372200001
ID de PubMed: 39265613

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