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
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