TY - JOUR
T1 - Fedratinib Improves Myelofibrosis-related Symptoms and Health-related Quality of Life in Patients with Myelofibrosis Previously Treated with Ruxolitinib
T2 - Patient-reported Outcomes from the Phase II JAKARTA2 Trial
AU - Harrison, Claire N.
AU - Schaap, Nicolaas
AU - Vannucchi, Alessandro M.
AU - Kiladjian, Jean Jacques
AU - Jourdan, Eric
AU - Silver, Richard T.
AU - Schouten, Harry C.
AU - Passamonti, Francesco
AU - Zweegman, Sonja
AU - Talpaz, Moshe
AU - Verstovsek, Srdan
AU - Tang, Derek
AU - Abraham, Pranav
AU - Lord-Bessen, Jennifer
AU - Rose, Shelonitda
AU - Guo, Shien
AU - Liao, Weiqin
AU - Mesa, Ruben A.
N1 - Funding Information:
The original study was supported by Sanofi S.A.; this reanalysis was funded by Celgene, a Bristol-Myers Squibb company.
Funding Information:
CNH reports consultancy for Celgene, Novartis, CTI, Roche, Promedior, Galacteo, Sierra Oncology, Constellation, Janssen, and Geron; Honoraria from Celgene, Novartis, Roche, AOP Pharma; and Speakers’ Bureau participation for Celgene, Novartis, CTI, and Janssen. NS reports no conflicts. AMV holds positions on advisory committees for Novartis, BMS/Celgene, Abbvie, Blueprint, and Incyte; and participates in speakers’ bureau for Novartis, BMS/Celgene, and Abbvie. J-JK holds positions on advisory committees for Novartis, AOP Orphan, BMS, and Abbvie. EJ reports advisory board participation for Novartis, BMS, and Abbvie; and honoraria from Novartis. RTS reports consultancy, honoraria, and advisory committee participation for PharmEssentia; and equity interest in BMS. HCS has no disclosures. FP participates in speakers’ bureau for Novartis and BMS/Celgene. SZ receives research funding and participates in advisory committees for Janssen, Celgene, Takeda, and Sanofi. MT consults for BMS, IMAGO, and Celgene; received research funding from NS Pharma, Incyte, Stemline, Janssen, Promedior, Gilead, CTI Biopharma, Novartis, Samus Therapeutics, Asana, and Constellation; participates in advisory boards for BMS and Constellation; and received funding for travel and accommodations expenses from BMS and Celgene. SV reports Honoraria from Celgene. RAM reports consultancy for Novartis, Blueprint, Protagonist, Sierra, AbbVie, Geron, Genentech; and research support from Incyte, AbbVie, CTI, Imago. SR, PA, JLB, and DT report employment and equity ownership, Bristol Myers Squibb. SG and WL are employees of Evidera.
Publisher Copyright:
© 2021 Wolters Kluwer Health. All rights reserved.
PY - 2021/5/29
Y1 - 2021/5/29
N2 - Myelofibrosis symptoms compromise health-related quality of life (HRQoL). Ruxolitinib can reduce myelofibrosis symptom severity, but many patients discontinue ruxolitinib due to loss of response or unacceptable toxicity. Fedratinib is an oral, selective JAK2 inhibitor approved in the United States for treatment of patients with intermediate-2 or high-risk myelofibrosis. The single-Arm, phase II JAKARTA2 trial assessed fedratinib 400 mg/d (starting dose) in patients with myelofibrosis previously treated with ruxolitinib. Patient-reported changes in myelofibrosis symptom severity using the modified Myelofibrosis Symptom Assessment Form (MFSAF), and overall HRQoL and functional status using the EORTC QLQ-C30, were evaluated at each cycle. Clinically meaningful changes from baseline HRQoL scores were based on effect sizes. Ninety patients were MFSAF-evaluable. Myelofibrosis symptoms were mild-To-moderate at baseline. Patients showed statistically significant and clinically meaningful improvements in total symptom scores from baseline on the MFSAF at all post baseline visits through the end of cycle 6 (EOC6). Baseline global health status/QoL and functional domain scores on the EORTC QLQ-C30 were meaningfully worse than in the general population. At EOC6, 44% of patients reported clinically meaningful improvements in global health status/QoL, and 30%-53% of patients experienced clinically meaningful improvement in QLQ-C30 functional domains across post baseline timepoints. Over 80% of ongoing patients perceived fedratinib as beneficial on the Patient's Global Impression of Change questionnaire. Fedratinib effects were consistent among prognostically relevant patient subgroups. Patients with myelofibrosis previously treated with ruxolitinib experienced clinically meaningful improvements in myelofibrosis symptom burden, overall HRQoL, and functional status in the first 6 months of fedratinib treatment.
AB - Myelofibrosis symptoms compromise health-related quality of life (HRQoL). Ruxolitinib can reduce myelofibrosis symptom severity, but many patients discontinue ruxolitinib due to loss of response or unacceptable toxicity. Fedratinib is an oral, selective JAK2 inhibitor approved in the United States for treatment of patients with intermediate-2 or high-risk myelofibrosis. The single-Arm, phase II JAKARTA2 trial assessed fedratinib 400 mg/d (starting dose) in patients with myelofibrosis previously treated with ruxolitinib. Patient-reported changes in myelofibrosis symptom severity using the modified Myelofibrosis Symptom Assessment Form (MFSAF), and overall HRQoL and functional status using the EORTC QLQ-C30, were evaluated at each cycle. Clinically meaningful changes from baseline HRQoL scores were based on effect sizes. Ninety patients were MFSAF-evaluable. Myelofibrosis symptoms were mild-To-moderate at baseline. Patients showed statistically significant and clinically meaningful improvements in total symptom scores from baseline on the MFSAF at all post baseline visits through the end of cycle 6 (EOC6). Baseline global health status/QoL and functional domain scores on the EORTC QLQ-C30 were meaningfully worse than in the general population. At EOC6, 44% of patients reported clinically meaningful improvements in global health status/QoL, and 30%-53% of patients experienced clinically meaningful improvement in QLQ-C30 functional domains across post baseline timepoints. Over 80% of ongoing patients perceived fedratinib as beneficial on the Patient's Global Impression of Change questionnaire. Fedratinib effects were consistent among prognostically relevant patient subgroups. Patients with myelofibrosis previously treated with ruxolitinib experienced clinically meaningful improvements in myelofibrosis symptom burden, overall HRQoL, and functional status in the first 6 months of fedratinib treatment.
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U2 - 10.1097/HS9.0000000000000562
DO - 10.1097/HS9.0000000000000562
M3 - Article
AN - SCOPUS:85105717345
VL - 5
JO - HemaSphere
JF - HemaSphere
SN - 2572-9241
IS - 5
M1 - e562
ER -