TY - JOUR
T1 - Health-related quality of life and symptoms in patients with myelofibrosis treated with ruxolitinib versus best available therapy
AU - Harrison, Claire N.
AU - Mesa, Ruben A.
AU - Kiladjian, Jean Jacques
AU - Al-Ali, Haifa Kathrin
AU - Gisslinger, Heinz
AU - Knoops, Laurent
AU - Squier, Margaret
AU - Sirulnik, Andres
AU - Mendelson, Estella
AU - Zhou, Xiaolei
AU - Copley-Merriman, Catherine
AU - Hunter, Deborah S.
AU - Levy, Richard S.
AU - Cervantes, Francisco
AU - Passamonti, Francesco
AU - Barbui, Tiziano
AU - Barosi, Giovanni
AU - Vannucchi, Alessandro M.
PY - 2013/7
Y1 - 2013/7
N2 - Patients with myelofibrosis (MF) have significant debilitating symptoms, physical disabilities, and poor health-related quality of life (HRQoL). Here, we report post-hoc analyses of the impact of ruxolitinib, a potent and selective JAK1 and JAK2 inhibitor, on disease-related symptoms and HRQoL in MF patients from the large phase 3 COMFORT-II study (N = 219). During the follow-up period of 48 weeks, HRQoL and MF-associated symptoms improved from baseline for ruxolitinib-treated patients but remained the same or worsened for best available therapy (BAT)-treated patients. Based on the European Organization for Research and Treatment of Cancer QoL Questionnaire core 30 items (EORTC QLQ-C30), treatment-induced differences in physical and role functioning, fatigue, and appetite loss significantly favoured ruxolitinib versus BAT from week 8 (P < 0·05) up to week 48 (P < 0·05). Ruxolitinib resulted in significantly higher response rates in global health status/QoL and Functional Assessment of Cancer Therapy-Lymphoma (FACT-Lym) summary scores versus BAT at most time points (P < 0·05). Significant improvements in the Lymphoma subscale (including symptoms of pain, fever, itching, fatigue, weight loss, loss of appetite, and other patient concerns), FACT-General, FACT-Lym trial outcome index, and FACT-Lym total were also observed with ruxolitinib versus BAT starting at week 8 and continuing thereafter. Overall, these data demonstrated that ruxolitinib improved HRQoL in MF patients and further support the use of ruxolitinib for the treatment of symptomatic MF.
AB - Patients with myelofibrosis (MF) have significant debilitating symptoms, physical disabilities, and poor health-related quality of life (HRQoL). Here, we report post-hoc analyses of the impact of ruxolitinib, a potent and selective JAK1 and JAK2 inhibitor, on disease-related symptoms and HRQoL in MF patients from the large phase 3 COMFORT-II study (N = 219). During the follow-up period of 48 weeks, HRQoL and MF-associated symptoms improved from baseline for ruxolitinib-treated patients but remained the same or worsened for best available therapy (BAT)-treated patients. Based on the European Organization for Research and Treatment of Cancer QoL Questionnaire core 30 items (EORTC QLQ-C30), treatment-induced differences in physical and role functioning, fatigue, and appetite loss significantly favoured ruxolitinib versus BAT from week 8 (P < 0·05) up to week 48 (P < 0·05). Ruxolitinib resulted in significantly higher response rates in global health status/QoL and Functional Assessment of Cancer Therapy-Lymphoma (FACT-Lym) summary scores versus BAT at most time points (P < 0·05). Significant improvements in the Lymphoma subscale (including symptoms of pain, fever, itching, fatigue, weight loss, loss of appetite, and other patient concerns), FACT-General, FACT-Lym trial outcome index, and FACT-Lym total were also observed with ruxolitinib versus BAT starting at week 8 and continuing thereafter. Overall, these data demonstrated that ruxolitinib improved HRQoL in MF patients and further support the use of ruxolitinib for the treatment of symptomatic MF.
KW - Health-related quality of life
KW - JAK1/JAK2 inhibitor
KW - Myelofibrosis
KW - Ruxolitinib
UR - http://www.scopus.com/inward/record.url?scp=84879840304&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84879840304&partnerID=8YFLogxK
U2 - 10.1111/bjh.12375
DO - 10.1111/bjh.12375
M3 - Article
C2 - 23672349
AN - SCOPUS:84879840304
SN - 0007-1048
VL - 162
SP - 229
EP - 239
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 2
ER -