Health-related quality of life and symptoms in patients with myelofibrosis treated with ruxolitinib versus best available therapy

被引:68
作者
Harrison, Claire N. [1 ]
Mesa, Ruben A. [2 ]
Kiladjian, Jean-Jacques [3 ,4 ]
Al-Ali, Haifa-Kathrin [5 ]
Gisslinger, Heinz [6 ]
Knoops, Laurent [7 ,8 ]
Squier, Margaret [9 ]
Sirulnik, Andres [9 ]
Mendelson, Estella [9 ]
Zhou, Xiaolei [10 ]
Copley-Merriman, Catherine [10 ]
Hunter, Deborah S. [11 ]
Levy, Richard S. [11 ]
Cervantes, Francisco [12 ]
Passamonti, Francesco [13 ]
Barbui, Tiziano [14 ]
Barosi, Giovanni [15 ]
Vannucchi, Alessandro M. [16 ]
机构
[1] Guys Hosp, Guys & St Thomas NHS Fdn Trust, London SE1 9RT, England
[2] Mayo Clin, Scottsdale, AZ USA
[3] Hop St Louis, Paris, France
[4] Univ Paris, F-75252 Paris, France
[5] Univ Leipzig, D-04109 Leipzig, Germany
[6] Med Univ Vienna, Vienna, Austria
[7] Catholic Univ Louvain, Clin Univ St Luc, B-1200 Brussels, Belgium
[8] Catholic Univ Louvain, de Duve Inst, B-1200 Brussels, Belgium
[9] Novartis Pharmaceut, E Hanover, NJ USA
[10] RTI Hlth Solut, Res Triangle Pk, NC USA
[11] Incyte Corp, Wilmington, DE USA
[12] Hosp Clin Barcelona, Inst Invest Biomed August Pi & Sunyer, Barcelona, Spain
[13] Osped Circolo & Fdn Macchi, Varese, Italy
[14] AO Osped Riuniti Bergamo, Bergamo, Italy
[15] Policlin San Matteo Fdn, Ist Ricovero & Cura Carattere Sci, Pavia, Italy
[16] Univ Florence, Florence, Italy
关键词
ruxolitinib; myelofibrosis; JAK1/JAK2; inhibitor; health-related quality of life; INTERNATIONAL WORKING GROUP; MYELOPROLIFERATIVE DISORDERS; IWG-MRT; LEUKEMIA; LYMPHOMA; ONCOLOGY; PLACEBO; FATIGUE;
D O I
10.1111/bjh.12375
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 48weeks, 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<005) up to week 48 (P<005). 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<005). 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.
引用
收藏
页码:229 / 239
页数:11
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