Pazopanib in the treatment of advanced renal cell carcinoma

被引:30
作者
Cella, David [1 ]
Beaumont, Jennifer L. [2 ]
机构
[1] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Feinberg Sch Med, Dept Med Social Sci, 633 N St Clair,19th Floor, Chicago, IL 60611 USA
[2] Northwestern Univ, Feinberg Sch Med, Dept Med Social Sci, Chicago, IL 60611 USA
关键词
clinical experience; health-related quality of life; metastatic renal cell carcinoma; patient-reported outcomes; pazopanib; tyrosine kinase inhibitors;
D O I
10.1177/1756287215614236
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Pazopanib is an orally available multitargeted tyrosine kinase inhibitor (a class of targeted therapies) that inhibits tumor angiogenesis and cell proliferation. The safety and efficacy of pazopanib (noninferior to sunitinib for progression-free survival) in patients with advanced or metastatic renal cell carcinoma (mRCC) have been demonstrated in several clinical trials. However, in addition to therapeutic efficacy, treatment choices should also take into account health-related quality of life (HRQoL) aspects of cancer therapy. Here, we summarize the HRQoL findings related to pazopanib use, based on patient-reported outcome measures; pazopanib has been shown to be superior to sunitinib on several HRQoL domains (including patient preference). A further consideration for treatment choice is how well the findings from clinical trials correlate with evidence from general clinical practice. This review therefore includes descriptions of real-world experience of pazopanib use in the treatment of patients with mRCC, following its approval by medical regulatory authorities in a number of countries. Naturalistic observational studies demonstrate that the efficacy of pazopanib in patients with mRCC is consistent with clinical trial findings. Similarly, consistent results were observed for the safety profile of pazopanib between observational studies and clinical trials, with most treatment-associated adverse events being mild to moderate in severity, and manageable.
引用
收藏
页码:61 / 69
页数:9
相关论文
共 39 条
[1]
Beaumont J., 2014, J CLIN ONCOL S5, V32
[2]
Health-related quality of life in patients with advanced renal cell carcinoma receiving pazopanib or placebo in a randomised phase III trial [J].
Cella, D. ;
Pickard, A. S. ;
Duh, M. S. ;
Guerin, A. ;
Mishagina, N. ;
Antras, L. ;
Neary, M. P. ;
McCann, L. ;
Hodge, R. ;
Sternberg, C. N. .
EUROPEAN JOURNAL OF CANCER, 2012, 48 (03) :311-323
[3]
Combining anchor and distribution-based methods to derive minimal clinically important differences on the functional assessment of cancer therapy (FACT) anemia and fatigue scales [J].
Cella, D ;
Eton, DT ;
Lai, JS ;
Peterman, AH ;
Merkel, DE .
JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2002, 24 (06) :547-561
[4]
Cella D., 2013, J CLIN ONCOL S6, V31
[5]
Prospective non-interventional multicentre observational trial of first-line anti-cancer treatment in patients with metastatic renal cell cancer in Belgium [J].
Cornelis, N. ;
Vermassen, T. ;
Schallier, D. ;
Machiels, J. -P. ;
Gil, T. ;
Debruyne, P. R. ;
D'hondt, R. ;
Bols, A. ;
Schrijvers, D. ;
Mebis, J. ;
Lumen, N. ;
Rottey, S. .
ACTA CLINICA BELGICA, 2014, 69 (05) :335-340
[6]
Persistence and Compliance Among US Patients Receiving Pazopanib or Sunitinib as First-Line Therapy for Advanced Renal Cell Carcinoma: A Retrospective Claims Analysis [J].
DaCosta, Stacey A. ;
McPheeters, Jeffrey T. ;
Burton, Tanya M. ;
Nagar, Saurabh P. ;
Hackshaw, Michelle D. .
JOURNAL OF MANAGED CARE & SPECIALTY PHARMACY, 2015, 21 (06) :515-522
[7]
Randomized, Controlled, Double-Blind, Cross-Over Trial Assessing Treatment Preference for Pazopanib Versus Sunitinib in Patients With Metastatic Renal Cell Carcinoma: PISCES Study [J].
Escudier, Bernard ;
Porta, Camillo ;
Bono, Petri ;
Powles, Thomas ;
Eisen, Tim ;
Sternberg, Cora N. ;
Gschwend, Juergen E. ;
De Giorgi, Ugo ;
Parikh, Omi ;
Hawkins, Robert ;
Sevin, Emmanuel ;
Negrier, Sylvie ;
Khan, Sadya ;
Diaz, Jose ;
Redhu, Suman ;
Mehmud, Faisal ;
Cella, David .
JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (14) :1412-+
[8]
Galvis V., 2013, EUR J CANC S2, V49
[9]
Gernone A, 2014, TUMORI J, V100, pE165, DOI [10.1177/1636.17942, 10.1700/1636.17942]
[10]
GlaxoSmithKline, 2014, US PROD INF PAZ