Measuring health-related quality of life in patients with rare disease

被引:28
作者
Lenderking, William R. [1 ]
Anatchkova, Milena [2 ]
Pokrzywinski, Robin [2 ]
Skalicky, Anne [3 ]
Martin, Mona L. [3 ]
Gelhorn, Heather [2 ]
机构
[1] Evidera, Patient Ctr Res, 500 Totten Pond Rd,Fifth Floor, Waltham, MA 02451 USA
[2] Evidera, Patient Ctr Res, Bethesda, MD USA
[3] Evidera, Patient Ctr Res, Seattle, WA USA
关键词
Rare disease; HRQoL; Clinical outcome assessment (COA); Item banks; Measure adaptation; FDA; Embedded interviews; Disease-specific; Multi-dimensional responder index;
D O I
10.1186/s41687-021-00336-8
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
BackgroundThere has been a growing emphasis on health-related quality of life (HRQoL) as an important outcome in rare disease drug development, although its assessment may be useful outside the drug development context, including in clinical applications or natural history studies. Central to assessing quality of life in health research is utilizing outcome measures that capture symptoms and impacts of the disease and treatment that are important and relevant to patients. Identifying and implementing valid and reliable tools to measure HRQoL in rare diseases poses unique challenges that often require creative solutions. Main body: In this commentary, we explore some of the challenges in HRQoL assessment in rare disease, propose solutions, and consider regulatory issues. Some of the solutions discussed entail the use of item banks, adapting existing measures from phenotypically similar disease contexts, use of multi-domain measurement indices, and adapting methods for assessing content validity of existing measures. Current regulatory considerations are discussed and resources outlined. Conclusion: Quality of life may be the most important endpoint for patients with rare diseases, and the challenges of valid assessment require effort and innovative thinking specific to each context to improve measurement and clinical outcomes.
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页数:7
相关论文
共 26 条
[11]   Patient-reported Symptoms of Tenosynovial Giant Cell Tumors [J].
Gelhorn, Heather L. ;
Tong, Sandra ;
McQuarrie, Kelly ;
Vernon, Christina ;
Hanlon, Jennifer ;
Maclaine, Grant ;
Lenderking, William ;
Ye, Xin ;
Speck, Rebecca M. ;
Lackman, Richard D. ;
Bukata, Susan V. ;
Healey, John H. ;
Keedy, Vicki L. ;
Anthony, Stephen P. ;
Wagner, Andrew J. ;
Von Hoff, Daniel D. ;
Singh, Arun S. ;
Becerra, Carlos R. ;
Hsu, Henry H. ;
Lin, Paul S. ;
Tap, William D. .
CLINICAL THERAPEUTICS, 2016, 38 (04) :778-793
[12]  
Gorlin RJ, 2000, AM J MED GENET, V91, P368, DOI 10.1002/(SICI)1096-8628(20000424)91:5<368::AID-AJMG10>3.0.CO
[13]  
2-9
[14]   Assessing the impact on caregivers caring for patients with rare pediatric lysosomal storage diseases: development of the Caregiver Impact Questionnaire [J].
Harrington, Magdalena ;
Hareendran, Asha ;
Skalicky, Anne ;
Wilson, Hilary ;
Clark, Marci ;
Mikl, Jaromir .
JOURNAL OF PATIENT-REPORTED OUTCOMES, 2019, 3 (01)
[15]  
HealthMeasures Neuro-QoL&TRADE, QUAL LIF NEUR DISS QUAL LIF NEUR DISS
[16]  
HealthMeasures PROMIS®, PATIENT REPORTED OUT
[17]   Patient-Reported Outcomes in Orphan Drug Labels Approved by the US Food and Drug Administration [J].
Hong, Yoon Duk ;
Villalonga-Olives, Ester ;
Perfetto, Eleanor M. .
VALUE IN HEALTH, 2019, 22 (08) :925-930
[18]   Childhood disorders of neurodegeneration with brain iron accumulation (NBIA) [J].
Kurian, Manju A. ;
McNeill, Alasdair ;
Lin, Jean-Pierre ;
Maher, Eamonn R. .
DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY, 2011, 53 (05) :394-404
[19]   To what degree are orphan drugs patient-centered? A review of the current state of clinical research in rare diseases [J].
Lanar, Sally ;
Acquadro, Catherine ;
Seaton, James ;
Savre, Isabelle ;
Arnould, Benoit .
ORPHANET JOURNAL OF RARE DISEASES, 2020, 15 (01)
[20]   Diagnostic and clinical experience of patients with pantothenate kinase-associated neurodegeneration [J].
Marshall, Randall D. ;
Collins, Abigail ;
Escolar, Maria L. ;
Jinnah, H. A. ;
Klopstock, Thomas ;
Kruer, Michael C. ;
Videnovic, Aleksandar ;
Robichaux-Viehoever, Amy ;
Burns, Colleen ;
Swett, Laura L. ;
Revicki, Dennis A. ;
Bender, Randall H. ;
Lenderking, William R. .
ORPHANET JOURNAL OF RARE DISEASES, 2019, 14 (1)