BURDEN OF SYSTEMIC LIGHT-CHAIN (AL) AMYLOIDOSIS- A SYSTEMATIC LITERATURE REVIEW

Author(s)

Mehta S1, Cooke C1, Gao X1, Labotka R2, Berg D2, Parameswaran H3, Lin HM2
1Pharmerit International, Bethesda, MD, USA, 2Millennium Pharmaceuticals, Inc., a wholly owned subsidiary of Takeda Pharmaceutical Company Limited, Cambridge, MA, USA, 3Medical College of Wisconsin, Milwaukee, WI, USA

OBJECTIVES: To conduct a systematic literature review on relapsed or refractory AL amyloidosis, focusing on clinical outcomes, epidemiology, health-related quality-of-life (HRQoL) and economic aspects. METHODS: MEDLINE and EMBASE databases were searched for English-language articles published in the last 10 years using search terms including “Primary/Systemic amyloidosis”, “epidemiology/prevalence/incidence”, “therapeutics/drug therapy/outcome”, ”patient-reported/quality-of-life/satisfaction and “economics/cost” etc. Search results were manually reviewed, and relevant studies were selected for inclusion as appropriate. Additional references were obtained from clinical conferences and the reference lists of selected articles.  RESULTS: CONCLUSIONS: Limited epidemiologic and health outcomes data exist in the literature for relapsed or refractory AL amyloidosis. Treatment options are insufficient. New therapies which offer better clinical outcomes with less toxicity are needed to improve patient care.

Conference/Value in Health Info

2015-05, ISPOR 2015, Philadelphia, PA, USA

Value in Health, Vol. 18, No. 3 (May 2015)

Code

PCN138

Topic

Health Service Delivery & Process of Care

Topic Subcategory

Health Care Research, Treatment Patterns and Guidelines

Disease

Oncology, Rare and Orphan Diseases

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