Neurology and Therapy · 2023 · 20 citations · 33 references
MedicineNeurologyPharmacotherapyGene TherapyMolecular PathologyNeuropathologyInterferon-based TherapyNeurological Gene TherapyPeripheral Neuropathy ManagementSafety Of Gene TherapyFamilial Amyloid PolyneuropathyHereditary AmyloidosisRna Interference TherapeuticsWild-type Transthyretin Amyloidosis
Hereditary transthyretin (ATTRv; v for variant) amyloidosis, also known as hATTR amyloidosis, is a progressive and fatal disease associated with rapid deterioration of physical function and patients' quality of life (QOL). Vutrisiran, a subcutaneously administered RNA interference (RNAi) therapeutic that reduces hepatic production of transthyretin, was assessed in patients with ATTRv amyloidosis with polyneuropathy in the pivotal HELIOS-A study. The phase 3 open-label HELIOS-A study investigated the efficacy and safety of vutrisiran in patients with ATTRv amyloidosis with polyneuropathy, compared with an external placebo group from the APOLLO study of the RNAi therapeutic patisiran. Measures of QOL and physical function were assessed. At month 18, vutrisiran improved Norfolk Quality of Life-Diabetic Neuropathy (Norfolk QOL-DN) total score (least squares mean difference [LSMD] in change from baseline [CFB]: –21.0; p = 1.84 × 10 –10 ) and Norfolk QOL-DN domain scores, compared with external placebo. This benefit relative to external placebo was evident across all baseline polyneuropathy disability (PND) scores and most pronounced in patients with baseline PND scores I–II. Compared with external placebo, vutrisiran also demonstrated benefit in EuroQoL-Visual Analog Scale (EQ-VAS) score (LSMD in CFB: 13.7; nominal p = 2.21 × 10 –7 ), 10-m walk test (LSMD in CFB: 0.239 m/s; p = 1.21 × 10 –7 ), Rasch-built Overall Disability Score (LSMD in CFB: 8.4; p = 3.54 × 10 –15 ), and modified body mass index (mBMI) (LSMD in CFB: 140.7; p = 4.16 × 10 –15 ) at month 18. Overall, Norfolk QOL-DN, EQ-VAS, and mBMI improved from pretreatment baseline with vutrisiran, whereas all measures worsened from baseline in the external placebo group. At month 18, Karnofsky Performance Status was stable/improved from baseline in 58.2/13.1% with vutrisiran versus 34.7/8.1% with external placebo. Vutrisiran treatment provided significant clinical benefits in multiple measures of QOL and physical function in patients with ATTRv amyloidosis with polyneuropathy. Benefits were most pronounced in patients with earlier-stage disease, highlighting the importance of early diagnosis and treatment. ClinicalTrials.gov: NCT03759379.
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Jayaprakash K. Nair, Jennifer L. S. Willoughby, Amy Chan et al. · Journal of the American Chemical Society · 2014 · 1.1K citations
Tafamidis for transthyretin familial amyloid polyneuropathy
Teresa Coelho, Luı́s F. Maia, Ana Silva et al. · Neurology · 2012 · 795 citations · Full text
Medicine, Neurology, Pharmacotherapy +14
Repurposing Diflunisal for Familial Amyloid Polyneuropathy
John L. Berk, Ole B. Suhr, Laura Obici et al. · JAMA · 2013 · 701 citations · Full text