Literature DB >> 33186633

Hepatotoxicity following administration of onasemnogene abeparvovec (AVXS-101) for the treatment of spinal muscular atrophy.

Deepa Chand1, Franziska Mohr2, Hugh McMillan3, Francis Fonyuy Tukov4, Kyle Montgomery2, Aaron Kleyn2, Rui Sun2, Sitra Tauscher-Wisniewski2, Petra Kaufmann2, Gerd Kullak-Ublick5.   

Abstract

BACKGROUND & AIMS: Spinal muscular atrophy (SMA) is an autosomal recessive, childhood-onset motor neuron disease. Onasemnogene abeparvovec (OA) is a gene therapy designed to address SMA's root cause. In pivotal mouse toxicology studies, the liver was identified as a major site of OA toxicity. Clinical data reflect elevations in serum aminotransferase concentrations, with some reports of serious acute liver injury. Prophylactic prednisolone mitigates these effects. Herein, we aim to provide pragmatic, supportive guidance for identification, management, and risk mitigation of potential drug-induced liver injury.
METHODS: Data from 325 patients with SMA who had received OA through 31 December 2019, in 5 clinical trials, a managed access program (MAP), and a long-term registry (RESTORE), and through commercial use, were analyzed. Liver-related adverse events, laboratory data, concomitant medications, and prednisolone use were analyzed.
RESULTS: Based on adverse events and laboratory data, 90 of 100 patients had elevated liver function test results (alanine aminotransferase, and/or aspartate aminotransferase, and/or bilirubin concentrations). Of these, liver-associated adverse events were reported for 34 of 100 (34%) and 10 of 43 (23%) patients in clinical trials and MAP/RESTORE, respectively. Two patients in MAP had serious acute liver injury, which resolved completely. While all events in the overall population resolved, prednisolone treatment duration varied (range: 33-229 days), with a majority receiving prednisolone for 60-120 days. More than 60% had elevations in either alanine aminotransferase, aspartate aminotransferase, or bilirubin concentrations prior to dosing. Greater than 40% received potentially hepatotoxic concomitant medications.
CONCLUSIONS: Hepatotoxicity is a known risk associated with OA use. Practitioners should identify contributing factors and mitigate risk through appropriate monitoring and intervention. LAY
SUMMARY: Onasemnogene abeparvovec is a type of medicine called a "gene therapy," which is used to treat babies and young children who have a rare, serious inherited condition called "spinal muscular atrophy" (SMA). It works by supplying a fully functioning copy of the survival motor neuron or SMN gene, which then helps the body produce enough SMN protein. However, it can cause an immune response that could lead to an increase in enzymes produced by the liver. This article provides information about the liver injury and how to prevent and recognize if it happens, so that it may be treated properly.
Copyright © 2020 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  AAV9; Gene therapy; Hepatotoxicity; Onasemnogene abeparvovec; Safety

Mesh:

Substances:

Year:  2020        PMID: 33186633     DOI: 10.1016/j.jhep.2020.11.001

Source DB:  PubMed          Journal:  J Hepatol        ISSN: 0168-8278            Impact factor:   25.083


  27 in total

Review 1.  Curing SMA: Are we there yet?

Authors:  Aoife Reilly; Lucia Chehade; Rashmi Kothary
Journal:  Gene Ther       Date:  2022-05-26       Impact factor: 5.250

2.  Eliminating Panglossian thinking in development of AAV therapeutics.

Authors:  Radoslaw Kaczmarek; Glenn F Pierce; Declan Noone; Brian O'Mahony; David Page; Mark W Skinner
Journal:  Mol Ther       Date:  2021-11-10       Impact factor: 11.454

3.  Biodistribution of onasemnogene abeparvovec DNA, mRNA and SMN protein in human tissue.

Authors:  Gretchen Thomsen; Arthur H M Burghes; Caroline Hsieh; Janet Do; Binh T T Chu; Stephanie Perry; Basam Barkho; Petra Kaufmann; Douglas M Sproule; Douglas E Feltner; Wendy K Chung; Vicki L McGovern; Robert F Hevner; Miriam Conces; Christopher R Pierson; Mariacristina Scoto; Francesco Muntoni; Jerry R Mendell; Kevin D Foust
Journal:  Nat Med       Date:  2021-10-04       Impact factor: 53.440

Review 4.  A Historical Review of Brain Drug Delivery.

Authors:  William M Pardridge
Journal:  Pharmaceutics       Date:  2022-06-16       Impact factor: 6.525

5.  Hypercompact adenine base editors based on transposase B guided by engineered RNA.

Authors:  Do Yon Kim; Yuhee Chung; Yujin Lee; Dongmin Jeong; Kwang-Hyun Park; Hyun Jung Chin; Jeong Mi Lee; Seyeon Park; Sumin Ko; Jeong-Heon Ko; Yong-Sam Kim
Journal:  Nat Chem Biol       Date:  2022-08-01       Impact factor: 16.174

Review 6.  Spinal muscular atrophy.

Authors:  Eugenio Mercuri; Charlotte J Sumner; Francesco Muntoni; Basil T Darras; Richard S Finkel
Journal:  Nat Rev Dis Primers       Date:  2022-08-04       Impact factor: 65.038

Review 7.  Onasemnogene Abeparvovec: A Review in Spinal Muscular Atrophy.

Authors:  Hannah A Blair
Journal:  CNS Drugs       Date:  2022-08-12       Impact factor: 6.497

8.  Five-Year Extension Results of the Phase 1 START Trial of Onasemnogene Abeparvovec in Spinal Muscular Atrophy.

Authors:  Jerry R Mendell; Samiah A Al-Zaidy; Kelly J Lehman; Markus McColly; Linda P Lowes; Lindsay N Alfano; Natalie F Reash; Megan A Iammarino; Kathleen R Church; Aaron Kleyn; Matthew N Meriggioli; Richard Shell
Journal:  JAMA Neurol       Date:  2021-07-01       Impact factor: 18.302

9.  Developing a second-generation clinical candidate AAV vector for gene therapy of familial hypercholesterolemia.

Authors:  Lili Wang; Ilayaraja Muthuramu; Suryanarayan Somanathan; Hong Zhang; Peter Bell; Zhenning He; Hongwei Yu; Yanqing Zhu; Anna P Tretiakova; James M Wilson
Journal:  Mol Ther Methods Clin Dev       Date:  2021-05-05       Impact factor: 6.698

Review 10.  Novel vectors and approaches for gene therapy in liver diseases.

Authors:  Sheila Maestro; Nicholas D Weber; Nerea Zabaleta; Rafael Aldabe; Gloria Gonzalez-Aseguinolaza
Journal:  JHEP Rep       Date:  2021-04-30
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