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Indirect Comparison of Lenadogene Nolparvovec Gene Therapy Versus Natural History in Patients with Leber Hereditary Optic Neuropathy Carrying the m.11778G>A MT-ND4 Mutation

INTRODUCTION: Lenadogene nolparvovec is a promising novel gene therapy for patients with Leber hereditary optic neuropathy (LHON) carrying the m.11778G>A ND4 mutation (MT-ND4). A previous pooled analysis of phase 3 studies showed an improvement in visual acuity of patients injected with lenadogen...

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Autores principales: Carelli, Valerio, Newman, Nancy J., Yu-Wai-Man, Patrick, Biousse, Valerie, Moster, Mark L., Subramanian, Prem S., Vignal-Clermont, Catherine, Wang, An-Guor, Donahue, Sean P., Leroy, Bart P., Sergott, Robert C., Klopstock, Thomas, Sadun, Alfredo A., Rebolleda Fernández, Gema, Chwalisz, Bart K., Banik, Rudrani, Girmens, Jean François, La Morgia, Chiara, DeBusk, Adam A., Jurkute, Neringa, Priglinger, Claudia, Karanjia, Rustum, Josse, Constant, Salzmann, Julie, Montestruc, François, Roux, Michel, Taiel, Magali, Sahel, José-Alain
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834474/
https://www.ncbi.nlm.nih.gov/pubmed/36449262
http://dx.doi.org/10.1007/s40123-022-00611-x
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author Carelli, Valerio
Newman, Nancy J.
Yu-Wai-Man, Patrick
Biousse, Valerie
Moster, Mark L.
Subramanian, Prem S.
Vignal-Clermont, Catherine
Wang, An-Guor
Donahue, Sean P.
Leroy, Bart P.
Sergott, Robert C.
Klopstock, Thomas
Sadun, Alfredo A.
Rebolleda Fernández, Gema
Chwalisz, Bart K.
Banik, Rudrani
Girmens, Jean François
La Morgia, Chiara
DeBusk, Adam A.
Jurkute, Neringa
Priglinger, Claudia
Karanjia, Rustum
Josse, Constant
Salzmann, Julie
Montestruc, François
Roux, Michel
Taiel, Magali
Sahel, José-Alain
author_facet Carelli, Valerio
Newman, Nancy J.
Yu-Wai-Man, Patrick
Biousse, Valerie
Moster, Mark L.
Subramanian, Prem S.
Vignal-Clermont, Catherine
Wang, An-Guor
Donahue, Sean P.
Leroy, Bart P.
Sergott, Robert C.
Klopstock, Thomas
Sadun, Alfredo A.
Rebolleda Fernández, Gema
Chwalisz, Bart K.
Banik, Rudrani
Girmens, Jean François
La Morgia, Chiara
DeBusk, Adam A.
Jurkute, Neringa
Priglinger, Claudia
Karanjia, Rustum
Josse, Constant
Salzmann, Julie
Montestruc, François
Roux, Michel
Taiel, Magali
Sahel, José-Alain
author_sort Carelli, Valerio
collection PubMed
description INTRODUCTION: Lenadogene nolparvovec is a promising novel gene therapy for patients with Leber hereditary optic neuropathy (LHON) carrying the m.11778G>A ND4 mutation (MT-ND4). A previous pooled analysis of phase 3 studies showed an improvement in visual acuity of patients injected with lenadogene nolparvovec compared to natural history. Here, we report updated results by incorporating data from the latest phase 3 trial REFLECT in the pool, increasing the number of treated patients from 76 to 174. METHODS: The visual acuity of 174 MT-ND4-carrying patients with LHON injected in one or both eyes with lenadogene nolparvovec from four pooled phase 3 studies (REVERSE, RESCUE and their long-term extension trial RESTORE; and REFLECT trial) was compared to the spontaneous evolution of an external control group of 208 matched patients from 11 natural history studies. RESULTS: Treated patients showed a clinically relevant and sustained improvement in their visual acuity when compared to natural history. Mean improvement versus natural history was − 0.30 logMAR (+ 15 ETDRS letters equivalent) at last observation (P < 0.01) with a maximal follow-up of 3.9 years after injection. Most treated eyes were on-chart as compared to less than half of natural history eyes at 48 months after vision loss (89.6% versus 48.1%; P < 0.01) and at last observation (76.1% versus 44.4%; P < 0.01). When we adjusted for covariates of interest (gender, age of onset, ethnicity, and duration of follow-up), the estimated mean gain was − 0.43 logMAR (+ 21.5 ETDRS letters equivalent) versus natural history at last observation (P < 0.0001). Treatment effect was consistent across all phase 3 clinical trials. Analyses from REFLECT suggest a larger treatment effect in patients receiving bilateral injection compared to unilateral injection. CONCLUSION: The efficacy of lenadogene nolparvovec in improving visual acuity in MT-ND4 LHON was confirmed in a large cohort of patients, compared to the spontaneous natural history decline. Bilateral injection of gene therapy may offer added benefits over unilateral injection. TRIAL REGISTRATION NUMBERS: NCT02652780 (REVERSE); NCT02652767 (RESCUE); NCT03406104 (RESTORE); NCT03293524 (REFLECT); NCT03295071 (REALITY). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40123-022-00611-x.
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spelling pubmed-98344742023-01-13 Indirect Comparison of Lenadogene Nolparvovec Gene Therapy Versus Natural History in Patients with Leber Hereditary Optic Neuropathy Carrying the m.11778G>A MT-ND4 Mutation Carelli, Valerio Newman, Nancy J. Yu-Wai-Man, Patrick Biousse, Valerie Moster, Mark L. Subramanian, Prem S. Vignal-Clermont, Catherine Wang, An-Guor Donahue, Sean P. Leroy, Bart P. Sergott, Robert C. Klopstock, Thomas Sadun, Alfredo A. Rebolleda Fernández, Gema Chwalisz, Bart K. Banik, Rudrani Girmens, Jean François La Morgia, Chiara DeBusk, Adam A. Jurkute, Neringa Priglinger, Claudia Karanjia, Rustum Josse, Constant Salzmann, Julie Montestruc, François Roux, Michel Taiel, Magali Sahel, José-Alain Ophthalmol Ther Original Research INTRODUCTION: Lenadogene nolparvovec is a promising novel gene therapy for patients with Leber hereditary optic neuropathy (LHON) carrying the m.11778G>A ND4 mutation (MT-ND4). A previous pooled analysis of phase 3 studies showed an improvement in visual acuity of patients injected with lenadogene nolparvovec compared to natural history. Here, we report updated results by incorporating data from the latest phase 3 trial REFLECT in the pool, increasing the number of treated patients from 76 to 174. METHODS: The visual acuity of 174 MT-ND4-carrying patients with LHON injected in one or both eyes with lenadogene nolparvovec from four pooled phase 3 studies (REVERSE, RESCUE and their long-term extension trial RESTORE; and REFLECT trial) was compared to the spontaneous evolution of an external control group of 208 matched patients from 11 natural history studies. RESULTS: Treated patients showed a clinically relevant and sustained improvement in their visual acuity when compared to natural history. Mean improvement versus natural history was − 0.30 logMAR (+ 15 ETDRS letters equivalent) at last observation (P < 0.01) with a maximal follow-up of 3.9 years after injection. Most treated eyes were on-chart as compared to less than half of natural history eyes at 48 months after vision loss (89.6% versus 48.1%; P < 0.01) and at last observation (76.1% versus 44.4%; P < 0.01). When we adjusted for covariates of interest (gender, age of onset, ethnicity, and duration of follow-up), the estimated mean gain was − 0.43 logMAR (+ 21.5 ETDRS letters equivalent) versus natural history at last observation (P < 0.0001). Treatment effect was consistent across all phase 3 clinical trials. Analyses from REFLECT suggest a larger treatment effect in patients receiving bilateral injection compared to unilateral injection. CONCLUSION: The efficacy of lenadogene nolparvovec in improving visual acuity in MT-ND4 LHON was confirmed in a large cohort of patients, compared to the spontaneous natural history decline. Bilateral injection of gene therapy may offer added benefits over unilateral injection. TRIAL REGISTRATION NUMBERS: NCT02652780 (REVERSE); NCT02652767 (RESCUE); NCT03406104 (RESTORE); NCT03293524 (REFLECT); NCT03295071 (REALITY). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s40123-022-00611-x. Springer Healthcare 2022-11-30 2023-02 /pmc/articles/PMC9834474/ /pubmed/36449262 http://dx.doi.org/10.1007/s40123-022-00611-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research
Carelli, Valerio
Newman, Nancy J.
Yu-Wai-Man, Patrick
Biousse, Valerie
Moster, Mark L.
Subramanian, Prem S.
Vignal-Clermont, Catherine
Wang, An-Guor
Donahue, Sean P.
Leroy, Bart P.
Sergott, Robert C.
Klopstock, Thomas
Sadun, Alfredo A.
Rebolleda Fernández, Gema
Chwalisz, Bart K.
Banik, Rudrani
Girmens, Jean François
La Morgia, Chiara
DeBusk, Adam A.
Jurkute, Neringa
Priglinger, Claudia
Karanjia, Rustum
Josse, Constant
Salzmann, Julie
Montestruc, François
Roux, Michel
Taiel, Magali
Sahel, José-Alain
Indirect Comparison of Lenadogene Nolparvovec Gene Therapy Versus Natural History in Patients with Leber Hereditary Optic Neuropathy Carrying the m.11778G>A MT-ND4 Mutation
title Indirect Comparison of Lenadogene Nolparvovec Gene Therapy Versus Natural History in Patients with Leber Hereditary Optic Neuropathy Carrying the m.11778G>A MT-ND4 Mutation
title_full Indirect Comparison of Lenadogene Nolparvovec Gene Therapy Versus Natural History in Patients with Leber Hereditary Optic Neuropathy Carrying the m.11778G>A MT-ND4 Mutation
title_fullStr Indirect Comparison of Lenadogene Nolparvovec Gene Therapy Versus Natural History in Patients with Leber Hereditary Optic Neuropathy Carrying the m.11778G>A MT-ND4 Mutation
title_full_unstemmed Indirect Comparison of Lenadogene Nolparvovec Gene Therapy Versus Natural History in Patients with Leber Hereditary Optic Neuropathy Carrying the m.11778G>A MT-ND4 Mutation
title_short Indirect Comparison of Lenadogene Nolparvovec Gene Therapy Versus Natural History in Patients with Leber Hereditary Optic Neuropathy Carrying the m.11778G>A MT-ND4 Mutation
title_sort indirect comparison of lenadogene nolparvovec gene therapy versus natural history in patients with leber hereditary optic neuropathy carrying the m.11778g>a mt-nd4 mutation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9834474/
https://www.ncbi.nlm.nih.gov/pubmed/36449262
http://dx.doi.org/10.1007/s40123-022-00611-x
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