Literature DB >> 35913563

Efficacy and safety of lumasiran for infants and young children with primary hyperoxaluria type 1: 12-month analysis of the phase 3 ILLUMINATE-B trial.

Wesley Hayes1, David J Sas2, Daniella Magen3, Hadas Shasha-Lavsky4, Mini Michael5, Anne-Laure Sellier-Leclerc6, Julien Hogan7, Taylor Ngo8, Marianne T Sweetser8, John M Gansner8, Tracy L McGregor8, Yaacov Frishberg9.   

Abstract

BACKGROUND: Primary hyperoxaluria type 1 (PH1) is a rare genetic disease that causes progressive kidney damage and systemic oxalosis due to hepatic overproduction of oxalate. Lumasiran demonstrated efficacy and safety in the 6-month primary analysis period of the phase 3, multinational, open-label, single-arm ILLUMINATE-B study of infants and children < 6 years old with PH1 (ClinicalTrials.gov: NCT03905694 (4/1/2019); EudraCT: 2018-004,014-17 (10/12/2018)). Outcomes in the ILLUMINATE-B extension period (EP) for patients who completed ≥ 12 months on study are reported here.
METHODS: Of the 18 patients enrolled in the 6-month primary analysis period, all entered the EP and completed ≥ 6 additional months of lumasiran treatment (median (range) duration of total exposure, 17.8 (12.7-20.5) months).
RESULTS: Lumasiran treatment was previously reported to reduce spot urinary oxalate:creatinine ratio by 72% at month 6, which was maintained at 72% at month 12; mean month 12 reductions in prespecified weight subgroups were 89%, 68%, and 71% for patients weighing < 10 kg, 10 to < 20 kg, and ≥ 20 kg, respectively. The mean reduction from baseline in plasma oxalate level was reported to be 32% at month 6, and this improved to 47% at month 12. Additional improvements were also seen in nephrocalcinosis grade, and kidney stone event rates remained low. The most common lumasiran-related adverse events were mild, transient injection-site reactions (3 patients (17%)).
CONCLUSIONS: Lumasiran treatment provided sustained reductions in urinary and plasma oxalate through month 12 across all weight subgroups, with an acceptable safety profile, in infants and young children with PH1. A higher resolution version of the Graphical abstract is available as Supplementary information.
© 2022. The Author(s).

Entities:  

Keywords:  Hyperoxaluria, Primary; Infant; Nephrocalcinosis; RNA interference, Lumasiran

Year:  2022        PMID: 35913563     DOI: 10.1007/s00467-022-05684-1

Source DB:  PubMed          Journal:  Pediatr Nephrol        ISSN: 0931-041X            Impact factor:   3.651


  23 in total

1.  International registry for primary hyperoxaluria.

Authors:  John C Lieske; Carla G Monico; W Scott Holmes; Erik J Bergstralh; Jeffrey M Slezak; Audrey L Rohlinger; Julie B Olson; Dawn S Milliner
Journal:  Am J Nephrol       Date:  2005-06-15       Impact factor: 3.754

Review 2.  Primary hyperoxaluria.

Authors:  Pierre Cochat; Gill Rumsby
Journal:  N Engl J Med       Date:  2013-08-15       Impact factor: 91.245

3.  Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria.

Authors:  Katharina Hopp; Andrea G Cogal; Eric J Bergstralh; Barbara M Seide; Julie B Olson; Alicia M Meek; John C Lieske; Dawn S Milliner; Peter C Harris
Journal:  J Am Soc Nephrol       Date:  2015-02-02       Impact factor: 10.121

4.  End Points for Clinical Trials in Primary Hyperoxaluria.

Authors:  Dawn S Milliner; Tracy L McGregor; Aliza Thompson; Bastian Dehmel; John Knight; Ralf Rosskamp; Melanie Blank; Sixun Yang; Sonia Fargue; Gill Rumsby; Jaap Groothoff; Meaghan Allain; Melissa West; Kim Hollander; W Todd Lowther; John C Lieske
Journal:  Clin J Am Soc Nephrol       Date:  2020-03-12       Impact factor: 8.237

5.  Vitamin B6 in primary hyperoxaluria I: first prospective trial after 40 years of practice.

Authors:  Heike Hoyer-Kuhn; Sina Kohbrok; Ruth Volland; Jeremy Franklin; Barbara Hero; Bodo B Beck; Bernd Hoppe
Journal:  Clin J Am Soc Nephrol       Date:  2014-01-02       Impact factor: 8.237

6.  Genotype-phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome.

Authors:  Jérôme Harambat; Sonia Fargue; Cécile Acquaviva; Marie-France Gagnadoux; Françoise Janssen; Aurélia Liutkus; Chebl Mourani; Marie-Alice Macher; Daniel Abramowicz; Christophe Legendre; Antoine Durrbach; Michel Tsimaratos; Hubert Nivet; Eric Girardin; Anne-Marie Schott; Marie-Odile Rolland; Pierre Cochat
Journal:  Kidney Int       Date:  2009-12-16       Impact factor: 10.612

7.  Primary hyperoxaluria type 1 in The Netherlands: prevalence and outcome.

Authors:  Christiaan S van Woerden; Jaap W Groothoff; Ronald J A Wanders; Jean-Claude Davin; Frits A Wijburg
Journal:  Nephrol Dial Transplant       Date:  2003-02       Impact factor: 5.992

8.  Long-term complications of systemic oxalosis in children-a retrospective single-center cohort study.

Authors:  Efrat Ben-Shalom; Ruth Cytter-Kuint; Choni Rinat; Rachel Becker-Cohen; Shimrit Tzvi-Behr; Jenny Goichberg; Vardit Peles; Yaacov Frishberg
Journal:  Pediatr Nephrol       Date:  2021-03-02       Impact factor: 3.714

9.  Phase 1/2 Study of Lumasiran for Treatment of Primary Hyperoxaluria Type 1: A Placebo-Controlled Randomized Clinical Trial.

Authors:  Yaacov Frishberg; Georges Deschênes; Jaap W Groothoff; Sally-Anne Hulton; Daniella Magen; Jérôme Harambat; William G Van't Hoff; Ulrike Lorch; Dawn S Milliner; John C Lieske; Patrick Haslett; Pushkal P Garg; Akshay K Vaishnaw; Sandeep Talamudupula; Jiandong Lu; Bahru A Habtemariam; David V Erbe; Tracy L McGregor; Pierre Cochat
Journal:  Clin J Am Soc Nephrol       Date:  2021-05-13       Impact factor: 10.614

10.  Nephrocalcinosis is a risk factor for kidney failure in primary hyperoxaluria.

Authors:  Xiaojing Tang; Eric J Bergstralh; Ramila A Mehta; Terri J Vrtiska; Dawn S Milliner; John C Lieske
Journal:  Kidney Int       Date:  2014-09-17       Impact factor: 10.612

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