Delphi consensus on gene therapy of spinal muscular atrophy with onasemnogene abeparvovec in Germany, Austria and Switzerland - part II - expert based recommendations for surveillance and management of side-effects

Publikation: Beitrag in Fachzeitschrift › Forschungsartikel › Beigetragen › Begutachtung

Beitragende

  • collaborators and members of the INTEGRATE ATMP consortium - (Autor:in)
  • Klinik und Poliklinik für Kinder- und Jugendmedizin, Abteilung für Neuropädiatrie
  • Universitätsklinikum Heidelberg
  • Charité – Universitätsmedizin Berlin
  • Dr. von Haunerschen Kinderspital
  • Medizinische Universität Innsbruck
  • Klinik Favoriten - Kaiser Franz Josef Krankenhaus
  • Kepler Universitätsklinikum
  • Universität des Saarlandes
  • Universitätsklinikum Aachen
  • DRK Kliniken Berlin
  • Universitätsklinikum Gießen und Marburg GmbH
  • Medizinische Hochschule Hannover (MHH)
  • Ostschweizer Kinderspital
  • Universitätsklinikum Tübingen
  • Universitätsklinikum Jena
  • Centre Hospitalier Universitaire Vaudois (CHUV)
  • Universitätsklinikum Hamburg-Eppendorf (UKE)
  • Katholisches Klinikum Bochum gGmbH
  • Universität Duisburg-Essen
  • Deutsche Muskelstiftung
  • Inselspital - Universitätsspital Bern
  • Universitätsklinikum Freiburg
  • Paracelsus Medizinischen Privatuniversität
  • Klinikum Kassel GmbH
  • Universitätsklinikum Münster
  • Deutsche Gesellschaft für Muskelkranke (DGM) e.V.
  • Universitäts-Kinderspital Zürich – Eleonorenstiftung
  • SMA Europe e. V.
  • Universitätsklinikum der Friedrich-Alexander-Universität Erlangen-Nürnberg
  • Asklepios Klinik Hamburg Nord-Heidberg
  • Universitätsmedizin Göttingen

Abstract

BACKGROUND: Systematic protocols for long-term surveillance of children with spinal muscular atrophy treated with onasemnogene abeparvovec are lacking. Together with best practice recommendations for safety monitoring and management, such recommendations should increase patient safety and confidence levels of healthcare providers.

OBJECTIVE: Based on systematic literature review and evidence grading from part 1, this initiative aims to develop a structured treatment plan applicable across all treatment centers in Germany, Austria and Switzerland. Additionally, it seeks to establish consensus recommendations for the clinical management of safety alerts.

METHODS: Part 2 describes the methodology used to formulate Delphi consensus statements, the development of a structured treatment plan for OA treatment, and the anonymous consensus voting process with standardized follow-up in case of disagreement.

RESULTS: A total of 12 consensus statements were developed, addressing diagnostic work-up, safety evaluation, and best practice management of common adverse drug reactions associated with OA gene therapy. All statements achieved >95% consensus in the anonymous Delphi voting. Additionally, two consensus recommendations for handling of positive newborn screening result achieved consensus of 97% and 87%, respectively. A structured treatment plan for gene therapy was consented with 100% agreement, as were standardized recommendations for laboratory testing and a consensus-based algorithm for management of liver transaminase elevations.

CONCLUSIONS: Delphi-based expert recommendations, developed in co-creation with patient representatives, provide a framework to minimize complications associated with gene therapy and establish the basis for standardized post-marketing data collections. The methodology used in this Delphi-consensus-group can serve as a blueprint for future gene therapy approvals.

Details

OriginalspracheEnglisch
FachzeitschriftJournal of neuromuscular diseases
PublikationsstatusElektronische Veröffentlichung vor Drucklegung - 27 Aug. 2026
Peer-Review-StatusJa

Externe IDs

PubMedCentral PMC13522257
Scopus 105051769306

Schlagworte