- Paul, Friedemann;
- Marignier, Romain;
- Palace, Jacqueline;
- Arrambide, Georgina;
- Asgari, Nasrin;
- Bennett, Jeffrey L;
- Cree, Bruce Anthony Campbell;
- De Sèze, Jérôme;
- Fujihara, Kazuo;
- Kim, Ho Jin;
- Hornby, Rebecca;
- Huda, Saif;
- Kissani, Najib;
- Kleiter, Ingo;
- Kuwabara, Satoshi;
- Lana-Peixoto, Marco;
- Law, Lisa;
- Leite, M Isabel;
- Pandit, Lekha;
- Pittock, Sean J;
- Quan, Chao;
- Ramanathan, Sudarshini;
- Rotstein, Dalia;
- Saiz, Albert;
- Sato, Douglas Kazutoshi;
- Vaknin-Dembinsky, Adi
Background and objectives
Neuromyelitis optica spectrum disorder (NMOSD) is a rare debilitating autoimmune disease of the CNS. Three monoclonal antibodies were recently approved as maintenance therapies for aquaporin-4 immunoglobulin G (AQP4-IgG)-seropositive NMOSD (eculizumab, inebilizumab, and satralizumab), prompting the need to consider best practice therapeutic decision-making for this indication. Our objective was to develop validated statements for the management of AQP4-IgG-seropositive NMOSD, through an evidence-based Delphi consensus process, with a focus on recommendations for eculizumab, inebilizumab, and satralizumab.Methods
We recruited an international panel of clinical experts in NMOSD and asked them to complete a questionnaire on NMOSD management. Panel members received a summary of evidence identified through a targeted literature review and provided free-text responses to the questionnaire based on both the data provided and their clinical experience. Responses were used to generate draft statements on NMOSD-related themes. Statements were voted on over a maximum of 3 rounds; participation in at least 1 of the first 2 rounds was mandatory. Panel members anonymously provided their level of agreement (6-point Likert scale) on each statement. Statements that failed to reach a predefined consensus threshold (≥67%) were revised based on feedback and then voted on in the next round. Final statements were those that met the consensus threshold (≥67%).Results
The Delphi panel comprised 24 experts, who completed the Delphi process in November 2021 after 2 voting rounds. In round 1, 23/25 statements reached consensus and were accepted as final. The 2 statements that failed to reach consensus were revised. In round 2, both revised statements reached consensus. Twenty-five statements were agreed in total: 11 on initiation of or switching between eculizumab, inebilizumab, and satralizumab; 3 on monotherapy/combination therapy; 7 on safety and patient population considerations; 3 on biomarkers/patient-reported outcomes; and 1 on research gaps.Discussion
An established consensus method was used to develop statements relevant to the management of AQP4-IgG-seropositive NMOSD. These international statements will be valuable for informing individualized therapeutic decision-making and could form the basis for standardized practice guidelines.