Management of amyotrophic lateral sclerosis in clinical practice: Results of the expert consensus using the Delphi methodology

被引:0
作者
Cassereau, J. [1 ]
Bernard, E. [2 ,3 ]
Genestet, S. [4 ]
Chebbah, M. [5 ]
Le Clanche, S. [5 ]
Verschueren, A. [6 ]
Couratier, P. [7 ]
机构
[1] CHU Angers, Serv Neurol, CRC SLA Angers, 4 Rue Larrey, F-49933 Angers, France
[2] Univ Lyon, Hosp Civils Lyon, Hop Neurol P Wertheimer, Ctr SLA Lyon, 59 Blvd Pinel, F-69677 Bron, France
[3] Univ Claude Bernard Lyon I, Inst NeuroMyoGene, CNRS UMR5310, INSERM,U1217,Fac Med Rockefeller, 8 Ave Rockefeller, F-69373 Lyon 08, France
[4] CHRU Brest, Hop Cavale Blanche, Explorat Fonct Neurol, CRC SLA & Malad Motoneurone, Blvd Tanguy Prigent, F-29609 Brest, France
[5] Dept Affaires Med, Publ Hlth Expertise, 10 Blvd Sebastopol, F-75004 Paris, France
[6] CHU Marseille, Hop la Timone, Ctr Reference Malad Neuromusculaires & SLA, Marseille, France
[7] CHU Limoges, Ctr Reference Malad Rares SLA & Autres Malad Neuro, Serv Neurol, Neurosci Tete Cou & Os,Hop Dupuytren 1, 2 Ave Martin Luther King, F-87000 Limoges, France
关键词
France; Amyotrophic lateral sclerosis; Delphi panel; Expert consensus; Gold Coast criteria; ALS clinical practice; AMX0035; LONG-TERM SURVIVAL; CRITERIA; DIAGNOSIS; SYSTEM;
D O I
10.1016/j.neurol.2023.07.011
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Amyotrophic lateral sclerosis (ALS) is a rare disease characterized by a progressive and irreversible degeneration of upper and lower motor neurons leading to death. In France, limited data exist describing the criteria used in clinical practice for diagnosis and follow-up, and how novel therapies may fit in. The objective of this Delphi panel was to obtain an overview of current French practices in ALS diagnosis, management, and follow-up by determining the scales and criteria used in clinical practice outside of clinical trials, as well as the place of a future treatment like AMX0035, acting on endoplasmic reticulum (ER) stress and mitochondrial dysfunction, in the current therapeutic strategies. A questionnaire was administered to 24 ALS healthcare providers practicing in ALS centers in France. Two rounds of remote voting were organized, before proposition of final consensus statements. Consensus was considered reached when at least 66% of the voters agreed. Consensus were obtained to define the new Gold Coast criteria as the ones used in clinical practice to establish the diagnosis of ALS, thus replacing the revised El Escorial criteria, considered too complex and now mainly used to characterize the patient populations to be included in clinical trials. The clinical factors considered to establish ALS diagnosis are mainly the demonstration of progression of the motor deficit and elimination of differential diagnoses. The ALSFRS-R scale is used in daily clinical practice to assess patient's functional impairment in terms of number of points lost, with the bulbar, respiratory, and fine motor subscores being the most important to evaluate independently. A critical medical need was identified regarding the provision of new therapeutic alternatives in ALS. The panel members would support the earliest management of patients. In this landscape, based on data from a very encouraging phase II (Centaur trial), AMX0035 represents a new tool of choice in current treatment strategies for all patients for whom experts are confident in the diagnosis of ALS, in combination with riluzole. These results will need to be confirmed by the ongoing phase III trial (Phoenix trial).# 2023 Elsevier Masson SAS. All rights reserved.
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页码:1134 / 1144
页数:11
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