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Overcoming therapeutic challenges: Successful management of a supposedly triple seronegative, refractory generalized myasthenia gravis patient with efgartigimod.
Sorrenti, Benedetta; Laurini, Christian; Bosco, Luca; Strano, Camilla Mirella Maria; Scarlato, Marina; Gastaldi, Matteo; Filippi, Massimo; Previtali, Stefano Carlo; Falzone, Yuri Matteo.
Afiliação
  • Sorrenti B; Neuroimmunology Research Unit, IRCCS Mondino Foundation, Pavia, Italy.
  • Laurini C; Neuroimmunology Research Unit, IRCCS Mondino Foundation, Pavia, Italy.
  • Bosco L; Neuroimmunology Research Unit, IRCCS Mondino Foundation, Pavia, Italy.
  • Strano CMM; Institute of Experimental Neurology, Division of Neuroscience, IRCCS San Raffaele Scientific Institute, Milan, Italy.
  • Scarlato M; Neuroimmunology Research Unit, IRCCS Mondino Foundation, Pavia, Italy.
  • Gastaldi M; Neurorehabilitation Unit, Quarenghi Clinical Institute, San Pellegrino Terme,, Italy.
  • Filippi M; Neuroimmunology Research Unit, IRCCS Mondino Foundation, Pavia, Italy.
  • Previtali SC; Neuroimmunology Research Unit, IRCCS Mondino Foundation, Pavia, Italy.
  • Falzone YM; Vita-Salute San Raffaele University, Milan, Italy.
Eur J Neurol ; 31(7): e16306, 2024 Jul.
Article em En | MEDLINE | ID: mdl-38716750
ABSTRACT
BACKGROUND AND

PURPOSE:

This study was undertaken to highlight neonatal Fc receptor inhibition (efgartigimod) as a valuable therapeutic option for patients with refractory seronegative myasthenia gravis (MG) and to emphasize the concept that seronegative MG is greatly constrained by the limitations of currently available diagnostic methods and therapeutic measures.

METHODS:

We describe the first refractory, generalized MG (gMG) patient successfully treated with efgartigimod after testing negative on standard autoantibody detection tests.

RESULTS:

Our patient presented with severe fluctuating bulbar and generalized weakness, resulting in multiple myasthenic crises requiring intubation. After a 28-year medical history of multiple failed lines of treatment, our patient was started on efgartigimod. Over five treatment cycles, a definite improvement in her clinical condition was observed (Myasthenia Gravis Foundation of America class IIIb to IIb; MG-Activities of Daily Living score 11 to 0; MG-Quality of Life 15 score 30 to 0; Quantitative MG score 28 to 6). Standard autoantibody detection tests failed to detect known pathogenic autoantibodies, but cell-based assay (CBA) identified autoantibodies against clustered adult acetylcholine receptor (AChR).

CONCLUSIONS:

In light of recent approvals of efgartigimod by the European Medicines Agency and US Food and Drug Administration exclusively for AChR-positive gMG forms, our case highlights evidence suggesting that such an approach might be shortsighted and could limit therapeutic options for patients with refractory seronegative gMG. Additionally, introducing more sensitive analytical techniques, exemplified by CBA, may help bridge the gap between seronegative and seropositive patients. This represents an urgent unmet need for gMG patients, as the antibody profile dramatically influences the therapeutic approach.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Miastenia Gravis Limite: Adult / Female / Humans / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Miastenia Gravis Limite: Adult / Female / Humans / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article