Overcoming therapeutic challenges: Successful management of a supposedly triple seronegative, refractory generalized myasthenia gravis patient with efgartigimod

Author:

Sorrenti Benedetta1,Laurini Christian1,Bosco Luca12,Strano Camilla Mirella Maria1,Scarlato Marina3,Gastaldi Matteo1ORCID,Filippi Massimo14567ORCID,Previtali Stefano Carlo12ORCID,Falzone Yuri Matteo12

Affiliation:

1. Neuroimmunology Research Unit IRCCS Mondino Foundation Pavia Italy

2. Institute of Experimental Neurology, Division of Neuroscience, IRCCS San Raffaele Scientific Institute Milan Italy

3. Neurorehabilitation Unit Quarenghi Clinical Institute San Pellegrino Terme, Italy

4. Vita‐Salute San Raffaele University Milan Italy

5. Neuroimaging Research Unit, Institute of Experimental Neurology, Division of Neuroscience IRCCS San Raffaele Scientific Institute Milan Italy

6. Neurorehabilitation Unit IRCCS San Raffaele Scientific Institute Milan Italy

7. Neurophysiology Service IRCCS San Raffaele Scientific Institute Milan Italy

Abstract

AbstractBackground and purposeThis 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.MethodsWe describe the first refractory, generalized MG (gMG) patient successfully treated with efgartigimod after testing negative on standard autoantibody detection tests.ResultsOur 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).ConclusionsIn 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.

Publisher

Wiley

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