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Abstract Details

Efficacy and limitations of cyclophosphamide in refractory myasthenia gravis
Neuromuscular and Clinical Neurophysiology (EMG)
P5 - Poster Session 5 (5:30 PM-6:30 PM)
12-028

To determine the efficacy of cyclophosphamide (CPP) in refractory myasthenia gravis (MG) in the Mexican population.

MG is the most common disease of the neuromuscular junction. "Refractory MG" defines that patient without improvement or worsening after treatment with steroids and at least two immunosuppressants. Treatment is recommended with chronic IVIG and PLEX, CPP and rituximab. CPP is an alkylating agent of DNA that causes important interferences in the processes of transcription and DNA replication and have been use in refractory MG with positive results.

We included all the patients with refractory MG treated at our institution with CPP: 30-50 mg/kg monthly for at least 6 months. The efficacy was assessed clinically with the Osserman scale, with a difference of 1 being significant. The assessment included the search for adverse effects. Frequency analysis was carried out. The results obtained were expressed in percentages, some data were described using measures of central tendency. The relapse-free and remission-free period was also calculated using the Kaplan-Meyer statistic.

8 patients were identified (7F:1M). According to Osserman scale in 75% of the patients (6/8 cases) there was clinical improvement. The remaining 25% maintained in the initial grade, even after six months of treatment. One of the patients showed relapse at six months of follow-up; while the rest of the cases remained stable after six months of follow-up. According to the Kaplan-Meyer analysis the median survival-free period of relapse was 9 (6.2-11.5) months and the median remission onset was 4 (1-8) months.

CPP was effective in reducing the symptoms of patients with refractory MG. The initial improvement of symptoms and maintaining of it with the application of CPP is within the first months. It has an adequate safety profile with mild adverse effects reported. Also, the response to treatment was independent of the characteristics of the patients.
Authors/Disclosures

PRESENTER
No disclosure on file
Enrique Gomez Figueroa, MD, MSc Dr. Gomez Figueroa has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Biogen Mexico. Dr. Gomez Figueroa has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Astra Zeneca Mexico. Dr. Gomez Figueroa has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Johnson & Johnson LATAM.
No disclosure on file