News

Phenytoin trial in optic neuritis hints at neuroprotection

View on the News

Interpret neuroprotection results with caution

The absence of regular, early outcome assessments around 1-2 months after initiation of treatment makes it hard to interpret the results because they would have helped to rule out a primarily anti-inflammatory effect of the treatment by tracking retinal nerve fiber layer (RNFL) swelling and possible optic nerve inflammation, especially given that there was higher baseline RNFL thickness and worse low-contrast visual acuity in the patients who received phenytoin. If the true RNFL thickness at baseline in the affected eye of patients in the phenytoin group was higher than those in the placebo group, it could have accounted for the findings even though the investigators made a prespecified adjustment for it.

Although the results of this study are a major advancement and undeniably encouraging, future studies need to include more frequent OCT sampling, as well as more detailed OCT-segmentation-derived retinal measures such as ganglion cell plus inner plexiform layer thickness, which do not swell during acute optic neuritis, mitigating the need for statistical corrections involving the unaffected eye.

Dr. Shiv Saidha and Dr. Peter A. Calabresi are from the division of neuroimmunology and neurological infections at Johns Hopkins University, Baltimore. These comments were taken from an accompanying editorial (Lancet Neurol. 2016 Jan 25. doi: 10.1016/S1474-4422(16)00024-7). Dr. Saidha declared receiving funding support, consulting fees, grant support, speaking honoraria, and advisory board positions with the pharmaceutical industry, including companies that market MS drugs. Dr. Calabresi declared consultancies, research funding, and advisory board positions with the pharmaceutical industry, including companies that market MS drugs.


 

FROM LANCET NEUROLOGY

References

Patients with acute demyelinating optic neuritis who received the anticonvulsant drug phenytoin lost 30% less of their retinal nerve fiber layer than did placebo-treated patients in a randomized, phase II study.

“The results of this clinical trial support the concept of neuroprotection using phenytoin to inhibit voltage-gated sodium channels in patients with acute optic neuritis,” wrote Dr. Rhian Raftopoulos of the National Hospital for Neurology and Neurosurgery, London, and coauthors (Lancet Neurol. 2016 Jan 25. doi: 10.1016/S1474-4422(16)00004-1).

Courtesy National Eye Institute

The study in 86 individuals with acute optic neuritis randomized 29 participants to receive 4 mg/kg per day of oral phenytoin, 13 to 6 mg/kg per day of oral phenytoin, and 44 to placebo for 3 months; all were randomized within 14 days of vision loss. One-third of the patients had previously been diagnosed with multiple sclerosis or were diagnosed at presentation, and 74% had at least one brain lesion on MRI.

Treatment with phenytoin resulted in a decline of mean retinal nerve fiber layer thickness in the affected eye from 130.62 mcm at baseline to 81.46 mcm at 6 months, compared with a decline from 125.20 mcm to 74.29 mcm in the placebo group, representing an adjusted mean difference of 7.15 mcm that reached statistical significance.

The researchers also noted a significant 34% reduction in macular volume loss in the treatment arm, compared with placebo, representing an adjusted mean difference of 0.20 mm3. However, the treatment had no significant effect on low-contrast visual acuity and visual evoked potentials.

The most common adverse event in the treatment arm was maculopapular rash, which was judged as severe in one patient treated with phenytoin.

The study was supported by the U.S. National Multiple Sclerosis Society, the Multiple Sclerosis Society of Great Britain and Northern Ireland, Novartis, the U.K. National Institute for Health Research, and the NIHR UCLH/UCL Biomedical Research Centre. Several authors declared personal fees, trial funding, grants, and consultancies for pharmaceutical companies, including Novartis.

Recommended Reading

New case of MS possibly related to tocilizumab
MDedge Neurology
Study bolsters argument for sodium channel role in MS cerebellar dysfunction
MDedge Neurology
Cortical atrophy, lesion burden in MS linked to Epstein-Barr virus
MDedge Neurology
Glatiramer acetate didn’t affect birth outcomes in women with multiple sclerosis
MDedge Neurology
Tapered approach better for discontinuing natalizumab in MS patients
MDedge Neurology
Fludarabine added to interferon hints at benefits for breakthrough MS
MDedge Neurology
USPSTF: Screen all adults for depression
MDedge Neurology
Study confirms value of watching JCV serology during natalizumab treatment
MDedge Neurology
Molecular Biomarkers May Predict Conversion to MS
MDedge Neurology
Three lesions needed for MRI diagnosis of MS
MDedge Neurology