Conference Coverage

Peginterferon beta-1a MS data show positive early and long-term results


 

AT THE AAN 2015 ANNUAL MEETING

References

The rates of flu-like symptoms over 3 years were also similar (62%-64%) in the two groups, and influenza-like illness was reported in 55% of those dosed every 2 weeks and in 45% of those dosed every 4 weeks. In addition to influenza-like illness, pyrexia was the most common flu-like symptom reported over 3 years (43%-45%).

About 65%-69% of those in the two groups reported injection-site reactions, with erythema the most common (62%-64%), followed by pain (17%-18%) and pruritus (12%-16%).

Lab abnormalities were comparable with both dosing schedules: Over 3 years, white blood cell counts were reduced in 6% of those on the 2-week schedule, compared with 8% among those on the 4-week schedule. Lymphocyte counts were reduced in 12% and 9% of those on the 2-week and 4-week schedules, respectively. In addition, 8% of those on the 2-week dose and 6% of those on the 4-week dose had low hemoglobin (100 g/L or less) over the 3 years.

Rates of anti-IFN and anti-PEG antibodies associated with both schedules were low, Dr. Kremenchutzkysaid. Over 3 years, 7%-9% tested positive for IFN binding antibody at least once, and 4%-6% of the total were “persistent positive.” Another 9% of those on the 4-week schedule and 6% of those on the 2-week schedule were anti-PEG antibody positive at least once, and 3%-5% of the patients in total had persistent levels. Titers were high in less than 1% of the total.

In ATTAIN, efficacy endpoints were secondary, and included ARR, which was reduced by 25.1% over 3 years among those receiving the dose every 2 weeks, compared with every 4 weeks (P = .0199). By 144 weeks, 30.5% of those on the 2-week schedule and 41.1% of those on the 4-week schedule had experienced a relapse, a significant difference (P = .0070), Dr. Kremenchutzky said.

The proportion of those with CDP by 144 weeks was 15.5% among those on the 4-week schedule, vs. 9.2% among those on the 2-week schedule (P = .0098), he added.

The studies were funded by Biogen Idec. Dr. Newsome and Dr. Kremenchutzky both disclosed having been compensated for activities with Biogen Idec and other companies that market MS drugs.

emechcatie@frontlinemedcom.com

Pages

Recommended Reading

Epilepsy Drug May Preserve Eyesight for Patients With MS
MDedge Neurology
Tips for Coping With Multiple Sclerosis
MDedge Neurology
Switch to Oral Fingolimod May Improve MS Outcomes
MDedge Neurology
Conference News Update—Federation of American Societies for Experimental Biology
MDedge Neurology
Can FLAIR MRI Show Treatment Efficacy?
MDedge Neurology
Using the GAD-7 Scale in Multiple Sclerosis Patients
MDedge Neurology
Concurrent Autoimmune Diseases in MS
MDedge Neurology
Does Pharmacy-Directed Treatment Management Improve Care?
MDedge Neurology
MSC Consensus Paper on DMTs in MS
MDedge Neurology
Robert Fox, MD
MDedge Neurology