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OnabotulinumtoxinA effectively controls chronic migraine

Audrey Abella
08 Jul 2020

Long-term use of onabotulinumtoxinA led to reductions in monthly headache days (MHDs) in adults with chronic migraine (CM), according to post hoc analyses of the COMPEL* study presented at the AHS 2020 virtual scientific meeting.

“Frequent migraine attacks limit work and leisure activities, affect socioeconomic status, and impair quality of life,” said the researchers. [Cephalalgia 2015;35:563-578; Cephalalgia 2011;31:301-315] Studies have attested the clinical efficacy and tolerability of onabotulinumtoxinA in this setting. [Headache 2010;50:921-936; J Headache Pain 2017;18:75]

COMPEL evaluated 716 adults with CM (mean age 43 years, 85 percent female) receiving onabotulinumtoxinA 155 U every 12 weeks for 108 weeks. Of these, 52 percent completed the trial. Mean baseline MHDs and monthly moderate/severe HDs were 22 and 18 days, respectively.

 

Responder rates

At week(W) 108, 62 percent noted that their mean MHDs were halved, which was higher than the W24 percentage of 40 percent. Improvements were also observed among those reporting ≥25, ≥75, and 100-percent reduction in mean MHDs. “[These reflect the] consistent and progressive reductions in headache day responder rates [with onabotulinumtoxinA],” said the researchers. [AHS 2020, poster session]

This trend was also observed among those who completed all treatment cycles. The percentage of participants whose MHDs were halved increased from 47 percent at W24 to 62 percent at W108.

The fraction of W24 responders sustaining ≥25, ≥50, and ≥75-percent MHD reduction through W108 were 85, 76, and 61 percent, respectively. These data suggest that most achieved a sustained response throughout the study duration, noted the researchers.

Less than 5 percent of participants ceased treatment due to treatment-related adverse events, the most common being neck pain, followed by eyelid ptosis and musculoskeletal stiffness.

 

Treatment-controlled CM

In another subanalysis, those who achieved treatment-controlled** CM (tcCM) following onabotulinumtoxinA use increased over time (from 56 percent at W24 to 74 percent by W108). [AHS 2020, poster session]

At W108, mean MHD was 5.8, which according to the researchers, was far below the <15 MHD criteria. The 7.8 MHD at W24 was already a far cry from the tcCM definition criteria, reflecting the efficacy of the study drug early on, they noted.

Moderate/severe MHDs substantially dropped (mean change, –12.1; p<0.001), while a majority met the ≥50-percent responder rate at W108 (83 percent).

These data were mirrored among those with sustained*** tcCM (50 percent of participants with MHD data across all timepoints) by W108 (mean MHDs, 4.5; mean change in moderate/severe MHDs, –11.9; p<0.001; and percentage of participants with ≥50-percent reduction in MHDs, 89 percent).

“[These data show that] a high proportion of individuals achieved tcCM and/or sustained tcCM throughout the 2-year study. A reduction in MHDs to <15 is clinically meaningful, as supported by the high and increasing ≥50-percent responder rates and the large reductions in moderate/severe MHDs in these individuals,” said the researchers.

Although nearly half discontinued treatment (which may have influenced the upsurge in responder rates), the collective results support the long-term benefits of onabotulinumtoxinA in this setting, they said. Further exploration is warranted to ascertain the effects of onabotulinumtoxinA in CM.

 

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