From the Journals

Short steroid taper tested with tocilizumab for giant cell arteritis


 

TOPLINE:

A combination of tocilizumab (Actemra) and 8 weeks of tapering prednisone was effective for inducing and maintaining disease remission in adults with giant cell arteritis (GCA).

METHODOLOGY:

  • In a single-center, single-arm, open-label pilot study, 30 adults (mean age, 73.7 years) with GCA received 162 mg of tocilizumab as a subcutaneous injection once a week for 52 weeks, plus prednisone starting between 20 mg and 60 mg with a prespecified 8-week taper off the glucocorticoid.
  • Patients had to be at least 50 years of age and could have either new-onset (diagnosis within 6 weeks of baseline) or relapsing disease (diagnosis > 6 weeks from baseline).
  • The primary endpoint was sustained, prednisone-free remission at 52 weeks, defined by an erythrocyte sedimentation rate of less than 40 mm/h, C-reactive protein level less than 10 mg/L, and adherence to the prednisone taper; secondary endpoints included the proportions of patients in remission and relapse, cumulative prednisone dose, and glucocorticoid toxicity.

TAKEAWAY:

  • At 52 weeks, 23 patients (77%) met the criteria for sustained remission after weaning off prednisone within 8 weeks of starting tocilizumab; 7 relapsed after a mean of 15.8 weeks.
  • Of the patients who relapsed, six underwent a second prednisone taper for 8 weeks with a mean initial daily dose of 32.1 mg, four regained and maintained remission, and two experienced a second relapse and withdrew from the study.
  • The mean cumulative prednisone dose at week 52 was 1,051.5 mg for responders and 1,673.1 mg for nonresponders.
  • All 30 patients had at least one adverse event; four patients had a serious adverse event likely related to tocilizumab, prednisone, or both.

IN PRACTICE:

Studies such as this “are highly valuable as proof of concept, but of course cannot be definitive guides to treatment decisions without a comparator group,” according to authors of an editorial accompanying the study.

SOURCE:

The study, by Sebastian Unizony, MD, Harvard Medical School, Boston, and colleagues, was published in The Lancet Rheumatology .

LIMITATIONS:

The small size and open-label design with no control group were limiting factors; more research is needed to confirm the findings before this treatment strategy can be recommended for clinical practice.

DISCLOSURES:

The study was funded by Genentech. Two authors reported financial relationships with pharmaceutical companies outside of this report.

A version of this article first appeared on Medscape.com.

Recommended Reading

Ginger consumption may mitigate neutrophil dysfunction and inflammation
MDedge Rheumatology
Are cellular therapies the future of autoimmune disease?
MDedge Rheumatology
Tapering lupus drugs in stable patients: Large study outlines risks, benefits
MDedge Rheumatology
PET scan at diagnosis may help to predict aneurysm risk in patients with giant cell arteritis
MDedge Rheumatology
More evidence shows COVID-19’s link to risk for autoimmune disease
MDedge Rheumatology
Are women and men with rheumatism treated equally?
MDedge Rheumatology
Anti-acid meds lower strength of systemic sclerosis drug
MDedge Rheumatology
Anemia, iron deficit common in rheumatic disease pregnancy
MDedge Rheumatology
Approximately 20% of U.S. adults are diagnosed with arthritis
MDedge Rheumatology
Researchers link two genes to Raynaud’s disease
MDedge Rheumatology