December 02, 2016
1 min read
Save

No immune-related adverse events found in 40% of patients who received immune checkpoint inhibitors

You've successfully added to your alerts. You will receive an email when new content is published.

Click Here to Manage Email Alerts

We were unable to process your request. Please try again later. If you continue to have this issue please contact customerservice@slackinc.com.

WASHINGTON — Despite most patients having an autoimmune disease at the time of checkpoint inhibition, no immune-related adverse events or disease exacerbation were found in 40% of patients who received immune checkpoint inhibitors, according to a systematic review of case reports presented at the American College of Rheumatology Annual Meeting.

Noha Abdel-Wahab, MD, PhD, in the Department of General Internal Medicine at the University of Texas MD Anderson Cancer Center, and colleagues performed a systematic review of 14 reports that described a total of 45 cases of patients with cancer and autoimmune disease diagnosed before initiation of checkpoint inhibitor therapy. The researchers collected information on patient characteristics, checkpoint inhibitor type, immune-related adverse events (IRAEs), overall management, clinical outcome and whether treatment re-challenge was reported.

Of the 45 cases, 86.8% had concomitant treatment — including corticosteroids, disease-modifying antirheumatic drugs and biologics — for their autoimmune disease (AID). Slightly more than half of patients (53.9%) still had an AID at the time of checkpoint inhibitor therapy, 88.9% of which was ipilimumab. After receiving therapy, 40% of patients reported de novo IRAEs; 28.9% reported exacerbation of a pre-existing AID; 8.9% reported both; and 40% did not report any adverse events. Also, 27.8% of patients had hypophysitis and a separate, but not mutually exclusive, 27.8% of patients had colitis with de novo IRAEs. Physicians recommended discontinuation of therapy in 33.3% of cases and IRAE resolution occurred in most patients.

There was one death by toxic epidermal necrolysis and another from severe colitis. There was also one case of treatment re-challenge in a patient with ulcerative colitis who developed exacerbation after ipilimumab use. After re-challenge, the patient reported grade 3 anterior panhypopitutarism and tracheobronchitis. More studies are needed to establish the efficacy of ipilimumab, the researchers wrote.

Reference:

Abdel-Wahab N, et al. Abstract #1342. Presented at: American College of Rheumatology Annual Meeting; Nov. 11-16, 2016; Washington.

Disclosure: The researchers report no relevant financial disclosures.