AI Article Synopsis

  • Steroid-refractory acute graft-versus-host disease (aGVHD) is a serious issue post-stem cell transplantation, leading to high rates of morbidity and mortality.
  • A study evaluated combination therapy with inolimomab and etanercept in 21 patients with severe aGVHD, finding a 48% overall response rate at day 28, but nearly all patients eventually died (90%) mainly due to refractory aGVHD and infections.
  • This treatment approach did not significantly improve the poor survival rates, with only 29% and 10% of patients surviving at 6 months and 2 years, respectively.

Article Abstract

Steroid-refractory acute graft-versus-host disease (aGVHD) remains an important cause of morbidity and mortality after allogeneic stem cell transplantation (SCT). A protocol on the management of aGVHD was introduced in our center that incorporated a prospective study on combination therapy with inolimomab (anti-IL-2Rα) and etanercept (anti-tumor necrosis factor-α) for steroid-refractory aGVHD. We evaluated the efficacy and safety in 21 consecutively treated patients. The patients had developed refractory aGVHD after SCT (n = 16) or donor lymphocyte infusion (n = 5), and aGVHD was classified as severe in all patients, mostly due to gastrointestinal involvement stages 2 to 4. No drug-related side effects were observed apart from the infections expected to occur in these severely immunocompromised patients. Overall response at day 28 of second-line therapy was 48% (10/21), with 6 and 4 patients achieving a complete and partial response, respectively. Eventually, 19 patients died (90%), with early mortality (<6 months) predominantly resulting from refractory aGVHD and secondary infections and late mortality resulting from relapse of the underlying disease. With a median follow-up of 55 days, the estimated rates of 6-month and 2-year overall survival were dismal, 29% and 10%, respectively. In conclusion, the combination of inolimomab and etanercept for steroid-refractory aGVHD failed to improve the dismal prognosis of severe steroid-refractory aGVHD.

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Source
http://dx.doi.org/10.1016/j.bbmt.2015.08.039DOI Listing

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