Efficacy and safety of protein C concentrate to treat purpura fulminans and thromboembolic events in severe congenital protein C deficiency

Thromb Haemost. 2016 Jul 4;116(1):58-68. doi: 10.1160/TH15-10-0786. Epub 2016 Apr 7.

Abstract

Severe congenital protein C (PC) deficiency (SCPCD) is associated with disseminated intravascular coagulation (DIC), purpura fulminans (PF), and vascular thromboembolic events (TE), often leading to organ failure and death. PC replacement therapy offers a safe, effective treatment for thromboembolic complications of SCPCD and secondary prophylaxis for recurrent DIC, PF, and TEs. A prospective, multi-centre, open-label, phase 2/3 study was conducted to demonstrate the safety and efficacy of protein C concentrate for treatment of PF and acute TEs. Fifteen enrolled patients with SCPCD received protein C concentrate; 11 received treatment for acute TEs (PF, 18 events; PF and other coumarin-related vascular thromboembolic events [coumarin-induced skin necrosis; CISN], 1 event; venous thrombosis, 5 events). Pre-defined efficacy criteria for treatment of acute TEs were compared with a historical control arm (i. e. patients receiving conventional therapy without protein C replacement). PF/CISN was demonstrated by pre-defined primary and secondary efficacy ratings. Primary ratings of protein C concentrate-treated episodes were significantly higher (p=0.0032) than in the historical control. For 19 PF/CISN episodes in 11 patients, 94.7 % of treatments were rated effective and 5.3 % effective with complications (not related to protein C concentrate). In a secondary efficacy rating, all treatments were rated effective (68.4 % excellent; 21.1 % good; 10.5 % fair). For 5/24 vascular thrombosis episodes, 80 % of treatments were rated excellent and 20 % were rated good. No treatment-related adverse events or serious adverse events occurred. In conclusion, protein C concentrate provides an efficacious, safe treatment for PF, CISN, and other TEs in SCPCD patients.

Keywords: Disseminated intravascular coagulation; congenital thrombotic disease due to protein C deficiency; protein C deficiency; purpura fulminans; therapeutics.

Publication types

  • Clinical Trial, Phase II
  • Clinical Trial, Phase III
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Child, Preschool
  • Disseminated Intravascular Coagulation / drug therapy
  • Disseminated Intravascular Coagulation / etiology
  • Disseminated Intravascular Coagulation / prevention & control
  • Female
  • Humans
  • Infant, Newborn
  • Male
  • Prospective Studies
  • Protein C / adverse effects
  • Protein C / pharmacokinetics
  • Protein C / therapeutic use*
  • Protein C Deficiency / complications
  • Protein C Deficiency / congenital
  • Protein C Deficiency / drug therapy*
  • Purpura Fulminans / drug therapy*
  • Purpura Fulminans / etiology
  • Purpura Fulminans / prevention & control
  • Secondary Prevention
  • Thromboembolism / drug therapy*
  • Thromboembolism / etiology
  • Thromboembolism / prevention & control
  • Treatment Outcome
  • Young Adult

Substances

  • Protein C

Supplementary concepts

  • Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Recessive