Carfilzomib-induced thrombotic microangiopathy. A case report

J Oncol Pharm Pract. 2022 Apr;28(3):754-758. doi: 10.1177/10781552211067433. Epub 2021 Dec 14.

Abstract

Introduction: Drug-induced thrombotic microangiopathy (DITMA) is an acquired condition resulting from exposure to a drug that induces the formation of platelet-rich thrombi in small arterioles or capillaries secondary to drug-dependent antibodies or direct tissue toxicity. Carfilzomib is a selective proteasome inhibitor approved to treat selected patients with Multiple Myeloma (MM). It is one of the drugs with the strongest evidence for a causal association with non-antibody-mediated DITMA.

Case report: A 75-year-old man presented to the emergency department for the outbreak of vomit, asthenia, oliguria and dark stool emission. He was recently diagnosed with multiple myeloma, treated with lenalidomide, dexamethasone and carfilzomib. Laboratory exams were significant for microangiopathic haemolytic anaemia, thrombocytopenia and new-onset renal failure. ADAMTS-13 levels were in range, and no infectious signs were found both in blood nor in stool test.

Management & outcome: A carfilzomib induced thrombotic microangiopathy was soon suspected. Thus, since daily haemodialysis and supportive care did not seem to get a fast enough recovery, the patient was treated with eculizumab with a good general outcome.

Discussion: Drug-induced thrombotic microangiopathy is a rare and often life-threatening acquired condition whose diagnosis can be challenging and whose therapy is not always limited to supportive treatment and drug avoidance. Carfilzomib, along with other proteasome inhibitors, is one of the described potential drugs which can trigger such a manifestation.

Keywords: Drug-induced thrombotic microangiopathy; carfilzomib; multiple myeloma.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Humans
  • Male
  • Multiple Myeloma* / complications
  • Multiple Myeloma* / drug therapy
  • Oligopeptides / adverse effects
  • Proteasome Inhibitors / adverse effects
  • Thrombotic Microangiopathies* / chemically induced

Substances

  • Oligopeptides
  • Proteasome Inhibitors
  • carfilzomib