Risk factors for developing cardiac toxicities in cancer patients treated with panitumumab combination therapy

Future Oncol. 2020 Jul;16(19):1359-1370. doi: 10.2217/fon-2020-0050. Epub 2020 May 18.

Abstract

Aim: To evaluate the incidence and risk of cardiac toxicities associated with panitumumab in advanced cancer of Caucasian patients. Materials & methods: The incidence of cardiac toxicity was assessed by simple incidence rates and rates per 100 person-years. Univariate and multivariate Cox regression was conducted. Results: Panitumumab-containing therapy significantly increased the risk of developing cardiac arrhythmias (p = 0.036), but not for any cardiac event (p = 0.24) or ischemic event (p = 0.087). The absolute rate of developing cardiac arrhythmia was 10.0 events versus 7.5 events per 100 person-years. Pre-existing hypertension (p = 0.033), history of cardiac disease (p = 0.055) or panitumumab usage (p = 0.046) were risk factors for cardiac arrhythmias. Conclusion: The addition of panitumumab to chemotherapy increases the risk of developing cardiac arrhythmia, but not for any cardiac toxicity or ischemic events.

Keywords: cancer; cardiac toxicity; panitumumab; risk factors.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antineoplastic Agents, Immunological / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Cardiotoxicity / epidemiology
  • Cardiotoxicity / etiology*
  • Cardiotoxicity / pathology
  • China / epidemiology
  • Clinical Trials, Phase III as Topic
  • Colorectal Neoplasms / drug therapy*
  • Colorectal Neoplasms / immunology
  • Colorectal Neoplasms / metabolism
  • ErbB Receptors / antagonists & inhibitors
  • Female
  • Humans
  • Incidence
  • Male
  • Middle Aged
  • Panitumumab / adverse effects*
  • Randomized Controlled Trials as Topic
  • Retrospective Studies
  • Risk Factors
  • Young Adult

Substances

  • Antineoplastic Agents, Immunological
  • Panitumumab
  • EGFR protein, human
  • ErbB Receptors