Survey of cutaneous adverse reactions to targeted cancer therapies: value of dermatological advice

G Ital Dermatol Venereol. 2020 Oct;155(5):658-661. doi: 10.23736/S0392-0488.18.06033-9. Epub 2018 May 11.

Abstract

Background: Target-therapy offers a better efficacy for several cancers, with less toxic adverse effects, if compared with traditional chemotherapy. However cutaneous complications are increased in number and complexity. The severity of these reactions positively correlates with efficacy, and the management of these reactions is challenging.

Methods: This was a multicenter cross-sectional study on a consecutive series of adult patients with incident cutaneous reactions linked to targeted cancer therapies observed in five referral centers for cancer treatment in the province of Bergamo and Brescia in northern Italy. Each center was asked to collect data on the first 5 consecutive cases of severe adverse cutaneous events observed during a one-week surveillance period.

Results: From June to October 2012, 25 patients with cutaneous adverse reactions linked to targeted therapies were included in the study. The main prescribed drugs were cetuximab (52%) and erlotinib (20%) and the most common reactions were folliculitis/pustules (40%) and rash/erythema (40%). Hand-foot reaction syndrome was present in 8% of patients. A total of 30% of patients treated for a cutaneous reaction underwent a consultation by a dermatologist. In these patients the rate of oncologic therapy continuation without regimen modifications was higher (100%), while it was progressively lower in patients treated by oncologists (71%) or without any specific treatment (60%).

Conclusions: Adverse reaction should be recognized by both dermatologists and oncologists and a multidisciplinary approach is mandatory.

Publication types

  • Multicenter Study

MeSH terms

  • Aged
  • Cross-Sectional Studies
  • Directive Counseling
  • Drug Eruptions / etiology*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Molecular Targeted Therapy / adverse effects*
  • Neoplasms / drug therapy*