Isotretinoin plus clindamycin seem highly effective against severe erlotinib-induced skin rash in advanced non-small cell lung cancer

J Thorac Oncol. 2010 Oct;5(10):1662-3. doi: 10.1097/JTO.0b013e3181ec1729.

Abstract

Introduction: Erlotinib is useful in advanced non-small cell lung cancer although compliance and efficacy are diminished by skin rash in a high proportion of patients, often necessitating dose reduction or drug withdrawal. No effective treatment for the rash is available.

Methods: We carried out a preliminary investigation on isotretinoin and clindamycin. Among 56 advanced lung cancer patients treated with erlotinib, 31 (53%) developed rash. Seven (35%) of the 20 G2/G3 cases agreed to treatment with clindamycin (450 mg/d, days 1-10; 300 mg/d, days 11-20) plus isotretinoin (20 mg/d, days 11-20) after being informed of the experimental nature of the combination.

Results: In 6 of 7 (86%) patients, the rash resolved (G1/G0) without dose reduction; in the other patient (G3), the erlotinib dose also had to be reduced. Median time to resolution was 14 days (range 7-20 days). No rash-treatment adverse events occurred during 20 days of administration.

Conclusions: Isotretinoin plus clindamycin promises to be the first effective treatment for erlotinib rash and is being tested further.

MeSH terms

  • Anti-Bacterial Agents / therapeutic use
  • Carcinoma, Non-Small-Cell Lung / drug therapy*
  • Carcinoma, Non-Small-Cell Lung / pathology
  • Clindamycin / therapeutic use*
  • Dermatologic Agents / therapeutic use
  • ErbB Receptors / antagonists & inhibitors
  • Erlotinib Hydrochloride
  • Exanthema / chemically induced
  • Exanthema / drug therapy*
  • Humans
  • Isotretinoin / therapeutic use*
  • Lung Neoplasms / drug therapy*
  • Lung Neoplasms / pathology
  • Protein Kinase Inhibitors / adverse effects
  • Quinazolines / adverse effects*
  • Survival Rate
  • Treatment Outcome

Substances

  • Anti-Bacterial Agents
  • Dermatologic Agents
  • Protein Kinase Inhibitors
  • Quinazolines
  • Clindamycin
  • Erlotinib Hydrochloride
  • ErbB Receptors
  • Isotretinoin