Onychopathy induced by temsirolimus, a mammalian target of rapamycin inhibitor

L Peuvrel1, G Quéreux, A Brocard

  • 1Department of Dermatology-Cancerology, Nantes University Hospital, and CIC biothérapie INSERM 0305, Nantes, France.

Dermatology (Basel, Switzerland)
|May 23, 2012
PubMed

Insights

Temsirolimus, a mammalian target of rapamycin (mTOR) inhibitor, can cause nail dystrophy. This study details two cases of yellow nail discoloration and fragility in patients treated with temsirolimus.

Area of Science:

  • Oncology
  • Dermatology
  • Pharmacology

Background:

  • Mammalian target of rapamycin (mTOR) inhibitors are increasingly used in oncology.
  • Mucocutaneous toxicities, including nail disorders, are common side effects of mTOR inhibitors but are not well-characterized.
  • Temsirolimus is an mTOR inhibitor used in cancer treatment.

Observation:

  • Two patients developed significant nail dystrophy after 6-7 months of temsirolimus treatment.
  • Nail changes included fragility, distal onycholysis, and yellow discoloration affecting all 20 nails.
  • One patient also experienced painful paronychia, which improved with topical steroids but not the underlying nail dystrophy.

Findings:

  • This is the first report of yellow nail discoloration associated with temsirolimus therapy.
  • The nail dystrophy presented as a comprehensive 20-nail dystrophy with characteristic features.
  • Topical steroids were effective for paronychia but not for the nail dystrophy itself.

Implications:

  • This case series highlights a previously unreported side effect of temsirolimus, emphasizing the need for vigilant monitoring of nail health in patients undergoing mTOR inhibitor therapy.
  • Understanding and characterizing these nail toxicities can lead to improved patient management and supportive care strategies.
  • Further research is warranted to elucidate the mechanisms behind temsirolimus-induced nail changes and to develop targeted interventions.