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Published on: August 27, 2019
Onychopathy induced by temsirolimus, a mammalian target of rapamycin inhibitor
Abstract:
Temsirolimus belongs to the mammalian target of rapamycin (mTOR) inhibitors, targeted therapies for which indications are booming in oncology. While their tolerance is usually good, mucocutaneous toxicity is the most common, including stomatitis, rashes, edemas, pruritus, dry skin and nail disorders. The latter are common in clinical practice but have not yet been well characterized. We report 2 cases of patients who developed, after 6-7 months with temsirolimus, a dystrophy of the 20 nails with fragility, distal onycholysis, yellow discoloration, associated in 1 case with painful paronychia. Topical steroids improved the paronychia, without changing the nail dystrophy. To our knowledge, the occurrence of yellow nail discoloration with temsirolimus has never been reported before. We review the cutaneous and mucosal toxicities induced by temsirolimus and everolimus, two mTOR inhibitors used as anticancer agents and by their parent molecule sirolimus.
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.
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