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Secondary cutaneous malignancy after treatment of basal cell carcinoma with hedgehog pathway inhibitor: a systematic review.
- Source :
-
Archives of dermatological research [Arch Dermatol Res] 2024 Oct 26; Vol. 316 (10), pp. 716. Date of Electronic Publication: 2024 Oct 26. - Publication Year :
- 2024
-
Abstract
- Several studies have been published describing development of cutaneous malignancy after vismodegib therapy; no systematic review has been conducted to interpret these data. Our objective was to systemically review reported cases of same-site or different-site cutaneous malignancy after smoothened inhibitor (SMOi) therapy for primary basal cell carcinoma (BCC). PubMed, CINAHL, and Scopus were systematically searched January 1, 2012 - March 28, 2024. Inclusion criteria: primary BCC, SMOi therapy, and biopsy-proven secondary malignancy. Exclusion criteria: non-human subjects. Bias was assessed using Risk of Bias in Nonrandomized Studies of Interventions (ROBINS-I) tool. Twenty-three cases describing same-site secondary malignancy were included. Average patient age was 67.2 years, mean treatment time 8.4 months, and average latency period to secondary malignancy development of 10.2 months. Five cases describing different-site secondary cutaneous malignancies were included. Mean patient age was 80.4 years, mean treatment time 2.9 months, and mean latency period 4.5 months. Twenty-seven cases were associated with vismodegib, while one case described vismodegib then sonidegib therapy. Pathologies included squamous cell carcinoma, BCC, basosquamous carcinoma, and malignant melanoma. The mechanism(s) by which same-site and different-site secondary malignancy occur are not known; mechanisms may differ depending on location type and secondary tumor type. We discuss multiple mechanistic hypotheses including pharmacologic selective pressure leading to hedgehog pathway mutant cells and activation of pro-growth signaling, and potential protective effect of hedgehog inhibition from melanoma given reports of rapid growth after SMOi discontinuation. This study is limited by the small number of reported cases. Additional research is needed to investigate these hypotheses.<br /> (© 2024. This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply.)
- Subjects :
- Humans
Aged
Smoothened Receptor antagonists & inhibitors
Neoplasms, Second Primary pathology
Neoplasms, Second Primary chemically induced
Aged, 80 and over
Signal Transduction drug effects
Biphenyl Compounds therapeutic use
Middle Aged
Antineoplastic Agents adverse effects
Antineoplastic Agents therapeutic use
Female
Male
Carcinoma, Basal Cell drug therapy
Carcinoma, Basal Cell pathology
Skin Neoplasms drug therapy
Skin Neoplasms pathology
Anilides adverse effects
Anilides therapeutic use
Anilides administration & dosage
Pyridines adverse effects
Pyridines therapeutic use
Pyridines administration & dosage
Hedgehog Proteins antagonists & inhibitors
Hedgehog Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1432-069X
- Volume :
- 316
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- Archives of dermatological research
- Publication Type :
- Academic Journal
- Accession number :
- 39460789
- Full Text :
- https://doi.org/10.1007/s00403-024-03471-6