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Dig Dis Sci ; 66(12): 4436-4440, 2021 12.
Artículo en Inglés | MEDLINE | ID: mdl-33428042

RESUMEN

BACKGROUND: Limited data suggest that non-melanoma skin cancer (NMSC) risk is higher in patients with inflammatory bowel disease (IBD) particularly in those on a tumor necrosis factor-α antagonist (TNF antagonist). It remains unknown whether TNF antagonist exposure alters the clinical course of NMSC in patients with IBD or if this therapy should be discontinued. AIMS: To assess the impact of TNF antagonist exposure on NMSC severity, recurrence and need for ancillary treatments. METHODS: Patients with IBD seen at London Health Sciences Centre, London, Canada were assessed for a history of NMSC and pre-diagnosis TNF antagonist exposure. NMSC severity (low risk and high risk), ancillary NMSC therapies, including chemo or radiotherapy, and changes to IBD therapy were assessed. RESULTS: Eleven of 472 patients with IBD reviewed were diagnosed with NMSC. Sixty-four percent (7/11) were on a TNF antagonist at the time of NMSC diagnosis. All patients with TNF antagonist exposure, (7/7) presented with a high-risk lesion based on National Comprehensive Cancer Network (NCCN) clinical practice guidelines. The incidence of positive margins was 42.9% (3/7) and 14.3% (1/7) required ancillary therapy. No metastatic disease was seen. TNF antagonist therapy was discontinued in a single patient due to NMSC diagnosis. Recurrent NMSC lesions were not seen in any of the TNF antagonist exposed patients. CONCLUSIONS: In this case series, TNF antagonist exposure may be associated with a severe NMSC clinical course. Larger studies are needed to confirm whether TNF antagonist discontinuation should be considered in the setting of NMSC diagnosis in IBD.


Asunto(s)
Enfermedades Inflamatorias del Intestino/complicaciones , Recurrencia Local de Neoplasia/inducido químicamente , Neoplasias Cutáneas/inducido químicamente , Inhibidores del Factor de Necrosis Tumoral/efectos adversos , Femenino , Humanos , Enfermedades Inflamatorias del Intestino/tratamiento farmacológico , Masculino , Persona de Mediana Edad , Recurrencia Local de Neoplasia/patología , Fenotipo , Estudios Retrospectivos , Piel/patología , Neoplasias Cutáneas/patología
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