A More Severe Non-melanoma Skin Cancer Phenotype Is Seen in Patients with Inflammatory Bowel Disease on Tumor Necrosis Factor-α Antagonists
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作者:
Townsend, Cassandra M.
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Western Univ, Dept Med, Div Gastroenterol, 339 Windermere Rd A10-221a, London, ON N6A 5A5, CanadaWestern Univ, Dept Med, Div Gastroenterol, 339 Windermere Rd A10-221a, London, ON N6A 5A5, Canada
Townsend, Cassandra M.
[1
]
Khanna, Reena
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Western Univ, Dept Med, Div Gastroenterol, 339 Windermere Rd A10-221a, London, ON N6A 5A5, CanadaWestern Univ, Dept Med, Div Gastroenterol, 339 Windermere Rd A10-221a, London, ON N6A 5A5, Canada
Khanna, Reena
[1
]
Wilson, Aze Suzanne
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Western Univ, Dept Med, Div Gastroenterol, 339 Windermere Rd A10-221a, London, ON N6A 5A5, Canada
Western Univ, Dept Med, Div Clin Pharmacol, London, ON, Canada
Western Univ, Dept Physiol & Pharmacol, London, ON, CanadaWestern Univ, Dept Med, Div Gastroenterol, 339 Windermere Rd A10-221a, London, ON N6A 5A5, Canada
Wilson, Aze Suzanne
[1
,2
,3
]
机构:
[1] Western Univ, Dept Med, Div Gastroenterol, 339 Windermere Rd A10-221a, London, ON N6A 5A5, Canada
[2] Western Univ, Dept Med, Div Clin Pharmacol, London, ON, Canada
[3] Western Univ, Dept Physiol & Pharmacol, London, ON, Canada
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-alpha 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.
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Piedmont Hosp, Atlanta, GA USAPiedmont Hosp, Atlanta, GA USA
Calloway, Alexis
Dalal, Robin
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Vanderbilt Univ, Div Gastroenterol Hepatol & Nutr, Dept Med, Med Ctr, 1211 21st Ave South,Med Arts Bldg Suite 220, Nashville, TN 37232 USAPiedmont Hosp, Atlanta, GA USA
Dalal, Robin
Beaulieu, Dawn B.
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Vanderbilt Univ, Div Gastroenterol Hepatol & Nutr, Dept Med, Med Ctr, 1211 21st Ave South,Med Arts Bldg Suite 220, Nashville, TN 37232 USAPiedmont Hosp, Atlanta, GA USA
Beaulieu, Dawn B.
Duley, Caroline
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Vanderbilt Univ, Div Gastroenterol Hepatol & Nutr, Dept Med, Med Ctr, 1211 21st Ave South,Med Arts Bldg Suite 220, Nashville, TN 37232 USAPiedmont Hosp, Atlanta, GA USA
Duley, Caroline
Annis, Kimberly
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Vanderbilt Univ, Div Gastroenterol Hepatol & Nutr, Dept Med, Med Ctr, 1211 21st Ave South,Med Arts Bldg Suite 220, Nashville, TN 37232 USAPiedmont Hosp, Atlanta, GA USA
Annis, Kimberly
Gaines, Lawrence
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Vanderbilt Univ, Div Gastroenterol Hepatol & Nutr, Dept Med, Med Ctr, 1211 21st Ave South,Med Arts Bldg Suite 220, Nashville, TN 37232 USAPiedmont Hosp, Atlanta, GA USA
Gaines, Lawrence
Slaughter, Chris
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Vanderbilt Univ, Div Gastroenterol Hepatol & Nutr, Dept Med, Med Ctr, 1211 21st Ave South,Med Arts Bldg Suite 220, Nashville, TN 37232 USAPiedmont Hosp, Atlanta, GA USA
Slaughter, Chris
Schwartz, David A.
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Vanderbilt Univ, Div Gastroenterol Hepatol & Nutr, Dept Med, Med Ctr, 1211 21st Ave South,Med Arts Bldg Suite 220, Nashville, TN 37232 USAPiedmont Hosp, Atlanta, GA USA
Schwartz, David A.
Horst, Sara
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Vanderbilt Univ, Div Gastroenterol Hepatol & Nutr, Dept Med, Med Ctr, 1211 21st Ave South,Med Arts Bldg Suite 220, Nashville, TN 37232 USAPiedmont Hosp, Atlanta, GA USA
机构:
Cedars Sinai Med Ctr, Dept Med, Los Angeles, CA 90048 USACedars Sinai Med Ctr, Dept Med, Los Angeles, CA 90048 USA
Lew, Daniel
Yoon, Soon Man
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Cedars Sinai Med Ctr, F Widjaja Fdn Inflammatory Bowel & Immunobiol Res, Los Angeles, CA 90048 USACedars Sinai Med Ctr, Dept Med, Los Angeles, CA 90048 USA
Yoon, Soon Man
Yan, Xiaofei
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Cedars Sinai Med Ctr, F Widjaja Fdn Inflammatory Bowel & Immunobiol Res, Los Angeles, CA 90048 USACedars Sinai Med Ctr, Dept Med, Los Angeles, CA 90048 USA
Yan, Xiaofei
Robbins, Lori
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Cedars Sinai Med Ctr, Dept Gastroenterol, Los Angeles, CA 90048 USACedars Sinai Med Ctr, Dept Med, Los Angeles, CA 90048 USA
Robbins, Lori
Haritunians, Talin
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Cedars Sinai Med Ctr, F Widjaja Fdn Inflammatory Bowel & Immunobiol Res, Los Angeles, CA 90048 USACedars Sinai Med Ctr, Dept Med, Los Angeles, CA 90048 USA
Haritunians, Talin
Liu, Zhenqiu
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Cedars Sinai Med Ctr, F Widjaja Fdn Inflammatory Bowel & Immunobiol Res, Los Angeles, CA 90048 USACedars Sinai Med Ctr, Dept Med, Los Angeles, CA 90048 USA
Liu, Zhenqiu
Li, Dalin
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Cedars Sinai Med Ctr, F Widjaja Fdn Inflammatory Bowel & Immunobiol Res, Los Angeles, CA 90048 USACedars Sinai Med Ctr, Dept Med, Los Angeles, CA 90048 USA
Li, Dalin
McGovern, Dermot P. B.
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Cedars Sinai Med Ctr, F Widjaja Fdn Inflammatory Bowel & Immunobiol Res, Los Angeles, CA 90048 USACedars Sinai Med Ctr, Dept Med, Los Angeles, CA 90048 USA