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1.
J Drugs Dermatol ; 20(3): 260-267, 2021 03 01.
Article in English | MEDLINE | ID: mdl-33683072

ABSTRACT

BACKGROUND: Minimally invasive alternative approaches to treat non-melanoma skin cancers remain limited and unproven. OBJECTIVE: We aim to assess the efficacy of varying combinations of anti-tumor agents—imiquimod 5% cream, 5-fluorouracil 2% solution, and tretinoin 0.1% cream—with brief cryotherapy in treating non-melanoma skin cancers. METHODS: This retrospective study included 690 cases of non-melanoma skin cancers in 480 patients who received a diagnosis of a basal cell carcinoma or squamous cell carcinoma during a ten-year period. During treatment period, patients applied 30 applications of one of three combinations (imiquimod/tretinoin, 5-fluorouracil/tretinoin, or imiquimod/5-fluorouracil/tretinoin) and had cryotherapy every 2 weeks. Each patient had a clinical examination at least three years post-treatment or documented treatment failure. Clearance was defined by a lack of persistence or recurrence for 3 years following the completion of treatment. The likelihood of lesion clearance was evaluated using multivariable logistic regression analysis. RESULTS: A total of 186 cases (97; basal cell carcinoma and 89; squamous cell carcinoma) in 133 patients [37% women and 63% men; median (interquartile range) age, 77 (69, 83) years] met the inclusion criteria. Multivariable logistic regression analysis adjusting for clinical and lesion variables demonstrated that, relative to the imiquimod/5-fluorouracil/tretinoin treatment approach, imiquimod/ tretinoin (odds ratio, 0.05; 95% confidence interval, 0.00-0.99) and 5-fluorouracil/tretinoin (0.02; 0.00–0.45) were associated with lower likelihoods of lesion clearance. Likewise, morpheaform basal cell carcinoma had a lower probability of clearance (0.05; 0.00–0.72). CONCLUSIONS: The combination of imiquimod/5-fluorouracil/tretinoin with cryotherapy had high clearance rates and was the most effective treatment regimen. J Drugs Dermatol. 2021;20(3):260-267. doi:10.36849/JDD.5427.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/administration & dosage , Carcinoma, Basal Cell/therapy , Carcinoma, Squamous Cell/therapy , Cryotherapy/methods , Neoplasm Recurrence, Local/epidemiology , Skin Neoplasms/therapy , Administration, Cutaneous , Aged , Aged, 80 and over , Antineoplastic Combined Chemotherapy Protocols/economics , Carcinoma, Basal Cell/economics , Carcinoma, Basal Cell/epidemiology , Carcinoma, Squamous Cell/economics , Carcinoma, Squamous Cell/epidemiology , Combined Modality Therapy/economics , Combined Modality Therapy/methods , Cost-Benefit Analysis , Cryotherapy/economics , Female , Fluorouracil/administration & dosage , Fluorouracil/economics , Humans , Imiquimod/administration & dosage , Imiquimod/economics , Male , Middle Aged , Neoplasm Recurrence, Local/economics , Neoplasm Recurrence, Local/prevention & control , Retrospective Studies , Skin Neoplasms/economics , Skin Neoplasms/epidemiology , Treatment Outcome , Tretinoin/administration & dosage , Tretinoin/economics
2.
J Drugs Dermatol ; 17(5): 582-585, 2018 May 01.
Article in English | MEDLINE | ID: mdl-29742194

ABSTRACT

Gemcitabine, a pyrimidine nucleoside analogue, is an oncologic agent used in the treatment of cutaneous T-cell lymphoma (CTCL). Common dermatologic reactions associated with gemcitabine include alopecia, mild skin rash, and mucositis but skin necrosis is exceptional. Herein we present an unusual case of widespread skin necrosis mimicking toxic epidermal necrolysis in a 45-year-old woman receiving gemcitabine therapy for stage IIIA cutaneous T-cell lymphoma. This is the first reported case of a TEN-like reaction subsequent to gemcitabine treatment. J Drugs Dermatol. 2018;17(5):582-585.


Subject(s)
Antimetabolites, Antineoplastic/adverse effects , Deoxycytidine/analogs & derivatives , Lymphoma, T-Cell, Cutaneous/drug therapy , Skin Neoplasms/drug therapy , Stevens-Johnson Syndrome/diagnosis , Deoxycytidine/adverse effects , Diagnosis, Differential , Female , Humans , Middle Aged , Stevens-Johnson Syndrome/etiology , Gemcitabine
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