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1.
J Drugs Dermatol ; 16(5): 432-436, 2017 May 01.
Article in English | MEDLINE | ID: mdl-28628678

ABSTRACT

Background: Ingenol mebutate gel 0.015% provides high clearance rates for actinic keratosis (AK) on the face and scalp but causes transient local skin responses (LSRs).

Objective: This study sought to determine whether the application of 1% dimethicone would decrease ingenol mebutate-associated LSRs and/or affect efficacy during the treatment of multiple AKs on the face.

Methods: Ingenol mebutate gel 0.015% was applied for 3 days to two 25 cm2 areas, each containing 3 to 8 AKs on the face of each subject, followed by application of 1% dimethicone lotion in an investigator-blinded manner to one randomly selected AK-containing area until LSRs were no longer present.

Results: In total, 20 subjects were enrolled and completed the study. Topical 1% dimethicone lotion applied during and after treatment of facial AK with ingenol mebutate gel 0.015% reduced mean total LSR scores at days 8 and 15 compared with ingenol mebutate gel only, although the difference was not statistically significant. Efficacy was equivalent between the two treatment arms.

Limitations: The study evaluated a relatively small number of subjects, all of whom were white.

Conclusions: The application of 1% dimethicone following ingenol mebutate gel 0.015% produced a trend toward lower severity of some LSRs, with no difference in efficacy.

J Drugs Dermatol. 2017;16(5):432-436.

.


Subject(s)
Dimethylpolysiloxanes/administration & dosage , Diterpenes/administration & dosage , Keratosis, Actinic/diagnosis , Keratosis, Actinic/drug therapy , Skin Cream/administration & dosage , Administration, Cutaneous , Aged , Aged, 80 and over , Dermatologic Agents/administration & dosage , Dermatologic Agents/adverse effects , Dimethylpolysiloxanes/adverse effects , Diterpenes/adverse effects , Drug Compounding , Drug Therapy, Combination , Face/pathology , Female , Gels , Humans , Male , Middle Aged , Skin Cream/adverse effects , Treatment Outcome
2.
Cutis ; 99(3): E36-E39, 2017 Mar.
Article in English | MEDLINE | ID: mdl-28398427

ABSTRACT

Disseminated superficial actinic porokeratosis (DSAP) is a chronic condition characterized by numerous atrophic papules and patches with a distinctive peripheral keratotic ridge, typically found on sun-exposed areas. Treatment of DSAP is warranted not only for cosmetic and symptomatic benefits but also to prevent malignant transformation. Successful treatment of DSAP often is difficult and frequently requires the use of multiple modalities. Ingenol mebutate gel 0.05% is a topical medication primarily used for the treatment of actinic keratosis (AK) by inducing cell death. We report a case of DSAP treated effectively with ingenol mebutate gel 0.05%.


Subject(s)
Dermatologic Agents/therapeutic use , Diterpenes/therapeutic use , Porokeratosis/drug therapy , Administration, Cutaneous , Adult , Dermatologic Agents/administration & dosage , Diterpenes/administration & dosage , Female , Gels , Humans , Porokeratosis/pathology , Treatment Outcome
3.
Article in English | MEDLINE | ID: mdl-27601928

ABSTRACT

BACKGROUND: Ingenol mebutate gel is a topical field treatment for actinic keratosis (AK). The treatment elicits application-site reactions in most patients. This analysis evaluated the relationship between the severity of reactions and the speed of their resolution. METHODS: Patients in Phase III studies were treated for AKs on the face (n=218), scalp (n=56), and trunk and extremities (n=209). All of the patients were treated with either ingenol mebutate gel 0.015% once daily for three consecutive days (face/scalp) or ingenol mebutate gel 0.05% once daily for two consecutive days (trunk/extremities). Local skin reactions (LSRs) were assessed on a 5-point scale from 0 to 4 in six categories, yielding composite scores in the range of 0 to 24. RESULTS: The composite LSR score on the day after the last application of ingenol mebutate gel was an important predictor of the speed of resolution of LSRs. The rate of resolution was greatest for AKs treated on the face, followed by the scalp, and then the trunk and extremities. All patients were expected to have minimal LSR scores for the face and scalp at 2 weeks, and for the trunk and extremities at 4 weeks. CONCLUSION: The absolute reduction in LSR scores was proportional to the composite LSR score on the day after the last application of ingenol mebutate gel treatment. The rate of resolution for LSRs was dependent on the anatomic site treated as well as the day 4 composite score.

5.
Cutis ; 95(1): 47-51, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25671445

ABSTRACT

Ingenol mebutate gel is a topical field treatment of actinic keratosis (AK). One of several proposed mechanisms of action for ingenol mebutate is induction of cell death in proliferating keratinocytes, suggesting a preferential action on AKs rather than healthy skin. Local skin reactions (LSRs) during 2 sequential 4-week cycles of AK treatment with ingenol mebutate gel 0.015% on the face or scalp were evaluated to test the hypothesis that reapplication of the study product would produce lower LSR scores than during the first treatment cycle. In this unblinded study, 20 participants with AKs on the face or scalp were treated with ingenol mebutate gel 0.015% once daily for 3 days in 2 sequential 4-week cycles. Composite LSR scores were evaluated during both cycles. The composite LSR score during the second cycle was found to be significantly lower than the first cycle (P=.0002). The proportion of participants who experienced LSRs in the second treatment cycle was less than the first cycle. Ingenol mebutate gel 0.015% may cumulatively reduce the burden of sun-damaged skin over 2 treatment cycles by targeting and removing transformed keratinocytes.


Subject(s)
Diterpenes/therapeutic use , Keratosis, Actinic/drug therapy , Administration, Topical , Aged , Aged, 80 and over , Diterpenes/administration & dosage , Female , Gels , Humans , Male , Middle Aged , Treatment Outcome
6.
Dermatol Surg ; 39(2): 240-7, 2013 Feb.
Article in English | MEDLINE | ID: mdl-23279092

ABSTRACT

BACKGROUND: Little is known about patient preferences for preoperative consultation in dermatologic surgery. OBJECTIVE: To determine patient preferences for separate- versus same-day preoperative consultation and factors that may be associated with these preferences. METHODS AND MATERIALS: Patients who underwent Mohs micrographic surgery (MMS) or excision at our institution within 24 months were retrospectively surveyed regarding their preferences for a separate- or same-day preoperative consultation. Procedure, tumor attributes, complications, and medications were recorded. RESULTS: Sixty-seven percent of patients preferred same-day preoperative consultation and surgery. Patients preferring same-day surgery were more likely to have a larger preoperative tumor size, whereas those preferring separate-day surgery were more likely to have had a history of complications. LIMITATIONS: This was a retrospective study performed at a single academic center. CONCLUSION: A majority of patients preferred same-day preoperative consultation and surgery. Tumor size and prior complications should be considered in preoperative planning for dermatologic surgery.


Subject(s)
Dermatologic Surgical Procedures , Patient Preference , Referral and Consultation , Aged , Ambulatory Surgical Procedures , Decision Making , Demography , Female , Humans , Male , Postoperative Complications , Retrospective Studies , Surveys and Questionnaires
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