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Phase 1 Study of Topical Perillyl Alcohol Cream for Chemoprevention of Skin Cancer

Perillyl alcohol (POH) is a natural product derived from plants such as cherry and lavendin. Previous studies have indicated that topical POH inhibits ultraviolet (UV) B-induced skin carcinogenesis in vivo, and it may be an effective chemopreventive agent for skin cancer. We performed a 1-mo, first-...

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Published in:Nutrition and cancer 2008, Vol.60 (3), p.325-330
Main Authors: Stratton, S.P, Saboda, K.L, Myrdal, P.B, Gupta, A, McKenzie, N.E, Brooks, C, Salasche, S.J, Warneke, J.A, Ranger-Moore, J, Bozzo, P.D
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cited_by cdi_FETCH-LOGICAL-c454t-756912eb685055b0c09d8529cffdb834089c320528d6d930da915ea74af73743
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creator Stratton, S.P
Saboda, K.L
Myrdal, P.B
Gupta, A
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Brooks, C
Salasche, S.J
Warneke, J.A
Ranger-Moore, J
Bozzo, P.D
description Perillyl alcohol (POH) is a natural product derived from plants such as cherry and lavendin. Previous studies have indicated that topical POH inhibits ultraviolet (UV) B-induced skin carcinogenesis in vivo, and it may be an effective chemopreventive agent for skin cancer. We performed a 1-mo, first-in-man, Phase 1 trial of topically administered POH cream in human subjects. Endpoints included safety and evaluation of any histopathological changes in skin after 1 mo use of POH cream. We randomized 25 subjects with normal, healthy skin with little or no sun damage and no history of skin cancer in a double-blind fashion to receive topical POH (0.76% wt/wt) on 1 forearm with placebo cream applied to the other forearm twice daily for 30 days. Subjects were monitored for toxicity, and a 4 mm punch biopsy in the treated area was performed at the end of study for histopathological evaluation. The topical cream was well tolerated. No serious cutaneous toxicities, systemic toxicities, or histopathological abnormalities were observed. A total of 8 subjects (32%) reported mild adverse events possibly or probably related to use of cream including reversible appearance of 1 to 2 small papules. However, there was no significant difference between lesions appearing on the POH treated forearm vs. the placebo-treated forearm.
doi_str_mv 10.1080/01635580701840391
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Previous studies have indicated that topical POH inhibits ultraviolet (UV) B-induced skin carcinogenesis in vivo, and it may be an effective chemopreventive agent for skin cancer. We performed a 1-mo, first-in-man, Phase 1 trial of topically administered POH cream in human subjects. Endpoints included safety and evaluation of any histopathological changes in skin after 1 mo use of POH cream. We randomized 25 subjects with normal, healthy skin with little or no sun damage and no history of skin cancer in a double-blind fashion to receive topical POH (0.76% wt/wt) on 1 forearm with placebo cream applied to the other forearm twice daily for 30 days. Subjects were monitored for toxicity, and a 4 mm punch biopsy in the treated area was performed at the end of study for histopathological evaluation. The topical cream was well tolerated. No serious cutaneous toxicities, systemic toxicities, or histopathological abnormalities were observed. 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Previous studies have indicated that topical POH inhibits ultraviolet (UV) B-induced skin carcinogenesis in vivo, and it may be an effective chemopreventive agent for skin cancer. We performed a 1-mo, first-in-man, Phase 1 trial of topically administered POH cream in human subjects. Endpoints included safety and evaluation of any histopathological changes in skin after 1 mo use of POH cream. We randomized 25 subjects with normal, healthy skin with little or no sun damage and no history of skin cancer in a double-blind fashion to receive topical POH (0.76% wt/wt) on 1 forearm with placebo cream applied to the other forearm twice daily for 30 days. Subjects were monitored for toxicity, and a 4 mm punch biopsy in the treated area was performed at the end of study for histopathological evaluation. The topical cream was well tolerated. No serious cutaneous toxicities, systemic toxicities, or histopathological abnormalities were observed. 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Psychology</subject><subject>Humans</subject><subject>Lavandula</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mentha spicata</subject><subject>Middle Aged</subject><subject>Monoterpenes - administration &amp; dosage</subject><subject>Monoterpenes - adverse effects</subject><subject>neoplasms</subject><subject>plant extracts</subject><subject>plant-based foods</subject><subject>quantitative structure-activity relationships</subject><subject>Skin - drug effects</subject><subject>Skin - pathology</subject><subject>skin cancer</subject><subject>skin diseases</subject><subject>Skin Neoplasms - prevention &amp; control</subject><subject>topical application</subject><subject>Treatment Outcome</subject><subject>Tumors</subject><subject>Tumors of the skin and soft tissue. 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identifier ISSN: 0163-5581
ispartof Nutrition and cancer, 2008, Vol.60 (3), p.325-330
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language eng
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source Taylor and Francis:Jisc Collections:Taylor and Francis Read and Publish Agreement 2024-2025:Medical Collection (Reading list)
subjects Administration, Topical
Adult
anticarcinogenic activity
Antineoplastic Agents - administration & dosage
Antineoplastic Agents - adverse effects
Biological and medical sciences
chemoprevention
cherries
Citrus
Dermatology
Double-Blind Method
essential oils
Feeding. Feeding behavior
Female
Forearm
Fundamental and applied biological sciences. Psychology
Humans
Lavandula
Male
Medical sciences
Mentha spicata
Middle Aged
Monoterpenes - administration & dosage
Monoterpenes - adverse effects
neoplasms
plant extracts
plant-based foods
quantitative structure-activity relationships
Skin - drug effects
Skin - pathology
skin cancer
skin diseases
Skin Neoplasms - prevention & control
topical application
Treatment Outcome
Tumors
Tumors of the skin and soft tissue. Premalignant lesions
Vertebrates: anatomy and physiology, studies on body, several organs or systems
title Phase 1 Study of Topical Perillyl Alcohol Cream for Chemoprevention of Skin Cancer
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