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Preclinical Development and Clinical Use of Perillyl Alcohol for Chemoprevention and Cancer Therapy

Overview
Journal Am J Cancer Res
Specialty Oncology
Date 2015 Jul 16
PMID 26175929
Citations 47
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Abstract

Perillyl alcohol (POH) is a naturally occurring dietary monoterpene isolated from the essential oils of lavender, peppermint, and other plants. Medical interest in this compound was generated by research findings showing that POH was able to inhibit the growth of tumor cells in cell culture and exert cancer preventive and therapeutic activity in a variety of animal tumor models. Based on this promising preclinical work, POH was formulated in soft gelatine capsules and orally administered to cancer patients several times a day on a continuous basis. However, such clinical trials in humans yielded disappointing results, also because the large number of capsules that had to be swallowed caused hard-to-tolerate intestinal side effects, causing many patients to withdraw from treatment due to unrelenting nausea, fatigue, and vomiting. As a result, efforts to treat cancer patients with oral POH were abandoned and did not enter clinical practice. Intriguingly, clinical trials in Brazil have explored intranasal POH delivery as an alternative to circumvent the toxic limitations of oral administration. In these trials, patients with recurrent malignant gliomas were given comparatively small doses of POH via simple inhalation through the nose. Results from these studies show this type of long-term, daily chemotherapy to be well tolerated and effective. In this review, we will present the vicissitudes of POH's evaluation as an anticancer agent, and its most recent success in therapy of patients with malignant brain tumors.

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References
1.
Bishayee A, Thoppil R, Waghray A, Kruse J, Novotny N, Darvesh A . Dietary phytochemicals in the chemoprevention and treatment of hepatocellular carcinoma: in vivo evidence, molecular targets, and clinical relevance. Curr Cancer Drug Targets. 2012; 12(9):1191-232. View

2.
Stratton S, Saboda K, Myrdal P, Gupta A, McKenzie N, Brooks C . Phase 1 study of topical perillyl alcohol cream for chemoprevention of skin cancer. Nutr Cancer. 2008; 60(3):325-30. DOI: 10.1080/01635580701840391. View

3.
Bailey H, Levy D, Harris L, Schink J, Foss F, Beatty P . A phase II trial of daily perillyl alcohol in patients with advanced ovarian cancer: Eastern Cooperative Oncology Group Study E2E96. Gynecol Oncol. 2002; 85(3):464-8. DOI: 10.1006/gyno.2002.6647. View

4.
Pardeshi C, Belgamwar V . Direct nose to brain drug delivery via integrated nerve pathways bypassing the blood-brain barrier: an excellent platform for brain targeting. Expert Opin Drug Deliv. 2013; 10(7):957-72. DOI: 10.1517/17425247.2013.790887. View

5.
Hohl R, Lewis K . Differential effects of monoterpenes and lovastatin on RAS processing. J Biol Chem. 1995; 270(29):17508-12. DOI: 10.1074/jbc.270.29.17508. View