Summary. Introduction. Dow Stough, MD

Similar documents
Effect of dutasteride 0.5 mg/d in men with androgenetic alopecia recalcitrant to finasteride

Combined treatment with oral finasteride and topical minoxidil in male androgenetic alopecia: a randomized and comparative study in Chinese patients

Male pattern baldness is the most common type of balding among males. It affects roughly, 50% of men by the age of 50,

Natural Hair Transplant Medical Center, Inc Dove Street, Suite #250, Newport Beach, CA Phone

Key words: Androgenetic alopecia, Þ nasteride, topical gel

FINASTERIDE (PROPECIA, PROSCAR) SIDE EFFECT & CONSENT FORM

FEMALE PATTERN HAIR LOSS

1001 West Broadway, Vancouver, BC V6H 4B1. Topical Finasteride

Lack of efficacy of finasteride in postmenopausal women with androgenetic alopecia. J Am Acad Dermatol 43:

EVIDENCE-BASED DERMATOLOGY: REVIEW. Efficacy and Safety of Finasteride Therapy for Androgenetic Alopecia

EFFECTS OF REVIVOGEN SCALP THERAPY ON TESTOSTERONE METABOLISM IN RECONSTRUCTED HUMAN EPIDERMIS

Priyam Bhaskar Rai, Pragya Khushwaha*, Nitish Jain, Swati Gupta

MALE PATTERN BALDNESS

Clinical impact of type I and type II 5 alpha-reductase inhibition in prostatic disease: review and update 아주대학교김선일

M0BCore Safety Profile. Pharmaceutical form(s)/strength: 5 mg SE/H/PSUR/0002/006 Date of FAR:

PROPECIA Tablets Merck Sharp & Dhome

REPRODUCTIVE ENDOCRINOLOGY

PHYSICIANS CIRCULAR FINASTERIDE PROSCAR. Tablet 5-Alpha Reductase Inhibitor

International Journal of Clinical Pharmacology and Therapeutics, Vol. No. /2014 (1-8)

Androgenes and Antiandrogenes

An Analysis on Whether or not Baldness can be Reversed Spencer Waldman Spencer Waldman will graduate with a BS in Biology in September 2017.

Elements for a Public Summary. Overview of disease epidemiology

PACKAGE LEAFLET: INFORMATION FOR THE USER. FINASTERIDE 1 MG FILM-COATED TABLETS (finasteride)

STUDY OF THE EFFECT OF AN EXTRACT OF Serenoa repens on the production of the 5-α reductasa enzyme

PROPECIA PRODUCT MONOGRAPH. Finasteride tablets, USP. Film-coated Tablets 1 mg. Type II 5α-reductase inhibitor. Date of Revision: October 1, 2018

PRODUCT MONOGRAPH SANDOZ FINASTERIDE A

Prostate enlargement, also known as benign prostatic hyperplasia

PROPECIA (Finasteride) Tablets, 1 mg

Efficacy and Safety of Long-TermTreatment with the Dual 5a-Reductase Inhibitor Dutasteride in Men with Symptomatic Benign Prostatic Hyperplasia

PRODUCT MONOGRAPH. pms-finasteride. Finasteride Tablets, House Standard Film-coated Tablets 1 mg. Type II 5 α-reductase Inhibitor

SANDOZ FINASTERIDE A

HIGHLIGHTS OF PRESCRIBING INFORMATION

PRODUCT MONOGRAPH SANDOZ FINASTERIDE A

PROPECIA (finasteride) Tablets, 1 mg

PRODUCT INFORMATION. PROPECIA (finasteride) Tablets NAME OF THE MEDICINE

It is estimated that 24% to 90% of US men older than the age of

PRODUCT MONOGRAPH. Finasteride tablets BP. 1 mg. Type II 5α-reductase inhibitor

Comparison of Clinical Efficacy of Finasteride and Dutasteride as 5-alpha Reductase Inhibitor

Safety and Tolerability of the Dual 5a-Reductase Inhibitor Dutasteride in thetreatment of Benign Prostatic Hyperplasia

AUSTRALIAN PRODUCT INFORMATION PROPECIA (finasteride) Tablets QUALITATIVE AND QUANTITATIVE COMPOSITION

UC Davis Dermatology Online Journal

Therapeutic Guidelines - IADVL

PRODUCT INFORMATION. PROPECIA (finasteride) Tablets NAME OF THE MEDICINE

Report on the Deliberation Results

The effect of dutasteride on intraprostatic dihydrotestosterone concentrations in men with benign prostatic hyperplasia

Reproductive DHT Analyte Information

PRODUCT INFORMATION. Apo-Finasteride 1 (Finasteride Film-coated Tablets 1 mg)

DUPROST Capsules (Dutasteride)

2. QUALITATIVE AND QUANTITATIVE COMPOSITION

Safety and Tolerability of the Dual 5-Alpha Reductase Inhibitor Dutasteride in the Treatment of Androgenetic Alopecia

FINASTERIDE- finasteride tablet, film coated Actavis Pharma, Inc

FINCAR Tablets (Finasteride)

Clinical Study Synopsis

Testosterone Hormone Replacement Drug Class Prior Authorization Protocol

Maximum Hair Minimum Loss

2. QUALITATIVE AND QUANTITATIVE COMPOSITION

EUROPEAN UROLOGY 57 (2010)

SUMMARY OF PRODUCT CHARACTERISTICS

Secrets of Abang Sado : Effects of testosterone therapy. Azraai Nasruddin

Update on the use of dutasteride in the management of benign prostatic hypertrophy

UnitedHealthcare Pharmacy Clinical Pharmacy Programs

SUMMARY OF PRODUCT CHARACTERISTICS

Estudos.

SUMMARY OF PRODUCT CHARACTERISTICS 1 NAME OF THE MEDICINAL PRODUCT 2 QUALITATIVE AND QUANTITATIVE COMPOSITION

Affirming Care of the Transgender Patient

Issues. What is a low testosterone? Who needs testosterone therapy? Benefits/adverse effects of testosterone replacement Treatment options

The legally binding text is the original French version TRANSPARENCY COMMITTEE OPINION. 20 June 2012

Elements for a public summary

Enlarged prostate (EP), also known as benign prostatic

TESTOFEN HUMAN CLINICAL TRIAL GENCOR PACIFIC, INC. Copyright 2006 by Gencor Pacific, Inc.

The Science of. NUTRICULA Longevity Journal

PRODUCT INFORMATION TESTOVIRON DEPOT. (testosterone enanthate)

NEW ZEALAND DATA SHEET. 2. QUALITATIVE AND QUANTITATIVE COMPOSITION Each film coated tablet contains 1 mg of finasteride.

EFFECTS OF CLEAROGEN ACNE LOTION ON TESTOSTERONE METABOLISM IN RECONSTRUCTED HUMAN EPIDERMIS

european urology 55 (2009)

Clinical Significance of 5 -Reductase Activity

ANNEX 3 TO THE DRAFT REPORT OF THE OECD VALIDATION OF THE RAT HERSHBERGER BIOASSAY: PHASE 2

PROPECIA finasteride 1 mg tablet

Benign prostatic hyperplasia (BPH), which leads to an

Efficacy and tolerability of the dual 5a-reductase inhibitor, dutasteride, in the treatment of benign prostatic hyperplasia in African-American men

Current status of 5α-reductase inhibitors in the management of lower urinary tract symptoms and BPH

Impact of L-arginine on androgenetic alopecia: Current clinical data evaluation.

Estudos.

Dr Tarza Jamal Pharmacology Lecture 2

Finasteride 1mg film-coated tablets (Pharmacare )

TRT and LUTS. Mick Jagger, 70 years. PRISM IV Sept 2014

The capsules are opaque, yellow, oblong soft gelatin capsules filled with an oily and yellowish liquid, without printing.

Skin metabolism of steroid hormones as endogenous compounds?

The ICL Insider. Lab Testing: Testosterone. In This Issue. The Debate

Second Quarter 2018 Results Call Corporate Update & Financial Results. August 7, 2018

Natural estrogens estradiol estrone estriol

GSK Medicine: Study Number: Title: Rationale: Phase: Study Period: Study Design: Centres: Indication: Treatment: Objectives:

Testosterone Hormone Replacement Drug Class Prior Authorization Protocol

Drug Class Monograph

BEST FINASTERIDE IN INDIA

Dutasteride Avodart Softgel Capsule

social impairment. The following exclusion criteria applied: age under 18 years; weight under 45 kg or over 80 kg;

This is an English translation of the original Chinese instruction leaflet generated by Google Translate. No amendments were made.

Characterization and formulation of cocrystals

The study listed may include approved and non-approved uses, formulations or treatment regimens. The results reported in any single study may not

Transcription:

Original Contribution Blackwell Publishing ORIGINAL Inc CONTRIBUTION Dutasteride improves male pattern hair loss in a randomized study in identical twins Dow Stough, MD The Dermatology Clinic, Hot Springs, AR Summary Objectives This study compared the efficacy of dutasteride vs. placebo in the treatment of male pattern hair loss (androgenetic alopecia) in 17 pairs of identical twin males with androgenetic alopecia over a 1-year period. Methods In this randomized, double-blind, placebo-controlled, single-center study, one twin from each identical twin pair received dutasteride 0.5 mg/day for 12 months while the other received placebo for 12 months. Hair growth was evaluated using standardized clinical photographs, hair counts, and patient self-assessment questionnaires. Result Dutasteride significantly improved hair growth at 1-year compared to placebo based on the analysis of the investigator assessment and the patient self-assessment questionnaires. Sixteen of 17 sets of twins completed the study, of which 15 sets correctly predicted the use of dutasteride. Only one set could not determine the active drug from the placebo. Conclusion Through the use of identical twins, this randomized trial provides evidence that dutasteride significantly reduces hair loss progression in men with male pattern hair loss. Keywords: androgenetic alopecia, dutasteride, identical twins Introduction Male pattern hair loss (MPHL) affects 50% of men by the age of 50. 1,2 This condition is thought to be genetically controlled, occurring in males with an inherited propensity to the effects of dihydrotestosterone on scalp hair follicles. 3,4 Studies in monozygotic twins are commonly conducted to examine the influence of genetic and environmental factors on phenotypic traits. 5 Similarly, monozygotic twins are ideally suited to determine the extent of drug efficacy in the treatment of a condition, such as MPHL, whose expression is determined by genetics. 6 Identical twins share the same genetic makeup, so that comparison between Correspondence: Dow Stough, The Dermatology Clinic, 3633 Central Avenue, Suite N, Hot Springs, AR 71913. E-mail: dowstoughmd@cablelynx.com Accepted for publication November 5, 2006 the responses of each subject in a twin pair, such as when one receives active drug and the other placebo, allows for rigorous examination of the effects of drug treatment. This approach has been used for over 20 years. 6 9 Dutasteride is a potent, selective, orally active inhibitor of the enzyme 5α-reductase type 2 in humans, lowering serum and scalp dihydrotestosterone levels without having intrinsic androgenic, antiandrogenic, estrogenic, antiestrogenic, or progestational effects. 10 15 Dutasteride has been shown to significantly increase hair count and hair weight, improve the ratio of anagen to telogen hairs, improve scalp coverage based on assessment of standardized clinical (global) photography, and improve patients satisfaction with the appearance of their hair. 16 20 In this unique study, the efficacy of dutasteride was compared with placebo in genotypically identical twins with MPHL. The primary efficacy objective was to determine whether dutasteride reduced hair loss as determined by assessments of standardized clinical photographs in 2007 Blackwell Publishing Journal of Cosmetic Dermatology, 6, 9 13 9

comparison to placebo. Secondary efficacy objectives were to determine the effects of dutasteride on hair count and patient self-assessment changes in scalp hair at study initialization. This study thus assessed the effects of dutasteride treatment by monitoring the changes in phenotype in genotypically identical twins. Patients and methods Patients Seventeen pairs of Caucasian identical twin males between the ages of 18 and 50 participated in the study. These identical twins had a vertex grade of II, III, IV, or V MPHL, according to a modified Norwood/Hamilton classification scale. 1,17 As would be expected in a study of identical twins, demographics and baseline characteristics were similar between the two treatment groups. Both twins in each pair had the same Norwood/Hamilton classification and were in good physical and mental condition. Major exclusion criteria included a history of any significant illness or condition that might confound the results of the study or pose an additional risk in administering dutasteride to the patient; surgical correction of scalp hair loss; and the use of minoxidil or any 5α-reductase inhibitor within 12 months of study initiation. Institutional review board approval of the protocol was obtained prior to study initiation and all patients provided written informed consent prior to entry in the study. Study design This was a randomized, placebo-controlled, double-blind study conducted in a single center in the United States. After screening, each patient in each pair of twins was randomized to receive either dutasteride or placebo for 1 year. Patients were instructed not to alter their hairstyle or dye their hair during the study period. The primary efficacy assessment was by comparison of pre- and posttreatment standardized clinical (global) photographs of the vertex scalp, 17,20 using the Canfield photography system 20 at baseline, month 6, and month 12. This technique has been previously validated to generate reproducible results. 21 An experienced dermatologist assessed changes from baseline using a 7-point rating scale, ranging from greatly decreased hair growth to greatly increased hair growth, centered at no change. 17 Macrophotography for hair counts was done at baseline, month 6, and month 12 with the Canfield photography system. 20 A small dot tattoo was placed on the scalp at baseline to identify the center of a 1 cm 2 circular target area on the anterior leading edge of the vertex hair loss region to be used for hair counts. 22 Hair counts were obtained from macrophotographs at Canfield Scientific Inc. (Fairfield, NJ), using a technique that has been previously described. 17,20 Patients assessed the changes in their scalp hair using a validated, self-administered hair growth questionnaire 17,23 consisting of four questions on treatment efficacy and three questions on satisfaction with appearance of scalp hair. These questionnaires were completed at months 6 and 12. Any reports of adverse events were collected at each clinic visit during the 1-year treatment period. The intensity and the relationship to treatment of any reported adverse events were evaluated. Results Hair count month 6 At month 6, the summary of the hair count data indicated that there was an average of 11 fewer hairs in the placebotreated group vs. 6.8 more hairs in the dutasteridetreated subjects (Table 1). In 12 sets of twins, the mean hair count reached statistical significance indicating 19.8 more hairs in the dutasteride-treated subjects than in the placebo-treated subjects. Compliance was 94% with placebo and 99% with dutasteride. Because of technical problems related to the hair count evaluation, hair count data were uninterpretable in five sets of twins. Month 12 At month 12, there were 3.8 fewer hairs in the placebotreated vs. 16.5 more hairs in the dutasteride-treated subjects. In 11 sets of twins, the mean hair count indicated 22.2 more hairs in the dutasteride-treated subjects than in the placebo-treated subjects. However, this did not achieve statistical significance (P = 0.14) because of the large variability and the technical problems encountered with five sets of twins at months 6 and 12. Table 1 Mean change from baseline in hair counts*. Mean change Placebo Dutasteride Month 6 11.0 (n = 14) 6.8 (n = 13) Month 12 3.8 (n = 14) 16.5 (n = 11) *Five pairs of twins were not included in this analysis because of technical problems. 10 2007 Blackwell Publishing Journal of Cosmetic Dermatology, 6, 9 13

Table 2 Hair growth scoring. Rank Definition 1 Greatly worse 2 Moderately worse 3 Slightly worse 4 No change 5 Slightly improved 6 Moderately improved 7 Greatly improved Table 3 Mean change from baseline to month 12 in hair growth scores. Mean change Placebo Dutasteride Month 12 4.07 5.00 (n = 14) (n = 11) Figure 2 Twin subjects treated with placebo and dutasteride. of photographs from baseline to months 6 and 12. The score range was 1 7 as it related to questions about the subjects perception of hair growth. The patient questionnaire included an assessment beginning at baseline of their hair thinning, coverage, and appearance. Sixteen of 17 twin sets correctly identified their treatment by month 6. Adverse events No serious clinical or laboratory adverse experiences occurred during the study and possibly two treatmentrelated clinical adverse experiences were reported. These were characterized as decreased libido of mild to moderate severity. Figure 1 Twin subjects treated with dutasteride and placebo. Investigators assessment of hair growth Hair growth scores were derived from expert evaluation comparing 35-mm photographs from baseline to months 6 and 12. The score range was 1 7 with the ranking as illustrated (Table 2). The mean difference between the treatment groups in expert assessment of hair growth of 0.90 units achieved statistical significance at month 12 (P = 0.016). The mean score in the dutasteride group at month 12 was 5.0 (slightly improved) as indicated (Table 3). In the two sets of twins pictured in Figures 1 and 2, the dutasteride-treated subjects demonstrate more hair growth than the placebo-treated subject. Subjects assessment of hair growth The hair growth index, evaluated by the study subjects, rated perceptions of hair growth improvement via comparison Discussion Multiple studies have confirmed the benefit of 5α-reductase inhibitors in men with male pattern baldness. 17,24 Kaufman et al. demonstrated that long-term treatment with finasteride, 1 mg per day over a 5-year period, was well tolerated and led to sustained improvement in scalp hair growth and decreased the progression of hair loss without treatment. The 5α-reductase inhibitor finasteride was studied in MPHL in a randomized study involving identical twins. 25 In this study, finasteride significantly improved hair growth at 1 year compared to placebo (P < 0.05) based on an analysis of photographs of the vertex and frontal scalp. 25 The hair count change also demonstrated a positive effect compared to placebo (P < 0.05). 25 In the above-referenced study with finasteride, photographic endpoints demonstrated that none of the finasteride patients showed deterioration in their hair growth at 12 months. In contrast, the majority of placebo patients demonstrated visible worsening in scalp hair coverage based on global photographic assessment of the vertex scalp at month 4. 2007 Blackwell Publishing Journal of Cosmetic Dermatology, 6, 9 13 11

The normal course of androgenetic alopecia is progressive over time. 24 In this unique study of male identical twins with androgenetic alopecia (MPHL), treatment with dutasteride slowed the progression of hair loss and enhanced hair growth compared to treatment with placebo. This study supports previously published trials 26 showing that dutasteride significantly improves scalp hair growth based on assessments of standardized clinical photographs, hair count, and patients assessments of their scalp hair. Based on the two predefined photographic endpoints, none of the dutasteride patients showed deterioration in hair growth at 12 months. In contrast, the majority of placebo patients demonstrated visible worsening in scalp hair coverage based on global photographic assessment of the vertex scalp at month 12. The validated patient self-assessment hair growth questionnaire demonstrated that treatment with dutasteride, in comparison to placebo, led to improvement in patients scalp hair growth and increased satisfaction with the appearance of hair. Because MPHL is under genetic control and identical twins share the same genetic code, the comparison of paired data between twins is a highly efficient way of evaluating the efficacy of a treatment in a limited number of patients, as each twin serves as a control. Thus, despite the necessarily limited sample size of this study, efficacy in favor of dutasteride was demonstrated for the predefined endpoints. The separation between treatment groups was achieved. It should be noted that the phenotypic expression of MPHL, while similar in each twin pair, was not necessarily identical. This was evident by careful examination of baseline global photographs for each pair of twins. References 1 Norwood OT. Male pattern baldness: classification and incidence. South Med J 1975; 68: 1359 65. 2 Rhodes T, Girman CJ, Savin RC et al. Prevalence of male pattern hair loss in 18 49 year old men. Dermatol Surg 1998; 24: 1330 2. 3 Hamilton JB. Male hormone stimulation is prerequisite and an incitant in common baldness. Am J Anat 1942; 71: 451 80. 4 Hamilton JB. Patterned loss of hair in man: types and incidence. Ann N Y Acad Sci 1951; 53: 708 28. 5 Kroemer HC. What is the right statistical measure of twin concordance (or diagnostic reliability and validity?). Arch Gen Psychiatry 1997; 54: 1121 4. 6 Car AB, Marlin NG, Whitfield JB. Usefulness of the co-twin control design in investigations as exemplified in a study of effects of ascorbic acid on laboratory test results. Clin Chem 1981; 27: 1469 70. 7 Christian JC, Kang KW. Efficiency of human monozygotic twins in studies of blood lipids. Metabolism 1972; 21: 691 9. 8 Zaslavskaia RM, Zolotaia RD, Lil in ET. Partner control method of twin studies in evaluating the hemodynamic effects of nonachlazine. Farmakol Toksikol 1981; 44: 357 60. 9 Carr AB, Einstein R, Lai LY, Martin NG, Starmer GA. Vitamin C and the common cold: using identical twins as controls. Med J Aust 1981; 2: 411 2. 10 Gormley GJ. Finasteride: a clinical review. Biomed Pharmacother 1995; 49: 319 24. 11 Harris G, Azzolina B, Baginsky W et al. Identification and selective inhibition of an isozyme of steroid 5α-reductase in human scalp. Proc Natl Acad Sci USA 1992; 89: 10787 91. 12 Vermeulen A, Giagulli VA, De Schepper P, Buntinx A. Hormonal effects of a 5α-reductase inhibitor (finasteride) on hormonal levels in normal men and in patients with benign prostatic hyperplasia. Eur Urol 1991; 20 (Suppl. 1): 82 6. 13 McConnell JD, Wilson JD, George FW, Geller J, Pappas F, Stoner E. Finasteride, an inhibitor of 5α-reductase, suppresses prostatic dihydrotestosterone in men with benign prostatic hyperplasia. J Clin Endocrinol Metab 1992; 74: 505 8. 14 Dallob AL, Sadick NS, Unger W et al. The effect of finasteride, a 5α-reductase inhibitor, on scalp skin testosterone and dihydrotestosterone concentrations in patients with male pattern baldness. J Clin Endocrinol Metab 1994; 79: 703 6. 15 Drake L, Hordinsky M, Fiedler V et al. The effects of finasteride on scalp skin and serum androgen levels in men with androgenetic alopecia. J Am Acad Dermatol 1999; 41: 550 4. 16 Roberts JL, Fiedler V, Imperato-McGinley J et al. Clinical dose ranging studies with finasteride, a type 2 5α-reductase inhibitor, in men with male pattern hair loss. J Am Acad Dermatol 1999; 41: 555 63. 17 Kaufman KD, Olsen EA, Whiting D et al. Finasteride in the treatment of men with androgenetic alopecia. J Am Acad Dermotol 1998; 39: 578 88. 18 Leyden J, Dunlap F, Miller B et al. Finasteride in the treatment of men with frontal male pattern hair loss. J Am Acad Dermatol 1999; 40: 930 7. 19 McClellan KJ, Markham A. Finasteride: a review of its use in male pattern hair loss. Drugs 1999; 57: 111 26. 20 Canfield D. Photographic documentation of hair growth in androgenetic alopecia. Dermatol Clin 1996; 14: 713 21. 21 Kaufman K, Binkowitz B, Savin R, Canfield D. Reproducibility of global photographic assessments of patients with male pattern boldness in a clinical trial with finasteride. J Invest Dermatol 1995; 104: 659. 22 Van Neste D, Fuh V, Sanchez-Pedreno P et al. Finasteride increases anagen hair in men with androgenetic alopecia. Br J Dermatol 2000; 143: 804 10. 23 Barber BL, Kaufman KD, Kozloff RC, Girman CJ, Guess HA. A hair growth questionnaire for use in the evaluation 12 2007 Blackwell Publishing Journal of Cosmetic Dermatology, 6, 9 13

of therapeutic effects in men. J Dermatol Treat 1998; 9: 181 6. 24 Kaufman KD. Finasteride male pattern hair loss study group. Long-term (5 years) multinational experience with finasteride in the treatment of men with androgenetic alopecia (male pattern hair loss). Eur J Dermatol 2002; 12: 38 49. 25 Stough DB, Rao NA, Kaufman KD, Mitchell C. Finasteride improves male pattern hair loss in a randomized study in identical twins. Eur J Dermatol 2002; 12: 32 7. 26 Olsen EA, Hordinsky M, Whiting D et al. The importance of dual 5α-reductase inhibition in the treatment of male pattern hair loss: results of a randomized placebo-controlled study of dutasteride versus finasteride. J Am Acad Dermatol 2006; 55(6): 1014 23. 2007 Blackwell Publishing Journal of Cosmetic Dermatology, 6, 9 13 13