150 Combining Systemic Agents with Topical Therapies in the Treatment of Mild-to-Moderate Psoriasis.. Feldman Department of Dermatology, Center for DermatologyResearch, Wake Forest Unive
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Mild-to-Moderate
PSORIASIS
John Y M Koo University of California San Francisco Medical Center
San Francisco, California, U.S.A.
Mark G Lebwohl Mount Sinai School of Medicine New York, New York, U.S.A.
Chai Sue Lee University of California Davis Medical Center
Sacramento, California, U.S.A.
New York London
Trang 3Informa Healthcare USA, Inc.
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Trang 4Preface
The goal of this book is to provide guidance on state-of-the-art clinicalmanagement of mild-to-moderate psoriasis, utilizing the experiences of agroup of experts well known in the psoriasis field The treatments coveredinclude topical corticosteroids, calcipotriene, tazarotene, tar, anthralin,salicyclic acid, phototherapy, and lasers There is a chapter highlightingrecent advances in combination therapy We have also included chapters
on palmar plantar psoriasis, scalp psoriasis, inverse psoriasis, and nail riasis because these are areas of the body that are frequently resistant toordinary forms of therapy The editors are hopeful that the comprehensiveyet practical and problem-focused approach to the management of mild-to-moderate psoriasis makes this a reference that dermatologists, primary carephysicians, residents, medical students, and other health care professionalscan turn to again and again for the most updated guidance in taking care
pso-of patients with mild-to-moderate psoriasis
John Y M KooMark G LebwohlChai Sue Lee
iii
Trang 63 The Koo–Menter Psoriasis Instrument for Identifying
Candidate Patients for Systemic Therapy 9 John Y M Koo, Jonathan W Kowalski, Mark G Lebwohl, Chris M Kozma, and Alan Menter
Introduction 9
Overview 10
Components of the Koo–Menter Psoriasis
Instrument 10
Background on the PQOL-12 14
Application of the Original PQOL 14
Development of the PQOL-12 15
v
Trang 7Study 1: Multicentered Office-Based Study 15
Study 2: Using Data from the Randomized
Clinical Trial 24
Minimally Important Difference 26
Test–Retest Reliability of the PQOL-12 26
Calculating the PQOL-12 Score Within the KMPI 26 Discussion on KMPI 27
Conclusion 27
References 28
4 General Guidelines for Administration of Topical Agents
in the Treatment of Mild-to-Moderate Psoriasis 29 Jashin J Wu and Gerald D Weinstein
Factors of Psoriasis 30
Medications 32
References 38
5 Topical Corticosteroids 41 Jason Givan, Daniel Pearce, and Steven R Feldman
Introduction 41
Rationale for Psoriasis Therapy 42
Mechanism of Action and Biologic Potency 42
Delivery and Physiologic Potency 44
Practical Use of Topical Corticosteroids 52
Steroid Alternatives: Complementary, Not Really
Alternatives 53
Summary 54
References 55
6 Vitamin D3Analogs 59 Chai Sue Lee and John Y M Koo
Chemistry and Mechanism of Action 60
Calcipotriene Monotherapy 61
Calcipotriene in Children 61
Trang 8Calcipotriene vs Other Topical Agents 62
Combination Therapy 63
Calcipotriene and Topical Steroids 63
Calcipotriene and Tazarotene 64
Calcipotriene and Phototherapy 64
Calcipotriene and Systemic Agents 65
Combination Corticosteroid/Calcipotriene Therapy 76 Clinical Trials and Analyses of Fixed-Combination
Formulation of Betamethasone
Dipropionate/Calcipotriene 77
The Fixed-Dose Combination Is More Effective Than
Steroid or Calcipotriene Monotherapy 77
The Fixed-Dose Combination b.i.d Achieves Greater
PASI Reduction Within One Week vs Steroid
Monotherapy 77
Once-Daily Fixed-Dose Combination
Is Safe and Effective 78
Once-Daily Fixed-Dose Combination Is as Safe
and Effective as b.i.d Therapy 80
Once-Daily Fixed-Dose Therapy Achieves Higher Clearance and Fewer Adverse Events vs Monotherapy 81 Once-Daily Fixed-Dose Therapy Is Effective for Patients with Mild, Moderate, and Severe Psoriasis 81
Investigators and Patients’ Assessments of Once-Daily
Fixed-Dosed Therapy Agree 82
Long-Term, Once-Daily Fixed-Dose Therapy
Is Safe and Effective 83
Potential Benefits of Fixed-Dose
Combination Therapy 84
In Combination with Biologics 86
In Combination with Other Systemic Agents 87
Potential Effects on Compliance 87
Trang 9Conclusions 87
References 88
8 Tazarotene 91 Chai Sue Lee and John Y M Koo
Chemistry and Mechanism of Action 91
Tazarotene Monotherapy 93
Tazarotene vs Topical Steroids 93
Combination Therapy 94
Tazarotene and Topical Steroids 94
Tazarotene and Topical Steroid-Induced
Skin Atrophy 96
Tazarotene Chemical Compatibility with
a Topical Steroid 96
Tazarotene and Calcipotriene 97
Tazarotene and UVB Phototherapy 97
Tazarotene and PUVA Phototherapy 98
Tazarotene and Nail Psoriasis 99
Tazarotene Application in Psoriasis 99
10 Treatment of Mild-to-Moderate Psoriasis with Coal Tar,
Anthralin, Salicylic Acid, and Lactic Acid 115 Priya Sivanesan and John Y M Koo
Trang 1011 Phototherapy and Laser for the Treatment
of Mild-to-Moderate Psoriasis 125 Holly A Kerr, Henry W Lim, and Jennifer Trepte
Introduction 125
Mechanism of Action 126
Ultraviolet B 126
Psoralen and UVA 131
Targeted (Localized) Phototherapy 137
Ultraviolet A1 141
Conclusion 142
References 143
12 Combination Therapy 147 Wendy Myers, Jennifer Tan, and Alice B Gottlieb
The Rationale for Combination Therapy 147
Phototherapy Combinations 148
UV Phototherapy and Topical Medications 150
Combining Systemic Agents with Topical Therapies in the Treatment of Mild-to-Moderate Psoriasis 154
Future Therapies for the Combination Treatment
Trang 11Clobetasol Propionate Spray (Clobex Spray) 174 Clobetasol Propionate Shampoo (Clobex Shampoo) 175 Clobetasol Proprionate Lotion (Clobex Lotion) 176 Hydrogel Patch 176
Conclusions 181
References 181
15 Palmoplantar Psoriasis 183 Brian Bonish and Kenneth B Gordon
Descaling of the Scalp 199
Coal Tar and Dithranol 199
Trang 1217 Inverse Psoriasis 207 Robert A Lee and Abby S van Voorhees
Manifestations of Nail Psoriasis 222
Association with Psoriatic Arthritis 226
Associated Genetic Haplotypes 228
Nail Psoriasis: Childhood vs Adult Onset 228
Diagnostic Challenge: Isolated Nail Psoriasis and Its
Impersonators 229
Diagnostic Procedure: The Nail Biopsy 231
Measurement of Severity: The Nail Psoriasis
Trang 14Steven R Feldman Department of Dermatology, Center for DermatologyResearch, Wake Forest University School of Medicine, Winston-Salem,North Carolina, U.S.A.
Rianne M J P Gerritsen Department of Dermatology, RadboudUniversity Medical Center, Nijmegen, The Netherlands
Jason Givan Department of Dermatology, Center for DermatologyResearch, Wake Forest University School of Medicine, Winston-Salem,North Carolina, U.S.A
Kenneth B Gordon Feinberg School of Medicine, Evanston NorthwesternHealthcare and Northwestern University, Skokie, Illinois, U.S.A
xiii
Trang 15Alice B Gottlieb Department of Dermatology, Tuffs-New EnglandMedical Center, Boston, Massachusetts, U.S.A.
Holly A Kerr Department of Dermatology, Henry Ford Hospital,Detroit, Michigan, U.S.A
Marloes M Kleinpenning Department of Dermatology, Radboud
University Medical Center, Nijmegen, The Netherlands
John Y M Koo Department of Dermatology, Psoriasis and SkinTreatment Center, University of California San Francisco Medical Center,San Francisco, California, U.S.A
Jonathan W Kowalski Global Health Outcomes Research, Allergan Inc.,Irvine, California, U.S.A
Chris M Kozma University of South Carolina, Columbia,
South Carolina, U.S.A
Mark G Lebwohl Department of Dermatology, Mount Sinai School ofMedicine, New York, New York, U.S.A
Chai Sue Lee Department of Dermatology, University of CaliforniaDavis Medical Center, Sacramento, California, U.S.A
Robert A Lee Department of Dermatology, Hospital of the University ofPennsylvania, Philadelphia, Pennsylvania, U.S.A
Henry W Lim Department of Dermatology, Henry Ford Hospital,Detroit, Michigan, U.S.A
Alan Menter Division of Dermatology, Baylor University Medical Center,Dallas, Texas, U.S.A
Wendy Myers Department of Medicine, Division of Clinical
Pharmacology, Robert Wood Johnson Medical School, New Brunswick,New Jersey, U.S.A
Maithily A Nandedkar-Thomas Professional Dermatology Care, PC,Reston, Virginia, U.S.A
Daniel Pearce Department of Dermatology, Center for DermatologyResearch, Wake Forest University School of Medicine, Winston-Salem,North Carolina, U.S.A
Trang 16Richard K Scher Department of Dermatology, Columbia UniversityMedical Center, New York, New York, U.S.A.
Priya Sivanesan Department of Dermatology, University of CaliforniaSan Francisco, San Francisco, California, U.S.A
Jennifer Tan Department of Medicine, Division of Clinical
Pharmacology, Robert Wood Johnson Medical School, New Brunswick,New Jersey, U.S.A
Patricia Tinio Department of Dermatology, Mount Sinai School ofMedicine, New York, New York, U.S.A
Jennifer Trepte Department of Dermatology, Wayne State University,Detroit, Michigan, U.S.A
Peter C M van de Kerkhof Department of Dermatology, RadboudUniversity Medical Center, Nijmegen, The Netherlands
Abby S van Voorhees Department of Dermatology, Hospital of theUniversity of Pennsylvania, Philadelphia, Pennsylvania, U.S.A
Gerald D Weinstein Department of Dermatology, University of
California, Irvine, California, U.S.A
Jashin J Wu Department of Dermatology, University of California,Irvine, California, U.S.A
Trang 18Therapy of Mild-to-Moderate
Psoriasis—Introduction
Mark G Lebwohl
Department of Dermatology, Mount Sinai School of Medicine, New York,
New York, U.S.A
The therapy of mild-to-moderate psoriasis has come a long way from thedays of tar and anthralin, though the latter treatments are still occasionallyused The introduction of topical corticosteroids in the latter third of the20th century had a dramatic impact on the topical therapy of psoriasis,and topical corticosteroids remain one of the most important treatmentsavailable for mild to moderate disease Because superpotent corticosteroidsare associated with hypothalamic–pituitary–adrenal axis suppression, recentinnovations in topical corticosteroid development have emphasized morecosmetically elegant vehicles rather than more potent medications Mostrecently, the superpotent corticosteroid clobetasol propionate has beendeveloped in foam, spray, lotion, and shampoo vehicles Corticosteroidsare also available in creams, emollient creams, ointments, solutions, gels,and even tapes Therefore it should not be surprising that corticosteroids areextensively covered in this book and controversies such as tachyphylaxis aswell as issues such as compliance with therapy are raised by experts in the field
A major breakthrough in the treatment of mild to moderate psoriasisoccurred with the introduction of vitamin D analogs Calcipotriene, alsoknown as calcipotriol, was the first agent approved and it was followed
by additional vitamin D analogs including tacalcitol, calcitriol, and others
1
Trang 19Tazarotene, a retinoid developed for psoriasis, was the next class of agent
to be developed for this disease Other topical agents include the topical nomodulators, pimecrolimus, and tacrolimus These agents are not veryeffective on thick plaques of the elbows and knees, but are highly effective
immu-on facial and intertriginous skin, precisely those areas where use of topicalcorticosteroids is associated with the development of cutaneous atrophy andformation of striae and telangiectasia All of the above agents are reviewedcomprehensively in chapters written by leading authorities
What can the clinician do when monotherapy with topical agents isnot sufficiently effective but the disease is not severe enough to justifysystemic therapy? Combination therapy has proven to be more effectivethan monotherapy with selected agents Moreover, combination therapyoften eliminates the side effects of monotherapy For example, the combina-tion of topical corticosteroids and tazarotene is not only more effective thaneither treatment alone, but tazarotene protects against the atrophy of thecorticosteroid while the corticosteroid minimizes the irritation caused bytazarotene Likewise, the combination of calcipotriene with topical cortico-steroids is more effective than either agent alone, allowing reduced use ofthe corticosteroid and less irritation caused by the calcipotriene The use
of combination therapy has led to the development of yet another new agentthat combines calcipotriene with betamethasone dipropionate
When combination therapy is not adequate, use of intralesionalcorticosteroids may be effective, and when the latter is not sufficient, photo-therapy may be warranted New forms of phototherapy including narrow-band ultraviolet B (UVB) and localized targeted high output phototherapysuch as that afforded by the excimer laser are often effective for localizedrefractory plaques of psoriasis
Finally, unique body sites such as the nails or scalp may require ent vehicles and approaches to achieve good results All of these challengesare addressed by experts in Therapy of Mild-to-Moderate Psoriasis with thehope that our patients will benefit from this book