Combination therapy to treat moderate to severe psoriasis

被引:144
作者
Lebwohl, M
Menter, A
Koo, J
Feldman, SR
机构
[1] Mt Sinai Med Ctr, Dept Dermatol, New York, NY 10029 USA
[2] Baylor Univ, Med Ctr, Dallas, TX USA
[3] Univ Calif San Francisco, San Francisco, CA 94143 USA
[4] Wake Forest Univ, Sch Med, Winston Salem, NC 27109 USA
关键词
D O I
10.1016/j.jaad.2002.12.002
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
In patients with moderate-to-severe psoriasis, remission can be difficult to achieve and sustain. Both acutely acting and long-term maintenance agents are needed. Speed and efficiency of available monotherapies tend to be inversely proportional to safety. Combination, rotational, and sequential approaches are often more effective and safer than single-agent therapy. Combining agents with complementary adverse effect profiles is preferable. Apparent synergistic enhancement is seen with most paired combinations of the four major therapies: acitretin, phototherapy (ultraviolet B/psoralen plus ultraviolet A), cyclosporine, and methotrexate. Of those, only cyclosporine in combination with psoralen plus ultraviolet A is contraindicated because of increased cancer risk. Combinations of each of those major therapies with topical agents (retinoids, steroids, vitamin D derivatives, and others) have been used with varying efficacy and safety. The immunomodulators, hydroxyurea and thioguanine, have also shown some success in combination therapy. The new biologic agents with their novel modes of action and adverse effect profiles may prove to be important adjuncts in combination/rotational/sequential approaches. In some cases, monotherapy (with either systemic agents or phototherapy) adequately controls moderate to severe disease. A regimen using a single agent has the advantages of lower cost and greater adherence by the patient. For any number of reasons, however, including loss of efficacy, adverse effects, or cumulative or acute toxicity-and especially the inability to clear resistant lesions-a single modality will not be adequate. Using two or more therapies is thus the rule rather than the exception for most patients with moderate-to-severe psoriasis, but picking a combination that serves to balance safety and efficacy needs careful consideration, especially since no evidence-based treatment guidelines exist.
引用
收藏
页码:416 / 430
页数:15
相关论文
共 96 条
[31]   Rediscovering mycophenolic acid: a review of its mechanism, side effects, and potential uses [J].
Kitchin, JES ;
Pomeranz, MK ;
Washenik, K ;
Shupack, JL .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1997, 37 (03) :445-449
[32]   Systemic sequential therapy of psoriasis: A new paradigm for improved therapeutic results [J].
Koo, J .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1999, 41 (03) :S25-S28
[33]  
Koo John, 2000, Keio Journal of Medicine, V49, P20
[34]   Tazarotene plus UVB phototherapy in the treatment of psoriasis [J].
Koo, JYM ;
Lowe, NJ ;
Lew-Kaya, DA ;
Vasilopoulos, AI ;
Lue, JC ;
Sefton, J ;
Gibson, JR .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2000, 43 (05) :821-828
[35]   Investigator-masked comparison of tazarotene gel q.d. plus mometasone furoate cream q.d. vs. mometasone furoate cream b.i.d. in the treatment of plaque psoriasis [J].
Koo, JYM ;
Martin, D .
INTERNATIONAL JOURNAL OF DERMATOLOGY, 2001, 40 (03) :210-212
[36]   COMBINATION OF TOPICAL CALCIPOTRIOL (MC-903) AND UVB RADIATION FOR PSORIASIS-VULGARIS [J].
KRAGBALLE, K .
DERMATOLOGICA, 1990, 181 (03) :211-214
[37]  
Krueger G, 2001, ARCH DERMATOL, V137, P280
[38]  
KRUTMANN J, 1999, TXB PSORIASIS, P179
[39]   Cyclosporine consensus conference: With emphasis on the treatment of psoriasis [J].
Lebwohl, M ;
Ellis, C ;
Gottlieb, A ;
Koo, J ;
Krueger, G ;
Linden, K ;
Shupack, J ;
Weinstein, G .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1998, 39 (03) :464-475
[40]   ADDITION OF SHORT-CONTACT ANTHRALIN THERAPY TO AN ULTRAVIOLET-B PHOTOTHERAPY REGIMEN - ASSESSMENT OF EFFICACY [J].
LEBWOHL, M ;
BERMAN, B ;
FRANCE, DS .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1985, 13 (05) :780-784