Imiquimod to treat different cancers of the epidermis

被引:30
作者
Eklind, J
Maschke, J
Lidbrink, P
Hengge, UR
Tartler, U
机构
[1] Univ Dusseldorf, Dept Dermatol, D-4000 Dusseldorf, Germany
[2] Huddinge Univ Hosp, Dept Dermatol, Stockholm, Sweden
关键词
D O I
10.1046/j.1524-4725.2003.t01-1-29242.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
BACKGROUND. Topical immunomodulatory therapy with imiquimod has been recently used for the treatment of actinic keratoses, intraepithelial carcinoma, and small basal cell carcinoma (BCC) besides the licensed indication of extragenital warts (condyloma). METHODS. We treated several patients with particular epidermal neoplasias such as squamous cell cancer (SCC) and basal cell cancer of sclerodermiform type three times per week for 4 to 12 weeks. RESULTS. We report several novel aspects of the treatment of epidermal cancers with self-applied, nonpainful, immunomodulatory therapy. First, we treated-for the first time-two immunosuppressed renal transplant patients for invasive SCC with imiquimod. Interestingly, systemic immunosuppression did not adversely affect the response to therapy. Second, one patient with the high-risk and aggressive growth pattern of basal cell cancer (sclerodermiform histology) was cured from his disease at a particular location in the face, suggesting sufficient penetration despite scarring. No recurrence was detected in another patient who suffered from 29 BCCs until almost 2-years follow-up. Third, the treatment of actinic keratoses in the face is substantially shorter (in the order of 4 to 6 weeks) as opposed to other skin cancers. Immunomodulatory treatment with imiquimod led to the demarcation of in situ actinic keratosis lesions that could not be identified using the dermatologist's experience, probably because of the existence of exclusive alterations on the molecular level. CONCLUSION. Several novel aspects of immunomodulatory treatment with imiquimod and new indications such as selected cases of sclerodermiform BCC and SCC have been described. The texture of the skin at various different body locations may explain the varying sensitivities to imiquimod when facial skin is compared with skin on the extremities.
引用
收藏
页码:890 / 896
页数:7
相关论文
共 26 条
  • [1] Therapeutic response of basal cell carcinoma to the immune response modifier imiquimod 5% cream
    Beutner, KR
    Geisse, JK
    Helman, D
    Fox, TL
    Ginkel, A
    Owens, ML
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1999, 41 (06) : 1002 - 1007
  • [2] Treatment of genital warts with an immune-response modifier (imiquimod)
    Beutner, KR
    Spruance, SL
    Hougham, AJ
    Fox, TL
    Owens, ML
    Douglas, JM
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1998, 38 (02) : 230 - 239
  • [3] Co-expression of the squamous cell carcinoma antigens 1 and 2 in normal adult human tissues and squamous cell carcinomas
    Cataltepe, S
    Gornstein, ER
    Schick, C
    Kamachi, Y
    Chatson, K
    Fries, J
    Silverman, GA
    Upton, MP
    [J]. JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 2000, 48 (01) : 113 - 122
  • [4] Treatment of a large superficial basal cell carcinoma with 5% imiquimod: A case report and review of the literature
    Chen, TM
    Rosen, T
    Orengo, I
    [J]. DERMATOLOGIC SURGERY, 2002, 28 (04) : 344 - 346
  • [5] DRAKE LA, 1992, J AM ACAD DERMATOL, V26, P117
  • [6] FLUOROURACIL PASTE TREATMENT OF THIN BASAL-CELL CARCINOMAS
    EPSTEIN, E
    [J]. ARCHIVES OF DERMATOLOGY, 1985, 121 (02) : 207 - 213
  • [7] Long-term follow-up and histological changes of superficial nonmelanoma skin cancers treated with topical δ-aminolevulinic acid photodynamic therapy
    Fink-Puches, R
    Soyer-, HP
    Hofer, A
    Kerl, H
    Wolf, P
    [J]. ARCHIVES OF DERMATOLOGY, 1998, 134 (07) : 821 - 826
  • [8] Imiquimod 5% cream for the treatment of superficial basal cell carcinoma: A double-blind, randomized, vehicle-controlled study
    Geisse, JK
    Rich, P
    Pandya, A
    Gross, K
    Andres, K
    Ginkel, A
    Owens, M
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2002, 47 (03) : 390 - 398
  • [9] Hannuksela-Svahn A, 2000, ACTA DERM-VENEREOL, V80, P381
  • [10] Small anti-viral compounds activate immune cells via the TLR7 MyD88-dependent signaling pathway
    Hemmi, H
    Kaisho, T
    Takeuchi, O
    Sato, S
    Sanjo, H
    Hoshino, K
    Horiuchi, T
    Tomizawa, H
    Takeda, K
    Akira, S
    [J]. NATURE IMMUNOLOGY, 2002, 3 (02) : 196 - 200