Tazarotene 0.1% gel for refractory mycosis fungoides lesions: An open-label pilot study

被引:44
作者
Apisarnthanarax, N
Talpur, R
Ward, S
Ni, X
Kim, HW
Duvic, M
机构
[1] Univ Texas, MD Anderson Canc Ctr, Dept Dermatol, Houston, TX 77030 USA
[2] Univ Texas, MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
关键词
D O I
10.1016/j.jaad.2003.09.005
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Topical skin-directed therapies are used to induce remissions in early-stage mycosis fungoides (MF). They are rarely curative, and responding patients are subject to frequent relapses, emphasizing the need for alternative therapies. Objective. We sought to evaluate the efficacy and tolerability of topical tazarotene 0.1% gel as adjuvant therapy in the treatment of refractory MF lesions. Methods: A total of 20 adult patients with early patch or plaque MF limited to less than 20% body surface area (BSA) involvement whose lesions were either stable or refractory to therapy for at least 8 weeks enrolled in an open-label pilot study. Tazarotene 0.1% gel was applied to MF lesions once daily for 24 weeks. Continued concomitant use of other medications such as low- to mid-potency topical corticosteroids was permitted for the alleviation of skin irritation. Global improvement, overall disease severity, percent BSA involvement, and pruritus were evaluated every 4 weeks. Up to 6 index lesions were followed up for area, plaque elevation, scaling, and erythema scores. Skin biopsy specimens were to be taken at baseline, week 8, and week 24. Evaluable specimens were stained with hematoxylin and eosin, CD8 antibody, and CD45RO antibody. Results: In all, 20 patients enrolled, 19 received treatment, and 16 completed at least 4 weeks of topical treatment. By intent-to-treat analysis, 11 of 19 patients (58%) achieved at least a moderate (>50%) global improvement in BSA, and 35% of 99 index lesions cleared completely. Significant reductions (mean differences) were also found in the median lesional area score (-37, P = .0013), mean plaque elevation score (-.67, P = .016), mean scaling (-0.70, P = .033), and mean erythema score (-1.03, P = .002). Analysis of overall disease also disclosed statistical differences in percent of change for BSA involvement of 22% (P = .013) and of mean overall disease severity score of 34% (P = .011). Of 19 patients, 16 (84%) experienced mild or moderate local skin irritation manifested by peeling, erythema, burning, and tenderness that was managed successfully with topical steroids or reducing the frequency of treatment. Histopathology and immunohistochemistry results showed reductions in lymphocytic infiltrates and percentage of CD45RO(+) lymphocytes, and increases in the percentage of CD8(+) lymphocytes during the course of therapy. Conclusion: In this small pilot study, tazarotene 0.1% gel was a well-tolerated and effective adjuvant topical for the treatment of refractory MF lesions by clinical and histologic assessments.
引用
收藏
页码:600 / 607
页数:8
相关论文
共 26 条
[1]  
Apisarnthanarax N, 2001, Expert Rev Anticancer Ther, V1, P403, DOI 10.1586/14737140.1.3.403
[2]   Cutaneous T-cell lymphoma - New immunomodulators [J].
Apisarnthanarax, N ;
Duvic, M .
DERMATOLOGIC CLINICS, 2001, 19 (04) :737-+
[3]   Treatment of cutaneous T cell lymphoma: Current status and future directions [J].
Apisarnthanarax N. ;
Talpur R. ;
Duvic M. .
American Journal of Clinical Dermatology, 2002, 3 (3) :193-215
[4]   Phase 1 and 2 trial of bexarotene gel for skin-directed treatment of patients with cutaneous T-cell lymphoma [J].
Breneman, D ;
Duvic, M ;
Kuzel, T ;
Yocum, R ;
Truglia, J ;
Stevens, VJ .
ARCHIVES OF DERMATOLOGY, 2002, 138 (03) :325-332
[5]   SYSTEMIC THERAPY OF CUTANEOUS T-CELL LYMPHOMAS (MYCOSIS-FUNGOIDES AND THE SEZARY-SYNDROME) [J].
BUNN, PA ;
HOFFMAN, SJ ;
NORRIS, D ;
GOLITZ, LE ;
AELING, JL .
ANNALS OF INTERNAL MEDICINE, 1994, 121 (08) :592-602
[6]  
CONOVER WJ, 1980, PRACTICAL NON PARAME
[7]   Tazarotene-induced gene 3 is suppressed in basal cell carcinomas and reversed in vivo by tazarotene application [J].
Duvic, M ;
Ni, X ;
Talpur, R ;
Herne, K ;
Schulz, C ;
Sui, D ;
Ward, S ;
Joseph, A ;
Hazarika, P .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 121 (04) :902-909
[8]   Bexarotene is effective and safe for treatment of refractory advanced-stage cutaneous T-cell lymphoma: Multinational phase II-III trial results [J].
Duvic, M ;
Hymes, K ;
Heald, P ;
Breneman, D ;
Martin, AG ;
Myskowski, P ;
Crowley, C ;
Yocum, RC .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (09) :2456-2471
[9]  
Duvic M, 2001, ARCH DERMATOL, V137, P581
[10]   The pathogenesis of psoriasis and the mechanism of action of tazarotene [J].
Duvic, M ;
Asano, AT ;
Hager, C ;
Mays, S .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1998, 39 (04) :S129-S133