Treatment of vulvar intraepithelial neoplasia with topical imiquimod

被引:220
|
作者
van Seters, Manon [1 ,6 ]
van Beurden, Marc [6 ,8 ]
ten Kate, Fiebo J. W. [7 ]
Beckmann, Ilse [1 ]
Ewing, Patricia C. [4 ]
Eijkemans, Marinus J. C. [5 ]
Kagie, Marjolein J. [10 ]
Meijer, Chris J. M. [11 ]
Aaronson, Neil K. [9 ]
KleinJan, Alex [2 ]
Heijmans-Antonissen, Claudia [3 ]
Zijlstra, Freek J. [3 ]
Burger, Matthe P. M. [6 ]
Helmerhorst, Theo J. M. [1 ]
机构
[1] Erasmus Univ, Med Ctr, Dept Gynecol, Rotterdam, Netherlands
[2] Erasmus Univ, Med Ctr, Dept Pulmonol, Rotterdam, Netherlands
[3] Erasmus Univ, Med Ctr, Dept Anesthesiol, Rotterdam, Netherlands
[4] Erasmus Univ, Med Ctr, Dept Pathol, Rotterdam, Netherlands
[5] Erasmus Univ, Med Ctr, Dept Publ Hlth, Rotterdam, Netherlands
[6] Univ Amsterdam, Acad Med Ctr, Dept Gynecol, NL-1105 AZ Amsterdam, Netherlands
[7] Univ Amsterdam, Acad Med Ctr, Dept Pathol, NL-1105 AZ Amsterdam, Netherlands
[8] Netherlands Canc Inst, Dept Gynecol, Amsterdam, Netherlands
[9] Netherlands Canc Inst, Div Psychosocial Res & Epidemiol, Amsterdam, Netherlands
[10] Med Ctr Haaglanden, The Hague, Netherlands
[11] Free Univ Amsterdam, Med Ctr, Dept Pathol, Amsterdam, Netherlands
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2008年 / 358卷 / 14期
关键词
D O I
10.1056/NEJMoa072685
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Alternatives to surgery are needed for the treatment of vulvar intraepithelial neoplasia. We investigated the effectiveness of imiquimod 5% cream, a topical immune-response modulator, for the treatment of this condition. Methods: Fifty-two patients with grade 2 or 3 vulvar intraepithelial neoplasia were randomly assigned to receive either imiquimod or placebo, applied twice weekly for 16 weeks. The primary outcome was a reduction of more than 25% in lesion size at 20 weeks. Secondary outcomes were histologic regression, clearance of human papillomavirus (HPV) from the lesion, changes in immune cells in the epidermis and dermis of the vulva, relief of symptoms, improvement of quality of life, and durability of response. Reduction in lesion size was classified as complete response (elimination), strong partial response (76 to 99% reduction), weak partial response (26 to 75% reduction), or no response (lessthan/equal 25% reduction). The follow-up period was 12 months. Results: Lesion size was reduced by more than 25% at 20 weeks in 21 of the 26 patients (81%) treated with imiquimod and in none of those treated with placebo (P<0.001). Histologic regression was significantly greater in the imiquimod group than in the placebo group (P<0.001). At baseline, 50 patients (96%) tested positive for HPV DNA. HPV cleared from the lesion in 15 patients in the imiquimod group (58%), as compared with 2 in the placebo group (8%) (P<0.001). The number of immune epidermal cells increased significantly and the number of immune dermal cells decreased significantly with imiquimod as compared with placebo. Imiquimod reduced pruritus and pain at 20 weeks (P=0.008 and P=0.004, respectively) and at 12 months (P=0.04 and P=0.02, respectively). The lesion progressed to invasion (to a depth of <1 mm) in 3 of 49 patients (6%) followed for 12 months (2 in the placebo group and 1 in the imiquimod group). Nine patients, all treated with imiquimod, had a complete response at 20 weeks and remained free from disease at 12 months. Conclusions: Imiquimod is effective in the treatment of vulvar intraepithelial neoplasia. (Current Controlled Trials number, ISRCTN11290871.).
引用
收藏
页码:1465 / 1473
页数:9
相关论文
共 50 条
  • [31] Vulvar intraepithelial neoplasia
    Kaufman, RH
    10TH WORLD CONGRESS OF CERVICAL PATHOLOGY AND COLPOSCOPY, 1999, : 17 - 21
  • [32] Vulvar intraepithelial neoplasia
    Preti, Mario
    Scurry, James
    Marchitelli, Claudia E.
    Micheletti, Leonardo
    BEST PRACTICE & RESEARCH CLINICAL OBSTETRICS & GYNAECOLOGY, 2014, 28 (07) : 1051 - 1062
  • [33] Topical imiquimod treatment for human papillomavirus infection in patients with and without cervical/vaginal intraepithelial neoplasia
    Lin, Cheng-Tao
    Qiu, Jian-Tai
    Wang, Chin-Jung
    Chang, Shuenn-Dyh
    Tang, Yun-Hsin
    Wu, Pei-Ju
    Jung, Shih-Ming
    Huang, Chu-Chun
    Chou, Hung-Hsueh
    Jao, Mei-Shan
    Lai, Chyong-Huey
    TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2012, 51 (04): : 533 - 538
  • [34] Vulvar Intraepithelial Neoplasia: Evaluation of Treatment Modalities
    Ribeiro, Filipa
    Figueiredo, Ana
    Paula, Tereza
    Borrego, Jorge
    JOURNAL OF LOWER GENITAL TRACT DISEASE, 2012, 16 (03) : 313 - 317
  • [35] Patient characteristics of women treated with topical imiquimod for vulval intraepithelial neoplasia
    Harvey, G.
    Hughes, B.
    Christie, C.
    Brinkmann, D.
    AUSTRALASIAN JOURNAL OF DERMATOLOGY, 2018, 59 : 5 - 6
  • [36] Epidemiology, diagnosis and treatment of vulvar intraepithelial neoplasia
    Joura, EA
    CURRENT OPINION IN OBSTETRICS & GYNECOLOGY, 2002, 14 (01) : 39 - 43
  • [37] Differentiated Vulvar Intraepithelial Neoplasia Associated with Intraepithelial Neoplastic Spread and with Usual Vulvar Intraepithelial Neoplasia
    Mai, Kien T.
    MODERN PATHOLOGY, 2017, 30 : 299A - 299A
  • [38] TOPICAL TREATMENT OF VAGINAL INTRAEPITHELIAL NEOPLASIA
    HULL, MGR
    BOWENSIMPKINS, P
    PAINTIN, DB
    OBSTETRICS AND GYNECOLOGY, 1977, 49 (03): : 382 - 382
  • [39] Vulvar intraepithelial neoplasia and vulvar cancer
    Edwards, CL
    TortoleroLuna, G
    Linares, AC
    Malpica, A
    Baker, VV
    Cook, E
    Johnson, E
    Mitchell, MF
    OBSTETRICS AND GYNECOLOGY CLINICS OF NORTH AMERICA, 1996, 23 (02) : 295 - +
  • [40] Differentiated Vulvar Intraepithelial Neoplasia Associated with Intraepithelial Neoplastic Spread and with Usual Vulvar Intraepithelial Neoplasia
    Mai, Kien T.
    LABORATORY INVESTIGATION, 2017, 97 : 299A - 299A