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
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 32 条
  • [1] Translation, validation, and norming of the Dutch language version of the SF-36 Health Survey in community and chronic disease populations
    Aaronson, NK
    Muller, M
    Cohen, PDA
    Essink-Bot, ML
    Fekkes, M
    Sanderman, R
    Sprangers, MAG
    Velde, AT
    Verrips, E
    [J]. JOURNAL OF CLINICAL EPIDEMIOLOGY, 1998, 51 (11) : 1055 - 1068
  • [2] THE EUROPEAN-ORGANIZATION-FOR-RESEARCH-AND-TREATMENT-OF-CANCER QLQ-C30 - A QUALITY-OF-LIFE INSTRUMENT FOR USE IN INTERNATIONAL CLINICAL-TRIALS IN ONCOLOGY
    AARONSON, NK
    AHMEDZAI, S
    BERGMAN, B
    BULLINGER, M
    CULL, A
    DUEZ, NJ
    FILIBERTI, A
    FLECHTNER, H
    FLEISHMAN, SB
    DEHAES, JCJM
    KAASA, S
    KLEE, M
    OSOBA, D
    RAZAVI, D
    ROFE, PB
    SCHRAUB, S
    SNEEUW, K
    SULLIVAN, M
    TAKEDA, F
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (05) : 365 - 376
  • [3] ANDERSEN BL, 1983, OBSTET GYNECOL, V62, P457
  • [4] ANDERSEN BL, 1988, OBSTET GYNECOL, V71, P15
  • [5] SEXUAL FUNCTION AND SOMATOPSYCHIC REACTIONS IN VULVECTOMY-OPERATED WOMEN AND THEIR PARTNERS
    ANDREASSON, B
    MOTH, I
    JENSEN, SB
    BOCK, JE
    [J]. ACTA OBSTETRICIA ET GYNECOLOGICA SCANDINAVICA, 1986, 65 (01) : 7 - 10
  • [6] Imiquimod, a patient-applied immune-response modifier for treatment of external genital warts
    Beutner, KR
    Tyring, SK
    Trofatter, KF
    Douglas, JM
    Spruance, S
    Owens, ML
    Fox, TL
    Hougham, AJ
    Schmitt, KA
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1998, 42 (04) : 789 - 794
  • [7] Davis G, 2000, J REPROD MED, V45, P619
  • [8] Diaz-Arrastia C, 2001, CLIN CANCER RES, V7, P3031
  • [9] Intraepithelial and invasive squamous cell neoplasia of the vulva: Trends in incidence, recurrence, and survival rate in Norway
    Iversen, T
    Tretli, S
    [J]. OBSTETRICS AND GYNECOLOGY, 1998, 91 (06) : 969 - 972
  • [10] A simplified and reliable HPV testing of archival Papanicolaou-stained cervical smears: application to cervical smears from cancer patients starting with cytologically normal smears
    Jacobs, MV
    Zielinski, D
    Meijer, CJLM
    Poli, RP
    Voorhorst, FJ
    de Schipper, FA
    Runsink, AP
    Snijders, PJF
    Walboomers, JMM
    [J]. BRITISH JOURNAL OF CANCER, 2000, 82 (08) : 1421 - 1426