Use of p16-INK4A overexpression to increase the specificity of human papillomavirus testing: a nested substudy of the NTCC randomised controlled trial

被引:152
作者
Carozzi, Francesca [2 ]
Confortini, Massimo [2 ]
Dalla Palma, Paolo [3 ]
Del Mistro, Annarosa [4 ]
Gillio-Tos, Anna
De Marco, Laura
Giorgi-Rossi, Paolo [5 ]
Pontenani, Giovanni [2 ]
Rosso, Stefano
Sani, Cristina [2 ]
Sintoni, Catia [6 ]
Segnan, Nereo
Zorzi, Manuel [4 ]
Cuzick, Jack [7 ]
Rizzolo, Raffaella
Ronco, Guglielmo [1 ]
机构
[1] Ctr Canc Prevent, Canc Epidemiol Unit, I-10123 Turin, Italy
[2] Ctr Canc Study & Prevent, Florence, Italy
[3] Santa Chiara Hosp, Trento, Italy
[4] Venetian Oncol Inst IRCCS, Padua, Italy
[5] Laziosanita Agcy Publ Hlth, Rome, Italy
[6] Ravenna Hosp, AUSL Ravenna, Ravenna, Italy
[7] Queen Marys Sch Med & Dent & Canc Res UK, London, England
关键词
D O I
10.1016/S1470-2045(08)70208-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Human-papillomavirus (HPV) testing is more sensitive, but less specific, than conventional cytology for detecting high-grade cervical intraepithelial neoplasia. (CIN). We assessed whether HPV testing with triage by p16-INK4A overexpression. can increase specificity while maintaining sensitivity. Methods HPV-positive women were enrolled between June 10, 2003, and Dec 31, 2004 in a multicentre randomised controlled trial, which compared stand-alone HPV testing by Hybrid Capture 2 (experimental group) with conventional cytology, were referred for colposcopy. In seven of nine centres, cytospin preparations from these women were tested for p16-INK4A overexpression by immunostaining. The sensitivity and specificity for CIN grade 2 or more, determined at blind review of histology, were calculated for these women. We also estimated the relative sensitivity and relative referral to colposcopy that would have been obtained by HPV testing with p16-INK4A triage compared with conventional cytology. This trial is registered as a Standard Randomised Controlled Trial, number ISRCTN81678807. Findings 24661 women were randomly assigned to the experimental group. 1137 women (74% of those undergoing colposcopy in relevant centres), including 50 with CIN2 and 42 with CIN3 or cancer, had valid p16-INK4A immunostaining. For the endpoint of CIN2+, sensitivity and specificity of p16-INK4A (deemed positive with any number of stained cells-except endocervical, metaplastic, and atrophic cells if morphologically normal) in HPV-positive women of any age were 88% (81 of 92; 95% CI 80-94) and 61% (633 of 1045; 57-64), respectively. In the 35-60-year age group, the relative sensitivity of HPV testing and p16-INK4A triage versus conventional cytology for CIN2+ was 1.53 (95% CI 1.15-2.02) and relative referral was 1.08 (0.96-1.21). In the 25-34-year age group, relative sensitivity was 3.01 (1.82-5.17) and relative referral was 1.15 (0.96-1.37). In the latter age group, when 5% or more stained cells were deemed positive, the corresponding values were 2.06 (1.20-3.68) and 0.58 (0.46-0.73), respectively. Interpretation HPV testing with p16-INK4A triage produces a significant increase in sensitivity compared with conventional cytology, with no substantial increase in referral to colposcopy. Funding European Union, Italian Ministry of Health, Regional Health Administrations of Piemonte, Tuscany, Veneto, and Emilia-Romagna, and Public Health Agency of Lazio Region.
引用
收藏
页码:937 / 945
页数:9
相关论文
共 34 条
  • [31] Predictive significance of the alterations of p16INK4A, p14ARF, p53, and proliferating cell nuclear antigen expression in the progression of cervical cancer
    Wang, JL
    Zheng, BY
    Li, XD
    Ångström, T
    Lindström, MS
    Wallin, KL
    [J]. CLINICAL CANCER RESEARCH, 2004, 10 (07) : 2407 - 2414
  • [32] Wang SS, 2004, CANCER EPIDEM BIOMAR, V13, P1355
  • [33] Triage of women with ASCUS and LSIL cytology -: Use of qualitative assessment of p16INK4a positive cells to identify patients with high-grade ceivical intraepithelial neoplasia
    Wentzensen, Nicolas
    Bergeron, Christine
    Cas, Frederic
    Vinokurova, Svetlana
    Doeberitz, Magnus von Knebel
    [J]. CANCER CYTOPATHOLOGY, 2007, 111 (01) : 58 - 66
  • [34] WENZENSTEN N, 2005, CANC CANC CYTOPATHOL, V105, P461