Solares Concepción, Velasco Julio, Álvarez-Ruiz Eduardo, González-Fernández Laura, Encinas Ana-Isabel, Astudillo Aurora, Schneider José
Obstetrics & Gynecology Service, San Agustín Hospital, Avilés, Spain.
Pathology Service, San Agustín Hospital, Avilés, Spain.
Anticancer Res. 2015 Nov;35(11):6291-5.
To determine if positive dual staining of p16/Ki-67 in cytology samples from women with atypical squamous cells of undetermined significance (ASC-US), low-grade squamous intraepithelial lesion (LSIL) or normal cytological reports with presence of high-risk human papillomavirus (HPV), helps in predicting the risk of developing high-grade cervical lesions during one-year of follow-up after a normal initial colposcopy.
One-hundred and sixty women with ASC-US, LSIL or otherwise normal cytology, but with the presence of high-risk HPV, were referred to the colposcopy Unit of our Hospital. Cytology and HPV testing were repeated and dual staining of p16/Ki-67 performed on a new cytological specimen, and subsequently patients were colposcopically assessed and prospectively followed-up for one year, after which the colposcopy was repeated. An optional intermediate colposcopical assessment after six months was also offered.
Out of 143/160 women with a normal initial colposcopy, 13 were ultimately lost to follow-up. Out of the remaining 130, nine developed histologically verified cervical intraepithelial neoplasia or higher grade (CIN2+) lesions during the one-year follow-up period. Two thirds of them (6/9) were initially p16/Ki-67-positive.
Biomarker detection may identify women at higher risk of CIN2+, and these women may benefit from early colposcopic assessment. Women who test negatively for the biomarkers could eventually follow a less aggressive protocol.
确定在意义不明确的非典型鳞状细胞(ASC-US)、低级别鳞状上皮内病变(LSIL)或高危型人乳头瘤病毒(HPV)呈阳性的正常细胞学报告的女性细胞学样本中,p16/Ki-67双重染色是否有助于预测在初次阴道镜检查正常后的一年随访期间发生高级别宫颈病变的风险。
160名患有ASC-US、LSIL或细胞学检查正常但存在高危型HPV的女性被转诊至我院阴道镜检查科。重复进行细胞学和HPV检测,并在新的细胞学标本上进行p16/Ki-67双重染色,随后对患者进行阴道镜评估并进行为期一年的前瞻性随访,之后再次进行阴道镜检查。还提供了在6个月后进行的可选中间阴道镜评估。
在160名初次阴道镜检查正常的女性中,143名中有13名最终失访。在其余130名中,9名在一年随访期间发生了组织学证实的宫颈上皮内瘤变或更高级别(CIN2+)病变。其中三分之二(6/9)最初p16/Ki-67呈阳性。
生物标志物检测可识别CIN2+风险较高的女性,这些女性可能受益于早期阴道镜评估。生物标志物检测呈阴性的女性最终可能遵循不太激进的方案。