Köhler Christhardt, Le Xin, Dogan Nasuh Utku, Pfiffer Tatiana, Schneider Achim, Marnitz Simone, Bertolini Julia, Favero Giovanni
Department of Advanced Operative and Oncologic Gynecology, Asklepios Hospital, Hamburg, Germany.
Department of Advanced Operative and Oncologic Gynecology, Asklepios Hospital, Hamburg, Germany; Department of Obstetrics and Gynecology, Akdeniz University, Antalya, Turkey.
J Minim Invasive Gynecol. 2016 Jul-Aug;23(5):748-52. doi: 10.1016/j.jmig.2016.03.003. Epub 2016 Mar 11.
To evaluate the feasibility and accuracy of a commercially available test to detect E6/E7 mRNA of 14 subtypes of high-risk HPVs (APTIMA; Hologic, Bedford, MA) in the sentinel lymph nodes of CC patients laparoscopically operated.
Prospective pilot study.
The study was conducted in the Department of Advanced Operative and Oncologic Gynecology, Asklepios Hospital, Hamburg, Germany.
54 women with HPV-positive CC submitted to laparoscopic sentinel node biopsy alone or sentinel node biopsy followed by systematic pelvic and/or para-aortic endoscopic lymphadenectomy.
All removed sentinel lymph nodes (SLNs) underwent sample collection by cytobrush for the APTIMA assay before frozen section.
Results obtained with the HPV mRNA test were compared with the definitive histopathological analysis of the SLNs and additional lymph nodes removed.
A total of 125 SLNs (119 pelvic and 6 paraaortic) were excised with a mean number of 2.3 SLNs per patient. Final histopathologic analysis confirmed nodal metastases in 10 SLNs from 10 different patients (18%). All the histologically confirmed metastatic lymph nodes were also HPV E6/E7 mRNA positive, resulting in a sensitivity of 100%. Four histologically free sentinel nodes were positive for HPV E6/E7 mRNA, resulting in a specificity of 96.4%.
The HPV E6/E7 mRNA assay in the SLNs of patients with CC is feasible and highly accurate. The detection of HPV mRNA in 4 women with negative SLNs might denote a shift from microscopic identification of metastasis to the molecular level. The prognostic value of this findings awaits further verification.
评估一种市售检测方法检测腹腔镜手术的宫颈癌(CC)患者前哨淋巴结中14种高危人乳头瘤病毒(HPV)亚型E6/E7 mRNA的可行性和准确性(APTIMA;Hologic公司,贝德福德,马萨诸塞州)。
前瞻性试点研究。
该研究在德国汉堡Asklepios医院高级手术与肿瘤妇科进行。
54例HPV阳性的CC患者,单独接受腹腔镜前哨淋巴结活检或前哨淋巴结活检后行系统性盆腔和/或腹主动脉旁内镜下淋巴结清扫术。
所有切除的前哨淋巴结(SLN)在冰冻切片前通过细胞刷进行样本采集,用于APTIMA检测。
将HPV mRNA检测结果与SLN及额外切除淋巴结的最终组织病理学分析结果进行比较。
共切除125个SLN(119个盆腔淋巴结和6个腹主动脉旁淋巴结),平均每位患者2.3个SLN。最终组织病理学分析证实10例不同患者的10个SLN有淋巴结转移(18%)。所有组织学确诊的转移淋巴结HPV E6/E7 mRNA也呈阳性,敏感性为100%。4个组织学上无转移的前哨淋巴结HPV E6/E7 mRNA呈阳性,特异性为96.4%。
CC患者SLN中的HPV E6/E7 mRNA检测可行且高度准确。4例SLN阴性女性中检测到HPV mRNA可能意味着从转移的显微镜识别向分子水平的转变。这一发现的预后价值有待进一步验证。