Omar Clavero (Spain)

Catalan Institute of Oncology (ICO) - IDIBELL Cancer Epidemiology Research Programme

Presenter of 1 Presentation

Clinical Research / Diagnosis and Management of Cervical Cancer and Its’ Precursors ePoster

REPRODUCIBILITY OF THE NEW CLASSIFICATION OF CERVICAL ADENOCARCINOMAS (ID 1340)

Abstract

Introduction

HPV is identified in almost all squamous invasive cervical carcinomas and a high proportion of adenocarcinomas. HPV involvement in cervical adenocarcinoma is between 8.3% - 71.8% depending on the histological subtype. A new morphological classification of adenocarcinomas has been proposed where ADC are classified based on the presence or absence of HPV infection-related features (IECC, International Endocervical Adenocarcinoma Criteria and Classification, 2017). Two adenocarcinoma groups were established: HPV-associated (HPVA) and non-HPV associated (NHPVA).

The objective is to evaluate the reproducibility of IECC morphological criteria with a highly sensitive HPV testing in our own series of cervical adenocarcinomas.

Methods

We identified sixty-nine incident cases of endocervical adenocarcinoma identified through Tarragona and Girona cancer registries (Catalonia) between 1998-2007. All adenocarcinoma hematoxylin and eosin (HE) slides were reviewed by two expert pathologists and classified in accordance with the IECC system. HPV DNA was done using SPF-10 PCR/DEIA/LiPA25. Demographic and clinical information was retrieved from the cancer registry databases.

Results

The morphological diagnostic distribution was; HPVA (n=51): usual -type (56.5%), mucinous, not otherwise specified (10.1%); villoglandular (4.3%), mucinous, intestinal type (2.9%); NHPVA (n=18): clear cell adenocarcinoma (8.7%), gastric-type adenocarcinoma (7.2%), endometroid adenocarcinoma (5.8%), serous adenocarcinoma (2.9%) and mesonephric carcinoma (1.4%). The mean patient’s age in HPVA was 50.4, compared to 55.4 in NHPVA (p>0.05). HPV was identified in 68.6% of HPVA tumors and in 5.6% of NHPVA tumors (p<0.05). Tumor stage IV at diagnosis was 7.8% in HPVA and 16.7% in NHPVA (p>0.05). Finally, 27.5% of HPVA patients dead by cervical cancer compared to 33.3% of NHPVA (p>0.05).

Conclusions

Our results using IECC criteria with HE are supported by HPV detection results. The use of a specific immuno-marker p16, and HPV detection would help in complex diagnosis.

Hide