Clinical and Ultrasound Characteristics of the Microcystic Elongated and Fragmented (MELF) Pattern in Endometrial Cancer According to the International Endometrial Tumor Analysis (IETA) criteria.


Journal

International journal of gynecological cancer : official journal of the International Gynecological Cancer Society
ISSN: 1525-1438
Titre abrégé: Int J Gynecol Cancer
Pays: England
ID NLM: 9111626

Informations de publication

Date de publication:
01 2019
Historique:
accepted: 02 10 2018
received: 08 04 2018
revised: 04 09 2018
entrez: 15 1 2019
pubmed: 15 1 2019
medline: 7 1 2020
Statut: ppublish

Résumé

To describe sonographic features of the microcystic elongated and fragmented (MELF) pattern of myometrial invasion (MI) using the International Endometrial Tumor Analysis (IETA) criteria; to assess the effect of the MELF pattern on preoperative ultrasound evaluation of MI; and to determine the relationship of the MELF pattern to more advanced stage (≥ IB) and lymph node metastases in women with endometrioid endometrial cancer. We included 850 women with endometrioid endometrial cancer from the prospective IETA 4 study. Ultrasound experts performed all ultrasound examinations, according to the IETA protocol. Reference pathologists assessed the presence or absence of the MELF pattern. Sonographic features and accuracy of ultrasound assessment of MI were compared in cases with the presence and the absence of the MELF pattern. The MELF pattern was correlated to more advanced stage (≥IB) and lymph node metastases. The MELF pattern was present in 197 (23.2%) women. On preoperative ultrasound imaging the endometrium was thicker (p = 0.031), more richly vascularized (p = 0.003) with the multiple multifocal vessel pattern (p < 0.001) and the assessment of adenomyosis was more often uncertain (p < 0.001). The presence or the absence of the MELF pattern did not affect the accuracy of the assessment of MI. The MELF pattern was associated with deep myometrial invasion (≥ 50%) (p < 0.001), cervical stromal invasion (p = 0.037), more advanced stage (≥ IB) (p < 0.001) and lymph node metastases (p = 0.011). Tumors with the MELF pattern were slightly larger, more richly vascularized with multiple multifocal vessels and assessment of adenomyosis was more uncertain on ultrasound imaging. The MELF pattern did not increase the risk of underestimating MI in preoperative ultrasound staging. Tumors with the MELF pattern were more than twice as likely to have more advanced stage (≥ IB) and lymph node metastases.

Identifiants

pubmed: 30640693
pii: ijgc-2018-000045
doi: 10.1136/ijgc-2018-000045
doi:

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

119-125

Informations de copyright

© IGCS and ESGO 2019. No commercial re-use. See rights and permissions. Published by BMJ.

Auteurs

Linda S E Eriksson (LSE)

Department of Obstetrics and Gynecology, Karolinska University Hospital, Stockholm, Sweden linda.eriksson@sll.se.
Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.

Denis Nastic (D)

Department of Pathology and Cytology and Institution for Oncology-Pathology, Karolinska University Hospital and Karolinska Institutet, Stockholm, Sweden.

Filip Frühauf (F)

Gynecological Oncology Center, Department of Obstetrics and Gynecology, First Faculty of Medicine, Charles University, Prague, Czech Republic.

Daniela Fischerova (D)

Gynecological Oncology Center, Department of Obstetrics and Gynecology, First Faculty of Medicine, Charles University, Prague, Czech Republic.

Kristyna Nemejcova (K)

Department of Pathology, First Faculty of Medicine, Charles University, Prague, Czech Republic.

Francesca Bono (F)

Pathology Unit, San Gerardo Hospital, Monza, Italy.

Dorella Franchi (D)

Preventive Gynecology Unit, European Institute of Oncology, Milan, Italy.

Robert Fruscio (R)

Clinic of Obstetrics and Gynecology, University of Milan-Bicocca, San Gerardo Hospital, Monza, Italy.

Mariacristina Ghioni (M)

Division of Pathology, European Institute of Oncology, Milan, Italy.

Lucia A Haak (LA)

Institute for the Care of Mother and Child, Prague, Czech Republic.
Third Faculty of Medicine, Charles University, Prague, Czech Republic.

Vaclav Hejda (V)

Institute for the Care of Mother and Child, Praque, Czech Republic.

Raimundas Meskauskas (R)

National Centre of Pathology, Vilnius, Lithuania.

Gina Opolskiene (G)

Center of Obstetrics and Gynecology, Vilnius University Hospital, Santariskiu Clinic, Vilnius, Lithuania.

M Angela Pascual (MA)

Department of Obstetrics, Gynecology and Reproduction, Hospital Universitario Dexeus, Barcelona, Spain.

Antonia Testa (A)

Department of Obstetrics and Gynecology, Catholic University of the Sacred Heart, Rome, Italy.

Francisco Tresserra (F)

Department of Pathology and Cytology, Hospital Universitario Dexeus, Barcelona, Spain.

Gian Franco Zannoni (GF)

Department of Pathology, Catholic University of the Sacred Heart, Rome, Italy.

Joseph W Carlson (JW)

Department of Pathology and Cytology and Institution for Oncology-Pathology, Karolinska University Hospital and Karolinska Institutet, Stockholm, Sweden.

Elisabeth Epstein (E)

Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.
Department of Clinical Science and Education, Södersjukhuset, Stockholm, Sweden.

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