Lymph node dissection in endometrial cancer and clinical outcome: A population-based study in 5546 patients.


Journal

Gynecologic oncology
ISSN: 1095-6859
Titre abrégé: Gynecol Oncol
Pays: United States
ID NLM: 0365304

Informations de publication

Date de publication:
07 2019
Historique:
received: 02 01 2019
revised: 01 04 2019
accepted: 02 04 2019
pubmed: 28 4 2019
medline: 27 8 2019
entrez: 28 4 2019
Statut: ppublish

Résumé

According to current treatment guidelines, comprehensive surgical staging procedures in endometrial cancer confined to the uterus depend on uterine risk factors: a systematic lymph node dissection (LND) is recommended in high risk patients and should be omitted in low risk patients. Its role in intermediate and high intermediate risk patients is inconclusive. The aim of this analysis was to review the implementation of this risk-adopted strategy. Data were provided by the population-based Munich Cancer Registry. Patients with endometrial cancer diagnosed between 1998 and 2016 were included. Of 5446 eligible patients, 58.5%, 30.1% and 11.4% belonged to the low risk, intermediate/high-intermediate and high risk group, respectively. Lymph node dissection was performed in 20.2%, 53.0% and 63.7% within these groups. Lymph node involvement was diagnosed in 1.7%, 9.6% and 19.3%, respectively. Within these risk groups, there was no significant difference in the time to local recurrence, lymph node recurrence or distant metastases between patients with and without LND. After adjusting for age and comorbidity-status, no significant difference in overall survival was found. The application of a risk-adopted management of LND in early endometrial cancer in real-life is associated with a high rate of surgical under- and overtreatment. Corresponding survival data do not show a significant benefit of a systematic lymph node dissection. In order to improve the management and outcome of early endometrial cancer in the future, prospective trials, new surgical concepts and prognostic markers will be primary and necessary.

Sections du résumé

BACKGROUND
According to current treatment guidelines, comprehensive surgical staging procedures in endometrial cancer confined to the uterus depend on uterine risk factors: a systematic lymph node dissection (LND) is recommended in high risk patients and should be omitted in low risk patients. Its role in intermediate and high intermediate risk patients is inconclusive. The aim of this analysis was to review the implementation of this risk-adopted strategy.
MATERIALS AND METHODS
Data were provided by the population-based Munich Cancer Registry. Patients with endometrial cancer diagnosed between 1998 and 2016 were included.
RESULTS
Of 5446 eligible patients, 58.5%, 30.1% and 11.4% belonged to the low risk, intermediate/high-intermediate and high risk group, respectively. Lymph node dissection was performed in 20.2%, 53.0% and 63.7% within these groups. Lymph node involvement was diagnosed in 1.7%, 9.6% and 19.3%, respectively. Within these risk groups, there was no significant difference in the time to local recurrence, lymph node recurrence or distant metastases between patients with and without LND. After adjusting for age and comorbidity-status, no significant difference in overall survival was found.
CONCLUSIONS
The application of a risk-adopted management of LND in early endometrial cancer in real-life is associated with a high rate of surgical under- and overtreatment. Corresponding survival data do not show a significant benefit of a systematic lymph node dissection. In order to improve the management and outcome of early endometrial cancer in the future, prospective trials, new surgical concepts and prognostic markers will be primary and necessary.

Identifiants

pubmed: 31027900
pii: S0090-8258(19)30497-4
doi: 10.1016/j.ygyno.2019.04.002
pii:
doi:

Types de publication

Journal Article

Langues

eng

Pagination

65-71

Informations de copyright

Copyright © 2019 Elsevier Inc. All rights reserved.

Auteurs

M Pölcher (M)

Depeartment of Gynecologic Oncology and Minimally-invasive Surgery, Rotkreuzklinikum München, Frauenklinik Taxisstraße Munich, Germany. Electronic address: martin.poelcher@swmbrk.de.

M Rottmann (M)

Munich Cancer Registry, Institute for Medical Information Processing, Biometry and Epidemiology, Ludwig-Maximilians-University (LMU), Munich, Germany. Electronic address: rottmann@ibe.med.uni-muenchen.de.

S Brugger (S)

Depeartment of Gynecologic Oncology and Minimally-invasive Surgery, Rotkreuzklinikum München, Frauenklinik Taxisstraße Munich, Germany. Electronic address: sarah.brugger@swmbrk.de.

S Mahner (S)

Department of Obstetrics and Gynecology, University Hospital, LMU Munich, Germany. Electronic address: sven.mahner@med.uni-muenchen.de.

C Dannecker (C)

Department of Obstetrics and Gynecology, University Hospital, LMU Munich, Germany. Electronic address: christian.dannecker@med.uni-muenchen.de.

M Kiechle (M)

Department of Obstetrics and Gynecology, University Hospital, Technical University Munich, Germany. Electronic address: marion.kiechle@tum.de.

C Brambs (C)

Department of Obstetrics and Gynecology, University Hospital, Technical University Munich, Germany. Electronic address: christine.brambs@tum.de.

D Grab (D)

Department of Obstetrics and Gynecology Städtisches Klinikum Harlaching Munich, Germany. Electronic address: dieter.grab@klinikum-muenchen.de.

C Anthuber (C)

Department of Obstetrics and Gynecology Klinikum Starnberg, Germany. Electronic address: christoph.anthuber@klinikum-starnberg.de.

F von Koch (F)

Department of Obstetrics and Gynecology, Klinikum Dritter Orden, Munich, Germany. Electronic address: franz.koch@dritter-orden.de.

A Schnelzer (A)

Department of Obstetrics and Gynecology, RoMed Kliniken, Rosenheim, Germany. Electronic address: andreas.schnelzer@ro-med.de.

J Engel (J)

Munich Cancer Registry, Institute for Medical Information Processing, Biometry and Epidemiology, Ludwig-Maximilians-University (LMU), Munich, Germany. Electronic address: engel@ibe.med.uni-muenchen.de.

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