Surgical versus clinical staging prior to primary chemoradiation in patients with cervical cancer FIGO stages IIB-IVA: oncologic results of a prospective randomized international multicenter (Uterus-11) intergroup study.


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:
12 2020
Historique:
received: 17 08 2020
revised: 23 10 2020
accepted: 26 10 2020
entrez: 9 12 2020
pubmed: 10 12 2020
medline: 2 10 2021
Statut: ppublish

Résumé

Revised staging of patients with locally advanced cervical cancer is based on clinical examination, imaging, and potential surgical findings. A known limitation of imaging techniques is an appreciable rate of understaging. In contrast, surgical staging may provide more accurate information on lymph node involvement. The aim of this prospective study was to evaluate the impact of pre-treatment surgical staging, including removal of bulky lymph nodes, on disease-free survival in patients with locally advanced cervical cancer. Uterus-11 was a prospective international multicenter study including patients with locally advanced cervical cancer who were randomized 1:1 to surgical staging (experimental arm) or clinical staging (control arm) followed by primary platinum-based chemoradiation. Patients with histologically proven squamous cell carcinoma, adenocarcinoma, or adenosquamous cancer International Federation of Gynecology and Obstetrics (FIGO) 2009 stage IIB-IVA underwent gynecologic examination and pre-treatment imaging including abdominal computed tomography (CT) and/or abdominal magnetic resonance imaging (MRI). Patients had chest imaging (any of the following: X-ray, CT, or PET-CT). The primary endpoint was disease-free survival and the secondary endpoint was overall survival. An ad hoc analysis was performed after trial completion for cancer-specific survival. Randomization was conducted from February 2009 to August 2013. A total of 255 patients (surgical arm, n=130; clinical arm, n=125) with locally advanced cervical cancer were randomized. Of these, 240 patients were eligible for analysis. The two groups were comparable with respect to patient characteristics. The surgical approach was transperitoneal laparoscopy in most patients (96.6%). Laparoscopic staging led to upstaging in 39 of 120 (33%) patients. After a median follow-up of 90 months (range 1-123) in both arms, there was no difference in disease-free survival between the groups (p=0.084). For patients with FIGO stage IIB, surgical staging is superior to clinical staging with respect to disease-free survival (HR 0.51, 95% CI 0.30 to 0.86, p=0.011). In the post-hoc analysis, surgical staging was associated with better cancer-specific survival (HR 0.61, 95% CI 0.40 to 0.93, p=0.020). Our study did not show a difference in disease-free survival between surgical and clinical staging in patients with locally advanced cervical cancer. There was a significant benefit in disease-free survival for patients with FIGO stage IIB and, in a post-hoc analysis, a cancer-specific survival benefit in favor of laparoscopic staging. The high risk of distant metastases in both arms emphasizes the need for further evaluation.

Identifiants

pubmed: 33293284
pii: ijgc-2020-001973
doi: 10.1136/ijgc-2020-001973
pmc: PMC7788482
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

1855-1861

Commentaires et corrections

Type : CommentIn

Informations de copyright

© IGCS and ESGO 2020. Re-use permitted under CC BY-NC. No commercial re-use. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

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Auteurs

Simone Marnitz (S)

Department of Radiooncology, Medical Faculty of the University of Cologne, Cologne, Germany simone.marnitz-schulze@uk-koeln.de.

Audrey Tieko Tsunoda (AT)

Gynecologic Oncology Department, Hospital Erasto Gaertner, Curitiba, Brazil.

Peter Martus (P)

Institute for Clinical Epidemiology and Biometry, Eberhard Karls University Tübingen Faculty of Medicine, Tubingen, Germany.

Marcelo Vieira (M)

Department for Gynecologic Oncology, Hospital de Amor de Barretos, Barretos, Brazil.

Renato Jose Affonso Junior (RJ)

Department of Radiooncology, Hospital de Amor de Barretos, Barretos, Brazil.

João Nunes (J)

Gynecologic Oncology Department, Hospital Erasto Gaertner, Curitiba, Brazil.
Gynecologic Oncology Department, Instituto de Oncologia do Paraná, Curitiba, Brazil.

Volker Budach (V)

Department of Radiooncology, Charité Universitätsmedizin Berlin, Berlin, Germany.

Hermann Hertel (H)

Department of Obstetrics and Gynecology, Hannover Medical School, Hannover, Germany.

Alexander Mustea (A)

Department of Gynecology and Gynecologic Oncology, University of Bonn, Bonn, Germany.

Jalid Sehouli (J)

Department of Gynecology with Center for Oncological Surgery, Campus Virchow Klinikum, Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health, Berlin, Germany.

Jens-Peter Scharf (JP)

Department of Gynecology and Obstetrics, Sana-Clinics Berlin Lichtenberg, Berlin, Germany.

Uwe Ulrich (U)

Department of Gynecology and Obstetrics, Martin-Luther-Hospital Berlin, Berlin, Germany.

Andreas Ebert (A)

Outpatient Clinics for Women's Health, Berlin, Germany.

Iris Piwonski (I)

Institute of Pathology, Charite Medical Faculty Berlin, Berlin, Germany.

Christhardt Kohler (C)

Department of Gynecology, University of Cologne, Koln, Germany.
Department of Special Operative and Oncologic Gynecology, Asklepios-Clinic Hamburg-Altona, Asklepios Hospital Group, Hamburg, Germany.

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