Early tumor regrowth is a contributor to impaired survival in patients with completely resected advanced ovarian cancer. An exploratory analysis of the Intergroup trial AGO-OVAR 12.


Journal

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

Informations de publication

Date de publication:
02 2019
Historique:
received: 24 09 2018
revised: 30 10 2018
accepted: 06 11 2018
pubmed: 24 11 2018
medline: 23 2 2019
entrez: 24 11 2018
Statut: ppublish

Résumé

Surgical assessment of residual tumor provides the strongest prognostic information in advanced ovarian cancer (AOC), with the best outcome observed after complete resection. Postoperative radiological assessment before initiation of chemotherapy can supplement the information obtained by surgical assessment; however, it may also reveal conflicting findings. Patients with AOC enrolled in the AGO-OVAR 12 trial underwent baseline imaging before the first chemotherapy cycle. The findings from surgical and radiologic assessment for disease extend were compared. Additionally, an integrated approach was assessed. Complete data from all 3 assessment methods were available for 1345 patients. Of 689 patients with complete resection, tumor was observed in 28% and 22% of patients undergoing radiologic and integrated assessment, respectively. Patients with surgical- radiological and surgical-integrated concordant findings showed a 5-year overall survival (5Y-OS) of 72% and 71%, whereas patients with surgical-radiological and surgical-integrated discordant results showed inferior 5Y-OS of 47% and 49%, respectively. Patients with surgically assessed residual disease had a 5-YOS of 37%. The interval between surgery and baseline assessment was independently associated with discordance between assessment methods, which might reflect early tumor regrowth. Baseline tumor assessment before chemotherapy provides information that stratifies patients with complete resection into different prognostic groups. Integrating the data from different assessment methods might lead to improved definitions of prognostic groups. Further investigation to determine if earlier initiation of chemotherapy after debulking surgery could increase survival of patients with early tumor regrowth is warranted.

Identifiants

pubmed: 30466805
pii: S0090-8258(18)31406-9
doi: 10.1016/j.ygyno.2018.11.008
pii:
doi:

Substances chimiques

Indoles 0
Carboplatin BG3F62OND5
nintedanib G6HRD2P839
Paclitaxel P88XT4IS4D

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

235-242

Informations de copyright

Copyright © 2018. Published by Elsevier Inc.

Auteurs

F Heitz (F)

Department of Gynecology and Gynecologic Oncology, Kliniken Essen-Mitte, Evangelische Huyssens-Stiftung, Germany; Department for Gynecology, Charité - Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health. Electronic address: florian.heitz@gmx.net.

P Harter (P)

Department of Gynecology and Gynecologic Oncology, Kliniken Essen-Mitte, Evangelische Huyssens-Stiftung, Germany.

E Åvall-Lundqvist (E)

Linköping University and Karolinska Institute, Linköping, Sweden.

A Reuss (A)

Coordinating Center for Clinical Trials, Marburg, Germany.

P Pautier (P)

Institut Gustave Roussy, Villejuif, France.

G Cormio (G)

University of Bari and Gynecologic Oncology Unit, National Cancer Institute "Giovanni Paolo II", Bari, Italy.

N Colombo (N)

University of Milano-Bicocca and Instituto Europeo di Oncologia, Milan, Italy.

A Reinthaller (A)

Department of General Gynecology and Gynecologic Oncology, Gynecologic Cancer Unit - Comprehensive Cancer Center, Medical University of Vienna, Austria.

I Vergote (I)

University of Leuven, Leuven Cancer Institute, Leuven, Belgium.

A Poveda (A)

Instituto Valenciano de Oncología, Valencia, Spain.

P B Ottevanger (PB)

Radboud University Medical Center, Nijmegen, Netherlands.

L C Hanker (LC)

University of Schleswig-Holstein, Lübeck, Germany.

A Leminen (A)

Women's Hospital, Haartmaninkatu 2, Helsinki, Finland.

J Alexandre (J)

Hôpitaux Universitaires Paris Centre, Hôpital Cochin, Services de Cancérologie et d'Oncologie Gynécologique, 27, rue du Faubourg-Saint-Jacques, 75014 Paris, France.

U Canzler (U)

Department of Gynecology and Obstetrics, TU Dresden, Dresden, Germany.

J Sehouli (J)

Charité Campus Virchow-Klinikum, Berlin, Germany.

J Herrstedt (J)

Odense University Hospital, Odense and Zealand University Hospital Roskilde, Denmark.

B Fiane (B)

Department of Gynecology and Gynecologic Oncology, Stavanger University Hospital, Stavanger, Norway.

M Merger (M)

Clinical Research, Boehringer Ingelheim Pharma, Biberach An der Riss, Germany.

A du Bois (A)

Department of Gynecology and Gynecologic Oncology, Kliniken Essen-Mitte, Evangelische Huyssens-Stiftung, Germany.

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Classifications MeSH