Optimal Treatment Duration of Bevacizumab as Front-Line Therapy for Advanced Ovarian Cancer: AGO-OVAR 17 BOOST/GINECO OV118/ENGOT Ov-15 Open-Label Randomized Phase III Trial.


Journal

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
01 02 2023
Historique:
pubmed: 5 11 2022
medline: 1 2 2023
entrez: 4 11 2022
Statut: ppublish

Résumé

To compare standard versus extended duration of bevacizumab treatment in combination with front-line chemotherapy in women with newly diagnosed stage IIB-IV ovarian cancer. In this multicenter, open-label, randomized phase III trial (ClinicalTrials.gov identifier: NCT01462890), patients with newly diagnosed International Federation of Gynecology and Obstetrics stage IIB-IV epithelial ovarian, fallopian tube, or peritoneal cancer underwent primary cytoreductive surgery followed by six cycles of chemotherapy (paclitaxel 175 mg/m Between November 11, 2011, and August 6, 2013, 927 women were randomly assigned. There was no difference in PFS between treatment arms (hazard ratio, 0.99; 95% CI, 0.85 to 1.15; unstratified log-rank Longer treatment duration with bevacizumab for up to 30 months did not improve PFS or OS in patients with primary epithelial ovarian, fallopian tube, or peritoneal cancer. A bevacizumab treatment duration of 15 months remains the standard of care.

Identifiants

pubmed: 36332161
doi: 10.1200/JCO.22.01010
doi:

Substances chimiques

Bevacizumab 2S9ZZM9Q9V
Carboplatin BG3F62OND5
Paclitaxel P88XT4IS4D

Banques de données

ClinicalTrials.gov
['NCT01462890']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

893-902

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Auteurs

Jacobus Pfisterer (J)

Arbeitsgemeinschaft Gynaekologische Onkologie (AGO) Study Group and Gynecologic Oncology Center, Kiel, Germany.

Florence Joly (F)

Groupe d'Investigateurs National des Etudes des Cancers Ovariens et du sein (GINECO) and Centre François Baclesse, University Caen Normandie, Caen, France.

Gunnar Kristensen (G)

Nordic Society of Gynaecological Oncology (NSGO) and Oslo University Hospital, Oslo, Norway.

Joern Rau (J)

AGO Study Group and Coordinating Center for Clinical Trials, Philipps-University Marburg, Marburg, Germany.

Sven Mahner (S)

AGO Study Group and University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
Department of Obstetrics and Gynecology, University Hospital LMU Munich, Munich, Germany.

Patricia Pautier (P)

GINECO and Gustave Roussy Cancer Center, Villejuif, France.

Ahmed El-Balat (A)

AGO Study Group and University Hospital Frankfurt, Frankfurt, Germany.
Spital Uster, Uster, Switzerland.

Jean-Emmanuel Kurtz (JE)

GINECO and Institut de Cancérologie Strasbourg Europe, Strasbourg, France.

Ulrich Canzler (U)

AGO Study Group and University Hospital Carl Gustav Carus, Technische Universität Dresden and National Center for Tumor Diseases (NCT), Partner Site Dresden, Dresden, Germany.

Jalid Sehouli (J)

AGO Study Group and Charité-Universitätsmedizin Berlin, Campus Virchow Klinikum, Berlin, Germany.

Martin L Heubner (ML)

AGO Study Group and University Hospital Essen, Essen, Germany.
Cantonal Hospital Baden AG, Baden, Switzerland.

Andreas D Hartkopf (AD)

AGO Study Group and University Hospital Tübingen, Tübingen, Germany.
University Hospital Ulm, Ulm, Germany.

Klaus Baumann (K)

AGO Study Group and University Hospital Gießen and Marburg, Site Marburg, Marburg, Germany.
Hospital Ludwigshafen, Ludwigshafen, Germany.

Annette Hasenburg (A)

AGO Study Group and University Hospital Freiburg, Freiburg, Germany.
University Medical Center Mainz, Mainz, Germany.

Lars C Hanker (LC)

AGO Study Group and University Hospital Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.

Antje Belau (A)

AGO Study Group and University Hospital Greifswald, Greifswald, Germany.
Frauenarztpraxis Dr. Belau, Greifswald, Germany.

Barbara Schmalfeldt (B)

AGO Study Group and Hospital Rechts der Isar, Technical University Munich, Munich, Germany.
University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

Dominik Denschlag (D)

AGO Study Group and Hochtaunus-Kliniken, Hospital Bad Homburg, Bad Homburg, Germany.

Tjoung-Won Park-Simon (TW)

AGO Study Group and Hannover Medical School, Hannover, Germany.

Frédéric Selle (F)

GINECO and Groupe Hospitalier Diaconesses Croix Saint-Simon, Paris, France.

Christian Jackisch (C)

AGO Study Group and Sana Hospital Offenbach, Offenbach, Germany.

Alexander Burges (A)

Department of Obstetrics and Gynecology, University Hospital LMU Munich, Munich, Germany.

Hans-Joachim Lück (HJ)

AGO Study Group and Gynäkologisch-Onkologische Praxis Hannover, Hannover, Germany.

Günter Emons (G)

AGO Study Group and University Medical Center Göttingen, Göttingen, Germany.

Werner Meier (W)

AGO Study Group and Evangelisches Krankenhaus Düsseldorf, Düsseldorf, Germany.
University Hospital Düsseldorf, Düsseldorf, Germany.

Martina Gropp-Meier (M)

AGO Study Group and Onkologie Ravensburg, Ravensburg, Germany.

Willibald Schröder (W)

AGO Study Group and GYNAEKOLOGICUM Bremen, Bremen, Germany.

Nikolaus de Gregorio (N)

AGO Study Group and University Hospital Ulm, Ulm, Germany.
SLK-Kliniken Heilbronn, Klinikum am Gesundbrunnen, Heilbronn, Germany.

Felix Hilpert (F)

AGO Study Group and University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Krankenhaus Jerusalem, Mammazentrum Hamburg, Hamburg, Germany.

Philipp Harter (P)

AGO Study Group and Evangelische Kliniken Essen-Mitte, Essen, Germany.

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Classifications MeSH