Epithelial Ovarian CancerGREATNCT04027868
Genomic BRCA and Extensive ovArian Cancer Testing
An observational study of Epithelial Ovarian Cancer and Peritoneal Cancer, run by ARCAGY/ GINECO GROUP at 137 sites in France.
Trial summary
This is a prospective observational French multicenter cohort in patients with ovarian and/or primitive peritoneal and/or fallopian tubes carcinoma, histologically confirmed, with an advanced stage at diagnosis (stage III to IV FIGO 2014). Read more about this study
- Who is it for?
- Ages 18 years and older, women only
- Conditions the study is for
- Epithelial Ovarian Cancer, Peritoneal Cancer, Fallopian Tube Cancer
- How many people
- 1,500 participants
- Where
- 137 sitesFrance
- Study dates
- 6 Dec 2019to 7 Nov 2022
- How long will I take part?
- 10 Years
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- Women only
- No healthy volunteers
- Adult, Older adult
Study population: Patients with ovarian and/or primitive peritoneal and/or fallopian tubes carcinoma, histologically confirmed, with an advanced stage at diagnosis (stage III to IV FIGO 2014)
Who may be able to join
- Patient older than 18 years.
- Patient with ovarian and/or primitive peritoneal and/or fallopian tubes carcinoma, histologically confirmed, with an advanced stage at diagnosis (stage III to IV FIGO 2014)
- Patient in first line therapy
- Available tumor sample fixed in formalin and included in paraffin (FFPE):
- in pre-chemotherapy, insofar as possible
- having a sufficient tumor surface, with a final cellularity of at least 20%
Show all 9Show fewer
- Identification of a molecular genetics' cancer platform participant in GREAT and an onco-geneticists team working with the investigator team
- Patient consenting her data to be collected and submitted through an automated processing
- Patient beneficiary from the French social security
Who cannot join
- Patient with a mucinous ovarian carcinoma
- Patient pregnant or breastfeeding
- Patient under legal protection (guardianship or court order) or unable to consent
Trial locations and contacts
137 sites in 1 country.
137 sites in 1 country
France137 sites
Centre de Radiothérapie et d'Oncologie de Moyenne Garonne (CROMG)
Agen, 47000
Hôpital Privé d'Aix en Provence
Aix-en-Provence, 13080
Centre Hospitalier Général d'Aix-en-Provence
Aix-en-Provence
CHU Amiens
Amiens
Clinique Victor PAUCHET
Amiens
Institut de Cancérologie de l'Ouest - ICO
Angers
Hôpital Privé d'Antony - Ramsay Santé
Antony, 92160
CH Arras
Arras
CH Auxerre
Auxerre
Institut Sainte Catherine
Avignon
Clinique Belharra
Bayonne, 64100
CH Côte Basque
Bayonne
Centre Hospitalier de Beauvais
Beauvais, 60021
CHRU Jean Minjoz
Besançon
Reims Icone
Bezannes, 51100
CH de Blois
Blois
Hôpital Avicenne
Bobigny, 93009
CHU de Bordeaux - Hôpital Pellegrin
Bordeaux
Clinique Tivoli
Bordeaux
Institut Bergonié
Bordeaux
Polyclinique Bordeaux Nord
Bordeaux
Centre Hospitalier Fleyriat - BOURG-EN-BRESSE
Bourg-en-Bresse
CHU Brest
Brest
Hôpital Femme Mère Enfant
Bron, 89500
Centre François Baclesse
Caen
Centre Maurice Tubiana
Caen
CH de Cahors
Cahors
CH Carcassonne
Carcassonne
Hôpital Général de Castres
Castres
Medipole de Savoie
Challes-les-Eaux
CH Chalon sur Saone
Chalon-sur-Saône
CH Metropole Savoie
Chambéry
Centre d'Oncologie et de Radiothérapie 37
Chambray-lès-Tours
Centre Hospitalier de Chateauroux
Châteauroux, 36000
CHPC - Hôpital Louis Pasteur
Cherbourg
CH Cholet
Cholet
Hôpital Antoine Béclère
Clamart
Centre Jean Perrin
Clermont-Ferrand
CH Alpes Léman
Contamine-sur-Arve
Centre Hospitalier Sud Francilien (Site Gilles de Corbeil)
Corbeil-Essonnes, 91106
Clinique des Cèdres
Cornebarrieu, 31700
Clinique de Flandre
Coudekerque-Branche
Groupe Hospitalier public du Sud de l'Oise (GHPSO)
Creil
CHI Creteil
Créteil
Centre Georges François Leclerc
Dijon
CHU Dijon
Dijon
Institut de Cancérologie de Bourgogne - GRReCC
Dijon
Clinique du Mousseau (CMCO) - Ramsay Santé
Évry, 91000
Centre Hospitalier Intercommunal de Fréjus Saint Raphael
Fréjus, 83600
GH Mutualiste de Grenoble
Grenoble
Hôpital Privé Drôme Ardèche - Clinique Pasteur
Guilherand-Granges, 07500
Centre Hospitalier Marne-la-Vallée
Jossigny
Centre Hospitalier Départemental de Vendée
La Roche-sur-Yon, 85925
CHU Grenoble Alpes - Site Nord (La Tronche)
La Tronche
Hôpital André Mignot
Le Chesnay
Les Hôpitaux de Chartres
Le Coudray
Hôpital Privé de l'Estuaire
Le Havre, 76600
CHU Bicêtre
Le Kremlin-Bicêtre
Centre Hospitalier du Mans
Le Mans
CH de Lens
Lens
Institut Hospitalier Franco-Britannique
Levallois-Perret
Polyclinique de Limoges - Clinique Chenieux
Limoges, 87039
CHU de Limoges - Hôpital Dupuytren
Limoges, 87042
Groupe Hospitalier Bretagne Sud - Hôpital du Scorff
Lorient
HCL - Hôpital de la Croix Rousse
Lyon, 60004
Clinique de l'infirmerie Protestante
Lyon, 69300
Centre Léon Bérard
Lyon
Clinique de la Sauvegarde
Lyon
Hôpital Privé Jean Mermoz
Lyon
APHM - Hôpital de la Timone
Marseille
Hôpital Nord
Marseille
Institut Paoli Calmettes
Marseille
Centre Hospitalier Layné
Mont-de-Marsan, 40024
Hôpital Nord Franche Comté
Montbéliard
CH de Montelimar
Montélimar
Centre de Cancérologe du Grand Montpellier
Montpellier
CHRU de Montpellier - Hôpital Saint-Eloi
Montpellier
ICM - Val d'Aurelle
Montpellier
Centre Azuréen de Cancérologie
Mougins, 06250
Oracle - Centre d'Oncologie de Gentilly
Nancy
Hôpital Privé du Confluent
Nantes
Clinique Hartmann
Neuilly-sur-Seine
Centre Antoine Lacassagne
Nice, 06000
Institut de Cancérologie du Gard - ONCOGARD
Nîmes, 30029
Institut de Cancérologie du Gard
Nîmes
CHR Orléans
Orléans
Hôpital de la Pitié Salpétrière
Paris, 75000
GH Saint Joseph
Paris
Groupe Hospitalier Diaconesses - Croix Saint-Simon
Paris
HEGP
Paris
Hôpital Bichat
Paris
Hôpital Cochin
Paris
Hôpital Lariboisière
Paris
Institut Curie
Paris
Institut Mutualiste Montsouris
Paris
CH Pau
Pau
Clinique Francheville
Périgueux
Centre Catalan d'Oncologie
Perpignan
CH Perpignan
Perpignan
HCL - Centre Hospitalier Lyon Sud
Pierre-Bénite, 69006
Centre CARIO-HPCA
Plérin
Hôpital de la Milétrie
Poitiers
CH René Dubos
Pontoise
CH Annecy Genevois
Pringy
Clinique de la Croix du Sud
Quint-Fonsegrives
Centre Eugène Marquis
Rennes
Hôpitaux Drôme Nord - Centre Hospitalier Romans
Romans-sur-Isère, 26100
Centre Henri Becquerel
Rouen, 76000
Clinique Mathilde
Rouen, 76100
Centre Frédéric Joliot
Rouen
Centre Hospitalier Yves Le Foll
Saint-Brieuc
Institut Curie - Site Saint Cloud
Saint-Cloud, 92210
Hôpital Privé de La Loire Saint-Etienne
Saint-Etienne, 42100
Centre Hospitalier Privé Saint Grégoire
Saint-Grégoire
Institut de Cancérologie de l'Ouest - ICO
Saint-Herblain
HIA Begin
Saint-Mandé
Clinique Mutualiste de l'Estuaire
Saint-Nazaire
CHU Saint-Etienne - Pôle de Cancérologie
Saint-Priest-en-Jarez
Centre Médicale Sainte Feyre Alfred Leune
Sainte-Feyre, 23000
Clinique Charcot
Sainte-Foy-lès-Lyon
Institut de Cancérologie Paris Nord
Sarcelles
CH Sens
Sens
CH Broussais
St-Malo
ICANS - Institut de cancérologie Strasbourg Europe
Strasbourg, 67037
Hôpital Foch
Suresnes
CHR Metz-Thionville / Hôpital de Mercy
Thionville, 45001
Hôpitaux du Léman
Thonon-les-Bains
Hôpital d'Instruction des Armées Saint-Anne
Toulon, 83800
Clinique Pasteur - Groupe Oncorad Garonne
Toulouse
Clinique Pasteur - Oncosud
Toulouse
Institut Claudius Regaud
Toulouse
CHU Bretonneau
Tours
Centre Hospitalier de Troyes
Troyes
CH Jean Bernard
Valenciennes
Clinique des Dentellières
Valenciennes
Institut de Cancérologie de Lorraine (ICL) - Centre Alexis Vautrin
Vandœuvre-lès-Nancy
Gustave Roussy
Villejuif
About this study
Official title: Cohort Study to Evaluate the Clinical Features of Patients With Epithelial Ovarian Cancer Depending on Tumoral Mutation of BRCA or Beyond BRCA Genomic Molecular Abnormalities
This is a prospective observational French multicenter cohort in patients with ovarian and/or primitive peritoneal and/or fallopian tubes carcinoma, histologically confirmed, with an advanced stage at diagnosis (stage III to IV FIGO 2014). The objective is to constitute a clinico-biological database that allows to correlate clinical and progressive features of ovarian cancer patients based on tumor genomics and molecular detected abnormalities.
Read the detailed description
This is a prospective observational French multicenter cohort in patients with ovarian and/or primitive peritoneal and/or fallopian tubes carcinoma, histologically confirmed, with an advanced stage at diagnosis (stage III to IV FIGO 2014). The objective is to constitute a clinico-biological database that allows to correlate clinical and progressive features of ovarian cancer patients based on tumor genomics and molecular detected abnormalities.
- Medical subject headings
- Carcinoma, Ovarian Epithelial, Fallopian Tube Neoplasms
What is being measured
The primary outcome is the main question the study is designed to answer.
Correlation between Progression Free Survival (PFS) and the detected tumor genetic abnormalities
Measured: From baseline until the date of progression or death, which ever occurs earlier, assessed up to 10 years
Secondary outcomes (6)
Correlation between age and the detected tumor genetic abnormalities
Measured: Baseline
Correlation between histology status and the detected tumor genetic abnormalities
Measured: Baseline
Correlation between FIGO stage and the detected tumor genetic abnormalities
Measured: Baseline
Correlation between surgery resection status and the detected tumor genetic abnormalities
Measured: Up to 10 years
Correlation between treatment response and the detected tumor genetic abnormalities
Measured: Up to 10 years
Correlation between Overall survival (OS) and the detected tumor genetic abnormalities
Measured: From baseline to death, assessed up to 10 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted22 Jul 2019
- Study start6 Dec 2019
- Primary completion7 Nov 2022
- Study completion7 Nov 2022
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Epithelial Ovarian CancerStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 1,500 participants (actual)
- Target duration
- 10 Years
Sponsor and investigators
- Lead sponsor
- ARCAGY/ GINECO GROUP
- Sponsor type
- University, hospital or other
- Collaborators
- AstraZeneca
- Responsible party
- Sponsor
- Investigators
- Thibault De La Motte Rouge, MD., Principal investigator, Centre Eugène Marquis, Rennes
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04027868
- Sponsor's protocol ID
- GINECO-OV128
- Other IDs
- 2019-A01190-57, 19.06.45
- Acronym
- GREAT
- Status last verified
- Jun 2026
- First submitted
- 18 Jul 2019
- Last updated
- 8 Jun 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 8 Jun 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Cohort Study to Evaluate the Clinical Features of Patients With Epithelial Ovarian Cancer Depending on Tumoral Mutation of BRCA or Beyond BRCA Genomic Molecular Abnormalities
- ClinicalTrials.gov ID
- NCT04027868
- Acronym / sponsor ID
- GREAT / GINECO-OV128
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 1,500 participants (actual)
- Lead sponsor
- ARCAGY/ GINECO GROUPUniversity, hospital or other
- Collaborators
- AstraZeneca
- Study start
- 6 Dec 2019 (actual)
- Primary completion
- 7 Nov 2022 (actual)
- Study completion
- 7 Nov 2022 (actual)
- First posted
- 22 Jul 2019 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is a prospective observational French multicenter cohort in patients with ovarian and/or primitive peritoneal and/or fallopian tubes carcinoma, histologically confirmed, with an advanced stage at diagnosis (stage III to IV FIGO 2014). The objective is to constitute a clinico-biological database that allows to correlate clinical and progressive features of ovarian cancer patients based on tumor genomics and molecular detected abnormalities.
Detailed description
This is a prospective observational French multicenter cohort in patients with ovarian and/or primitive peritoneal and/or fallopian tubes carcinoma, histologically confirmed, with an advanced stage at diagnosis (stage III to IV FIGO 2014). The objective is to constitute a clinico-biological database that allows to correlate clinical and progressive features of ovarian cancer patients based on tumor genomics and molecular detected abnormalities.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 10 Years
Who may qualify
- Ages
- 18 years and older
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients with ovarian and/or primitive peritoneal and/or fallopian tubes carcinoma, histologically confirmed, with an advanced stage at diagnosis (stage III to IV FIGO 2014)
Key inclusion criteria (9 listed)
- Patient older than 18 years.
- Patient with ovarian and/or primitive peritoneal and/or fallopian tubes carcinoma, histologically confirmed, with an advanced stage at diagnosis (stage III to IV FIGO 2014)
- Patient in first line therapy
- Available tumor sample fixed in formalin and included in paraffin (FFPE):
- Identification of a molecular genetics' cancer platform participant in GREAT and an onco-geneticists team working with the investigator team
Key exclusion criteria (3 listed)
- Patient with a mucinous ovarian carcinoma
- Patient pregnant or breastfeeding
- Patient under legal protection (guardianship or court order) or unable to consent
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Correlation between Progression Free Survival (PFS) and the detected tumor genetic abnormalities
Time frame: From baseline until the date of progression or death, which ever occurs earlier, assessed up to 10 years
6 secondary outcomes
Correlation between age and the detected tumor genetic abnormalities
Time frame: Baseline
Correlation between histology status and the detected tumor genetic abnormalities
Time frame: Baseline
Correlation between FIGO stage and the detected tumor genetic abnormalities
Time frame: Baseline
Correlation between surgery resection status and the detected tumor genetic abnormalities
Time frame: Up to 10 years
Correlation between treatment response and the detected tumor genetic abnormalities
Time frame: Up to 10 years
Correlation between Overall survival (OS) and the detected tumor genetic abnormalities
Time frame: From baseline to death, assessed up to 10 years
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 8 Jun 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Thibault De La Motte Rouge, MD. principal investigator
Centre Eugène Marquis, Rennes
137 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Epithelial Ovarian Cancer and Peritoneal Cancer, run by ARCAGY/ GINECO GROUP at 137 sites in France.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 9 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 8 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 137 sites in France. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Correlation between Progression Free Survival (PFS) and the detected tumor genetic abnormalities (time frame: From baseline until the date of progression or death, which ever occurs earlier, assessed up to 10 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Jun 2026; AzTrials last refreshed its copy on 4 Nov 2026.