ClinicalTrials.gg
CompletedNCT06660147KELI-PAOLAUpdated Jun 23, 2026

Validation of KELIM as a Predictive/Prognostic Factor for Maintenance Treatment With iPARP in First-Line Ovarian Cancer

An observational study in Ovarian Cancer, sponsored by ARCAGY/ GINECO GROUP. Completed at 24 sites in 2 countries. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-06-23.

Sponsored by ARCAGY/ GINECO GROUP · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
243
Ages
18 Years and older
Sex
Female
01

Study summary

This study aims to understand whether it is possible to predict the effectiveness of maintenance treatment with PARP inhibitors following first-line chemotherapy in ovarian cancer, and thus better target the patients who benefit from this treatment

02

Conditions studied

  • Ovarian Cancer

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Keywords

  • parp inhibitor
  • kelim
  • maintenance treatment
03

In context

Ovarian Neoplasms

3,381 studies on the registry are indexed under Ovarian Neoplasms; 790 are open to participants now.

This study's enrollment of 243 is above the median of 200 across 616 observational studies indexed under Ovarian Neoplasms.

Browse Ovarian Neoplasms studies →

Lead sponsor

ARCAGY/ GINECO GROUP is the lead sponsor of 51 studies on the registry; 6 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patients randomised in the PAOLA-1 study :

Patients with advanced FIGO stage IIIB-IV high grade serous or endometrioid ovarian, fallopian tube, or peritoneal cancer treated with standard first line treatment combining platinum based chemotherapy plus bevacizumab followed by a maintenance treatment by bevacizumab and Olaparib or placebo.

Eligibility criteria

Inclusion Criteria: Patients randomised in the PAOLA-1 study -

Exclusion Criteria:Opposition to the use of your data for research purposes.

-

05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
243 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. predictive and prognostic value of the KELIM score

    To evaluate the predictive and prognostic value of the KELIM score in patients receiving maintenance treatment with a PARP inhibitor as part of the PAOLA-1 clinical trial.

    Time frame: 18 months

07

Study locations

24 sites
  • ICO Paul Papin
    Angers, 49055, France
  • Sainte-Catherine Institut du Cancer Avignon-Provence
    Avignon, 84918, France
  • CHRU Besançon - Hôpital Jean Minjoz
    Besançon, 25030, France
  • Polyclinique Bordeaux Nord
    Bordeaux, 33300, France
  • Centre François Baclesse
    Caen, 14076, France
  • Centre Jean Perrin
    Clermont-Ferrand, 63011, France
  • CHU Grenoble-Alpes - Site Nord (La Tronche)
    Grenoble, 38043, France
  • Centre Hospitalier Départemental de Vendée
    La Roche-sur-Yon, 85925, France
  • Centre Azuréen de Cancérologie
    Mougins, 06250, France
  • Hôpital Privé du Confluent
    Nantes, France
  • Groupe Hospitalier Diaconesses - Croix Saint-Simon
    Paris, 75012, France
  • Hôpital Cochin
    Paris, 75014, France
  • Hôpital Européen Georges Pompidou
    Paris, 75015, France
  • Institut Curie
    Paris, 75248, France
  • Clinique Francheville
    Périgueux, 24004, France
  • HCL - Centre Hospitalier Lyon Sud
    Pierre-Bénite, 69495, France
  • CHU de Poitiers - Hôpital de la Milétrie
    Poitiers, 86021, France
  • Centre Eugène Marquis
    Rennes, 35042, France
  • ICO - Centre René Gauducheau
    Saint-Herblain, 44805, France
  • Oncopole Claudius Regaud - IUCT Oncopole
    Toulouse, 31059, France
  • Clinique Pasteur
    Toulouse, 31300, France
  • ICL - Centre Alexis Vautrin
    Vandœuvre-lès-Nancy, 54519, France
  • Gustave Roussy
    Villejuif, 94805, France
  • Centre Hospitalier Princesse Grace
    Monaco, 98012, Monaco
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Dec 2023 to primary completion in Jan 2025, 13 months.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 14, 2024
First posted
Oct 28, 2024
StartActual
Dec 11, 2023
Primary completionActual
Jan 21, 2025
CompletionActual
Jan 21, 2025
Last update
Jun 23, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06660147
Lead sponsor
ARCAGY/ GINECO GROUP
Responsible party
Sponsor
First posted
Oct 28, 2024
Start date
Dec 11, 2023
Primary completion
Jan 21, 2025
Completion
Jan 21, 2025
Last update
Jun 23, 2026
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jun 2026. You cannot join it, but the record below documents what was studied.

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