Blood test score may guide ovarian cancer treatment decisions
NCT ID NCT06660147
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at whether a score called KELIM can predict how well ovarian cancer patients respond to maintenance treatment with PARP inhibitors after initial chemotherapy. Researchers will analyze data from 243 patients who took part in the PAOLA-1 trial. If KELIM proves useful, it could help doctors personalize treatment and avoid giving strong medications to those unlikely to benefit.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If KELIM proves reliable, doctors could better match ovarian cancer patients to PARP inhibitor treatment, avoiding unnecessary side effects and focusing therapy on those most likely to benefit.
- What could go wrong
- This is a retrospective analysis of existing data, not a new treatment trial. The KELIM score may not prove accurate enough to change clinical practice, and results may not apply to all patient groups.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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243 people
The number who actually took part.
- Started
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Dec 2023
- Finished
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Jan 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
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.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Patients randomised in the PAOLA-1 study - Exclusion Criteria:Opposition to the use of your data for research purposes. \-
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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CHRU Besançon - Hôpital Jean Minjoz
Besançon, 25030, France
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CHU Grenoble-Alpes - Site Nord (La Tronche)
Grenoble, 38043, France
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CHU de Poitiers - Hôpital de la Milétrie
Poitiers, 86021, France
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Centre Azuréen de Cancérologie
Mougins, 06250, France
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Centre Eugène Marquis
Rennes, 35042, France
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Centre François Baclesse
Caen, 14076, France
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Centre Hospitalier Départemental de Vendée
La Roche-sur-Yon, 85925, France
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Centre Hospitalier Princesse Grace
Monaco, 98012, Monaco
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Centre Jean Perrin
Clermont-Ferrand, 63011, France
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Clinique Francheville
Périgueux, 24004, France
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Clinique Pasteur
Toulouse, 31300, France
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Groupe Hospitalier Diaconesses - Croix Saint-Simon
Paris, 75012, France
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Gustave Roussy
Villejuif, 94805, France
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HCL - Centre Hospitalier Lyon Sud
Pierre-Bénite, 69495, France
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Hôpital Cochin
Paris, 75014, France
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Hôpital Européen Georges Pompidou
Paris, 75015, France
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Hôpital Privé du Confluent
Nantes, France
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ICL - Centre Alexis Vautrin
Vandœuvre-lès-Nancy, 54519, France
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ICO - Centre René Gauducheau
Saint-Herblain, 44805, France
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ICO Paul Papin
Angers, 49055, France
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Institut Curie
Paris, 75248, France
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Oncopole Claudius Regaud - IUCT Oncopole
Toulouse, 31059, France
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Polyclinique Bordeaux Nord
Bordeaux, 33300, France
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Sainte-Catherine Institut du Cancer Avignon-Provence
Avignon, 84918, France
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Other studies related to the condition(s) this trial covers.
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