Evidence map›Paper›PMID 38129136›Full record

Trial reportInternational journal of gynecological cancer : official journal of the International Gynecological Cancer Society2024

Updated progression-free survival and final overall survival with maintenance olaparib plus bevacizumab according to clinical risk in patients with newly diagnosed advanced ovarian cancer in the phase III PAOLA-1/ENGOT-ov25 trial.

Domenica Lorusso, Marie-Ange Mouret-Reynier, Philipp Harter, Claire Cropet, Cristina Caballero, Pia Wolfrum-Ristau, Toyomi Satoh, Ignace Vergote, Gabriella Parma, Trine J Nøttrup and 20 more

2 registry-linked trialsOpen access · hybridAbstract readClinical Trial, Phase IIIRandomized Controlled Trial
In one paragraph

Trial report in International journal of gynecological cancer : official journal of the International Gynecological Cancer Society, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 46 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 4 pooled it
15.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02477644 phase3completednot on this map

Randomized, Double-Blind, Phase III Trial Olaparib vs. Placebo Patients With Advanced FIGO Stage IIIB-IV High Grade Serious or Endometrioid Ovarian, Fallopian Tube, or Peritoneal Cancer Treated Standard First-Line Treatment

TypeinterventionalSponsorArcagy ResearchRan2015 to 2022Enrolled806ConditionsOvarian CancerArmsOlaparib, Placebo
NCT06622798 recruitingnot on this map

A Retrospective Study Exploring the Correlation Between HRD Score and PARPi Efficacy Based on Chinese Ovarian Cancer Patients

TypeobservationalSponsorSun Yat-Sen Memorial Hospital of Sun Yat-Sen UniversityRan2024 to 2026Enrolled470ConditionsExploring the Correlation of HRD Score Pairs with the Prognosis of Chinese Ovarian Cancer Patients and the Outcome of Maintenance Therapy with PARPiArmsNon-interventional
3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 4 syntheses or guidelines pooled it, 56 citations in OpenAlex.

  1. Pooled it
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  9. [Update on ovarian cancer].Pathologie (Heidelberg, Germany) · 2026
    Review
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  14. Ovarian cancer.Nature reviews. Disease primers · 2026
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

30 authors at 20 institutions in 9 countries.

Domenica LorussoIstituto Tumori Milano + Fondazione Policlinico Universitario A Gemelli IRCCS, Rome, Italy kettalorusso@libero.it.ORCID 0000-0003-0981-0598
Marie-Ange Mouret-ReynierDepartment of Medical Oncology, Centre Jean Perrin, Clermont Ferrand, France.
Philipp HarterDepartment of Gynaecology & Gynaecologic Oncology, Ev. Kliniken Essen-Mitte, Essen, Germany.ORCID 0000-0002-9663-5005
Claire CropetDepartment of Biostatistics, Centre Léon Bérard, Lyon, France.
Cristina CaballeroServicio de Oncología Médica, Hospital General Universitario de Valencia, Valencia, Spain.
Pia Wolfrum-RistauDepartment of Obstetrics and Gynecology, Paracelsus Medical University Salzburg, Salzburg, Austria.
Toyomi SatohDepartment of Obstetrics and Gynecology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan.ORCID 0000-0002-6929-5463
Ignace VergoteDepartment of Obstetrics and Gynaecology, University Hospital Leuven, Leuven Cancer Institute, Leuven, Belgium, European Union.
Gabriella ParmaGynecologic Oncology Program, European Institute of Oncology IRCCS, Milan, Italy.
Trine J NøttrupDepartment of Oncology, Copenhagen University Hospital - Rigshospitalet, Copenhagen, Denmark.
Coriolan LebretonGroupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens, (GINECO), France.ORCID 0000-0002-4275-1721
Peter A FaschingArbeitsgemeinschaft Gynäkologische Onkologie Studiengruppe, (AGO), Germany.
Carmela PisanoMulticenter Italian Trials in Ovarian Cancer and Gynecologic Malignancies, (MITO), Italy.
Luis MansoGrupo Español de Investigación en Cáncer de Ovario, (GEICO), Spain.
Hugues BourgeoisGroupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens, (GINECO), France.
Ingo RunnebaumArbeitsgemeinschaft Gynäkologische Onkologie Studiengruppe, (AGO), Germany.
Claudio ZamagniMulticenter Italian Trials in Ovarian Cancer and Gynecologic Malignancies, (MITO), Italy.
Anne-Claire Hardy-BessardGroupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens, (GINECO), France.
Andreas SchnelzerArbeitsgemeinschaft Gynäkologische Onkologie Studiengruppe, (AGO), Germany.
Michel FabbroGroupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens, (GINECO), France.
Barbara SchmalfeldtArbeitsgemeinschaft Gynäkologische Onkologie Studiengruppe, (AGO), Germany.
Dominique BertonGroupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens, (GINECO), France.
Antje BelauArbeitsgemeinschaft Gynäkologische Onkologie Studiengruppe, (AGO), Germany.
Jean-Pierre LotzGroupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens, (GINECO), France.
Martina Gropp-MeierArbeitsgemeinschaft Gynäkologische Onkologie Studiengruppe, (AGO), Germany.
Laurence GladieffGroupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens, (GINECO), France.
Hans-Joachim LückArbeitsgemeinschaft Gynäkologische Onkologie Studiengruppe, (AGO), Germany.
Sophie Abadie-LacourtoisieGroupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens, (GINECO), France.
Eric Pujade-LauraineGroupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens, (GINECO), France.
Isabelle Ray-CoquardGroupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens, (GINECO), France.ORCID 0000-0003-2472-8306
Arbeitsgemeinschaft Gynäkologische Onkologie Studiengruppe · DECentre Léon Bérard · FRInstitut de Cancérologie de l'Ouest · FRArcagy Gineco · FRAzienda USL di Bologna · ITCentre Jean Bernard · FRCentre Jean Perrin · FRCopenhagen University Hospital · DKEuropean Union · BEFondation pour la Recherche Médicale · FRGynecologic Oncology Group · USHospital General Universitario De Valencia · ESInstitut Bergonié · FRInstitut Claudius Regaud · FRInstitut de Recherche en Cancérologie de Montpellier · FRItalian Association for Cancer Research · ITParacelsus Medical University · ATResearch Institute Hospital 12 de Octubre · ESSorbonne Université · FRTUM Klinikum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveIn the PAOLA-1/ENGOT-ov25 trial (NCT02477644), adding maintenance olaparib to bevacizumab provided a substantial progression-free survival benefit in patients with newly diagnosed advanced ovarian cancer and homologous recombination deficiency (HRD)-positive tumors, irrespective of clinical risk. Subsequently, a clinically meaningful improvement in overall survival was reported with olaparib plus bevacizumab in the HRD-positive subgroup. We report updated progression-free survival and overall survival by clinical risk and HRD status.

methodsPatients in clinical response after first-line platinum-based chemotherapy plus bevacizumab received maintenance olaparib (up to 24 months) plus bevacizumab (up to 15 months in total) or placebo plus bevacizumab. This

resultsOf 806 randomized patients, 74% were higher-risk and 26% were lower-risk. In higher-risk HRD-positive patients, the hazard ratio (HR) for progression-free survival was 0.46 (95% confidence interval (95% CI) 0.34 to 0.61), with 5-year progression-free survival of 35% with olaparib plus bevacizumab versus 15% with bevacizumab alone; and the HR for overall survival was 0.70 (95% CI 0.50 to 1.00), with 5-year overall survival of 55% versus 42%, respectively. In lower-risk HRD-positive patients, the HR for progression-free survival was 0.26 (95% CI 0.15 to 0.45), with 5-year progression-free survival of 72% with olaparib plus bevacizumab versus 28% with bevacizumab alone; and the HR for overall survival was 0.31 (95% CI 0.14 to 0.66), with 5-year overall survival of 88% versus 61%, respectively. No benefit was seen in HRD-negative patients regardless of clinical risk.

conclusionThis

Indexed as

Ovarian NeoplasmsPiperazinesBevacizumabCarcinoma, Ovarian EpithelialFemaleHumansPhthalazinesProgression-Free SurvivalBevacizumabolaparibPhthalazinesPiperazinesOvarian Cancer

Identifiers

PMID38129136
PMCPMC10982633
OpenAlexW4390078374

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.