Evidence map›Paper›PMID 38118421›Full record

ArticleCell reports. Medicine2023

GIInger predicts homologous recombination deficiency and patient response to PARPi treatment from shallow genomic profiles.

Christian Pozzorini, Gregoire Andre, Tommaso Coletta, Adrien Buisson, Jonathan Bieler, Loïc Ferrer, Rieke Kempfer, Pierre Saintigny, Alexandre Harlé, Davide Vacirca and 26 more

Abstract read
In one paragraph

Article in Cell reports. Medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Impact of Tumor Genomic Profile on Adjuvant Chemotherapy Efficacy in Resected Pancreatic Adenocarcinoma: Results From the PRODIGE-24/CCTG PA6 Study.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
    Article
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  4. Review
  5. Article
  6. The future of mathematical oncology in the age of AI.NPJ systems biology and applications · 2026
    Review
  7. Article
  8. Review
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  10. Combination ofFrontiers in oncology · 2025
    Article
  11. Review
  12. Review
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

36 authors.

Christian PozzoriniSOPHiA GENETICS, La Piéce 12, 1180 Rolle, Switzerland.
Gregoire AndreSOPHiA GENETICS, La Piéce 12, 1180 Rolle, Switzerland.
Tommaso ColettaSOPHiA GENETICS, La Piéce 12, 1180 Rolle, Switzerland.
Adrien BuissonDepartment of Medical Oncology, Centre Léon Bérard, Lyon, France.
Jonathan BielerSOPHiA GENETICS, La Piéce 12, 1180 Rolle, Switzerland.
Loïc FerrerSOPHiA GENETICS, La Piéce 12, 1180 Rolle, Switzerland.
Rieke KempferSOPHiA GENETICS, La Piéce 12, 1180 Rolle, Switzerland.
Pierre SaintignyDepartment of Medical Oncology, Centre Léon Bérard, Lyon, France; University of Lyon, Université Claude Bernard Lyon 1, INSERM 1052, CNRS 5286, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Alexandre HarléInstitut de Cancérologie de Lorraine, Service de Biopathologie, CNRS UMR 7039 CRAN, Vandoeuvre-lès-Nancy, France.
Davide VacircaEuropean Institute of Oncology, Milan, Italy.
Massimo BarberisEuropean Institute of Oncology, Milan, Italy.
Pauline GilsonInstitut de Cancérologie de Lorraine, Service de Biopathologie, CNRS UMR 7039 CRAN, Vandoeuvre-lès-Nancy, France.
Cristin RomaIstituto Nazionale Tumori-IRCCS-Fondazione G. Pascale, Naples, Italy.
Alexandra SaittaSOPHiA GENETICS, La Piéce 12, 1180 Rolle, Switzerland.
Ewan SmithSOPHiA GENETICS, La Piéce 12, 1180 Rolle, Switzerland.
Floriane Consales BarrasSOPHiA GENETICS, La Piéce 12, 1180 Rolle, Switzerland.
Lucia RipolSOPHiA GENETICS, La Piéce 12, 1180 Rolle, Switzerland.
Martin FritzscheSOPHiA GENETICS, La Piéce 12, 1180 Rolle, Switzerland.
Ana Claudia MarquesSOPHiA GENETICS, La Piéce 12, 1180 Rolle, Switzerland.
Amjad AlkodsiSOPHiA GENETICS, La Piéce 12, 1180 Rolle, Switzerland.
Ray MarinSOPHiA GENETICS, La Piéce 12, 1180 Rolle, Switzerland.
Nicola NormannoIstituto Nazionale Tumori-IRCCS-Fondazione G. Pascale, Naples, Italy.
Christoph GrimmMedical University of Vienna, Vienna, Austria.
Leonhard MüllauerMedical University of Vienna, Vienna, Austria.
Philipp HarterKliniken Essen Mitte, Essen, Germany.
Sandro PignataIstituto Nazionale Tumori IRCCS Fondazione G. Pascale, and Multicenter Italian Trials in Ovarian Cancer and Gynecologic Malignancies (MITO), Naples, Italy.
Antonio Gonzalez-MartinCancer Center Clinica Universidad de Navarra, Madrid, Spain; GEICO, Madrid, Spain; Program In Solid Tumors, CIMA, Pamplona, Spain.
Ursula DenisonDepartment for Gynaecology and Obstetrics, Klinik Hietzing, Vienna, Austria.
Keiichi FujiwaraSaitama Medical University International Medical Center, Saitama, Japan.
Ignace VergoteUniversity Hospital Leuven, Leuven Cancer Institute, Leuven, Belgium.
Nicoletta ColomboEuropean Institute of Oncology, Milan, Italy.
Adrian WilligSOPHiA GENETICS, La Piéce 12, 1180 Rolle, Switzerland.
Eric Pujade-LauraineAssociation de Recherche Cancers Gynécologiques (ARCAGY), Paris, France.
Pierre-Alexandre JustService de Pathologie, APHM (Assistance Publique - Hôpitaux de Marseille), Marseille, Provence-Alpes-Côte d'Azur, France.
Isabelle Ray-CoquardCentre Léon BERARD, and University Claude Bernard Lyon I, Lyon, France; Groupe d'Investigateurs Nationaux pour l'Etude des Cancers Ovariens (GINECO), Lyon, France.
Zhenyu XuSOPHiA GENETICS, La Piéce 12, 1180 Rolle, Switzerland. Electronic address: zxu@sophiagenetics.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Homologous recombination deficiency (HRD) is a predictive biomarker for poly(ADP-ribose) polymerase 1 inhibitor (PARPi) sensitivity. Routine HRD testing relies on identifying BRCA mutations, but additional HRD-positive patients can be identified by measuring genomic instability (GI), a consequence of HRD. However, the cost and complexity of available solutions hamper GI testing. We introduce a deep learning framework, GIInger, that identifies GI from HRD-induced scarring observed in low-pass whole-genome sequencing data. GIInger seamlessly integrates into standard BRCA testing workflows and yields reproducible results concordant with a reference method in a multisite study of 327 ovarian cancer samples. Applied to a BRCA wild-type enriched subgroup of 195 PAOLA-1 clinical trial patients, GIInger identified HRD-positive patients who experienced significantly extended progression-free survival when treated with PARPi. GIInger is, therefore, a cost-effective and easy-to-implement method for accurately stratifying patients with ovarian cancer for first-line PARPi treatment.

Indexed as

Ovarian NeoplasmsFemaleGenomicsHomologous RecombinationHumansProgression-Free Survivalbiomarkerbreast cancercancerconvolutional neural networkhomologous recombination deficiencyHRDlow-pass whole-genome sequencinglpWGSovarian cancerPARPi

Identifiers

PMID38118421
PMCPMC10772634

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.