Evidence map›Paper›PMID 40507252›Full record

ReviewCancers2025

Unraveling Homologous Recombination Deficiency in Ovarian Cancer: A Review of Currently Available Testing Platforms.

Nicola Marconato, Orazio De Tommasi, Dino Paladin, Diego Boscarino, Giulia Spagnol, Carlo Saccardi, Tiziano Maggino, Roberto Tozzi, Marco Noventa, Matteo Marchetti

Abstract readReview
In one paragraph

Review in Cancers, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Morphological and molecular characterization of epithelial ovarian cancer: SEOM-SEAP consensus guidelines for biomarker integration in clinical practice.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Guideline
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. 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

10 authors.

Nicola MarconatoDepartment of Women and Children's Health, University of Padua, 35128 Padua, Italy.ORCID 0009-0005-3595-5979
Orazio De TommasiUnit of Gynecology and Obstetrics, Department of Women and Children's Health, University of Padua, 35128 Padua, Italy.
Dino PaladinAB ANALITICA S.r.l., Via Svizzera, 16, 35127 Padova, Italy.
Diego BoscarinoAB ANALITICA S.r.l., Via Svizzera, 16, 35127 Padova, Italy.ORCID 0009-0003-5774-1723
Giulia SpagnolUnit of Gynecology and Obstetrics, Department of Women and Children's Health, University of Padua, 35128 Padua, Italy.ORCID 0000-0003-3525-0571
Carlo SaccardiUnit of Gynecology and Obstetrics, Department of Women and Children's Health, University of Padua, 35128 Padua, Italy.ORCID 0000-0001-7476-997X
Tiziano MagginoUnit of Gynecology and Obstetrics, Department of Women and Children's Health, University of Padua, 35128 Padua, Italy.ORCID 0000-0002-5177-8205
Roberto TozziUnit of Gynecology and Obstetrics, Department of Women and Children's Health, University of Padua, 35128 Padua, Italy.ORCID 0000-0001-6123-1628
Marco NoventaUnit of Gynecology and Obstetrics, Department of Women and Children's Health, University of Padua, 35128 Padua, Italy.
Matteo MarchettiUnit of Gynecology and Obstetrics, Department of Women and Children's Health, University of Padua, 35128 Padua, Italy.ORCID 0000-0003-4427-0101

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Homologous recombination deficiency (HRD) is a key biomarker associated with increased sensitivity to PARP inhibitors (PARPi) in advanced epithelial ovarian cancer. Accurate identification of HRD status is essential for selecting patients most likely to benefit from these therapies. Current diagnostic approaches combine sequencing to detect mutations in homologous recombination repair genes-particularly BRCA1 and BRCA2-with genome-wide analysis of structural genomic alterations indicative of HRD. This review briefly outlines the biological basis of HRD and its clinical significance and then focuses on currently available assays for HRD assessment. We compare their molecular strategies, including the use of targeted gene panels and genomic instability metrics such as loss of heterozygosity, telomeric allelic imbalance, and large-scale state transitions. The review also highlights the strengths and limitations of each platform and discusses their role in guiding clinical decision-making. Challenges related to dynamic tumor evolution and the interpretation of HRD status in recurrent disease settings are also addressed.

Indexed as

advanced epithelial ovarian cancerhomologous recombination deficiencyhomologous recombination repairpoly-ADP-ribose polymerase inhibitorstest

Identifiers

PMID40507252
PMCPMC12153926

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.