Evidence map›Paper›PMID 35246547›Full record

ArticleNPJ breast cancer2022

Efficacy of platinum-based chemotherapy in metastatic breast cancer and HRD biomarkers: utility of exome sequencing.

Loïck Galland, Elise Ballot, Hugo Mananet, Romain Boidot, Julie Lecuelle, Juliette Albuisson, Laurent Arnould, Isabelle Desmoulins, Didier Mayeur, Courèche Kaderbhai and 7 more

Open access · goldAbstract read
In one paragraph

Article in NPJ breast cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 6% 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.

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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
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  7. International journal of oncology · 2025
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  13. Observational
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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

17 authors at 3 institutions in 1 country.

Loïck Galland *Department of Medical Oncology, Centre Georges François Leclerc, Dijon, France.
Elise Ballot *Platform of Transfer in Biological Oncology, Georges François Leclerc Cancer Center, Dijon, France.
Hugo MananetPlatform of Transfer in Biological Oncology, Georges François Leclerc Cancer Center, Dijon, France.
Romain BoidotDepartment of Pathology and Tumor Biology, Centre Georges François Leclerc, Dijon, France.
Julie LecuellePlatform of Transfer in Biological Oncology, Georges François Leclerc Cancer Center, Dijon, France.
Juliette AlbuissonDepartment of Pathology and Tumor Biology, Centre Georges François Leclerc, Dijon, France.
Laurent ArnouldDepartment of Pathology and Tumor Biology, Centre Georges François Leclerc, Dijon, France.
Isabelle DesmoulinsDepartment of Medical Oncology, Centre Georges François Leclerc, Dijon, France.
Didier MayeurDepartment of Medical Oncology, Centre Georges François Leclerc, Dijon, France.
Courèche KaderbhaiDepartment of Medical Oncology, Centre Georges François Leclerc, Dijon, France.
Silvia IlieDepartment of Medical Oncology, Centre Georges François Leclerc, Dijon, France.
Audrey HennequinDepartment of Medical Oncology, Centre Georges François Leclerc, Dijon, France.
Anthony BergeronDepartment of Pathology and Tumor Biology, Centre Georges François Leclerc, Dijon, France.
Valentin DerangèrePlatform of Transfer in Biological Oncology, Georges François Leclerc Cancer Center, Dijon, France.
François GhiringhelliDepartment of Medical Oncology, Centre Georges François Leclerc, Dijon, France.
Caroline TruntzerPlatform of Transfer in Biological Oncology, Georges François Leclerc Cancer Center, Dijon, France.
Sylvain LadoireDepartment of Medical Oncology, Centre Georges François Leclerc, Dijon, France. sladoire@cgfl.fr.ORCID http://orcid.org/0000-0002-0331-9194
Centre Georges François Leclerc · FRInserm · FRUniversité de Bourgogne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastatic breast cancer (MBC) is frequently managed by platinum-based chemotherapy during the disease course. The real benefit of these treatments is uncertain at advanced stages of the disease and in non-triple-negative subtypes. Since homologous recombination deficiency (HRD) could inform about tumor sensitivity to DNA-damaging agents, we aimed to determine biomarkers of genomic instability, and their link with platinum efficacy. In this single-center study, we report BRCA1/2 mutational status, HRD score and signature 3 levels, all obtained by tumor exome sequencing, in 86 patients with various subtypes of MBC and who received platinum-based chemotherapy. Overall response rate, disease control rate, PFS and PFS2/PFS1 ratio were evaluated to assess platinum-based chemotherapy efficacy. Among the 86 tumor samples analyzed, 7 harbored BRCA1/2 mutations. We found a subset of BRCA-proficient MBC with high HRD score or high S3 levels, comparable to BRCA-mutated tumors. However, these patients with high HRD score or high S3 tumor level do not seem to benefit more from platinum-based chemotherapy than the others, in terms of response rates and/or PFS, regardless of BC molecular subtype. By multivariate analysis, only the absence of liver metastases was independently associated with significantly better PFS on platinum-based chemotherapy. However, some of our exploratory analyses reveal that certain methods, when optimized, seem to associate with platinum benefit. Tumor exome sequencing methodology for quantifying HRD has to be approached systematically, and further validated and standardized prior to its clinical use. Further studies are warranted to confirm these results to guide platinum use in MBC.

Identifiers

PMID35246547
PMCPMC8897409
OpenAlexW4214935416

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Registered trials

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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.