Evidence map›Paper›PMID 36879128›Full record

ArticleNature medicine2023

Evolution of synchronous female bilateral breast cancers and response to treatment.

Anne-Sophie Hamy, Judith Abécassis, Keltouma Driouch, Lauren Darrigues, Mathias Vandenbogaert, Cecile Laurent, Francois Zaccarini, Benjamin Sadacca, Myriam Delomenie, Enora Laas and 23 more

Open access · hybridFull text read
In one paragraph

Article in Nature medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

13 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
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

33 authors at 10 institutions in 3 countries.

Anne-Sophie HamyDepartment of Medical Oncology, Institut Curie, Université Paris Cité, Paris, France.ORCID http://orcid.org/0000-0003-4430-3022
Judith AbécassisResidual Tumor & Response to Treatment Laboratory, RT2Lab, Translational Research Department, Paris, INSERM, U932 Immunity and Cancer, Institut Curie, Université de Paris, Paris, France.
Keltouma DriouchPharmacogenomics Unit, Department of Genetics, PSL University, Institut Curie, Paris, France.
Lauren DarriguesDepartment of Breast, Gynecological and Reconstructive Surgery, Institut Curie, Université de Paris Cité, Paris, France.
Mathias VandenbogaertTranslational Research Department, Institut Curie Research Center, PSL University, Paris, France.
Cecile LaurentResidual Tumor & Response to Treatment Laboratory, RT2Lab, Translational Research Department, Paris, INSERM, U932 Immunity and Cancer, Institut Curie, Université de Paris, Paris, France.
Francois ZaccariniDepartment of Breast, Gynecological and Reconstructive Surgery, Institut Curie, Université de Paris Cité, Paris, France.ORCID http://orcid.org/0000-0002-6476-4590
Benjamin SadaccaResidual Tumor & Response to Treatment Laboratory, RT2Lab, Translational Research Department, Paris, INSERM, U932 Immunity and Cancer, Institut Curie, Université de Paris, Paris, France.
Myriam DelomenieDepartment of Breast, Gynecological and Reconstructive Surgery, Institut Curie, Université de Paris Cité, Paris, France.
Enora LaasDepartment of Breast, Gynecological and Reconstructive Surgery, Institut Curie, Université de Paris Cité, Paris, France.
Odette MarianiBiological Resource Center, Department of Pathology, Department of Diagnostic and Theranostic Medicine, Institut Curie, PSL University, Paris, France.
Thanh LamDepartment of Breast, Gynecological and Reconstructive Surgery, Institut Curie, Université de Paris Cité, Paris, France.
Beatriz GrandalResidual Tumor & Response to Treatment Laboratory, RT2Lab, Translational Research Department, Paris, INSERM, U932 Immunity and Cancer, Institut Curie, Université de Paris, Paris, France.
Marick LaéBiological Resource Center, Department of Pathology, Department of Diagnostic and Theranostic Medicine, Institut Curie, PSL University, Paris, France.
Ivan BiechePharmacogenomics Unit, Department of Genetics, PSL University, Institut Curie, Paris, France.
Sophie VacherPharmacogenomics Unit, Department of Genetics, PSL University, Institut Curie, Paris, France.ORCID http://orcid.org/0000-0002-0042-6023
Jean-Yves PiergaDepartment of Medical Oncology, Institut Curie, Université Paris Cité, Paris, France.
Etienne BrainDepartment of Medical Oncology, Institut Curie, Université Paris Cité, Paris, France.
Celine VallotTranslational Research Department, Institut Curie Research Center, PSL University, Paris, France.
Judicael HottonDepartment of Surgical Oncology, Institut Godinot, Reims, France.
Wilfrid RicherTranslational Research Department, Institut Curie Research Center, PSL University, Paris, France.
Dario RochaTranslational Immunotherapy Team, INSERM U932, Institut Curie, PSL University, Paris, France.
Zakia TariqPharmacogenomics Unit, Department of Genetics, PSL University, Institut Curie, Paris, France.
Veronique BecetteBiological Resource Center, Department of Pathology, Department of Diagnostic and Theranostic Medicine, Institut Curie, PSL University, Paris, France.
Didier MeseureDepartment of Diagnostic and Theranostic Medicine, Institut Curie, University Paris-Sciences et Lettres, Paris, France.ORCID http://orcid.org/0000-0001-6730-6686
Laetitia LesageDepartment of Diagnostic and Theranostic Medicine, Institut Curie, University Paris-Sciences et Lettres, Paris, France.ORCID http://orcid.org/0000-0001-8592-2482
Anne Vincent-SalomonDepartment of Diagnostic and Theranostic Medicine, Institut Curie, University Paris-Sciences et Lettres, Paris, France.ORCID http://orcid.org/0000-0001-5754-5771
Natalie FilmannGerman Breast Group, Neu-Isenburg, Germany.
Jenny FurlanettoGerman Breast Group, Neu-Isenburg, Germany.
Sibylle LoiblGerman Breast Group, Neu-Isenburg, Germany.
Elise DumasResidual Tumor & Response to Treatment Laboratory, RT2Lab, Translational Research Department, Paris, INSERM, U932 Immunity and Cancer, Institut Curie, Université de Paris, Paris, France.
Joshua J WaterfallTranslational Research Department, Institut Curie Research Center, PSL University, Paris, France. joshua.waterfall@curie.fr.ORCID http://orcid.org/0000-0002-3762-5050
Fabien ReyalResidual Tumor & Response to Treatment Laboratory, RT2Lab, Translational Research Department, Paris, INSERM, U932 Immunity and Cancer, Institut Curie, Université de Paris, Paris, France. fabien.reyal@curie.fr.ORCID http://orcid.org/0000-0002-2318-3589
Inserm · FRUniversité Paris Cité · FRUniversité Paris Sciences et Lettres · FRInstitut Curie · FRGerman Breast group · DECardiovascular Center Bethanien · DECentre National de la Recherche Scientifique · FRDélégation Paris 5 · FRÉcole Polytechnique · FRInstitut Jean Godinot · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Synchronous bilateral breast cancer (sBBC) occurs after both breasts have been affected by the same germline genetics and environmental exposures. Little evidence exists regarding immune infiltration and response to treatment in sBBCs. Here we show that the impact of the subtype of breast cancer on levels of tumor infiltrating lymphocytes (TILs, n = 277) and on pathologic complete response (pCR) rates (n = 140) differed according to the concordant or discordant subtype of breast cancer of the contralateral tumor: luminal breast tumors with a discordant contralateral tumor had higher TIL levels and higher pCR rates than those with a concordant contralateral tumor. Tumor sequencing revealed that left and right tumors (n = 20) were independent regarding somatic mutations, copy number alterations and clonal phylogeny, whereas primary tumor and residual disease were closely related both from the somatic mutation and from the transcriptomic point of view. Our study indicates that tumor-intrinsic characteristics may have a role in the association of tumor immunity and pCR and demonstrates that the characteristics of the contralateral tumor are also associated with immune infiltration and response to treatment.

Indexed as

Breast NeoplasmsBreastFemaleGene Expression ProfilingHumansLymphocytes, Tumor-InfiltratingNeoadjuvant Therapy

Identifiers

PMID36879128
PMCPMC10033420
OpenAlexW4323320213

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read48
identifiers read6
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.