Evidence map›Paper›PMID 42584742›Full record

Observational studyBreast cancer research and treatment2026

Real-world clinical outcomes of patients with early-stage TNBC and BRCAm who were treated with adjuvant capecitabine in the United States.

Filipa Lynce, Meng Ru, Linlin Luo, Miguel Miranda, Xiaoqing Xu, Claudine Isaacs

Abstract readObservational Study
In one paragraph

Observational study in Breast cancer research and treatment, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Filipa LynceDana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA. Filipa_Lynce@DFCI.HARVARD.EDU.ORCID http://orcid.org/0000-0001-6615-7076
Meng RuOncology Outcomes Research, Oncology Business Unit, AstraZeneca, Gaithersburg, MD, USA.
Linlin LuoOncology Data Analytics, Oncology Business Unit, AstraZeneca, Gaithersburg, MD, USA.
Miguel MirandaOncology Outcomes Research, Oncology Business Unit, AstraZeneca, Cambridge, UK.
Xiaoqing XuOncology Outcomes Research, Oncology Business Unit, AstraZeneca, Gaithersburg, MD, USA.
Claudine IsaacsLombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeClinical benefit from adjuvant capecitabine in patients with early-stage triple-negative breast cancer (eTNBC) and deleterious BRCA1/BRCA2 mutation (BRCAm) is not well characterized. This retrospective, observational study explored the real-world effectiveness of adjuvant capecitabine in patients with eTNBC by BRCAm status.

methodsData from adults diagnosed with eTNBC from 2016 to 2024 were captured from electronic health records in the US Flatiron Health database. Patients who initiated adjuvant capecitabine within 6 months after primary surgery and had documented BRCA status (by germline/tumor testing) were included.

resultsOf 882 patients who received adjuvant capecitabine, 53 (6%) had BRCAm, and 829 (94%) had non-BRCAm tumors. Median age at eTNBC diagnosis was lower in patients with BRCAm versus non-BRCAm (47 vs. 55 years). Most patients received capecitabine after neoadjuvant treatment (BRCAm: n = 49/53, 92%; non-BRCAm: n = 755/829, 91%), and most received adjuvant capecitabine monotherapy (BRCAm: n = 52/53, 98%; non-BRCAm: n = 790/829, 95%). Survival rates from surgery to 36 months were numerically lower in patients with BRCAm versus non-BRCAm (invasive disease-free survival: 59% vs. 72%; distant disease-free survival: 59% vs. 73%; overall survival: 67% vs. 80%); these differences were maintained in sensitivity analyses of patients with profiles aligned with the CREATE-X clinical trial criteria.

conclusionThis analysis showed a trend for worse real-world survival in patients with BRCAm versus non-BRCAm eTNBC who received adjuvant capecitabine. Although descriptive, these findings suggest an unmet need for patients with BRCAm eTNBC despite adjuvant capecitabine treatment; this could be addressed through wider BRCA testing and subsequent targeted therapy for patients with BRCAm.

Indexed as

Antimetabolites, AntineoplasticBRCA1 ProteinBRCA2 ProteinCapecitabineTriple Negative Breast NeoplasmsAdultAgedChemotherapy, AdjuvantFemaleHumansMiddle AgedNeoplasm StagingRetrospective StudiesTreatment OutcomeUnited StatesAntimetabolites, AntineoplasticBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, humanCapecitabineAdjuvantBRCACapecitabineReal-world evidenceTriple-negative breast cancerUS

Identifiers

PMID42584742
PMCPMC13468742

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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.