Evidence map›Paper›PMID 38916888›Full record

ArticleJAMA network open2024

Clinical Outcomes for BRCA Pathogenic Variant Carriers With Breast Cancer Undergoing Breast Conservation.

Kerollos Nashat Wanis, Henry M Kuerer, Susie X Sun, Kelly K Hunt, Alexa C Glencer, Mediget Teshome, Anthony Lucci, Roi Weiser, Helen Johnson, Benjamin D Smith and 3 more

Abstract read
In one paragraph

Article in JAMA network open, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Breast-Conserving Surgery inLife (Basel, Switzerland) · 2025
    Review
  5. Article
  6. Article
  7. 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

13 authors.

Kerollos Nashat WanisDepartment of Breast Surgical Oncology, MD Anderson Cancer Center, Houston, Texas.
Henry M KuererDepartment of Breast Surgical Oncology, MD Anderson Cancer Center, Houston, Texas.
Susie X SunDepartment of Breast Surgical Oncology, MD Anderson Cancer Center, Houston, Texas.
Kelly K HuntDepartment of Breast Surgical Oncology, MD Anderson Cancer Center, Houston, Texas.
Alexa C GlencerDepartment of Breast Surgical Oncology, MD Anderson Cancer Center, Houston, Texas.
Mediget TeshomeDepartment of Breast Surgical Oncology, MD Anderson Cancer Center, Houston, Texas.
Anthony LucciDepartment of Breast Surgical Oncology, MD Anderson Cancer Center, Houston, Texas.
Roi WeiserDepartment of Breast Surgical Oncology, MD Anderson Cancer Center, Houston, Texas.
Helen JohnsonDepartment of Breast Surgical Oncology, MD Anderson Cancer Center, Houston, Texas.
Benjamin D SmithDepartment of Breast Radiation Oncology, MD Anderson Cancer Center, Houston, Texas.
Angelica M GutierrezDepartment of Breast Medical Oncology, MD Anderson Cancer Center, Houston, Texas.
Simona F ShaitelmanDepartment of Breast Radiation Oncology, MD Anderson Cancer Center, Houston, Texas.
Banu K ArunDepartment of Breast Medical Oncology, MD Anderson Cancer Center, Houston, Texas.

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
U OF TEXAS HLTH SCI CTR HOUSTON CENTER FOR CLINICAL AND TRANSLATIONAL SCIENCESUL1RR024148 · NCRR · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MCPHERSON, DAVID D · 2006 to 2010
$27.9M
NCI NIH HHS P30 CA016672NCRR NIH HHS UL1 RR024148
6 · The paper itself

Abstract

Importance: Although most women with BRCA-associated breast cancer choose bilateral mastectomy, current guidelines support breast-conserving therapy as an option. As the indications for genetic testing expand and targeted therapies emerge, understanding the outcomes of breast-conserving therapy in the population of patients choosing breast conservation is important. Objective: To describe the clinical outcomes of women with BRCA-associated breast cancer who were treated with breast-conserving therapy, including the risks of ipsilateral and contralateral cancer events and bilateral mastectomy-free survival. Design, Setting, and Participants: This cohort study conducted at a single-institution academic national comprehensive cancer center included 172 women identified from a prospectively maintained database who had pathogenic BRCA1/2 variants and were treated with breast-conserving therapy from January 1, 1977, to December 31, 2021. Main Outcomes and Measures: Clinical and pathologic characteristics for patients with BRCA1 and BRCA2 were compared, and estimates of overall survival, bilateral mastectomy-free survival, distant disease-free survival, risk of ipsilateral breast cancer, and risk of contralateral cancer were computed. Results: The cohort included 172 women (mean [SD] age, 47.1 [11.7] years), with 42 (24.4%) receiving a diagnosis of breast cancer prior to 40 years of age. Compared with BRCA2 variant carriers (80 [46.5%]), women with BRCA1 variants (92 [53.5%]) were younger at breast cancer diagnosis and tended to have more advanced tumors, which were more likely to be hormone receptor negative and higher grade. At a median follow-up of 11.8 years (IQR, 5.7-18.2 years), estimates of 10-year survival and risk were: overall survival, 88.5% (95% CI, 83.1%-94.2%); bilateral mastectomy-free survival, 70.7% (95% CI, 63.3%-78.9%); risk of an ipsilateral breast cancer event, 12.2% (95% CI, 5.8%-18.2%); and risk of contralateral cancer, 21.3% (95% CI, 13.3%-28.6%). Risks continued to increase after 10 years of follow-up. Conclusions and Relevance: In this cohort study, although women with breast cancer and pathogenic BRCA1/2 variants treated with breast-conserving therapy had above-average risks of ipsilateral and contralateral breast cancer events, most did not have another cancer event and remained bilateral mastectomy free. These findings may be useful for informing patients with BRCA variants choosing breast conservation.

Indexed as

Breast NeoplasmsMastectomy, SegmentalAdultBRCA1 ProteinBRCA2 ProteinCohort StudiesDisease-Free SurvivalFemaleHumansMiddle AgedTreatment OutcomeBRCA1 ProteinBRCA1 protein, humanBRCA2 ProteinBRCA2 protein, human

Identifiers

PMID38916888
PMCPMC11200147

What OpenQuestion holds

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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.