Evidence map›Paper›PMID 41642482›Full record

ArticleBreast cancer research and treatment2026

Refined risk stratification in residual triple-negative breast cancer after neoadjuvant therapy using residual cancer burden class and lymphovascular invasion.

Tae Hoon Lee, Hyunwoo Lee, Jeong Yun Jang, Won Park, Won Kyung Cho, Eun Yoon Cho, Jin Seok Ahn, Yeon Hee Park, Seok Jin Nam, Seok Won Kim and 2 more

Abstract read
In one paragraph

Article 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. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

12 authors.

Tae Hoon Lee *Department of Radiation Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul, 06351, Republic of Korea.ORCID http://orcid.org/0000-0002-4723-3931
Hyunwoo Lee *Department of Pathology and Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0001-7513-2882
Jeong Yun Jang *Department of Radiation Oncology, Konkuk University Medical Center, Konkuk University School of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0002-3167-0635
Won ParkDepartment of Radiation Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul, 06351, Republic of Korea.ORCID http://orcid.org/0000-0003-4686-2071
Won Kyung ChoDepartment of Radiation Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul, 06351, Republic of Korea.ORCID http://orcid.org/0000-0002-4736-8270
Eun Yoon ChoDepartment of Pathology and Translational Genomics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0003-4675-4492
Jin Seok AhnDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0002-2880-6730
Yeon Hee ParkDivision of Hematology-Oncology, Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0003-4156-9212
Seok Jin NamDivision of Breast Surgery, Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0003-1072-8954
Seok Won KimDivision of Breast Surgery, Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0002-6130-7570
Jeong Eon LeeDivision of Breast Surgery, Department of Surgery, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0003-0037-2456
Haeyoung KimDepartment of Radiation Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, 81 Irwon-ro, Gangnam-gu, Seoul, 06351, Republic of Korea. haeyoung0131.kim@samsung.com.ORCID http://orcid.org/0000-0003-1808-7573

Funding

National Research Foundation of Korea RS-2023-00252283Samsung Medical Center, Sungkyunkwan University SMO1240501
6 · The paper itself

Abstract

purposeThis study aimed to identify prognostic factors and to stratify recurrence risk using a prognostic model incorporating the identified factors in patients with residual triple-negative breast cancer (TNBC) following neoadjuvant systemic therapy (NST).

methodsA retrospective analysis was conducted using data from a prospectively collected single-institution database. Eligible patients had residual TNBC after NST and curative surgery between 2007 and 2020 and completed planned postoperative radiotherapy. Prognostic factors for disease-free survival (DFS) were identified using multivariable Cox proportional hazards regression. Risk groups were stratified according to the number of these factors.

resultsA total of 347 patients were included. With a median follow-up of 61.6 months, the 5-year DFS and overall survival rates were 62.5% and 73.9%, respectively. Lymphovascular invasion (LVI) positivity and residual cancer burden (RCB) class 3 were significant risk factors for worse DFS. The 5-year DFS rates were 82.9% (0 factor), 55.7% (1 factor), and 20.0% (2 factors) (p < 0.001). The new three-tiered stratification using LVI positivity and RCB class 3 demonstrated a higher concordance index compared to RCB class (bootstrap-estimated difference 0.038, 95% CI 0.006-0.070, p = 0.026). Adjuvant capecitabine was associated with improved 5-year DFS in patients with 1 risk factor (71.9% vs. 44.2%, p = 0.027), but not in those with 0 (83.1% vs. 81.7%, p = 0.548) or 2 factors (29.2% vs. 14.6%, p = 0.066).

conclusionPatients with residual TNBC can be stratified into risk groups based on LVI and RCB class. The effect of adjuvant treatment varied across these groups. This model may support more tailored adjuvant treatment decisions after NST.

Indexed as

Neoadjuvant TherapyNeoplasm Recurrence, LocalTriple Negative Breast NeoplasmsAdultAgedDisease-Free SurvivalFemaleHumansLymphatic MetastasisMiddle AgedNeoplasm InvasivenessNeoplasm, ResidualPrognosisRetrospective StudiesRisk AssessmentRisk FactorsLymphovascular invasionNeoadjuvant treatmentResidual cancer burdenTriple-negative breast cancer

Identifiers

PMID41642482
PMCPMC12876077

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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.