Evidence map›Paper›PMID 41149457›Full record

ArticleCurrent oncology (Toronto, Ont.)2025

Examining a Genomic Test in Predicting Extended Endocrine Benefit and Recurrence Risk in a Diverse Breast Cancer Population.

Ho Hyun Lee, Nicholas Siu-Li, Ian Pagano, Jami Aya Fukui

Abstract read
In one paragraph

Article in Current oncology (Toronto, Ont.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

4 authors.

Ho Hyun LeeDepartment of Medicine, John A. Burns School of Medicine, University of Hawai'i, Honolulu, HI 96813, USA.ORCID 0009-0007-0950-7798
Nicholas Siu-LiDepartment of Medicine, John A. Burns School of Medicine, University of Hawai'i, Honolulu, HI 96813, USA.ORCID 0000-0002-5934-4188
Ian PaganoTranslational and Clinical Research, University of Hawaii Cancer Center, Honolulu, HI 96813, USA.ORCID 0000-0002-6248-0113
Jami Aya FukuiTranslational and Clinical Research, University of Hawaii Cancer Center, Honolulu, HI 96813, USA.ORCID 0000-0002-0248-266X

Funding

University of Hawaii Cancer Center CCSGP30CA071789 · NCI · UNIVERSITY OF HAWAII AT MANOA · PI GERTRAUD MASKARINEC · 1996 to 2026
$56.2M
NCI NIH HHS P30 CA071789NCI NIH HHS P30CA071789-17S2
6 · The paper itself

Abstract

(1) Background: Extended endocrine therapy (EET) beyond five years can reduce distant recurrence in early-stage hormone receptor-positive (HR+) breast cancer. The Breast Cancer Index (BCI) predicts recurrence risk and EET benefits, yet racial/ethnic differences in its results remain unexplored. This study evaluates such differences in a diverse early-stage HR+ breast cancer population. (2) Methods: We retrospectively analyzed demographics, tumor characteristics and BCI scores of 159 women in Hawaii with early-stage HR+ breast cancer, self-identifying as Caucasian, Filipino, Japanese, Native Hawaiian, Other Asian/Pacific Islander, or Other. Tumor characteristics included size, grade, histology, lymph node/receptor status, Oncotype DX score, and laterality. Logistic regression used demographics and tumor features as predictor variables, with BCI's benefit prediction and recurrence risk as outcome variables. (3) Results: Japanese and other Asian/Pacific Islander patients had significantly lower odds of high recurrence risk compared to Caucasian patients. Higher recurrence risk was associated with greater odds of predicted EET. Racial/ethnic differences in EET benefit prediction were not statistically significant. (4) Conclusions: No racial/ethnic differences in EET benefit prediction suggest BCI's applicability in racially and ethnically diverse populations. Findings among Japanese and other Asian/Pacific Islanders point to potential biological or socioeconomic variation. Limitations include sample size and underrepresentation of certain groups. Future studies should address these gaps and adjust for known risk factors to further clarify BCI's racial and ethnic implications.

Indexed as

Antineoplastic Agents, HormonalBreast NeoplasmsGenomicsNeoplasm Recurrence, LocalAdultAgedFemaleHumansMiddle AgedRetrospective StudiesAntineoplastic Agents, Hormonalbreast cancerbreast cancer indexextended endocrine benefithormone receptor-positive breast cancerrace/ethnicityrecurrence risk

Identifiers

PMID41149457
PMCPMC12563413

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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.