Evidence map›Paper›PMID 34907993›Full record

ArticleJournal of the Chinese Medical Association : JCMA2022

The clinical impacts of molecular subtyping by multigene assay on hormone receptor-positive breast cancers.

Yeng-Ling Liu, Chih-Yi Hsu, Chin-Jung Feng, Pei-Ju Lien, Chi-Cheng Huang, Yen-Shu Lin, Yu-Ling Wang, Ta-Chung Chao, Chun-Yu Liu, Jen-Hwey Chiu and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of the Chinese Medical Association : JCMA, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 45% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Review
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 at 2 institutions in 1 country.

Yeng-Ling LiuComprehensive Breast Health Center, Taipei Veterans General Hospital, Taipei, Taiwan, ROC.
Chih-Yi HsuFaculty of Medicine, School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan, ROC.
Chin-Jung FengComprehensive Breast Health Center, Taipei Veterans General Hospital, Taipei, Taiwan, ROC.
Pei-Ju LienComprehensive Breast Health Center, Taipei Veterans General Hospital, Taipei, Taiwan, ROC.
Chi-Cheng HuangComprehensive Breast Health Center, Taipei Veterans General Hospital, Taipei, Taiwan, ROC.
Yen-Shu LinComprehensive Breast Health Center, Taipei Veterans General Hospital, Taipei, Taiwan, ROC.
Yu-Ling WangComprehensive Breast Health Center, Taipei Veterans General Hospital, Taipei, Taiwan, ROC.
Ta-Chung ChaoFaculty of Medicine, School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan, ROC.
Chun-Yu LiuFaculty of Medicine, School of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan, ROC.
Jen-Hwey ChiuComprehensive Breast Health Center, Taipei Veterans General Hospital, Taipei, Taiwan, ROC.
Yi-Fang TsaiComprehensive Breast Health Center, Taipei Veterans General Hospital, Taipei, Taiwan, ROC.
Ling-Ming TsengComprehensive Breast Health Center, Taipei Veterans General Hospital, Taipei, Taiwan, ROC.
Taipei Veterans General Hospital · TWNational Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMultigene assays, such as MammaPrint and BluePrint, provide additional information other than conventional immunohistochemistry (IHC) to help making decision of treatment. This study aims to compare the clinical correlation between molecular subtyping (MS) versus surrogate pathological subtyping (PS).

methodsA database from patients receiving MS evaluation in Taipei Veterans General Hospital from 2013 to 2018 was reviewed retrospectively. Patients were categorized as luminal A, luminal B, human epidermal growth factor receptor 2 (HER2) and basal type from MS results and also centrally assessed according to PS (estrogen receptor [ER], progesterone receptor [PgR], HER2, and Ki-67). The clinical correlation between two different subtyping methodologies was analyzed, and the application of chemotherapy was compared.

resultsFrom 2013 to 2018, a total of 130 patients received MS testing in our institute, and 132 tumor samples were sent for analysis. From MammaPrint, 64 (48.5%) and 55 (41.7%) samples were defined as low and high risks, respectively. The other 13 (9.8%) tumor samples were identified as late recurrence low risk. MS restratified 44 tumors as subtype shifting including 20 tumors from A to B in intrinsic subtypes and 24 tumors from B to A after MS evaluation. Chemotherapy was conducted in only one (1.3%) patient with MS-luminal A but in 87.8% (n = 43) of MS-luminal B subtypes.

conclusionThe MS results restratify the subtypes of hormone receptor positive breast cancer and dominate decision-making of adjuvant therapy. The role of surrogate biomarkers as an alternative tool needs further elucidation. The treatment outcome in different subtypes categorized by MS or PS will be the interesting focus of research.

Indexed as

Breast NeoplasmsBiomarkers, TumorFemaleHumansPrognosisReceptors, EstrogenRetrospective StudiesBiomarkers, TumorReceptors, Estrogen

Identifiers

PMID34907993
PMCPMC12755496
OpenAlexW4200173200

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.