Evidence map›Paper›PMID 33727697›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2021

Genetic differences between benign phyllodes tumors and fibroadenomas revealed through targeted next generation sequencing.

Cedric Chuan Young Ng, Nur Diyana Md Nasir, Benjamin Nathanael Loke, Timothy Kwang Yong Tay, Aye Aye Thike, Vikneswari Rajasegaran, Wei Liu, Jing Yi Lee, Peiyong Guan, Abner Herbert Lim and 15 more

Abstract read
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In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
–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

17 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Periductal Stromal Tumor of the Breast with aInternational journal of surgical pathology · 2023
    Article
  10. Gene Expression Profiling of Fibroepithelial Lesions of the Breast.International journal of molecular sciences · 2023
    Article
  11. Article
  12. Article
  13. Article
  14. Artificial intelligence modelling in differentiating core biopsies of fibroadenoma from phyllodes tumor.Laboratory investigation; a journal of technical methods and pathology · 2022
    Article
  15. Article
  16. Fibroepithelial tumours of the breast-a review.Virchows Archiv : an international journal of pathology · 2022
    Review
  17. Large borderline phyllodes breast tumor related to histopathology, diagnosis, and treatment management - case report.Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie
    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

25 authors.

Cedric Chuan Young Ng *Laboratory of Cancer Epigenome, National Cancer Centre Singapore, Singapore, Singapore.
Nur Diyana Md Nasir *Department of Anatomical Pathology, Singapore General Hospital, Singapore, Singapore.
Benjamin Nathanael Loke *Department of Anatomical Pathology, Singapore General Hospital, Singapore, Singapore.
Timothy Kwang Yong TayDepartment of Anatomical Pathology, Singapore General Hospital, Singapore, Singapore.
Aye Aye ThikeDepartment of Anatomical Pathology, Singapore General Hospital, Singapore, Singapore.
Vikneswari RajasegaranLaboratory of Cancer Epigenome, National Cancer Centre Singapore, Singapore, Singapore.
Wei LiuLaboratory of Cancer Epigenome, National Cancer Centre Singapore, Singapore, Singapore.
Jing Yi LeeLaboratory of Cancer Epigenome, National Cancer Centre Singapore, Singapore, Singapore.
Peiyong GuanLaboratory of Cancer Epigenome, National Cancer Centre Singapore, Singapore, Singapore.ORCID http://orcid.org/0000-0001-9958-0137
Abner Herbert LimLaboratory of Cancer Epigenome, National Cancer Centre Singapore, Singapore, Singapore.
Kenneth Tou En ChangDepartment of Pathology and Laboratory Medicine, KK Women's and Children's Hospital, Singapore, Singapore.ORCID http://orcid.org/0000-0001-5244-4285
Mihir Ananta GudiDepartment of Pathology and Laboratory Medicine, KK Women's and Children's Hospital, Singapore, Singapore.
Preetha MadhukumarDivision of Surgery and Surgical Oncology, National Cancer Center Singapore, Singapore, Singapore.
Benita Kiat Tee TanDivision of Surgery and Surgical Oncology, National Cancer Center Singapore, Singapore, Singapore.ORCID http://orcid.org/0000-0002-8573-4606
Veronique Kiak Mien TanDivision of Surgery and Surgical Oncology, National Cancer Center Singapore, Singapore, Singapore.
Chow Yin WongDivision of Surgery and Surgical Oncology, National Cancer Center Singapore, Singapore, Singapore.
Wei Sean YongDivision of Surgery and Surgical Oncology, National Cancer Center Singapore, Singapore, Singapore.
Gay Hui HoDivision of Surgery and Surgical Oncology, National Cancer Center Singapore, Singapore, Singapore.
Kong Wee OngDivision of Surgery and Surgical Oncology, National Cancer Center Singapore, Singapore, Singapore.
International Fibroepithelial Consortium
George Wai Cheong YipDepartment of Anatomy, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Boon Huat BayDepartment of Anatomy, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
Patrick TanDuke-NUS Medical School, Singapore, Singapore.
Bin Tean TehLaboratory of Cancer Epigenome, National Cancer Centre Singapore, Singapore, Singapore. teh.bin.tean@singhealth.com.sg.ORCID http://orcid.org/0000-0003-1514-1124
Puay Hoon TanDepartment of Anatomical Pathology, Singapore General Hospital, Singapore, Singapore. tan.puay.hoon@singhealth.com.sg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast fibroepithelial lesions are biphasic tumors which comprise the common benign fibroadenomas (FAs) and the rarer phyllodes tumors (PTs). This study analyzed 262 (42%) conventional FAs, 45 (7%) cellular FAs, and 321 (51%) benign PTs contributed by the International Fibroepithelial Consortium, using a previously curated 16 gene panel. Benign PTs were found to possess a higher number of mutations, and higher rates of cancer driver gene alterations than both groups of FAs, in particular MED12, TERT promoter, RARA, FLNA, SETD2, RB1, and EGFR. Cases with MED12 mutations were also more likely to have TERT promoter, RARA, SETD2, and EGFR. There were no significant differences detected between conventional FAs and cellular FAs, except for PIK3CA and MAP3K1. TERT promoter alterations were most optimal in discriminating between FAs and benign PTs. Our study affirms the role of sequencing and key mutations that may assist in refining diagnoses of these lesions.

Indexed as

AdultBreast NeoplasmsDiagnosis, DifferentialDNA Mutational AnalysisFemaleFibroadenomaHigh-Throughput Nucleotide SequencingHumansMutationPhyllodes Tumor

Identifiers

What OpenQuestion holds

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Read underepoch 390

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.