Evidence map›Paper›PMID 39921370›Full record

ArticleThe oncologist2025

The pathologic and genomic evolution of primary malignant phyllodes tumors of the breast: retrospective cohort study and case-control genomic analysis.

Carmine Valenza, Dario Trapani, Francesca Maria Porta, Edoardo Olmeda, Aurora Gaeta, Luca Boscolo Bielo, Federica Conversano, Tommaso Martino De Pas, Grazia Castellano, Celeste Santoro and 10 more

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Article in The oncologist, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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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

20 authors.

Carmine ValenzaDivision of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan 20141, Italy.
Dario TrapaniDivision of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan 20141, Italy.ORCID 0000-0003-1672-9560
Francesca Maria PortaDivision of Pathology, European Institute of Oncology, IRCCS, Milan 20141, Italy.
Edoardo OlmedaDepartment of Oncology and Hemato-Oncology, University of Milan, Milan 20122, Italy.
Aurora GaetaDepartment of Experimental Oncology, European Institute of Oncology, IRCCS, Milan 20141, Italy.
Luca Boscolo BieloDivision of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan 20141, Italy.
Federica ConversanoDivision of Pathology, European Institute of Oncology, IRCCS, Milan 20141, Italy.
Tommaso Martino De PasMedical Oncology Division, Cliniche Humanitas Gavazzeni, Bergamo 24125, Italy.
Grazia CastellanoDivision of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan 20141, Italy.
Celeste SantoroDivision of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan 20141, Italy.
Elena BattaiottoDivision of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan 20141, Italy.
Eltjona ManeDivision of Pathology, European Institute of Oncology, IRCCS, Milan 20141, Italy.
Sara CoppolaDivision of Melanoma, Soft Tissue Sarcomas and Rare Tumors, European Institute of Oncology, IRCCS, Milan 20141, Italy.
Fabio ConfortiMedical Oncology Division, Cliniche Humanitas Gavazzeni, Bergamo 24125, Italy.
Denise MattarDivision of Breast Surgery, European Institute of Oncology, IRCCS, Milan 20141, Italy.
Sara GandiniDepartment of Experimental Oncology, European Institute of Oncology, IRCCS, Milan 20141, Italy.
Paolo VeronesiDepartment of Oncology and Hemato-Oncology, University of Milan, Milan 20122, Italy.
Elena Guerini RoccoDepartment of Oncology and Hemato-Oncology, University of Milan, Milan 20122, Italy.
Elisabetta PennacchioliDivision of Melanoma, Soft Tissue Sarcomas and Rare Tumors, European Institute of Oncology, IRCCS, Milan 20141, Italy.
Giuseppe CuriglianoDivision of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan 20141, Italy.ORCID 0000-0003-1781-2518

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn patients with phyllodes tumors of the breast, the presence of mediator of RNA polymerase II transcription subunit 12 homolog mutations (MED12m) and a history of previous fibroadenoma may predict better outcomes. To aid in the prognostication of malignant phyllodes tumors of the breast (B-MPT), we assessed the prognostic value of fibroadenoma-like areas (supposed to have stemmed from a pre-existing fibroadenoma) and MED12m, in patients with resected primary B-MPTs.

methodsWe conducted a single-center, retrospective, cohort study including all consecutive patients aged ≥18 years old, with non-metastatic B-MPT, who underwent surgery from January 2000 to December 2021. The endpoints were the cumulative incidences of all recurrences, according to the presence of fibroadenoma-like areas, reviewed by 3 reference pathologists. A nested, case-control genomic analysis was performed to evaluate the association between MED12m, the presence of fibroadenoma-like areas, and cancer recurrences.

resultsEight-nine patients were included, with 47% of tumors exhibiting Fibroadenoma-Like Areas (FLA+). These areas were not significantly associated with local recurrence (5-year cumulative incidence in FLA+ vs FLA-: 13.0, 95%CI [4.6-25.9] vs 23.6, 95%CI [11.9-37.5]; P = .14) or distant recurrence (5-year cumulative incidence in FLA+ vs FLA-: 12.5, 95%CI [4.5-25.0] vs 8.9, 95%CI [2.8-19.5], P = .61), at a median follow-up of 6.7 years. MED12m was not associated with distant recurrences or the presence of fibroadenoma-like areas.

conclusionsHalf of B-MPTs are characterized by the presence of fibroadenoma-like areas. This pathologic feature is not significantly associated with lower distant and local recurrences nor with the presence of MED12 mutations.

Indexed as

Breast NeoplasmsMediator ComplexPhyllodes TumorAdultAgedCase-Control StudiesFemaleGenomicsHumansMiddle AgedMutationNeoplasm Recurrence, LocalPrognosisRetrospective StudiesMED12 protein, humanMediator Complexbreast tumorfibroadenomamalignant phyllodes tumors of the breastMED12

Identifiers

PMID39921370
PMCPMC11806198

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