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

  • 0Division of New Drugs and Early Drug Development for Innovative Therapies, European Institute of Oncology, IRCCS, Milan 20141, Italy.

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Summary

This summary is machine-generated.

Fibroadenoma-like areas in malignant phyllodes tumors of the breast do not significantly predict recurrence. Mediator of RNA polymerase II transcription subunit 12 homolog mutations (MED12m) also showed no association with recurrence or these areas.

Area Of Science

  • Oncology
  • Pathology
  • Genetics

Background

  • Malignant phyllodes tumors of the breast (B-MPT) require accurate prognostication.
  • Mediator of RNA polymerase II transcription subunit 12 homolog mutations (MED12m) and prior fibroadenoma history may influence outcomes.
  • Fibroadenoma-like areas (FLA) are hypothesized to indicate a pre-existing fibroadenoma.

Purpose Of The Study

  • To evaluate the prognostic significance of FLA in resected primary B-MPTs.
  • To assess the association between MED12m and cancer recurrences.
  • To determine if FLA and MED12m can aid in B-MPT prognostication.

Main Methods

  • Retrospective cohort study of 89 patients with non-metastatic B-MPT undergoing surgery (2000-2021).
  • Pathological review by 3 pathologists to identify FLA.
  • Nested case-control genomic analysis for MED12m association with FLA and recurrences.

Main Results

  • 47% of B-MPTs exhibited FLA.
  • FLA were not significantly associated with local recurrence (5-year cumulative incidence: 13.0% vs 23.6%) or distant recurrence (5-year cumulative incidence: 12.5% vs 8.9%).
  • MED12m showed no association with distant recurrences or the presence of FLA.

Conclusions

  • FLA are common in B-MPTs but do not significantly correlate with reduced local or distant recurrence rates.
  • MED12m is not associated with recurrence or FLA in this cohort.
  • FLA and MED12m do not appear to be significant prognostic markers for B-MPT recurrence.

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