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Evolving paradigms in multifocal breast cancer.

Roberto Salgado1, Philippe Aftimos2, Christos Sotiriou2

  • 1Department of Pathology, GZA Antwerp, Belgium; Breast Cancer Translational Research Laboratory, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium.

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Summary

Multifocal breast cancer involves multiple distinct tumors in the same breast. Current assessment focuses on the largest tumor, but this may overlook crucial biological diversity and heterogeneity, potentially biasing clinical trials.

Keywords:
Breast cancer subtypingClinical trialsInter-lesion heterogeneityMultifocal breast cancer

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Area of Science:

  • Oncology
  • Pathology
  • Clinical Medicine

Background:

  • The 7th edition of the TNM classification defines multifocal breast cancer as multiple, distinct, synchronous ipsilateral lesions.
  • Current practice, guided by the College of American Pathologists (CAP), often involves characterizing only the largest lesion.
  • This approach simplifies assessment but may not capture the full biological complexity of multifocal disease.

Purpose of the Study:

  • To review critical aspects of multifocal breast cancer assessment.
  • To highlight the clinical relevance of different intrinsic subtypes within multifocal lesions.
  • To discuss the implications of inter-lesion heterogeneity and potential bias in clinical trials.

Main Methods:

  • Review of current definitions and clinical practices for multifocal breast cancer.
  • Discussion of emerging research on inter-lesion heterogeneity.
  • Analysis of the impact of multifocal breast cancer diversity on clinical trial design and interpretation.

Main Results:

  • Multifocal breast cancer presents distinct lesions that can harbor different intrinsic subtypes and heterogeneity.
  • Current assessment strategies focusing solely on the largest lesion may obscure significant biological differences.
  • This simplification risks introducing bias into clinical trials by not accounting for the full spectrum of disease biology.

Conclusions:

  • The current approach to multifocal breast cancer assessment, while feasible, may be insufficient given evolving understanding.
  • Recognizing inter-lesion heterogeneity and subtype differences is crucial for accurate diagnosis and treatment.
  • Future strategies may need to adapt to incorporate the biological diversity of multifocal breast cancers for improved clinical trial validity and patient care.