Has tumor doubling time in breast cancer changed over the past 80 years? A systematic review

Cancer Med. 2021 Aug;10(15):5203-5217. doi: 10.1002/cam4.3939. Epub 2021 Jul 15.

Abstract

Over the past century, epidemiologic changes and implementation of screening may have had an impact on tumor doubling time in breast cancer. Our study was designed to evaluate changes in tumor doubling time in breast cancer over the past 80 years. A systematic review of published literature and meta-regression analysis was performed. An online electronic database search was undertaken using the PubMed platform from inception until June 2020. All studies that measured tumor doubling time in breast cancer were included. A total of 151 publications were retrieved. Among them, 16 full-text articles were included in the qualitative analysis. An exponential growth model was used for quantitative characterization of tumor growth rate. Tumor doubling time has remained stable over the past 80 years. Recent studies have not only identified "fast growing tumor" (grade 3, human epidermal growth factor receptor 2-positive, triple-negative, or tumor with an elevated Ki-67) but also "inactive breast cancer" feeding the ongoing debate of overdiagnosis due to screening programs. The stability of tumor doubling time over the past 80 years, despite increasing and changing risk factors, supports the validity for our screening guidelines. Prospective studies based on more precise measurement of tumor size and adjustment for tumor characteristics are necessary to more clearly characterize the prognostic and predictive impact of tumor doubling time in breast cancer.

Keywords: breast cancer; molecular subtypes; screening; tumor doubling time; tumor growth rate.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't
  • Systematic Review

MeSH terms

  • Breast Neoplasms / diagnosis
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology*
  • Cell Proliferation*
  • Female
  • Humans
  • Ki-67 Antigen / metabolism
  • Mass Screening
  • Overdiagnosis
  • Receptor, ErbB-2 / metabolism
  • Regression Analysis
  • Time Factors
  • Triple Negative Breast Neoplasms / pathology
  • Tumor Burden*

Substances

  • Ki-67 Antigen
  • ERBB2 protein, human
  • Receptor, ErbB-2

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