Exquisite sensitivity of TP53 mutant and basal breast cancers to a dose-dense epirubicin−cyclophosphamide regimen
2007

Sensitivity of TP53 Mutant Breast Cancers to Chemotherapy

Sample size: 80 publication 10 minutes Evidence: high

Author Information

Author(s): Bertheau Philippe, Turpin Elisabeth, Rickman David S, Espié Marc, de Reyniès Aurélien, Feugeas Jean-Paul, Plassa Louis-François, Soliman Hany, Varna Mariana, de Roquancourt Anne, Lehmann-Che Jacqueline, Beuzard Yves, Marty Michel, Misset Jean-Louis, Janin Anne, de Thé Hugues

Primary Institution: Laboratoire de Pathologie, Assistance Publique/Hôpitaux de Paris, Hôpital Saint Louis, Paris, France

Hypothesis

Does TP53 mutation status affect the response to dose-dense chemotherapy in breast cancer patients?

Conclusion

TP53 status is a key predictive factor for response to a dose-dense chemotherapy regimen in noninflammatory breast cancers.

Supporting Evidence

  • All 15 complete responses occurred among the 28 TP53-mutant tumors.
  • Nine out of ten highly aggressive basal subtypes experienced complete pathological responses.
  • TP53 status and basal subtype were independent predictors of a complete response.
  • Patients with unresponsive tumors and mutant TP53 status had significantly shorter overall survival.

Takeaway

Breast cancers with a specific mutation (TP53) are very sensitive to a strong chemotherapy treatment, which can help patients who usually have a poor outlook.

Methodology

Analyzed 80 noninflammatory breast cancers treated with a dose-dense regimen of epirubicin and cyclophosphamide, assessing TP53 status and chemotherapy response.

Potential Biases

Potential bias due to the exclusion of patients with inflammatory breast cancer.

Limitations

The study's findings may not apply to inflammatory breast cancers or other chemotherapy regimens.

Participant Demographics

Median age of participants was 48 years, with a range from 24 to 76 years.

Statistical Information

P-Value

0.0003

Statistical Significance

p<0.0001

Digital Object Identifier (DOI)

10.1371/journal.pmed.0040090

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