Primary chemotherapy with gemcitabine, epirubicin and taxol (GET) in operable breast cancer: a phase II study
2005

Chemotherapy Combination for Breast Cancer

Sample size: 41 publication Evidence: moderate

Author Information

Author(s): Conte P F, Donati S, Gennari A, Guarneri V, Orlandini C, Rondini M, Roncella M, Marini L, Collecchi P, Viacava P, Naccarato A G, Degli Esposti R, Bonardi S, Bottini A, Saracchini S, Tumolo S, Gullo G, Santoro A, Crino L

Primary Institution: University of Modena and Reggio Emilia

Hypothesis

The study aims to assess the activity and tolerability of the gemcitabine, epirubicin, and taxol combination in patients with operable breast cancer.

Conclusion

The gemcitabine, epirubicin, and taxol regimen is active and well tolerated as primary chemotherapy for operable breast cancer.

Supporting Evidence

  • The overall clinical response rate was 87.8%, with 26.8% complete responses.
  • A pathological complete response was observed in six patients (14.6%).
  • Grade 4 neutropenia was observed in 67.4% of the patients.

Takeaway

Doctors tested a combination of three medicines to help women with early breast cancer, and it worked well without too many side effects.

Methodology

Patients received gemcitabine, epirubicin, and taxol every 21 days for four cycles, and their responses were evaluated.

Limitations

The study had a limited sample size and did not document nodal status at study entry.

Participant Demographics

The median age of participants was 48 years, with the majority having stage II disease and positive hormone receptors.

Statistical Information

P-Value

P<0.05

Confidence Interval

95% CI 77.8–97.8

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1038/sj.bjc.6602723

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