Phase II trial of docetaxel in advanced or metastatic endometrial cancer: a Japanese Cooperative Study
2005

Docetaxel for Advanced Endometrial Cancer

Sample size: 33 publication 10 minutes Evidence: moderate

Author Information

Author(s): Katsumata N, Noda K, Nozawa S, Kitagawa R, Nishimura R, Yamaguchi S, Aoki D, Susumu N, Kuramoto H, Jobo T, Ueki K, Ueki M, Kohno I, Fujiwara K, Sohda Y, Eguchi F

Primary Institution: National Cancer Center Hospital, Tokyo, Japan

Hypothesis

Does docetaxel have antitumour activity in patients with advanced or recurrent endometrial carcinoma?

Conclusion

Docetaxel shows antitumour activity in patients with advanced or recurrent endometrial cancer, but the effect is temporary and often accompanied by significant neutropenia.

Supporting Evidence

  • Overall response rate was 31%, with complete response in 3% and partial response in 28%.
  • 94% of patients experienced grade 3 or 4 neutropenia.
  • The median duration of response was 1.8 months.
  • The median time to progression was 3.9 months.
  • Most patients had undergone prior surgery, with 88% having total abdominal hysterectomy.

Takeaway

This study tested a medicine called docetaxel to see if it helps people with a serious type of cancer. It worked for some, but many had side effects.

Methodology

Patients with advanced or recurrent endometrial cancer received docetaxel 70 mg/m² every three weeks for up to six cycles, with response and toxicity evaluated.

Potential Biases

Potential bias due to the single-arm design and lack of a control group.

Limitations

The study had a relatively small sample size and was limited to a specific patient population.

Participant Demographics

Median age was 59 years, with a range of 39 to 74 years; 42% had received prior chemotherapy.

Statistical Information

P-Value

p<0.05

Confidence Interval

95% CI, 16.1–50.0%

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1038/sj.bjc.6602817

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