J Gynecol Oncol.  2021 Jul;32(4):e64. 10.3802/jgo.2021.32.e64.

A phase II, open-labeled, single-arm study of dose-dense paclitaxel plus carboplatin in advanced or recurrent uterine endometrial cancer treatment: a KCOG-G1303, DOENCA trial

Affiliations
  • 1Department of Obstetrics and Gynecology, Kansai Rosai Hospital, Amagasaki, Japan
  • 2Department of Obstetrics and Gynecology, Kurume University School of Medicine, Kurume, Japan
  • 3Department of Gynecologic Oncology, National Hospital Organization Shizuoka Cancer Center, Nagaizumi, Japan
  • 4Department of Obstetrics and Gynecology, Mie University, Tsu, Japan
  • 5Department of Gynecologic Oncology, National Hospital Organization Shikoku Cancer Center, Matsuyama, Japan

Abstract


Objective
To determine the safety and efficacy of dose-dense (dd) paclitaxel (PTX) and carboplatin (CBDCA) in treating advanced or recurrent endometrial cancer.
Methods
Women aged 20–75 years with histologically confirmed endometrial cancer, the International Federation of Gynecology and Obstetrics (FIGO) stage III disease with some residual tumor, FIGO stage IV disease, recurrence after front-line curative treatment, or recurrence after second-line chemotherapy or radiotherapy were enrolled in this study. PTX (80 mg/m2) was administered intravenously (IV) to every participant on days 1, 8, and 15, and CBDCA (area under the curve of 5) was administered IV on day 1 once every 3 weeks until the disease progressed, unacceptable adverse events occurred, or consent was withdrawn. The primary endpoint was the response rate (RR), while the secondary endpoints were progression-free survival, overall survival, and adverse effects.
Results
Forty-eight participants were enrolled, and 46 were eligible to receive treatment. The patients' median age was 61 years (range, 43–76 years). Twenty-two participants had experienced recurrence, and the remaining patients had primary advanced endometrial cancer. There were 10 cases of serous carcinoma, 3 cases of endometrioid carcinoma G3, 2 cases of carcinosarcoma, and 2 cases of clear-cell carcinoma according to histology. Twenty-nine participants (63.0%) received ≥6 cycles of chemotherapy. The RR (complete, 13 cases; partial, 20 cases) was 71.3% (95% confidence interval: 59.0%–84.5%).
Conclusion
The dd PTX with CBDCA is feasible and available as a treatment option for advanced or recurrent endometrial cancer.

Keyword

Endometrial Cancer; Chemotherapy; Paclitaxel; Carboplatin
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