TY - JOUR
T1 - Paclitaxel and carboplatin in patients with completely or optimally resected carcinosarcoma of the uterus
T2 - A phase II trial by the Japanese uterine sarcoma group and the tohoku gynecologic cancer unit
AU - Otsuki, Ai
AU - Watanabe, Yoh
AU - Nomura, Hiroyuki
AU - Futagami, Masayuki
AU - Yokoyama, Yoshihito
AU - Shibata, Kiyosumi
AU - Kamoi, Seiryu
AU - Arakawa, Atsushi
AU - Nishiyama, Hiroshi
AU - Katsuta, Takahiro
AU - Kudaka, Wataru
AU - Shimada, Muneaki
AU - Sato, Naoki
AU - Kotera, Kouhei
AU - Katabuchi, Hidetaka
AU - Yaegashi, Nobuo
N1 - Publisher Copyright:
Copyright © 2014 by IGCS and ESGO.
PY - 2015/1/1
Y1 - 2015/1/1
N2 - Objective: This study aimed to evaluate the efficacy of paclitaxel and carboplatin in patients with completely or optimally resected uterine carcinosarcoma. Materials and Methods: We conducted a single-arm multicenter prospective phase II trial at 20 Japanese medical facilities. Eligible patients had histologically confirmed uterine carcinosarcoma without prior chemotherapy or radiotherapy. Patients received 6 courses of 175 mg/m2 paclitaxel over 3 hours, followed by a 30-minute intravenous administration of carboplatin at an area under the serum concentration-time curve of 6. Results: A total of 51 patients were enrolled in this study, 48 of whom underwent complete resection and 3 of whom underwent optimal resection. At 2 years, the progression-free survival and overall survival rates were 78.2% (95% confidence interval [CI], 64.1%Y87.3%) and 87.9% (95% CI, 75.1%Y94.4%), respectively. At 4 years, these rates were 67.9% (95% CI, 53.0%Y79.0%) and 76.0% (95% CI, 60.5%Y86.1%), respectively. Although 15 patients showed disease recurrence during the follow-up period (median, 47.8 months; range, 2.1Y72.8 months), a total of 40 (78.4%) patients completed the 6 courses of treatment that had been planned. Conclusions: The combination of paclitaxel and carboplatin was a feasible and effective postoperative adjuvant therapy for patients with completely or optimally resected uterine carcinosarcoma.
AB - Objective: This study aimed to evaluate the efficacy of paclitaxel and carboplatin in patients with completely or optimally resected uterine carcinosarcoma. Materials and Methods: We conducted a single-arm multicenter prospective phase II trial at 20 Japanese medical facilities. Eligible patients had histologically confirmed uterine carcinosarcoma without prior chemotherapy or radiotherapy. Patients received 6 courses of 175 mg/m2 paclitaxel over 3 hours, followed by a 30-minute intravenous administration of carboplatin at an area under the serum concentration-time curve of 6. Results: A total of 51 patients were enrolled in this study, 48 of whom underwent complete resection and 3 of whom underwent optimal resection. At 2 years, the progression-free survival and overall survival rates were 78.2% (95% confidence interval [CI], 64.1%Y87.3%) and 87.9% (95% CI, 75.1%Y94.4%), respectively. At 4 years, these rates were 67.9% (95% CI, 53.0%Y79.0%) and 76.0% (95% CI, 60.5%Y86.1%), respectively. Although 15 patients showed disease recurrence during the follow-up period (median, 47.8 months; range, 2.1Y72.8 months), a total of 40 (78.4%) patients completed the 6 courses of treatment that had been planned. Conclusions: The combination of paclitaxel and carboplatin was a feasible and effective postoperative adjuvant therapy for patients with completely or optimally resected uterine carcinosarcoma.
KW - Adjuvant chemotherapy
KW - Phase II trial
KW - Uterine carcinosarcoma
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U2 - 10.1097/IGC.0000000000000302
DO - 10.1097/IGC.0000000000000302
M3 - Article
C2 - 25347097
AN - SCOPUS:84927729340
SN - 1048-891X
VL - 25
SP - 92
EP - 97
JO - International Journal of Gynecological Cancer
JF - International Journal of Gynecological Cancer
IS - 1
ER -