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首页> 外文期刊>International journal of gynecological cancer: official journal of the International Gynecological Cancer Society >Combination chemotherapy of intraperitoneal carboplatin and intravenous paclitaxel in suboptimally debulked epithelial ovarian cancer.
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Combination chemotherapy of intraperitoneal carboplatin and intravenous paclitaxel in suboptimally debulked epithelial ovarian cancer.

机译:腹膜内卡铂和静脉紫杉醇联合化疗治疗亚最佳减灭的上皮性卵巢癌。

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摘要

The objective of this study was to retrospectively assess the efficacy and safety of combination chemotherapy of intraperitoneal (IP) carboplatin and intravenous (IV) paclitaxel in suboptimally debulked ovarian cancer. Between March 1998 and March 2006, 44 patients with histologically confirmed epithelial ovarian carcinoma or peritoneal carcinoma with a residual mass greater than 1 cm received combination chemotherapy of IV paclitaxel and IP carboplatin. Administration of IV paclitaxel at 175 mg/m(2) immediately followed by IP carboplatin at an area under the curve of 6 was scheduled every 3 weeks for at least six cycles. The diagnosis and stage were ovarian carcinoma stage II in 8, III in 25, and IV in 6 cases, and peritoneal carcinoma stage III in 5 cases. Eighty-three percent of patients completed more than six cycles of chemotherapy. The incidences of grade 3/4 hematologic toxicities were 41 (93%) for neutrocytopenia, 10 (41%) for thrombocytopenia, and 18 (23%) for anemia. Observed grade 3/4 nonhematologic toxicities were 1 (2%) for allergy, 1 (2%) for fatigue, 1 (2%) for vomiting, 1 (2%) for liver dysfunction, and 4 (9%) for peripheral neuropathy. Two patients (5%) encountered catheter problems (one obstruction and one infection). Overall response rate was 80% (16 complete response, 19 partial response, 3 stable disease, and 6 progressive disease). Median progression-free survival and overall survival were 24 and 31 months, respectively. Combination chemotherapy of IP carboplatin and IV paclitaxel is effective and safe in suboptimally debulked ovarian cancer, and further evaluation is warranted.
机译:这项研究的目的是回顾性评估腹膜内(IP)卡铂和静脉内(IV)紫杉醇联合化疗在亚最佳减灭性卵巢癌中的疗效和安全性。在1998年3月至2006年3月之间,对44例经组织学证实为残留上皮性卵巢癌或腹膜癌且残留量大于1厘米的患者接受了IV紫杉醇和IP卡铂联合化疗。计划每3周进行一次175 mg / m(2)的IV紫杉醇的给药,随后在6曲线下的区域进行IP卡铂的给药,至少六个周期。诊断和分期为卵巢癌II期8例,III期25例和IV期6例,腹膜癌III期5例。 83%的患者完成了六个以上的化疗周期。中性白细胞减少症的3/4级血液学毒性发生率为41(93%),血小板减少症为10(41%),贫血为18(23%)。观察到的3/4级非血液学毒性过敏为1(2%),疲劳为1(2%),呕吐为1(2%),肝功能障碍为1(2%),周围神经病为4(9%) 。两名患者(占5%)遇到导管问题(一例阻塞并一例感染)。总体缓解率为80%(16例完全缓解,19例部分缓解,3例稳定疾病和6例进行性疾病)。中位无进展生存期和总生存期分别为24和31个月。 IP卡铂和IV紫杉醇联合化疗在亚最佳减灭卵巢癌中是安全有效的,因此有必要进行进一步评估。

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