首页> 外文期刊>International journal of gynecological cancer: official journal of the International Gynecological Cancer Society >Long-term survival after paclitaxel plus platinum-based combination chemotherapy for extraovarian peritoneal serous papillary carcinoma: is it different from that for ovarian serous papillary cancer?
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Long-term survival after paclitaxel plus platinum-based combination chemotherapy for extraovarian peritoneal serous papillary carcinoma: is it different from that for ovarian serous papillary cancer?

机译:紫杉醇联合铂类联合化疗治疗卵巢外腹膜浆液性乳头状癌的长期生存:与卵巢浆液性乳头状癌有何不同?

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The purpose of this study was to compare the effect of paclitaxel plus platinum-based chemotherapy in the treatment of extraovarian peritoneal serous papillary carcinoma (EPSPC) and ovarian serous papillary cancer (OSPC). Only the patients treated with initial surgery plus postoperative adjuvant chemotherapy and having FIGO stage IIIC disease with omental and/or peritoneal involvement were analyzed. Thirty-two patients with EPSPC and 43 with OSPC were included in this study. The median age, mean CA-125, and volume of ascitis were higher in patients with EPSPC. There was no significant difference between the two groups with respect to other prognosticators. The median overall survival (OS) durations were 30 months (95% CI 24.8-35.3) in patients with EPSPC and 28 months (95% CI 21.1-34.9) in those with OSPC (P= 0.35). The 3-year OS rates in the patients and controls were 28% and 31%, respectively (P= 0.84). In patients with EPSPC, only optimal cytoreduction was significantly related to progression-free survival and OS durations as a prognostic factor. In the EPSPC group, 65.5% of the patients (19/29) had lymphatic involvement, compared to 88.4% (38/43) in the OSPC group (P= 0.02). As an adjuvant therapy, the paclitaxel plus platinum-based combination regimen had similar effects on survival in the EPSPC and OSPC groups.
机译:这项研究的目的是比较紫杉醇联合铂类化学疗法治疗卵巢外腹膜浆液性乳头状癌(EPSPC)和卵巢浆液性乳头状癌(OSPC)的效果。仅分析接受初次手术加术后辅助化疗且患有网膜和/或腹膜受累的FIGO IIIC期疾病的患者。本研究包括32例EPSPC患者和43例OSPC患者。 EPSPC患者的中位年龄,平均CA-125和腹水量更高。两组在其他预后方面无显着差异。 EPSPC患者的中位总体生存期(OS)为30个月(95%CI 24.8-35.3),而OSPC患者的中位总体生存期(OS)为28个月(95%CI 21.1-34.9)(P = 0.35)。患者和对照组的3年OS发生率分别为28%和31%(P = 0.84)。在EPSPC患者中,只有最佳的细胞减少与无进展生存期和OS持续时间作为预后因素显着相关。在EPSPC组中,有65.5%的患者(19/29)有淋巴管受累,而在OSPC组中则为88.4%(38/43)(P = 0.02)。作为辅助治疗,紫杉醇加铂类联合治疗方案对EPSPC和OSPC组的生存率具有相似的影响。

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