首页> 外文期刊>Gynecologic Oncology: An International Journal >CA125 regression in ovarian cancer patients treated with intravenous versus intraperitoneal platinum-based chemotherapy: A gynecologic oncology group study
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CA125 regression in ovarian cancer patients treated with intravenous versus intraperitoneal platinum-based chemotherapy: A gynecologic oncology group study

机译:卵巢癌患者接受静脉内和腹膜内铂类化学疗法治疗后CA125回归:妇科肿瘤学小组研究

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Objective: CA125 is a non-specific marker of peritoneal irritation which has the potential for false elevation during intraperitoneal treatment. The purpose of this study is to identify the rate of CA125 regression during intraperitoneal (IP) versus intravenous (IV) chemotherapy for ovarian cancer. Methods: GOG 114, a randomized control trial evaluating IP and IV treatment, includes an intensive CA125 measurement schema with weekly CA125 levels until ≤ 35 units/ml for both IP- and IV-treated patients. Rate of CA125 normalization, median CA125 values for each treatment cycle, as well as clinical and pathologic features were compared between the treatment groups. Baseline CA125 levels and rate of CA125 decline were evaluated with respect to overall survival. Results: CA125 data were available for 223 patients who received IV cisplatin/paclitaxel and for 231 patients who received IV carboplatin followed by IP cisplatin/paclitaxel. Standard prognostic criteria and baseline CA125 values were similar between the treatment groups. For treatment cycles in which IP-treatment was administered, there was no statistically significant difference in CA125 levels between IV- and IP-treated patients. The rate of CA125 normalization was similar between IV- and IP-treated patients (p = 0.55). Patients with low pre-chemotherapy CA125 levels which rapidly declined during treatment demonstrated a survival advantage (p < 0.0001). Conclusions: No difference in CA125 decline was identified between IP- and IV-treated patients undergoing a weekly CA125 monitoring schedule. This data supports the utilization of standard CA125 response criteria in the therapeutic monitoring for patients receiving IP treatment.
机译:目的:CA125是一种非特异性的腹膜刺激性标志物,在腹膜内治疗期间可能会引起假性升高。这项研究的目的是确定卵巢癌腹膜内(IP)与静脉内(IV)化疗期间CA125的消退率。方法:GOG 114(一项评估IP和IV治疗的随机对照试验)包括一个密集的CA125测量方案,其中IP和IV治疗患者的每周CA125水平直至≤35单位/ ml。比较各治疗组之间CA125正常化率,每个治疗周期的CA125中值以及临床和病理特征。评估基线CA125水平和CA125下降率,以评估其总体生存率。结果:223例接受IV顺铂/紫杉醇的患者和231例接受IV卡铂然后IP顺铂/紫杉醇的患者的CA125数据可用。治疗组之间的标准预后标准和基线CA125值相似。对于进行IP治疗的治疗周期,IV和IP治疗的患者之间CA125水平无统计学差异。在静脉注射和静脉注射的患者中,CA125的正常化率相似(p = 0.55)。化疗前CA125水平低且在治疗期间迅速下降的患者表现出生存优势(p <0.0001)。结论:在接受每周CA125监测计划的IP和IV治疗的患者之间,未发现CA125下降的差异。该数据支持在接受IP治疗的患者的治疗监测中使用标准CA125响应标准。

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