早期上皮性卵巢癌的淋巴结转移:一家三级医院的回顾性临床研究。

Menghan Zhu, Jun Li, Lijuan Lu, Jie Duan, Wei Jiang
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引用次数: 0

摘要

研究目的本研究旨在评估粗表早期上皮性卵巢癌(EOC)患者淋巴结(LN)转移的发生率并预测其风险因素:我们回顾性回顾了复旦大学附属妇产科医院2018年1月至2022年9月期间266例因明显早期EOC接受LN清扫术的患者的临床病理资料和随访信息:在266例患者中,44例(16.5%)出现LN转移,其中65.9%和59.1%分别出现在盆腔区域和主动脉旁区域。单变量分析显示,高级别浆液性癌(HGSC)、术前成像提示LN转移、双侧附件受累、淋巴管间隙侵犯(LVSI)、腹膜细胞学阳性和临床分期为IIA的患者LN阳性率较高。在临床分期为 IA/B、IC 和 IIA 的病例中,分别有 7.9%、10.2% 和 39.7% 发现了 LN 转移。多变量分析证实,HGSC、LVSI 和临床 IIA 期患者的 LN 阳性率明显更高。在临床 IIA 期 EOC 中,LN 阴性组和 LN 阳性组的 3 年无进展生存率(PFS)分别为 65.8%和 77.4%(P = 0.360)。在临床I期EOC中,LN阴性组和LN阳性组的3年无进展生存率分别为93.5%和59.4%(P<0.001):结论:高级别浆液性组织学、LVSI 和临床 IIA 期疾病是早期 EOC LN 受累的预测因素。此外,与临床 IIA 期 EOC 相比,LN 转移似乎与临床 I 期 EOC 较差的 PFS 相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Lymph node metastasis in grossly apparent early-stage epithelial ovarian cancer: A retrospective clinical study at a tertiary institute.

Objective: This study aimed to evaluate the incidence and predict the risk factors of lymph node (LN) metastasis among patients with grossly apparent early-stage epithelial ovarian cancer (EOC).

Methods: We retrospectively reviewed the clinicopathologic data and follow-up information of 266 patients who underwent LN dissection for apparent early-stage EOC between January 2018 and September 2022 at the Obstetrics and Gynecology Hospital of Fudan University.

Results: Among 266 patients, 44 (16.5%) showed LN metastasis, of which 65.9% and 59.1% presented in the pelvic region and para-aortic region, respectively. Univariate analysis revealed higher LN positivity in patients with high-grade serous carcinoma (HGSC), preoperative imaging suggestive of LN metastasis, bilateral adnexal involvement, lymphovascular space invasion (LVSI), positive peritoneal cytology, and clinical stage IIA. LN metastases were identified in 7.9%, 10.2%, and 39.7% of clinical stage IA/B, IC, and IIA disease cases, respectively. Multivariate analysis confirmed significantly higher LN positivity rates in patients with HGSC, LVSI, and clinical stage IIA. In clinical stage IIA EOC, the 3-year progression-free survival (PFS) rates were 65.8% and 77.4% (P = 0.360) for LN-negative and LN-positive groups, respectively. In clinical stage I EOC, the 3-year PFS rates were 93.5% and 59.4% (P < 0.001) for LN-negative and LN-positive groups, respectively.

Conclusions: High-grade serous histology, LVSI, and clinical stage IIA disease are predictive factors for LN involvement in early-stage EOC. In addition, LN metastasis appears to be associated with worse PFS in clinical stage I EOC compared with clinical stage IIA EOC.

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