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原发性细胞减灭术后早期化疗对晚期上皮性卵巢癌预后的影响。

Prognostic influence of an early time to chemotherapy following primary cytoreductive surgery for advanced epithelial ovarian cancer.

机构信息

Women's Cancer Center, Southern California, Los Angeles, CA, USA.

Math Question Center, Division of Continuing Education, Harvard University, Cambridge, MA, USA.

出版信息

J Gynecol Oncol. 2022 Nov;33(6):e80. doi: 10.3802/jgo.2022.33.e80. Epub 2022 Sep 8.

Abstract

OBJECTIVE

The current investigation analyzes the prognostic role of the time to chemotherapy (TTC) interval following primary cytoreductive surgery for patients with advanced epithelial ovarian cancer.

METHODS

Characteristics and outcome data for 509 consecutive patients with stage IIIB-IVB ovarian, fallopian tube, and peritoneal cancer who had primary cytoreductive surgery between January 2000 and December 2019 are utilized. A univariate Cox regression determined the association of categorical variables with progression-free survival (PFS) and overall survival (OS). Significant variables (p≤0.05) on univariate analysis were applied to Cox proportional hazard regression.

RESULTS

The median TTC was 19 days and overall follow-up was 62.2 months. The PFS and OS were 25.5 months and 78.4 months for the study cohort plus 28.4 months and OS 84.5 months for patients rendered grossly disease-free. An early TTC (7-14 vs. 15-21 vs. 22-28 vs. >28 days) was associated with an improved PFS (41.7 vs. 30.6 vs. 18.9 vs. 17.9 months; p<0.001) and OS (132.7 vs. 104.6 vs. 56.5 vs. 48.0 months; p<0.001). The performance status, histology, disease distribution, dimension of residual disease, and categorical plus continuous TTC were predictors of PFS and OS. The use of maintenance therapy was also a predictor of PFS, and the route of chemotherapy administration was a predictor of OS.

CONCLUSIONS

For advanced epithelial ovarian cancer, a TTC of less than 21-days was observed to independently improve the PFS and OS. A 7-14 days TTC trended towards a further extension of the OS.

摘要

目的

本研究分析了原发性细胞减灭术后化疗(TTC)时间间隔对晚期上皮性卵巢癌患者的预后作用。

方法

利用 2000 年 1 月至 2019 年 12 月期间接受原发性细胞减灭术的 509 例 IIIB-IVB 期卵巢、输卵管和腹膜癌患者的特征和结局数据。单因素 Cox 回归确定了分类变量与无进展生存期(PFS)和总生存期(OS)的相关性。单因素分析中具有统计学意义的变量(p≤0.05)应用于 Cox 比例风险回归。

结果

中位 TTC 为 19 天,总随访时间为 62.2 个月。研究队列的 PFS 和 OS 分别为 25.5 个月和 78.4 个月,而大体无疾病患者的 PFS 和 OS 分别为 28.4 个月和 84.5 个月。早期 TTC(7-14 天 vs. 15-21 天 vs. 22-28 天 vs. >28 天)与改善的 PFS(41.7 个月 vs. 30.6 个月 vs. 18.9 个月 vs. 17.9 个月;p<0.001)和 OS(132.7 个月 vs. 104.6 个月 vs. 56.5 个月 vs. 48.0 个月;p<0.001)相关。表现状态、组织学、疾病分布、残留疾病大小和分类加连续 TTC 是 PFS 和 OS 的预测因素。维持治疗的使用也是 PFS 的预测因素,而化疗途径是 OS 的预测因素。

结论

对于晚期上皮性卵巢癌,小于 21 天的 TTC 观察到独立改善 PFS 和 OS。7-14 天的 TTC 趋势进一步延长 OS。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0810/9634102/976806240a4d/jgo-33-e80-g001.jpg

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