卵巢透明细胞癌中癌症相关血栓栓塞症的生存期和生物标志物分析

IF 1.4 Q4 ONCOLOGY Molecular and clinical oncology Pub Date : 2024-11-12 eCollection Date: 2025-01-01 DOI:10.3892/mco.2024.2804
Tsubasa Ito, Morikazu Miyamoto, Naohisa Kishimoto, Jin Suminokura, Taira Hada, Soichiro Kakimoto, Kento Kato, Masashi Takano
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引用次数: 0

摘要

本研究旨在探讨癌症相关血栓栓塞(CAT)对卵巢透明细胞癌(OCCC)的生存和生物标志物的影响。本研究纳入了2000年1月至2019年12月期间在日本所泽防卫医科大学医院接受手术的卵巢透明细胞癌患者。回顾性比较了CAT、临床病理特征和预后之间的关联。此外,还对所有患者进行了免疫组化染色,以比较有 CAT 和无 CAT 患者之间的差异。在111例OCCC患者中,20例(18.0%)有CAT并发症。12名患者(10.8%)在初治前发现了CAT,8名患者(7.2%)在初治手术后发现了CAT。有CAT的患者肿瘤复发率(P=0.048)和铂类耐药率(P=0.025)较高,无进展生存期(PFS;P=0.025)较差。
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Survival and biomarker analysis for cancer‑associated thromboembolism in ovarian clear cell carcinoma.

The present study aimed to investigate the impact of cancer-associated thromboembolism (CAT) on the survival and biomarkers of ovarian clear cell carcinoma (OCCC). Patients with OCCC who underwent surgery at the National Defense Medical College Hospital (Tokorozawa, Japan) between January 2000 and December 2019 were included in the current study. Associations among CAT, clinicopathological features and prognosis were retrospectively compared. Furthermore, immunohistochemical staining was conducted in all patients to compare differences between patients with and without CAT. Among 111 patients with OCCC, 20 patients (18.0%) had CAT complications. CAT was detected in 12 patients (10.8%) before primary treatment and in 8 patients (7.2%) after primary surgery. Patients with CAT experienced more tumor recurrence (P=0.048) and platinum resistance (P=0.025), had worse progression-free survival (PFS; P<0.01) and overall survival (OS; P<0.01), and multivariate analysis showed that CAT was a prognostic factor for worse PFS [hazard ratio (HR)=2.10, P=0.039] and OS (HR=4.26, P<0.01). Moreover, immunohistochemical analysis revealed that more OCCC cases with CAT were positive for tissue factor (TF; P=0.030) and phosphorylated-Janus kinase 2 (JAK2; P=0.034) expression than those without CAT. In conclusion, CAT may be associated with platinum resistance and poor prognosis in patients with OCCC. Furthermore, TF and JAK2 could be considered potential novel therapeutic targets for OCCC complicated by CAT.

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