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高级别浆液性卵巢癌的生长动力学:对早期检测的意义。

Growth kinetics of high-grade serous ovarian cancer: implications for early detection.

作者信息

Narayanan Bharath, Buddenkotte Thomas, Smith Hayley, Shah Mitul, Freeman Susan, Hulse David, Funingana Gabriel, Alcaraz Marie-Lyne, Crispin-Ortuzar Mireia, Brenton James, Pharoah Paul, Pashayan Nora

机构信息

Department of Public Health and Primary Care, University of Cambridge, Cambridge, UK.

Department of Nuclear Medicine and Interventional Radiology, University Hospital of Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Br J Cancer. 2025 Jun 12. doi: 10.1038/s41416-025-03082-6.

Abstract

BACKGROUND

High-grade serous ovarian cancer (HGSOC) is the most lethal gynaecological cancer with patients routinely diagnosed at advanced stages. Evidence from randomized controlled trials indicates that annual screening may not reduce cancer-related deaths. We aim to characterise the growth kinetics of HGSOC to understand why early detection failed and under what conditions it might prove fruitful.

METHODS

We analysed data from 597 HGSOC patients and identified 34 cases with serial CT scans. We calculated the growth rates of lesions in the ovaries/pelvis and the omentum and estimated the time to metastasis using a Gompertz model. Finally, we simulated ultrasound and CA125 based screening in a virtual population of patients.

RESULTS

Growing lesions in the ovaries and the omentum doubled in volume every 2.2 months and 1.8 months respectively. The 11 cases with growing lesions in both sites had a median interval of 13.1 months between disease initiation and the onset of metastasis. Our simulations suggested that 27% of tumours would metastasise before screen detection. The remainder would provide a median window of 4.2 months for detection before metastasis.

CONCLUSION

Our results suggest that HGSOC lesions have short times to metastasis, preventing effective early detection using current screening approaches.

摘要

背景

高级别浆液性卵巢癌(HGSOC)是最致命的妇科癌症,患者通常在晚期才被诊断出来。随机对照试验的证据表明,年度筛查可能无法降低癌症相关死亡率。我们旨在描述HGSOC的生长动力学,以了解早期检测失败的原因以及在何种情况下可能会取得成效。

方法

我们分析了597例HGSOC患者的数据,并确定了34例有系列CT扫描的病例。我们计算了卵巢/盆腔和大网膜病变的生长率,并使用Gompertz模型估计转移时间。最后,我们在虚拟患者群体中模拟了基于超声和CA125的筛查。

结果

卵巢和大网膜中生长的病变体积分别每2.2个月和1.8个月翻倍。两个部位都有生长病变的11例患者,从疾病开始到转移发生的中位间隔时间为13.1个月。我们的模拟表明,27%的肿瘤在筛查发现之前就会发生转移。其余的肿瘤在转移前提供的中位检测窗口期为4.2个月。

结论

我们的结果表明,HGSOC病变转移时间短,使用当前的筛查方法无法进行有效的早期检测。

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