Estimating the Opportunity for Early Detection of Ovarian Cancer Using Individual-Patient Data from a Large Randomized Controlled Trial
- Marc D Ryser 1, Shannon T Holloway 1, Raphaël Morsomme 1, Andy Ryan 2, Sophia Apostolidou 2, Aleksandra Gentry-Maharaj 2, Kemal Caglar Gogebakan 3, Jane Lange 4, Jason Xu 1, Usha Menon 2, Ruth Etzioni 3
- 1Duke University, Durham, United States.
- 2University College London, London, United Kingdom.
- 3Fred Hutchinson Cancer Center, Seattle, WA, United States.
- 4Oregon Health and Science University Hospital, Portland, Oregon, United States.
- 0Duke University, Durham, United States.
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August 14, 2025
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View abstract on PubMed
Summary
This summary is machine-generated.Ovarian cancer screening effectiveness varies by cancer type and method. Multimodal screening (MMS) and ultrasound screening (USS) show different detection windows for high-grade serous cancers versus other types.
Area Of Science
- Oncology
- Screening Technologies
- Biostatistics
Background
- The UK Collaborative Trial of Ovarian Cancer Screening (UKCTOCS) evaluated multimodal screening (MMS) and transvaginal ultrasound screening (USS) for ovarian cancer (OC).
- The trial did not find a reduction in OC mortality with either screening method compared to no screening.
- UKCTOCS data offer a valuable resource for understanding OC interception opportunities.
Purpose Of The Study
- To estimate ovarian cancer natural history using Bayesian inference.
- To quantify the preclinical detectable phase (PCDP) for different OC subtypes and screening modalities.
Main Methods
- Utilized Bayesian inference on individual screening and cancer diagnosis records from the UKCTOCS trial.
- Analyzed data from 199,499 women, including 674,806 screens and 2,025 OC diagnoses.
- Compared PCDP for high-grade serous cancers (HGSCs) and non-HGSCs across MMS and USS arms.
Main Results
- The estimated PCDP for HGSCs was 1.7 years, significantly shorter than 7.8 years for non-HGSCs.
- PCDP for HGSCs was longer with MMS (2.2 years) than USS (0.8 years).
- PCDP for non-HGSCs was shorter with MMS (2.7 years) than USS (8.2 years).
Conclusions
- The window for intercepting ovarian cancer is highly dependent on histological subtype and the screening modality used.
- Enhancing early detection benefits requires extending the interception window by combining different screening tests.
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