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临床试验/NCT06129968
NCT06129968招募中不适用

Transforming Ovarian Cancer Diagnostic Pathways (TranSforming Ovarian caNcer diAgnosTic pAthways: A Hybrid Type 1 Effectiveness-implementation Study of a Novel Biomarker Based, Threshold Driven Pathway for Earlier Ovarian Cancer Diagnosis

Professor Sudha Sundar3 个研究点 分布在 1 个国家目标入组 34,000 人开始时间: 2024年1月23日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
34,000
试验地点
3
主要终点
Sensitivity of ROMA versus CA125 in early stage ovarian cancer

研究概览

简要总结

The goal of this observational cohort study is to compare the diagnostic accuracy and cost effectiveness of Risk of Malignancy Algorithm (ROMA) compared with CA125 in the diagnosis of ovarian cancer in patients attending their general practitioner (GP) with symptoms that sometimes might indicate ovarian cancer. The main questions it aims to answer are: • what is the accuracy of the ROMA algorithm which uses the blood tests CA125 and Human epididymis protein 4 (HE4) compared to CA125 in diagnosing ovarian cancer, particularly early-stage ovarian cancer, in women tested for suspected ovarian cancer from primary care? • What is the cost-effectiveness of ROMA versus CA125 testing in primary care to diagnose ovarian cancer? When a participant's GP orders a CA125 blood test, the blood will also be tested for HE4 and the ROMA algorithm calculated. The diagnostic accuracy of ROMA and CA125 will be compared to see if ROMA would be a better diagnostic test for ovarian cancer when used in the primary care setting.

详细描述

A woman's chances of surviving 5 years after Ovarian Cancer (OC) diagnosis drops from 90% if diagnosed at Stage 1 to 15% at Stage 4. Currently, GPs use a blood test called CA125 and ultrasound scan to decide whether to refer a woman to hospital for suspected OC. CA125 misses 50% of early-stage cancers (Stage 1 and 2); both tests cause unnecessary referrals. Recently, a blood test called Human epididymis protein 4 (HE4) in combination with CA125 in a formula called ROMA (Risk of Malignancy Algorithm) has been developed. ROMA is used by doctors in the US and Europe to guide referrals and recommended by the American College of Obstetrics and Gynaecology. A large Cochrane systematic review of 30,000+ patients across 50 papers shows ROMA detects more cancers at earlier stage than a combination of CA125 and ultrasound. All included studies were conducted in hospital where OC rates are high, however a model at 3% OC rate shows that ROMA is superior. Before the test can be introduced in NHS, it is necessary to confirm this evidence in a large primary care study and establish cost effectiveness. The wider NHS cancer programme funded SONATA project evaluates an integrated pathway from community to cancer specialists using ROMA. It includes National Health Service (NHS) pilots in primary and secondary care to establish how practice can be supported to change, evaluates facilitators and barriers to change as well as a community campaign to promote OC awareness. This study is one component of the SONATA project. In it, two large NHS labs will additionally test 41,000 blood samples from women whose GPs requested CA125 testing for suspected OC with ROMA to accurately identify the number of patients who can be detected earlier. This will enable the investigators to establish cost effectiveness of ROMA and definitive data on accuracy in primary care.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
Female
接受健康志愿者

入选标准

  • Women presenting to primary care with suspected ovarian cancer who are tested for the biomarker CA125 according to current standards of care for investigation of CA125 in the primary care setting.

排除标准

  • Patients presenting to primary care who do not have potential symptoms of ovarian cancer.
  • Women with symptoms sometimes associated with ovarian cancer not tested for ovarian cancer.

结局指标

主要结局

Sensitivity of ROMA versus CA125 in early stage ovarian cancer

时间窗: 12 months

Cancer diagnoses will be identified from hospital gynaecological oncology centre multidisciplinary team databases.

Specificity of ROMA versus CA125 in early stage ovarian cancer

时间窗: 12 months

Cancer diagnoses will be identified from hospital gynaecological oncology centre multidisciplinary team databases.

次要结局

  • Specificity of ROMA versus CA125 in all stages of ovarian cancer(12 months)
  • Incremental Cost Effectiveness Ratio (ICER) of ROMA versus CA125(12 months)
  • Sensitivity of ROMA versus CA125 in all stages of ovarian cancer(12 months)

研究者

发起方
Professor Sudha Sundar
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Professor Sudha Sundar

Professor of Gynaecological Cancer

Sandwell & West Birmingham Hospitals NHS Trust

研究点 (3)

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