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临床试验/NCT05228197
NCT05228197进行中(未招募)不适用

A Study to Assess the Clinical and Cost-effectiveness of the Galen Prostate Artificial Intelligence Histology System in Diagnosing Clinically Important Prostate Cancer on Prostate Biopsy Tissue.

Imperial College London6 个研究点 分布在 1 个国家目标入组 750 人开始时间: 2022年3月11日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
750
试验地点
6
主要终点
Galen Prostate AI

研究概览

简要总结

The primary objective is to determine whether the Galen Prostate AI system has sufficient diagnostic accuracy and health economic value to be used for triage of pathology slides within the NHS.

详细描述

In the UK, about 80-100,000 men every year undergo prostate biopsy to diagnose prostate cancer. This equates to approximately 4 million histology slides; this is estimated to increase to 160,000-200,000 men and up to 6 million slides by 2030 due to rising numbers of men being tested for prostate cancer.

Health Education England and the Royal College of Pathology point to a significant pathology work-force shortage with only 3% of departments having adequate staffing levels and a 10% vacancy rate filled by locums costing £26M every year. By 2021, there will be a 3% decrease of the pathology consultant workforce (40 full-time pathologists); a period of time in which other specialties are expected to see a 13% increase. However, to meet the rising numbers of referrals to pathology departments, it is projected that there will need to be a 3-5% annual growth in the number of pathologists.

Inter-observer variability can occur between pathologists in terms of reporting a diagnosis of clinically important and clinically unimportant prostate cancer by as much as 20% although the differences are smaller when highly expert uro-pathologists are compared. This can lead to inappropriate management of cases.

Galen Prostate AI is a CE-marked deep learning AI-algorithm for prostate needle biopsies that can identify cell types, tissue structures and morphological features for cancer diagnosis. The technology is based on multi-layered convolutional neural networks (CNNs) designed for image classification in which whole-slide imaging is analysed for the detection of tissue areas and then benign versus cancer versus other pathology classification. Compared to almost all competitors, Galen Prostate AI has been tested in ~10 times more tissue samples. Further, Galen Prostate AI is the only algorithm that extends beyond cancer detection/grading to other clinically relevant features (e.g., perineural invasion, high-grade prostatic intraepithelial neoplasia [PIN], inflammation). This AI-algorithm is believed to be the only one in routine clinical deployment - demonstrating technical feasibility and with proven clinical utility.

The proposed study will perform validation in the NHS, for the first time. It is important to stress that this type of algorithm has never been tested on a UK-based population, and in particular, a population that includes a cohort of MRI targeted biopsies, which is now the new diagnostic strategy as it detects clinically relevant prostate cancer in higher percentages than the routine systematic biopsy.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Cross Sectional

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Patients with a prostate (either cis-male gender or trans-female gender with no prior hormone use at all).
  • Age 18 years or above.
  • Undergoing prostate biopsy as a result of an elevated serum PSA or abnormal digital rectal exam, who have undergone a pre-biopsy multi-parametric MRI and advised to undergo prostate biopsies.
  • (Please note: the Calibration stage requires patients who have already undergone a biopsy and the pathology has been processed over the prior 0 to 12 months).

排除标准

  • Unwilling or unable to give consent.
  • Any duration or type or dose of androgen deprivation therapy in the 6 months prior to screening.
  • Any prior radiotherapy to the prostate or pelvis (including the prostate) or ablation or chemical treatment of the prostate for treating cancer: these types of treatment affect the anatomy of prostate tissue microstructure for which Galen Prostate AI is not currently validated. NB: any treatment for benign enlargement of the prostate is permitted.

结局指标

主要结局

Galen Prostate AI

时间窗: Maximum 6 weeks following enrolment

Sensitivity, specificity, positive and negative predictive value of Galen Prostate AI on a patient basis for prostate cancer rated Gleason score 7 (ISUP Grade Group \>/=2) or greater by consensus pathology review.

Composite Health Outcome (Cost-Utility Analysis)

时间窗: Maximum 6 weeks following enrolment

Will be presented in the form of an Incremental Cost-Effectiveness Ratio (ICER), a ratio of 'extra cost per extra unit of health outcome' for the intervention vs the comparator. Costs: medical equipment, mean cost per diagnosis, primary and secondary care appointments, healthcare professionals' costs, cost of the diagnostic tests and of follow-up testing, implementation costs of adopting the intervention in the NHS, cost of treatment, treatment of adverse effects from the test or treatment, and any monitoring needed before or after the treatment. Health outcomes: Quality-adjusted life years (QALY). QALYs will be calculated by estimating the years of life remaining for a patient following diagnosis and weighting each year with a quality-of-life score (EQ-5D questionnaire).

Composite Health Outcome (Cost-Consequence Analysis)

时间窗: Maximum 6 weeks following enrolment

Includes all the relevant cost and consequences for the Ibex-AI and comparator. Costs: medical equipment, mean cost per diagnosis, primary and secondary care appointments, healthcare professionals' costs, cost of the diagnostic tests and of follow-up testing. Consequences: test accuracy, diagnostic yield, and therapeutic yield.

次要结局

  • Galen Prostate AI (3)(Maximum 6 weeks following enrolment)
  • Pathology Reporting(Maximum 6 weeks following enrolment)
  • Galen Prostate AI (5)(Maximum 6 weeks following enrolment)
  • Galen Prostate AI (8)(Maximum 6 weeks following enrolment)
  • Databank Link(Maximum 6 weeks following enrolment)
  • Consent to Linkage(Maximum 6 weeks following enrolment)
  • Cost-Effectiveness(Maximum 6 weeks following enrolment)
  • Galen Prostate AI (1)(Maximum 6 weeks following enrolment)
  • Galen Prostate AI (6)(Maximum 6 weeks following enrolment)
  • Galen Prostate AI (2)(Maximum 6 weeks following enrolment)
  • Galen Prostate AI (4)(Maximum 6 weeks following enrolment)
  • Galen Prostate AI (7)(Maximum 6 weeks following enrolment)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (6)

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