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Artificial Intelligence vs. LIRADS in Diagnosing HCC on CT

Primary Purpose

HCC, Liver Cancer

Status
Recruiting
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Prototype artificial intelligence algorithm
LI-RADS
Sponsored by
The University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for HCC focused on measuring HCC, liver cancer, AI, deep learning, CT, imaging

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 1. Age >=18 years. 2. Defined as the at-risk population requiring regular liver ultrasonography surveillance. These include:

    1. Cirrhotic patients of any disease etiology,
    2. Chronic hepatitis B patients of age ≥40 years for men, age ≥50 years for women or with a family history of HCC.

      3. At least one new-onset focal liver nodule detected on liver ultrasonography.

      Exclusion Criteria:

      1. Liver nodules of <1 cm. Currently such nodules are not reported using LI-RADS criteria but are recommended for a repeat scan in 3-6 months. In patients with multiple liver nodules, the largest nodule will be assessed.
      2. Patients with contraindications for contrast CT imaging, including a history of contrast anaphylaxis and impaired renal function (glomerular filtration rate <30 ml/min).
      3. Patients with prior transarterial chemoembolization or other interventional procedures with intrahepatic injection of lipiodol. Lipiodol is extremely hyperdense on computed tomography and will preclude objective interpretation. Such patients were also excluded in the development of our prototype AI algorithm.

Sites / Locations

  • Department of Medicine, The University of Hong Kong, Queen Mary HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Prototype AI algorithm

LI_RADS interpretation

Arm Description

In-house prototype deep learning artificial intelligence algorithm

LI-RADS criteria will be assessed independently by two specified abdominal radiologists with at least 10 years of experience in cross-sectional abdominal imaging

Outcomes

Primary Outcome Measures

Diagnostic accuracy for HCC
Number of participants diagnosed with HCC using a composite clinical reference standard. A lesion will be considered positive for HCC based on histology (biopsy, surgical resection or explant) or achieving LR-5 criteria in subsequent imaging. A lesion will be considered negative for HCC if it demonstrated stability at imaging for at least 12 months, unequivocal spontaneous reduction, or disappearance in the absence of tumor treatment.

Secondary Outcome Measures

Other diagnostic performance parameters for HCC
Number of participants diagnosed with HCC using a composite clinical reference standard. A lesion will be considered positive for HCC based on histology (biopsy, surgical resection or explant) or achieving LR-5 criteria in subsequent imaging. A lesion will be considered negative for HCC if it demonstrated stability at imaging for at least 12 months, unequivocal spontaneous reduction, or disappearance in the absence of tumor treatment.
Interpretation time
Mean time for AI interpretation for recruited participants
Occurrence of technical failures
Number of technical failures overall

Full Information

First Posted
April 6, 2021
Last Updated
May 17, 2022
Sponsor
The University of Hong Kong
Collaborators
Education University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT04843176
Brief Title
Artificial Intelligence vs. LIRADS in Diagnosing HCC on CT
Official Title
A Prototype Artificial Intelligence Algorithm Versus Liver Imaging Reporting and Data System (LI-RADS) Criteria in Diagnosing Hepatocellular Carcinoma on Computed Tomography: a Randomized Trial
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 19, 2021 (Actual)
Primary Completion Date
December 31, 2025 (Anticipated)
Study Completion Date
June 30, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The University of Hong Kong
Collaborators
Education University of Hong Kong

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Liver cancer is the sixth most commonly diagnosed cancer and the fourth leading cause of cancer death worldwide. It is the 3rd most common cause of cancer death in Hong Kong. The five-year survival rates of liver cancer differ greatly with disease staging, ranging from 91.5% in early-stage to 11% in late-stage. The early and accurate diagnosis of liver cancer is paramount in improving cancer survival. Liver cancer is diagnosed radiologically via cross sectional imaging, e.g. computed tomography (CT), without the routine use of liver biopsy. However, with current internationally-recommended radiological reporting methods, up to 49% of liver lesions may be inconclusive, resulting in repeated scans and a delay in diagnosis and treatment. An artificial intelligence (AI) algorithm that that can accurately diagnosed liver cancer has been developed. Based on an interim analysis, the algorithm achieved a high diagnostic accuracy. The AI algorithm is now ready for implementation. This study aims to prospective validate this AI algorithm in comparison with the current standard of radiological reporting in a randomized manner in the at-risk population undergoing triphasic contrast CT. This research project is totally independent and separated from the actual clinical reporting of the CT scan by the duty radiologist. The primary study outcome is the diagnostic accuracy of liver cancer, which will be unbiasedly based on a composite clinical reference standard.
Detailed Description
Liver cancer is the sixth most commonly diagnosed cancer and the fourth leading cause of cancer death worldwide. The main disease burden is found in East Asia, in which the age-standardized incidence is 26.8 and 8.7 per 100,000 in men and women respectively. In 2017, among the top 10 most common cancers in Hong Kong, liver cancer had the highest case fatality rate of 84.6%. The five-year survival rates of hepatocellular carcinoma (HCC) differ greatly with disease staging, ranging from 91.5% in <2 cm with surgical resection to 11% in >5 cm with adjacent organ involvement. The early and accurate diagnosis of HCC is paramount in improving cancer survival. Unlike other common cancers, HCC is diagnosed by highly characteristic dynamic patterns on contrast-enhanced cross sectional imaging, without the need of pathological confirmation. The Liver Imaging Reporting and Data System (LI-RADS) was established to standardize the lexicon, interpretation and communication of radiological findings related to HCC. However, up to 49% of nodules identified in computed tomography (CT) in the at-risk population are categorized by LI-RADS as indeterminate, further delaying the establishment of diagnosis. There are currently studies pioneering the application of artificial intelligence (AI) in the field of medical imaging. A interdisciplinary research team of clinicians, radiologists and statistical scientists, based on the clinical and radiological database of over 4,000 liver images, and have developed an AI algorithm to accurately diagnose liver cancer on CT. Based on retrospective data, an interim analysis found the AI algorithm able to achieve a diagnostic accuracy of >97% and a negative predictive value of >99%. Can this novel prototype AI algorithm achieve a better performance in diagnosing HCC in the at-risk population when compared to LI-RADS? This question is especially relevant when the key to improved survival is early diagnosis, of which AI can potentially improve. Currently, errors in radiologist reporting are estimated to be 3-5% on a day-to-basis, equating to 40 million errors per annum worldwide. This prototype algorithm can be a solution to reduce human misinterpretation of radiological findings.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HCC, Liver Cancer
Keywords
HCC, liver cancer, AI, deep learning, CT, imaging

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Scanned images are randomized individually 1:1 to either the prototype AI algorithm or LI-RADS criteria interpretation by two specialist gastrointestinal radiologists
Masking
Investigator
Masking Description
. Both radiologists will be blinded to the clinical characteristics and subsequent management of participants, with any discordance in assessment resolved by consensus before reaching a final decision.
Allocation
Randomized
Enrollment
250 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Prototype AI algorithm
Arm Type
Active Comparator
Arm Description
In-house prototype deep learning artificial intelligence algorithm
Arm Title
LI_RADS interpretation
Arm Type
Placebo Comparator
Arm Description
LI-RADS criteria will be assessed independently by two specified abdominal radiologists with at least 10 years of experience in cross-sectional abdominal imaging
Intervention Type
Diagnostic Test
Intervention Name(s)
Prototype artificial intelligence algorithm
Intervention Description
Developed by the University of Hong Kong
Intervention Type
Diagnostic Test
Intervention Name(s)
LI-RADS
Intervention Description
The Liver Imaging Reporting and Data System (LI-RADS) was established to standardize the lexicon, interpretation and communication of radiological findings related to HCC
Primary Outcome Measure Information:
Title
Diagnostic accuracy for HCC
Description
Number of participants diagnosed with HCC using a composite clinical reference standard. A lesion will be considered positive for HCC based on histology (biopsy, surgical resection or explant) or achieving LR-5 criteria in subsequent imaging. A lesion will be considered negative for HCC if it demonstrated stability at imaging for at least 12 months, unequivocal spontaneous reduction, or disappearance in the absence of tumor treatment.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Other diagnostic performance parameters for HCC
Description
Number of participants diagnosed with HCC using a composite clinical reference standard. A lesion will be considered positive for HCC based on histology (biopsy, surgical resection or explant) or achieving LR-5 criteria in subsequent imaging. A lesion will be considered negative for HCC if it demonstrated stability at imaging for at least 12 months, unequivocal spontaneous reduction, or disappearance in the absence of tumor treatment.
Time Frame
12 months
Title
Interpretation time
Description
Mean time for AI interpretation for recruited participants
Time Frame
12 months
Title
Occurrence of technical failures
Description
Number of technical failures overall
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 1. Age >=18 years. 2. Defined as the at-risk population requiring regular liver ultrasonography surveillance. These include: Cirrhotic patients of any disease etiology, Chronic hepatitis B patients of age ≥40 years for men, age ≥50 years for women or with a family history of HCC. 3. At least one new-onset focal liver nodule detected on liver ultrasonography. Exclusion Criteria: Liver nodules of <1 cm. Currently such nodules are not reported using LI-RADS criteria but are recommended for a repeat scan in 3-6 months. In patients with multiple liver nodules, the largest nodule will be assessed. Patients with contraindications for contrast CT imaging, including a history of contrast anaphylaxis and impaired renal function (glomerular filtration rate <30 ml/min). Patients with prior transarterial chemoembolization or other interventional procedures with intrahepatic injection of lipiodol. Lipiodol is extremely hyperdense on computed tomography and will preclude objective interpretation. Such patients were also excluded in the development of our prototype AI algorithm.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wai-Kay Seto, MD
Phone
85222553579
Email
wkseto@hku.hk
First Name & Middle Initial & Last Name or Official Title & Degree
Keith Chiu, FRCR
Phone
85222553111
Email
kwhchiu@hku.hk
Facility Information:
Facility Name
Department of Medicine, The University of Hong Kong, Queen Mary Hospital
City
Hong Kong
Country
Hong Kong
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wai-Kay Seto, MD
Phone
+85222553579
Email
wkseto@hku.hk
First Name & Middle Initial & Last Name & Degree
Keith Chiu, FRCR
First Name & Middle Initial & Last Name & Degree
Lung Yi Mak, FRCP
First Name & Middle Initial & Last Name & Degree
Man-Fung Yuen, MD

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Available to bona fide researchers who approach to principal investigator

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Artificial Intelligence vs. LIRADS in Diagnosing HCC on CT

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