A Study Protocol for a Comprehensive Evaluation of Two Artificial Intelligence‐Based Tools in Title and Abstract Screening for the Development of Evidence‐Based Cancer Guidelines

ABSTRACT Background Conducting a systematic review (SR) is a time‐intensive process and represents the first phase in developing a clinical practice guideline (CPG). Completing a CPG through the Program in Evidence‐Based Care (PEBC), a globally acknowledged guideline program supported by Ontario Hea...

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Main Authors: Xiaomei Yao, Ashirbani Saha, Sharan Saravanan, Ashley Low, Jonathan Sussman
Format: Article
Language:English
Published: Wiley 2025-08-01
Series:Cancer Innovation
Subjects:
Online Access:https://doi.org/10.1002/cai2.70021
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author Xiaomei Yao
Ashirbani Saha
Sharan Saravanan
Ashley Low
Jonathan Sussman
author_facet Xiaomei Yao
Ashirbani Saha
Sharan Saravanan
Ashley Low
Jonathan Sussman
author_sort Xiaomei Yao
collection DOAJ
description ABSTRACT Background Conducting a systematic review (SR) is a time‐intensive process and represents the first phase in developing a clinical practice guideline (CPG). Completing a CPG through the Program in Evidence‐Based Care (PEBC), a globally acknowledged guideline program supported by Ontario Health (Cancer Care Ontario), typically takes about 2 years. Thus, expediting an SR can significantly reduce the overall time required to complete a CPG. Our recently published review identified two artificial intelligence (AI) tools, DistillerSR and EPPI‐Reviewer that reduced time in the title and abstract screening in an SR process when developing a CPG. However, the consistency and generalizability of these tools remain unclear within or across different SRs related to cancer. This study protocol aims to evaluate and compare the performance of DistillerSR and EPPI‐Reviewer against human reviewers for title and abstract screening (Stage I screening) in cancer CPG development. Methods We will conduct a retrospective simulation study to evaluate and compare the performance of DistillerSR and EPPI‐Reviewer across 10 previously published CPGs by PEBC. These CPGs include the five cancer types with the highest incidence (lung, breast, prostate, colorectal, and bladder). We will run 30 simulation trials for one CPG per AI tool. Primary outcomes are workload savings and time savings in Stage I screening. The secondary outcome is the percentage of missing articles among the final included articles. This informs the accuracy and comprehensiveness of the AI tools. Descriptive and inferential statistical analysis will be conducted to evaluate the outcomes. Results This is a study protocol. The data presented in the tables are illustrative examples rather than actual study results, in accordance with the journal s standard structure. All data included in the final study will be thoroughly validated. Discussion This will be the first study to investigate and compare the performance of DistillerSR and EPPI‐Reviewer in Stage I screening of SRs in CPGs across different cancer types. These findings will inform the reliable use of AI tools in future cancer‐related CPGs. The results from this retrospective study will need to be confirmed by prospective studies.
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spelling doaj-art-a5219cedab49431e82d0b737645bc1cd2025-08-20T03:28:48ZengWileyCancer Innovation2770-91912770-91832025-08-0144n/an/a10.1002/cai2.70021A Study Protocol for a Comprehensive Evaluation of Two Artificial Intelligence‐Based Tools in Title and Abstract Screening for the Development of Evidence‐Based Cancer GuidelinesXiaomei Yao0Ashirbani Saha1Sharan Saravanan2Ashley Low3Jonathan Sussman4Department of Health Research Methods, Evidence, and Impact McMaster University Hamilton Ontario CanadaDepartment of Oncology McMaster University Hamilton Ontario CanadaFaculty of Health Sciences McMaster University Hamilton Ontario CanadaFaculty of Health Sciences McMaster University Hamilton Ontario CanadaDepartment of Oncology McMaster University Hamilton Ontario CanadaABSTRACT Background Conducting a systematic review (SR) is a time‐intensive process and represents the first phase in developing a clinical practice guideline (CPG). Completing a CPG through the Program in Evidence‐Based Care (PEBC), a globally acknowledged guideline program supported by Ontario Health (Cancer Care Ontario), typically takes about 2 years. Thus, expediting an SR can significantly reduce the overall time required to complete a CPG. Our recently published review identified two artificial intelligence (AI) tools, DistillerSR and EPPI‐Reviewer that reduced time in the title and abstract screening in an SR process when developing a CPG. However, the consistency and generalizability of these tools remain unclear within or across different SRs related to cancer. This study protocol aims to evaluate and compare the performance of DistillerSR and EPPI‐Reviewer against human reviewers for title and abstract screening (Stage I screening) in cancer CPG development. Methods We will conduct a retrospective simulation study to evaluate and compare the performance of DistillerSR and EPPI‐Reviewer across 10 previously published CPGs by PEBC. These CPGs include the five cancer types with the highest incidence (lung, breast, prostate, colorectal, and bladder). We will run 30 simulation trials for one CPG per AI tool. Primary outcomes are workload savings and time savings in Stage I screening. The secondary outcome is the percentage of missing articles among the final included articles. This informs the accuracy and comprehensiveness of the AI tools. Descriptive and inferential statistical analysis will be conducted to evaluate the outcomes. Results This is a study protocol. The data presented in the tables are illustrative examples rather than actual study results, in accordance with the journal s standard structure. All data included in the final study will be thoroughly validated. Discussion This will be the first study to investigate and compare the performance of DistillerSR and EPPI‐Reviewer in Stage I screening of SRs in CPGs across different cancer types. These findings will inform the reliable use of AI tools in future cancer‐related CPGs. The results from this retrospective study will need to be confirmed by prospective studies.https://doi.org/10.1002/cai2.70021abstract screeningartificial intelligencecancer screeningclinical practice guidelinesDistillerSREPPI‐reviewer
spellingShingle Xiaomei Yao
Ashirbani Saha
Sharan Saravanan
Ashley Low
Jonathan Sussman
A Study Protocol for a Comprehensive Evaluation of Two Artificial Intelligence‐Based Tools in Title and Abstract Screening for the Development of Evidence‐Based Cancer Guidelines
Cancer Innovation
abstract screening
artificial intelligence
cancer screening
clinical practice guidelines
DistillerSR
EPPI‐reviewer
title A Study Protocol for a Comprehensive Evaluation of Two Artificial Intelligence‐Based Tools in Title and Abstract Screening for the Development of Evidence‐Based Cancer Guidelines
title_full A Study Protocol for a Comprehensive Evaluation of Two Artificial Intelligence‐Based Tools in Title and Abstract Screening for the Development of Evidence‐Based Cancer Guidelines
title_fullStr A Study Protocol for a Comprehensive Evaluation of Two Artificial Intelligence‐Based Tools in Title and Abstract Screening for the Development of Evidence‐Based Cancer Guidelines
title_full_unstemmed A Study Protocol for a Comprehensive Evaluation of Two Artificial Intelligence‐Based Tools in Title and Abstract Screening for the Development of Evidence‐Based Cancer Guidelines
title_short A Study Protocol for a Comprehensive Evaluation of Two Artificial Intelligence‐Based Tools in Title and Abstract Screening for the Development of Evidence‐Based Cancer Guidelines
title_sort study protocol for a comprehensive evaluation of two artificial intelligence based tools in title and abstract screening for the development of evidence based cancer guidelines
topic abstract screening
artificial intelligence
cancer screening
clinical practice guidelines
DistillerSR
EPPI‐reviewer
url https://doi.org/10.1002/cai2.70021
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