grant

Personalized Risk-AdaptIve Surveillance (PRAISE) - Implications of Algorithmic Bias

Organization UNIVERSITY OF WASHINGTONLocation SEATTLE, UNITED STATESPosted 1 Sept 2018Deadline 31 Aug 2026
NIHUS FederalResearch GrantFY2024Active Follow-upAddressAlgorithmsAreaAttentionBiological MarkersCRC screeningCancer SurvivorCancersChronic Granulocytic LeukemiaChronic Myelocytic LeukemiaChronic Myelogenous LeukemiaChronic Myeloid LeukemiaClinic VisitsClinicalClinical ManagementCohort StudiesCollaborationsCollectionColorectal CancerComplexConcurrent StudiesContinuity of CareContinuity of Patient CareContinuum of CareCouplingDataDecision MakingDecision TheoryDetectionDiagnosisDisease ProgressionDisease remissionDisparitiesDisparityEthnic GroupEthnic PeopleEthnic PopulationEthnic individualEthnicity PeopleEthnicity PopulationFaceFrequenciesFutureGoalsGuidelinesHealthHealth PolicyHeterogeneityIndividualIntuitionLife ExpectancyLong-Term SurvivorsMachine LearningMalignant NeoplasmsMalignant Ovarian NeoplasmMalignant Ovarian TumorMalignant TumorMalignant Tumor of the LungMalignant Tumor of the OvaryMalignant Tumor of the ProstateMalignant neoplasm of lungMalignant neoplasm of ovaryMalignant neoplasm of prostateMalignant prostatic tumorMeasurementMethodologyMethodsModelingMonitorMonitoring for RecurrenceMorbidityMorbidity - disease rateOutcomeOvary CancerPatient outcomePatient-Centered OutcomesPatient-Focused OutcomesPatientsPatternPerformancePoliciesPredicting RiskProstate CAProstate CancerProstate malignancyProstatic CancerPulmonary CancerPulmonary malignant NeoplasmRaceRacesRecommendationRecurrenceRecurrentRecurrent Malignant NeoplasmRecurrent Malignant TumorRecurrent diseaseRelapsed DiseaseRemissionResearchRiskScheduleSourceSubgroupTestingTimeUncertaintyUpdateWorkactive followupalgorithmic biasbio-markersbiologic markerbiomarkercancer carecancer recurrencecancer survivor carecancer survivorship careclinical practicecolorectal cancer detectioncolorectal cancer early detectioncolorectal cancer screeningcomparative effectivenesscomputer based predictioncostcost outcomesdecision making algorithmdetect colorectal cancerdisparities in racedisparity due to racedisparity in ethnicdoubtethnic based disparityethnic biasethnic disadvantageethnic disparityethnic inequalityethnic inequityethnic subgroupethnicity disparityethnicity groupfacesfacialfollow upfollow-upfollowed upfollowupforecasting riskhealth care policyhealthcare policyhigh riskimprovedindividual patientindividualized clinical decisionindividualized decisioninequality due to raceinequity due to raceinnovateinnovationinnovativeintuitivelongterm survivorslung cancermachine based learningmalignancymenmodel-based simulationmodels and simulationmortalityneoplasm/cancernovelovarian cancerparent grantpatient oriented outcomespatient subclasspatient subclusterpatient subgroupspatient subpopulationspatient subsetspatient subtypespersonalized clinical decisionpersonalized data-driven decisionpersonalized decisionpredict riskpredict riskspredicted riskpredicted riskspredicting risksprediction algorithmpredictive modelingpredictive riskpredicts riskrace based disparityrace based inequalityrace based inequityrace disparityrace related disparityrace related inequalityrace related inequityracialracial backgroundracial disparityracial inequalityracial inequityracial originracially unequalrisk predictionrisk prediction algorithmrisk prediction modelrisk predictionssimulationsurveillance strategysurvivorshipunnecessary treatment
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Full Description

ABSTRACT
Algorithmic bias is an emerging and highly relevant topic in health policy that draws attention to the idea that

seemingly well-performing predictive algorithms built using biased data can propagate systemic biases and

disparities existing in clinical practice. Our primary goal in the parent grant was to innovatively use machine

learning based risk prediction and value-of-information methodology to develop a personalized risk-adaptive

surveillance (PRAISE) framework and assess its impact on outcomes, including costs, time to recurrence and

survival, for colorectal cancer survivors who have been treated for their primary cancer and are under

surveillance for recurrence. Decision-making in the PRAISE framework is driven by dynamic risk predictions for

recurrence, which identify high-risk patients to target for more frequent surveillance testing. However, potential

sources of racial/ethnic disparities along the cancer care continuum from diagnosis to survivorship can lead to

distorted risk predictions during surveillance. Using distorted risk predictions can have implications for

decision-making, potentially propagating and exacerbating biases that exist in clinical practice and resulting in

poorer outcomes for certain subgroups. The overarching goal of the proposed research is to understand and

address algorithmic bias in the PRAISE framework. Specifically, we will first characterize heterogeneity in

current practice with respect to surveillance testing patterns, recurrence detection and survival across

racial/ethnic subgroups for patients diagnosed with and treated for colorectal cancer (Aim 1). This will help us

better understand the sources of bias in our data and will better inform our approach in Aim 2, where we will

use emerging and novel methods to mitigate racial/ethnic bias in our previously developed dynamic risk

prediction model for colorectal cancer recurrence. Finally, in Aim 3, we will develop an outcomes-based

framework to assess the implications of using a biased versus a bias-corrected risk prediction model to guide

surveillance testing among colorectal cancer survivors, specifically through their effect on decision-making and

subgroup-specific health and cost outcomes. This important work will motivate the use of new methods for

addressing bias in risk prediction models in cancer and other clinical areas.

Grant Number: 5R37CA218413-07
NIH Institute/Center: NIH

Principal Investigator: Aasthaa Bansal

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