grant

Leveraging machine learning to improve risk prediction for chemotherapy inducedneuropathy

Organization STANFORD UNIVERSITYLocation STANFORD, UNITED STATESPosted 1 Jun 2020Deadline 31 May 2026
NIHUS FederalResearch GrantFY202421+ years oldActive Follow-upAddressAdjuvant ChemotherapyAdjuvant Drug TherapyAdultAdult HumanAffectAgeAwarenessBiometricsBiometryBiostatisticsBreastCancer TreatmentCancersCaringCharacteristicsChemotherapy-induced peripheral neuropathyChronicClinicalClinical DataClinical TrialsColorectal CancerCommunity HealthComplexComputer softwareDecision MakingDevelopmentDiagnosisDisablingDoseDose LimitingDrug TherapyElectronic Health RecordExtremitiesGoalsHealth Services EvaluationHealth Services ResearchImpairmentIndividualInterviewJournalsLifeLimb structureLimbsLoss of SensationMachine LearningMagazineMalignant Neoplasm TherapyMalignant Neoplasm TreatmentMalignant NeoplasmsMalignant TumorMedical Care ResearchMental DepressionMethodsModelingMotorNatureNeuropathyNewly DiagnosedNon-TrunkNumbnessObesityOncologyOncology CancerOutcomePNS DiseasesPainPainfulPatient CarePatient Care DeliveryPatient PreferencesPatientsPeer ReviewPeripheral Nerve DiseasesPeripheral Nervous System DiseasesPeripheral Nervous System DisordersPeripheral NeuropathyPersonsPharmacotherapyPlatinumPlatinum BlackPredicting RiskPreventionProbabilistic ModelsProbability ModelsProviderPt elementPublicationsQOLQuality of lifeRaceRacesReportingRiskRisk AssessmentRisk EstimateRisk FactorsSample SizeScientific PublicationSoftwareStatistical ModelsSymptomsTestingThinkingTimeToxic effectToxicitiesTranslationsTreatment PeriodTreatment ProtocolsTreatment RegimenTreatment ScheduleVinca Alkaloid CompoundVinca Alkaloidsactive followupadiposityadulthoodagesanaloganti-cancer therapyassociated symptomcancer carecancer epidemiologycancer invasivenesscancer survivor carecancer survivorship carecancer therapycancer typecancer-directed therapycare for patientscare of patientscare servicescare systemscaring for patientschemotherapychemotherapy induced neuropathyclinical decision-makingco-morbidco-morbid symptomco-morbidityco-occuring symptomcommunity based practicecommunity-based healthcomorbid symptomcomorbiditycomputer based predictionconcurrent symptomcooccuring symptomcorpulencedepressiondevelopmentaldisabilitydrug safetydrug treatmentelderly patientelectronic health care recordelectronic health medical recordelectronic health plan recordelectronic health registryelectronic medical health recordexperienceexperimentexperimental researchexperimental studyexperimentsfall riskfollow upfollow-upfollowed upfollowupforecasting riskhealth care settingshealthcare settingshigh riskimprovedmachine based learningmachine learning based methodmachine learning methodmachine learning methodologiesmalignancymath abilitymath achievementmath competencemath competencymath proficiencymathematic abilitymathematic achievementmathematic compentencemathematic compentencymathematic proficiencymathematical abilitymathematical achievementmathematical compentencemathematical compentencymathematical proficiencymedication safetyneoplasm/cancerneuron toxicityneuronal toxicityneuropathicneurotoxicitynumber sensenumeracyolder patientpharmaceutical safetypredict riskpredict riskspredicted riskpredicted riskspredicting riskspredictive modelingpredictive riskpredicts riskproficient in mathquantitative literacyracialracial backgroundracial originrisk predictionrisk predictionsservices researchside effectstatistical linear mixed modelsstatistical linear modelssurvivorshipsymptom associationsymptom comorbiditytaxanethoughtstooltranslationtreatment choicetreatment daystreatment duration
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Full Description

Project Summary/Abstract
Chemotherapy-induced peripheral neuropathy (CIPN) affects more than two-thirds of adults with

invasive cancer who receive select adjuvant chemotherapies (e.g., taxanes, platinum analogs).

Severe CIPN symptoms can lead to chemotherapy dose reductions, treatment delays, or

changes in treatment regimens; thereby affecting the potential curative effects of chemotherapy.

For some patients, CIPN symptoms can persist over time, contributing to lower quality of life.

Little is known about risk factors for CIPN. Chemotoxicity risk scores have been developed

and evaluated for use among elderly patients receiving chemotherapy. However, these tools

generally report moderate predictive accuracy (60%-70%), small sample sizes, and short-term

follow up. We are aware of no publicly available, validated risk models to assess risk of severe

and chronic CIPN among diverse patients at risk for this potentially disabling side effect.

The goal of this proposal is to identify patients at risk for CIPN and to understand how

patients and provider interpret and use CIPN risk information in clinical decision-making.

Focusing on more than 8,500 insured adults (18+) diagnosed with invasive, stage I-III breast

and II-IIIA colorectal cancers (2013-2021) who received adjuvant chemotherapy treatment with

known risk for CIPN, we will develop and validate predictive models to quantify the risk of

severe CIPN and incident chronic CIPN and assess how CIPN risk information might be used to

inform clinical decision-making about cancer treatment and survivorship care planning.

We hypothesize that CIPN risk is a high priority for patients in thinking about treatment

choice and survivorship care planning. In addition, we hypothesize that the relative importance

of CIPN risk for patient and provider decision-making will vary by patient characteristics (e.g.,

age, cancer stage). We anticipate that the risk of severe and chronic CIPN can be predicted

with a high degree of accuracy using electronic health records and machine learning methods.

The study team has significant and complementary expertise in health services research,

biostatistics and predictive modeling, oncology practice, cancer epidemiology,

pharmacotherapy, drug safety and the patient care experience. To our knowledge, this will be

one of the first studies to develop and validate a CIPN predictive model that can be used by

oncology teams to inform treatment and care planning decisions and improve patient-valued

outcomes. Translation and replication of the findings will be catalyzed through publication in

peer-reviewed journals and the development and distribution of free software to facilitate testing

and adaptation of the resulting risk models across diverse systems of care.

Grant Number: 5R01CA249127-05
NIH Institute/Center: NIH

Principal Investigator: Alyce Adams

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