grant

Neurocognitive Changes from Long-Term Androgen Deprivation Therapy in Prostate Cancer Patients

Organization YALE UNIVERSITYLocation NEW HAVEN, UNITED STATESPosted 13 Aug 2018Deadline 31 Jul 2026
NIHUS FederalResearch GrantFY2023AccelerationActive Follow-upAdjuvant TherapyAnxietyBiological MarkersBrainBrain Nervous SystemBrain imagingBreast Cancer TreatmentCancer PatientCancer TreatmentCaringCerebrumCharacteristicsClinicalClinical ManagementClinical assessmentsCognitionCognitiveCognitive DisturbanceCognitive ImpairmentCognitive declineCognitive deficitsCognitive function abnormalConsensusControl GroupsDiseaseDisorderDisturbance in cognitionEarly DiagnosisEarly treatmentElderlyEncephalonEvaluationFundingFutureGoalsHormonalImaging DeviceImaging InstrumentImaging ToolImpaired cognitionImpairmentIndividualInterventionIntervention StrategiesKnowledgeLifeMR ImagingMR TomographyMRIMRIsMagnetic Resonance ImagingMalignant Neoplasm TherapyMalignant Neoplasm TreatmentMalignant Tumor of the ProstateMalignant neoplasm of prostateMalignant prostatic tumorMedical Imaging, Magnetic Resonance / Nuclear Magnetic ResonanceMedical RehabilitationMental DepressionMetastasisMetastasizeMetastatic LesionMetastatic MassMetastatic NeoplasmMetastatic Prostate CancerMetastatic TumorNCI OrganizationNMR ImagingNMR TomographyNational Cancer InstituteNeoplasm MetastasisNeurocognitiveNeuropsychologic TestsNeuropsychological TestsNuclear Magnetic Resonance ImagingOutcomePSA levelParticipantPatientsPilot ProjectsPopulationProstate CAProstate CancerProstate Carcinoma MetastaticProstate malignancyProstatic CancerQOLQuality of Life AssessmentQuality of lifeQuestionnairesRehabilitationRehabilitation therapyResearchRiskSecondary NeoplasmSecondary TumorSeveritiesStructureSystemTechniquesTestingThickThicknessThinkingTimeTreatment PeriodTreatment ProtocolsTreatment RegimenTreatment ScheduleVulnerable PopulationsWomanWorkYale Cancer CenterZeugmatographyactive followupadjuvant treatmentadvanced ageandrogen ablation therapyandrogen blockade therapyandrogen deprivation therapyandrogen deprivation treatmentanti-cancer therapyanticancer therapyarmassociated symptombio-markersbiologic markerbiomarkerbrain visualizationcancer metastasiscancer therapycancer-directed therapycerebralchemotherapyclinical decision-makingco-morbid symptomco-occuring symptomcognitive assessmentcognitive changecognitive defectscognitive dysfunctioncognitive functioncognitive losscognitive neurosciencecognitive processcognitive recoverycognitive testingcohortcomorbid symptomcomputerizedconcurrent symptomcooccuring symptomdepressionearly detectionearly therapyeldersfollow upfollow-upfollowed upfollowupfunctional statusgeriatricgray matterindividual heterogeneityindividual variabilityindividual variationinterventional strategylate lifelater lifemenmulti-modalitymultimodalityneuralneural correlateneurocognitive testolder adultolder personpilot studypreservationprostate specific antigen levelrecruitrehab therapyrehabilitativerehabilitative therapysenior citizenside effectsubstantia albasubstantia griseasymptom associationsymptom comorbiditythoughtstreatment daystreatment durationtreatment grouptreatment guidelinestumor cell metastasisvulnerable groupvulnerable individualvulnerable peoplewhite matter
Sign up free to applyApply link · pipeline · email alerts
— or —

Get email alerts for similar roles

Weekly digest · no password needed · unsubscribe any time

Full Description

ABSTRACT/SUMMARY
The goal of this proposal is to examine the component and neural processes of cognitive impairment in

prostate cancer patients undergoing androgen deprivation therapy (ADT). We will combine neurocognitive

testing, clinical assessments, and brain imaging to examine cognitive impairment and its impact on quality of

life and identify the structural and functional brain changes that predict the severity of cognitive deficits. Early

detection of cognitive side effects of ADT would facilitate clinical decision making in the treatment and care of

prostate cancer patients.

ADT has proven efficacy in the treatment of many patients with metastatic prostate cancer. However,

there is a lack of consensus in the indications for and optimal duration of ADT in prostate cancer patients

without metastatic disease. Evidence grows to suggest that ADT may cause cognitive deficits that can have a

negative impact on the quality of life in these patients. However, extant studies using traditional

neuropsychological testing batteries have not consistently characterized ADT-induced cognitive impairment. It

remains unclear whether or when these cognitive deficits will occur in a patient undergoing ADT, whether these

deficits pertain broadly or only to specific cognitive domains, and whether the deficits are reversible.

Furthermore, there are no established biomarkers that may predict cognitive deficits induced by ADT. Our

preliminary findings suggest that cerebral changes may predate clinical manifestations of ADT-induced

cognitive impairment. As many prostate cancer patients will receive ADT for many years or for life, according to

current treatment protocols, it is of critical importance to identify individuals at risk for cognitive impairment.

To this end, we propose to employ longitudinal neurocognitive and clinical assessments, as well as

brain imaging, to identify cognitive impairment due to ADT and its impact on quality of life, to examine whether

these changes depend on treatment duration and are reversible after a short duration of treatment, and to

investigate cerebral markers that may predict cognitive impairment in a large cohort of prostate cancer patients

undergoing ADT and control patients not receiving ADT. Our over-arching goal is to thoroughly evaluate the

impact of ADT on cognition early during treatment. Studies of cognitive impairment in women receiving

chemotherapy have influenced our thoughts about early treatment of breast cancer. Similarly, the findings from

this study could enhance our understanding of the risks associated with ADT and inform clinical management

of men with prostate cancer.

Grant Number: 5R01CA218501-06
NIH Institute/Center: NIH

Principal Investigator: Herta Chao

Sign up free to get the apply link, save to pipeline, and set email alerts.

Sign up free →

Agency Plan

7-day free trial

Unlock procurement & grants

Upgrade to access active tenders from World Bank, UNDP, ADB and more — with email alerts and pipeline tracking.

$29.99 / month

  • 🔔Email alerts for new matching tenders
  • 🗂️Track tenders in your pipeline
  • 💰Filter by contract value
  • 📥Export results to CSV
  • 📌Save searches with one click
Start 7-day free trial →