Implementing HIV/Cervical Cancer Prevention CASCADE Clinical Trials in Uganda (CASCADE UGANDA)
Project Number5UG1CA275412-03
Contact PI/Project LeaderMWESIGWA, BETTY
Awardee OrganizationMAKERERE UNIVERSITY WALTER REED PROJECT
Description
Abstract Text
PROJECT SUMMARY/ABSTRACT
Uganda is one of 8 countries with the highest burden of cervical cancer (CXCA) among women living with HIV
(WLWH) with an HIV-attributable age-standardized incidence rate of 10–20 per 100,000. Strategies for Cervical
Cancer (CXCA) prevention include targeted Human Papillomavirus (HPV) vaccination, screening of women aged
25-49 years by visual inspection with acetic acid (VIA) or HPV DNA testing, and precancer treatment by
cryotherapy or ablation. However, there is limited and sparse availability of and access to CXCA interventions
which is compounded by low-uptake of ‘screen and treat’ strategies. Scalable, affordable, point-of-care, clinically
proven novel interventions (including HPV self-sampling techniques, HPV molecular biomarker tests, precancer
diagnostics and imaging techniques, and ablative and excisional treatments) are imperative. Further, the
effectiveness of these novel clinically proven interventions remains unknown which limits implementation in
intended-use settings in the US and low- and middle-income countries (LMICs). To support on-going efforts to
roll-out novel screen and treat strategies, the Makerere University WalterReed Project (MUWRP) in partnership
with the U.S. Military HIV Research Program (MHRP) propose to participate in the HIV/Cervical Cancer
Prevention ‘CASCADE’ Clinical Trials Network as a UG1 Clinical Research Site (UG1 CRS) to implement
pragmatic clinical trials in Uganda. We will: 1) leverage MUWRP’s expertise and experience in clinical trials and
CXCA prevention among WLWH to provide valuable insight and input on study feasibility, clinical significance
and local context during concept and protocol development; 2) accrue CASCADE targets in a timely manner and
retain ≥ 95% of study participants leveraging MUWRP’s pluripotent experience, clinical research infrastructure
and resources; and 3) provide competent leadership to ensure procedural fidelity to protocols and all applicable
regulations and guidelines. MUWRP will also support UG1 Research Bases and U24 Coordination Center to
obtain ethical and regulatory approvals for CASCADE trials, and implement clinical trial protocols with fidelity.
MUWRP is an ideal and rational choice for a UG1 CRS as MUWRP has: 1) access to over 37,000 WLWH in
urban, semi-urban, and rural settings at 114 health facilities supported by MUWRP’s Comprehensive HIV/AIDS
Prevention, Care and Treatment in Central Uganda (CARE) program funded by the U.S. President's Emergency
Plan for AIDS Relief (PEPFAR); 2) extensive experience conducting HIV clinical research and CXCA screening
and precancer treatment in the African Cohort Study, and CARE supported CXCA program; and 3) internationally
renowned scientists with experience and expertise in conducting clinical trials involving WLWH in Uganda and
other LMICs. MUWRP’s expertise and capacity will support all four research focus areas of the CASCADE
Network. MUWRP and MHRP will generate evidence that ultimately informs CXCA policy and screen and treat
strategies for WLWH.
Public Health Relevance Statement
PROTOCOL NARRATIVE
The Makerere University WalterReed Project (MUWRP) in partnership with the U.S. Military HIV Research
Program (MHRP) proposes to implement CASCADE clinical trials in central Uganda as a UG1 Clinical Research
Site. Leveraging MUWRP’s clinical research experience, resources and pluripotent infrastructure and resources,
as well as MUWRP’s Comprehensive HIV/AIDS Prevention, Care and Treatment in Central Uganda (CARE)
program; funded by U.S. President’s Emergency Plan For AIDS Relief (PEPFAR); MUWRP and MHRP
investigators will: 1) support UG1 Research Bases to develop concepts and protocols by providing insight and
input in study feasibility, clinical significance (with a local context), 2) efficiently accrue and retain participants for
all clinical trials; and 3) provide operational leadership to clinical and research staff implementing protocols at
selected study sites in Uganda. CASCADE clinical trials and activities conducted by MUWRP and MHRP (entitled
‘Implementing HIV/Cervical Cancer Prevention ‘CASCADE’ Clinical Trials in Uganda (CASCADE-UGANDA)) will
generate invaluable evidence for novel interventions for CXCA screening and precancer treatment.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AIDS preventionAblationAccreditationAcetic AcidsAcquired Immunodeficiency SyndromeAddressAfricanAgeAreaAwarenessCancer BurdenCancer InterventionCancer Prevention InterventionCaringClinicClinic VisitsClinicalClinical ResearchClinical TrialsClinical Trials NetworkCohort StudiesCold TherapyCommunitiesCommunity NetworksCompetenceConduct Clinical TrialsCountryDNADevelopmentDiagnostic ProcedureDiagnostic Reagent KitsEducationEffectivenessEmergency SituationEnsureEnvironmentEthicsExcisionFeasibility StudiesFundingGoalsGood Clinical PracticeGuidelinesHIVHealthHealth PersonnelHealth care facilityHuman Papilloma Virus VaccinationHuman PapillomavirusImaging TechniquesIncidenceInfrastructureInternationalInterventionLaboratoriesLeadershipLesionMalignant NeoplasmsMalignant neoplasm of cervix uteriMilitary PersonnelMolecularParticipantPerceptionPhasePoliciesPragmatic clinical trialPrevention strategyProceduresProspective StudiesProtocols documentationRampRegulationResearchResearch InfrastructureResearch PersonnelResource-limited settingResourcesSamplingScientistScreening for cancerSiteStandardizationSupervisionTechniquesTestingThermal Ablation TherapyTrainingTranslatingUgandaUniversitiesVisualWomanWomen's Groupagedbasecancer preventioncarcinogenesiscervical cancer preventionclinical research siteclinical trial protocolclinically significantcommunity collaborationcommunity engagementcommunity organizationscomorbidityexperiencehuman subject protectioninsightinterestlow and middle-income countriesmolecular markernovelparticipant retentionpoint of carepragmatic trialpremalignantprogramsprotocol developmentrecruitretention raterural settingscale upscreeningskillssocial stigmauptakeurban setting
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