Integration of HPV Vaccination and HPV-based Cervical Screening Into ARV Clinics: the H2VICTORY Trial

ConditionHPV Infection
Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexFemale
Age25-35
SponsorInternational Agency for Research on Cancer

About this trial

A 3-dose HPV vaccination scheme has shown to be safe and immunogenic in people living with HIV (PLWH), although evidence on 1-dose, which is important to improve coverage, is scarce. Available HPV vaccines only prevent new infections. Since a large fraction of WLWH is already infected with HPV (\>50%), vaccines' efficacy to prevent HPV infections (and therefore cervical disease) in this population is limited. Current WHO cervical cancer screening guidelines recommend treatment of the transformation zone (TZ) of WLWH who harbor HPV infections either at initial screening or one year later. Therefore, HPV vaccination at the time of the screening may improve vaccines efficacy conferring protection to newly growing cells of the treated TZ against HPV infections/re-infections. Consequently, a dual-intervention of HPV vaccination and HPV-based cervical screening in WLWH may alleviate the burden of HPV-related disease by improving HPV vaccination efficacy while extending cervical screening intervals. Nevertheless, implementing the dual-intervention may be challenging particularly in some contexts without well-established cervical cancer screening such as sub-Saharan African (SSA) countries. However, in these countries, at least 60% of PLWH regularly attend ARV clinics to be monitored and receive ARV treatment (cART). Therefore, integrating the dual-intervention into ARV clinics seems to be an efficient approach to reduce loss to follow-up while improving overall coverages of HPV vaccination and cervical screening. Such integration may also facilitate the implementation of a platform for the delivery of other HPV-related preventive measures such as HPV therapeutic vaccines.

Nevertheless, little is known about the efficacy of HPV vaccination in WLWH to prevent HPV infections and HPV-related diseases, especially in young adults. Moreover, evidence on how best to conduct cervical cancer prevention, particularly recently released WHO guidelines, through ARV clinics is limited. Therefore, IARC/WHO in collaboration with HRP/WHO and colleagues in SSA proposes to conduct a hybrid effectiveness-implementation trial (H2VICTORY) to evaluate the effectiveness of the dual-intervention of HPV vaccination and HPV-based cervical screening to reduce HPV infections (and therefore, the risk of cervical cancer) in WLWH aged 25-35 years while conducting implementation research to identify facilitators and barriers for adoption and sustainability of proven evidence-based cervical cancer prevention approaches integrated into ARV clinics across sub-Saharan Africa.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Women living with HIV (WLWH)

Aged 25-35 years

Attending ARV clinics

Mentally competent to give informed consent

Disqualifiers

Pregnancy

Less than 3 months postpartum

Women without a cervix (e.g., hysterectomy)

Plans to move to another city in the next 2 years or any other reason to prevent finalizing the study

Trial design

Design model

Parallel

Treatments tested in this trial

  • HPV vaccine

    Biological/Vaccine

    Licensed HPV vaccines (bivalent, quadrivalent, or nonvalent) available in the country of the study site

  • HPV testing

    Diagnostic test

    HPV testing with partial genotyping of HPV16/18 (and/or 45) to be used as a primary cervical screening test for all participants regardless of the study arm

  • HAV vaccine

    Biological/Vaccine

    Hepatitis A virus (HAV) vaccine to be offered as a placebo

Treatment groups

8,000 Participants
are divided into 3 treatment groups
Group A: 3-doses HPV vaccinationExperimental treatment 2 interventions
Group B: 1-dose HPV vaccinationExperimental treatment 3 interventions
Group C: PlaceboPlacebo comparator 2 interventions

Trial outcomes

Primary outcomes

1

HPV infection

HPV prevalent infections at 24 months since initial screening

Time frame
24 months

Secondary outcomes

1

HPV antibodies

Neutralizing antibodies of HPV at entry and at 24 months

Time frame
24 months
2

CD4

CD4 counts at entry and at 24 months

Time frame
24 months
3

HIV viral load

HIV viral load at entry and at 24 months

Time frame
24 months
4

Adverse events (AEs)

Adverse events

Time frame
24 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

International Agency for Research on Cancer

Lead sponsor

University of New Mexico

Collaborator

University of Stellenbosch

Collaborator

University of KwaZulu

Collaborator

Coptic Hope Center

Collaborator

Emory University

Collaborator

Ministry of Health, Swaziland

Collaborator

Baylor College of Medicine Children's Foundation

Collaborator

Sefako Makgatho Health Sciences University

Collaborator

Aga Khan University

Collaborator

World Health Organization

Collaborator

This trial is not recruiting at the moment. You can still explore other options: