Outcome at 5 Years of Early Treated HIV Infected Infants in the PEDIACAM Project (PEDIACAM)

January 28, 2025 updated by: ANRS, Emerging Infectious Diseases

Outcome at 5 Years of Early Treated HIV Infected Infants on Antiretroviral Multi-therapy in the PEDIACAM ANRS12140 Project in Cameroon

This study aims to assess the long-term outcomes of children infected with HIV, having participated in the ANRS 12140 PediacamI study, in terms of: clinical and immunovirological response to ARV therapy, long-term ARV tolerance, and the impact of family environment and lifestyle on adherence to ARV treatment.

Study Overview

Status

Active, not recruiting

Conditions

Detailed Description

The follow-up of HIV infected children is an important part of their access to antiretroviral drugs. This therapeutic follow-up has an impact on infant morbidity and mortality and remains challenging due to its complexity (multi-drug therapy), the use of galenic forms that are not well adapted to children, the risks of toxicity and their prolonged administration, and the evolution of this syndrome in the patients' parents. Currently, while access to ARV is being ameliorated for children in Sub-Saharan Africa, little information is available on medium to long-term evolution of early treated HIV infected infants on ARV treatment. In Cameroon, the PEDIACAM ANRS 12140 study assessed for a period of 2 years, the impact and feasibility of early ARV treatment in HIV infected children and their humoral responses to EPI vaccines.

This first study (PEDIACAM ANRS 12140) began in November 2007 and consisted of two phases. During the first phase all children born from HIV+ mothers in the maternity wards of the participating hospitals were invited to participate. For every infant born from an HIV+ mother, an infant born from an HIV- mother was matched. A total of 2052 pairs of infants were recruited and they were all followed up to the age of 14 weeks. All infants born from seropositive mothers had a PCR HIV diagnostic test at the age of 6 weeks.

The second phase began after the age of 14 weeks. It consisted of four groups of infants: a group of HIV+ infants born from HIV+ mothers and followed from birth (n=69); a group of HIV- infants born from HIV+ mothers and followed from birth (n=205); a control group including a subset of the HIV- children born from HIV- mothers that had been followed since birth (n=196); and a final group that was added at this phase including HIV+ children that had not been followed up since birth but who had been diagnosed before the age of 7 months at any of the trial sites (n=141). During this phase, children were followed up to the age of 2 years. During these two years (phase I and phase II) the following criteria were evaluated: feasibility of early ARV treatment in infants, treatment tolerance, efficacy and adherence, clinical and immuno-virological prognosis of HIV infection in infants, rate of MTCT according to prevention strategies and humoral response to vaccines,.

The prolongation to 5 years of follow-up of the children participating in Phase II of the study constitutes the present study, ANRS 12225 PEDIACAM II. This follow up includes HIV non-infected children and is a unique opportunity to describe the medium to long-term clinical and immunovirological prognosis of the HIV infection in children and to further identify factors associated with treatment failure.

This second part of PEDIACAM, is a prospective longitudinal, observational, national multi-centered study including two groups of infants: one group of HIV infected infants treated early, and one group of HIV non-infected infants (born to either HIV infected or HIV non-infected mothers). Participation in the study will be proposed to all the infants included in phase II of PEDIACAM ANRS 12140, if possible before the age of 2 years. Only children whose parents or legal guardians consent to this continuation of the follow-up will be included. The children participating in the study will be seen for consultation every 6 months until the last child included reaches the age of 5 years. In the course of each visit, a clinical examination will be carried out as well as a complete laboratory examination. Antiretroviral treatment will be in line with the national recommendations and guidelines.

Four hundred sixty (460) children including 148 HIV-infected and 312 HIV-uninfected have been included in ANRS 12225 - Pediacam II study. We hypothesize for the next three years follow up period a low rate of missing HIV-infected children (death or loss to follow up) of about 5% and 20% for HIV-uninfected children. With such hypothesis, we will have at the end of the study, information of 140 HIV-infected and 250 HIV-uninfected children for our analysis

This cohort will enable us to answer the questions that arise regarding the long-term outcomes of HIV infected children in terms of clinical prognosis and immunology, and the impact of family environment and lifestyle on ARV treatment adherence. It will also aid in structuring the follow-up of children treated with ARVs in Cameroon. Furthermore, this study will continue to observe the response to vaccines. It will enable the identification of possible failures in the vaccination program and will enable us to propose, if necessary, an adjustment of the vaccine calendar.

Study Type

Observational

Enrollment (Estimated)

460

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • Cameroon
      • Douala, Cameroon
        • Hôpital Laquintinie
      • Yaounde, Cameroon
        • Centre Hospitalier d'Essos
      • Yaounde, Cameroon
        • Centre Mère et Enfant de la Fondation Chantal Biya

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

No older than 5 years (Child)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Children

Description

Inclusion Criteria:

  • infants having participated in the ANRS 12140 PEDIACAM study
  • HIV+ or HIV-
  • signed consent
  • born from HIV+ mothers having received perinatal ARV therapy or not
  • or HIV- mothers

Exclusion Criteria:

  • unsigned consent form

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
children VIH+
children infected with HIV
Chlidren VIH-
uninfected children born from HIV-positive or HIV-negative mothers

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Number of clinical/biological events related to HIV infection
Time Frame: 5 years
5 years

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Number clinical/biological events grade 3 or higher and their potential relationship to ARV therapy, HIV infection or vaccines
Time Frame: 5 years
5 years
Emergence of genotypic mutations of viral resistance to treatment in infants with virologic failure
Time Frame: 5 years
Virologic failure is defined by a value of viral load > 400 copies / ml measured by RT-PCR after 6 months of treatment
5 years
Survival of infants
Time Frame: 5 years
5 years
Age at switch to second line of ARV treatment
Time Frame: 5 years
The duration of therapy without changes in treatment will also be monitored.
5 years
Clinical and immunovirological response to treatment
Time Frame: 5 years
Success is defined as viral load < 400 copies/ml and a rise in CD4 count of at least 20% at 6 months of treatment, and no recorded drops in CD4 counts of more than 25%
5 years
Regularity of consultations and relationship of the person bringing the child to consultation.
Time Frame: 5 years
5 years
Death of parent or sibling
Time Frame: 5 years
5 years
Changes in living situation.
Time Frame: 5 years
Changes of address and living space, separation of parents, changes of members of the family living with the infant (siblings, cousins, uncles, grandparents), transfer of the infant to public institutions or adoption, will all be monitored in the scheduled visits throughout the 5 year follow-up.
5 years
Communication of child's HIV status to family and community
Time Frame: 5 years
5 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

ANRS, Emerging Infectious Diseases

Collaborators

Assistance Publique - Hôpitaux de Paris
Institut National de la Santé Et de la Recherche Médicale, France
Institut Pasteur
Centre Pasteur du Cameroun
Centre Mère et Enfant de la Fondation Chantal Biya
Centre Hospitalier D'essos
Hospital General De Douala

Investigators

  • Principal Investigator: Mathurin Tejiokem, Dr, Centre Pasteur du CAmeroun
  • Principal Investigator: Albert Faye, Pr, Hôpital Universitaire Robert-Debré

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Helpful Links

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 1, 2007

Primary Completion (Estimated)

July 1, 2025

Study Completion (Estimated)

July 1, 2025

Study Registration Dates

First Submitted

January 21, 2014

First Submitted That Met QC Criteria

January 21, 2014

First Posted (Estimated)

January 23, 2014

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 28, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • ANRS 12140 -12225

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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