A Phase I Evaluation of Azidothymidine (AZT) in Children With Acquired Immune Deficiency Syndrome (AIDS) or AIDS Related Complex (ARC)

Inclusion Criteria

Concurrent Treatment:

Allowed:

• Nutritional support not exceeding 120 calories/kg/day (hyperalimentation or dietary supplements including vitamin, folate, iron supplements).

Exclusion Criteria

Co-existing Condition:

Children with the following conditions are excluded:

• Asymptomatic with T-lymphocyte deficiency.
• Asymptomatic viremic patients or those not meeting definition criteria of AIDS related complex (ARC) or AIDS.
• Clinical evidence of active infection of acute nature or active significant or clinically apparent opportunistic infection at time of entry into study.
• Hemoglobinopathy including sickle cell anemia.
• Congenital infections such as toxoplasmosis or herpes simplex virus infection in the first month after birth or cytomegalovirus infection in the first 6 months after birth.

Children with the following conditions are excluded:

• Asymptomatic with T-lymphocyte deficiency.
• Asymptomatic viremic patients or those not meeting definition criteria of AIDS related complex (ARC) or AIDS.
• Clinical evidence of active infection of acute nature or active significant or clinically apparent opportunistic infection at time of entry into study.
• Hemoglobinopathy including sickle cell anemia.
• Congenital infections such as toxoplasmosis or herpes simplex virus infection in the first month after birth or cytomegalovirus infection in the first 6 months after birth.

Prior Medication:

Excluded:

• Suramin.
• Ribavirin.
• HPA 23.
• Phosphonoformate.
• Ansamycin.
• Interleukin 2.
• Interferon.
• Excluded within 30 days of study entry:
• All cytolytic chemotherapeutic agents, immunomodulating agents including steroids and immunoglobulin preparations.
• Antivirals (acyclovir, ganciclovir).

Prior Treatment:

Excluded within 4 weeks of study entry:

• Lymphocyte transfusions for immune reconstitution.
• Excluded within 3 months of study entry:
• Bone marrow transplant.

Child who is seropositive for HIV antibody or has HIV viremia and presents with one or more of following clinical criteria and at least one of the laboratory criteria may be considered an ARC patient for purpose of study:

• Clinical criteria:
• Persistent oral candidiasis despite appropriate therapy.
• Wasting syndrome characterized by failure to thrive and malnutrition.
• Recurrent or chronic unexplained diarrhea.
• Lymphadenopathy (more than 1 cm) at 2 or more noncontiguous sites.
• Hepatomegaly with or without splenomegaly.
• Encephalopathy with loss of developmental milestones and cortical atrophy present on computed tomography (CT) examination.
• Recurrent bacterial infections (bacteremia, pneumonia, septic arthritis, meningitis).
• Cutaneous anergy as defined by lack of delayed cutaneous hypersensitivity to selected antigens.
• Laboratory criteria:
• Hypergammaglobulinemia (IgG or IgA) defined as immunoglobulin values exceeding the maximum age-adjusted level.
• Decreased number of total T-lymphocytes (2 SD from mean).
• Absolute depression in T-helper cells to less than 500/mm3.
• Depressed (equal to or more than 2 SD from normal mean) in vitro mitogen response to at least one antigen.
• One positive HIV culture within 3 months of study entry into the study or blood obtained and culture pending.
• Life expectancy greater than 6 months.
• Ambulatory and free of opportunistic infection at time of entry.
• Reliably diagnosed disease at least moderately indicative of underlying cellular immunodeficiency and no known cause of underlying cellular immunodeficiency or other reduced resistance reported to be associated with that disease.
• Disease accepted as sufficiently indicative of underlying cellular immunodeficiency by CDC. In absence of these opportunistic diseases, a histologically confirmed diagnosis of chronic lymphoid interstitial pneumonitis will be considered indicative of AIDS unless test(s) for HIV are negative.

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety