NCT Number: NCT00022035
Vaccine Therapy in Preventing Flu in Children With Acute Lymphoblastic Leukemia
RATIONALE: Flu vaccine may help the body build an immune response and decrease the occurrence of flu in children who are receiving chemotherapy for acute lymphoblastic leukemia.
PURPOSE: Clinical trial to study the effectiveness of vaccine therapy in preventing flu in children who have acute lymphoblastic leukemia.
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Conditions
Age range
1 year–20 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Primary location
Hackensack University Medical Center, Hackensack, New Jersey, United States
About this study
OBJECTIVES:
- Determine the immune response, in terms of the formation of protective antibody titers to influenza, in children with acute lymphoblastic leukemia treated with split-virus trivalent influenza vaccine.
- Correlate the formation of protective antibody titers following immunization with the absolute neutrophil counts and absolute lymphocyte counts in these patients at the time of vaccination.
OUTLINE: This is a multicenter study. Patients are stratified according to current treatment for acute lymphoblastic leukemia (consolidation chemotherapy vs maintenance chemotherapy vs off therapy for the past 6 months).
Patients receive split-virus trivalent influenza vaccine intramuscularly once or twice at 4 weeks apart for 2 doses.
Patients are followed at week 5. Patients receiving 2 doses of vaccine are also followed at week 9.
PROJECTED ACCRUAL: A total of 175 patients (50 receiving consolidation therapy, 75 receiving maintenance therapy, and 50 off therapy) will be accrued for this study within 2 years.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
DISEASE CHARACTERISTICS:
- Diagnosis of acute lymphoblastic leukemia
- In first remission after completion of induction chemotherapy
- Currently on active treatment OR
- Completed treatment within the past 6 months
PATIENT CHARACTERISTICS:
Age:
- 1 to 20 at time of diagnosis
Performance status:
- Not specified
Life expectancy:
- Not specified
Hematopoietic:
- Not specified
Hepatic:
- Not specified
Renal:
- Not specified
Pulmonary:
- No acute respiratory distress
Other:
- No history of Guillain-Barre syndrome
- No history of hypersensitivity to chicken eggs, egg products, or components of influenza virus vaccine, including thimerosal
- No febrile illness with fever over 100.4 degrees F
- Not pregnant or nursing
- Fertile patients must use effective contraception
PRIOR CONCURRENT THERAPY:
Biologic therapy:
- Not specified
Chemotherapy:
- See Disease Characteristics
Endocrine therapy:
- Not specified
Radiotherapy:
- Not specified
Surgery:
- Not specified
Other:
- At least 7 days since prior antibiotic or antiviral therapy except prophylactic antibiotics
Treatment and study plan
Sponsors and collaborators
Lead sponsor
Roswell Park Cancer Institute
Other
Collaborators
- National Cancer Institute (NCI)
Registry information
Official study title
Influenza Vaccine Immunogenicity in Children During and After Therapy for Acute Lymphoblastic Leukemia
Important dates
- Study start
- 2000
- Primary completion
- 2002
- First posted
- Jan 27, 2003
- Registry last updated
- Jan 31, 2013
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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