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Evaluation of Influenza H1N1 Vaccine in Adults With Lymphoid Malignancies on Chemotherapy

Evaluation of Pandemic H1N1(2009) Influenza Vaccine in Adults With Lymphoid Malignancies on Active Systemic Treatment or Post Stem Cell Transplantation

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01016548
Enrollment
42
Registered
2009-11-19
Start date
2009-11-30
Completion date
2010-06-30
Last updated
2010-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Influenza A Virus, H1N1 Subtype, Lymphoma, Multiple Myeloma

Keywords

Lymphoma, Multiple myeloma, Leukemia, Lymphocytic, Chronic, B-Cell, Influenza A Virus, H1N1 Subtype, Influenza Vaccines, Bone Marrow Transplantation

Brief summary

The purpose of this study is to determine whether adults with hematologic malignancies on active systemic therapy or shortly after bone marrow transplantation need one or two doses of adjuvanted vaccine to achieve best possible rates of protection. An additional research question is whether baseline biomarkers of the cellular and humoral immune systems are associated with an antibody response to vaccination.

Detailed description

The novel influenza H1N1 virus responsible for a world-wide pandemic throughout 2009 (H1N1(2009)) is expected to cause a second wave of infection during the 2009/10 winter season. Vaccines against H1N1(2009) will be available in early November, 2009. Adults with hematologic disorders are at high risk of influenza-related complications, including death. Given that the vaccination dosing for the pandemic vaccine has been developed on healthy individuals, it is unknown whether this subgroup of patients will respond similarly. We will evaluate the safety and efficacy of the pandemic vaccine in patients with lymphoid malignancies receiving active systemic treatment, or who have recently undergone stem cell transplantation. Patients will be randomized to one or two doses of the approved adjuvanted vaccine; immune responses will be measured to identify the optimal regimen. Also, we will look for an association between biomarkers of the immune system and a response to the vaccine; this will be done by measuring baseline CD3, 4, 8, 19, and 56 cells by flow cytometry.

Interventions

BIOLOGICALAS03-adjuvanted H1N1 pandemic influenza vaccine

One dose constitutes 0.5mL of suspended vaccine via the intramuscular route.

Sponsors

Princess Margaret Hospital, Canada
CollaboratorOTHER
University Health Network, Toronto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Male or female, ages 20-65 * Diagnosis of lymphoproliferative disorder * One of the following types of systemic treatment: active chemo/immunotherapy at enrollment or completed within the last 3 months, OR auto/allo stem cell transplant recipient within the past 12 months * Able to provide consent and comply with trial requirements

Exclusion criteria

* Systemic hypersensitivity to hen's eggs, thimerosal, gentamicin * History of life-threatening reaction to prior influenza vaccination * Thrombocytopenia or bleeding disorder contraindicating IM injection * Pregnancy * Laboratory-confirmed infection with H1N1(2009) * IVIG infusion within the last three months

Design outcomes

Primary

MeasureTime frame
Seroconversion rates.Day 0, 21, 42

Secondary

MeasureTime frame
Adverse events to vaccination.Day 7, 21, 28.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026