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Vaccination response in lymphoma patients treated with CHOP and rituximab

Vaccination response in lymphoma patients treated with CHOP and rituximab - RIVAC

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON32777
Enrollment
140
Registered
2009-03-23
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

B-cell malignancy lymph node cancer

Interventions

all patients will receive the pneumococcal conjugate vaccine Prevnar®, the Hib conjugate vaccine Act-Hib®, the influenza virus vaccine Influvac® and the pneumococcal polysaccharide vaccine Pneumovax

Sponsors

Sint Antonius Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Patients with non-Hodgkin's lymphoma, treated with rituximab (approximately 6-8 cycles) and who are in remission. - Completion of rituximab therapy in the last twelve months before start of the study - Age 18 years or older - Signing of informed consent

Exclusion criteria

Exclusion criteria: - Vaccination with Hib or pneumococcal vaccine in the last fifteen months before start of the study - Fever at time of vaccination - Previous/known allergic reaction to any of the components of the vaccines given

Design outcomes

Primary

MeasureTime frame
Antibody titres against S. pneumoniae and H. influenzae type b (in µg/mL) and the influenza virus before and after vaccination. The association between the reconstitution of immune function after treatment with rituximab (in terms of amount of B-cells and immunoglobulin levels) and the rise in antibody titre.

Secondary

MeasureTime frame
o The effect of the use of growth factor during chemotherapy on the response to vaccination o The relationship between time since last rituximab-dose and the rise in antibody titre

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)