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PEPtalk: postexposure prophylaxis against varicella in children with cancer
Jessica Bate1, Julia Chisholm, Paul T Heath
1Division of Clinical Sciences, St George's, University of London, London, UK.
Insights
Postexposure prophylaxis (PEP) for varicella zoster virus (VZV) in UK and Ireland children with cancer is inconsistent. A trial comparing VZIG and aciclovir for VZV PEP is needed.
Area of Science:
- Pediatric Oncology
- Infectious Disease Prevention
- Immunology
Background:
- Children undergoing cancer treatment are immunocompromised and at high risk for severe varicella zoster virus (VZV) infections.
- Effective postexposure prophylaxis (PEP) is crucial for preventing VZV complications in this vulnerable population.
Purpose of the Study:
- To assess the current practices and attitudes regarding VZV PEP in children with malignancy in the UK and Ireland.
- To identify the population at risk, frequency of VZV exposure, and clinical management strategies.
Main Methods:
- Observational study involving a retrospective serostatus survey, VZIG dispensing data collation, and an online survey of pediatric oncologists.
- Data collected from children diagnosed with malignancy and healthcare providers in the UK and Ireland.
Main Results:
- Approximately 24% of children diagnosed with malignancy annually are VZV seronegative.
- Around 250 children with cancer receive VZV PEP annually, with half receiving VZIG and the other half oral aciclovir.
- No consensus exists among oncologists regarding the preferred VZV PEP, highlighting a lack of evidence.
Conclusions:
- Current VZV PEP practices for children with cancer in the UK and Ireland are varied.
- A randomized controlled trial is necessary to compare the efficacy and acceptability of VZIG versus aciclovir for VZV PEP.
Objectives:
To describe postexposure prophylaxis (PEP) against varicella zoster virus (VZV) in children being treated for malignancy in the UK and Ireland: the population at risk, frequency of exposure, clinical practice and attitudes among healthcare providers.
Design:
An observational study in three parts: (1) a retrospective survey of serostatus at diagnosis of malignancy, (2) collation of varicella zoster immune globulin (VZIG) dispensing data over a 3-year period and (3) an online survey of paediatric oncologists' clinical practice and beliefs in relation to VZV disease and its prevention.
Setting:
UK and Ireland.
Participants:
Children diagnosed with malignancy in 2009 (serostatus survey) or receiving VZIG between April 2006 and March 2009 (VZIG dispensing study). Paediatric oncologists and haematologists working in tertiary paediatric oncology centres and related shared care units in the UK and Ireland (physician survey).
Results:
Of 1500 children diagnosed with malignancy each year, at least 24% are VZV seronegative. Few centres make efforts to prevent household exposure by vaccinating VZV-susceptible family members. Exposures to VZV result in the administration of PEP to approximately 250 children with cancer annually: half receive an intramuscular injection of VZIG while the remainder receive a course of oral aciclovir. The choice of PEP is made by doctors. There is no consensus among paediatric oncologists as to which is the better option, reflecting the lack of a secure evidence base.
Conclusions:
A randomised controlled trial to compare the effectiveness and acceptability of VZIG and aciclovir as PEP against varicella is both desirable and feasible.
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