June 20, 2012 in Cancer Universal hepatitis B virus
screening before chemotherapy for lymphoma reduces costs in most settings,
according to a study published online June 18 in the Journal of Clinical Oncology. (HealthDay) --
Universal hepatitis B virus (HBV) screening before chemotherapy for lymphoma
reduces costs in most settings, according to a study published online June 18 in the Journal of Clinical Oncology. Noting
that potentially fatal HBV reactivation can be largely prevented with antiviral
prophylaxis, Urszula Zurawska, M.D., from the University of Toronto ,
and colleagues developed a decision model to compare the clinical outcomes,
costs, and cost-effectiveness of three HBV screening strategies for patients
with lymphoma before rituximab plus cyclophosphamide, doxorubicin, vincristine,
and prednisone (R-CHOP) chemotherapy. The strategies were: screen all patients
for hepatitis B surface antigen (HBsAg; Screen-All), screen patients at
high-risk for HBV infection (Screen-HR), and screen no one (Screen-None).
Antiviral therapy was administered to screened patients who tested positive
until six months after completion of chemotherapy. Those not screened were
given antiviral therapy only if HBV hepatitis occurred. Costs were given in
Canadian dollars and a third-party payer perspective was adopted. The
researchers found that the dominant strategy was Screen-All, costing $32,589,
compared with $32,598 for Screen-HR and $32,657 for Screen-None. Screen-All was
also associated with the highest one-year survival rate (84.99 percent), compared
with Screen-HR and Screen-None (84.96 and 84.86 percent, respectively). The
prevalence of HBsAg positivity in the low-risk population influenced analysis;
when this value was ≤0.20 percent the Screen-HR became the least costly. "In
patients receiving R-CHOP for lymphoma, screening all patients for HBV reduces
the rate of HBV reactivation (10-fold) and is less costly than screening only
high-risk patients or screening no patients," the authors write. One
author disclosed financial ties to Gilead Sciences. More information: Abstract Full
Text Journal reference: Journal of Clinical Oncology
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