TY - JOUR
T1 - Infections in patients taking Rituximab for hematologic malignancies
T2 - Two-year cohort study
AU - Lanini, Simone
AU - Molloy, Aoife C.
AU - Prentice, Archibald G.
AU - Ippolito, Giuseppe
AU - Kibbler, Christopher C.
PY - 2013/7/12
Y1 - 2013/7/12
N2 - Background: Rituximab (R) is a chimeric human-murine anti-CD20 monoclonal antibody used to treat B-cell lymphomas. Despite R remarkable activity against malignant cells, there are concerns that R may facilitate the occurrence of infections. This study is aimed to define risk factors for infections, and the potential interaction with time since therapy, in patients undergoing R containing regimens.Methods: The study has been designed as a multiple failure events historical cohort including all patients who received a R contain regimen at London Royal Free Hospital between May 2007 and April 2009.Result: One-hundred-eighty-one infections occurred among the 113 enrolled patients (overall incidence rate 3.30 per 1000 person-days). Multivariate analysis showed that lymphocyte counts at nadir, graft versus host disease, HIV sero-status and the type of malignancy were all independently associated with the risk of infection. In addition the analysis of the interaction with the time since the start of therapy provided evidence that different risk factors may increase risk of infections in different times.Conclusion: This study provides preliminary data to describe the association between several patients' baseline characteristics and infections during therapy with R.
AB - Background: Rituximab (R) is a chimeric human-murine anti-CD20 monoclonal antibody used to treat B-cell lymphomas. Despite R remarkable activity against malignant cells, there are concerns that R may facilitate the occurrence of infections. This study is aimed to define risk factors for infections, and the potential interaction with time since therapy, in patients undergoing R containing regimens.Methods: The study has been designed as a multiple failure events historical cohort including all patients who received a R contain regimen at London Royal Free Hospital between May 2007 and April 2009.Result: One-hundred-eighty-one infections occurred among the 113 enrolled patients (overall incidence rate 3.30 per 1000 person-days). Multivariate analysis showed that lymphocyte counts at nadir, graft versus host disease, HIV sero-status and the type of malignancy were all independently associated with the risk of infection. In addition the analysis of the interaction with the time since the start of therapy provided evidence that different risk factors may increase risk of infections in different times.Conclusion: This study provides preliminary data to describe the association between several patients' baseline characteristics and infections during therapy with R.
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U2 - 10.1186/1471-2334-13-317
DO - 10.1186/1471-2334-13-317
M3 - Article
C2 - 23849292
AN - SCOPUS:84880002376
SN - 1471-2334
VL - 13
JO - BMC Infectious Diseases
JF - BMC Infectious Diseases
IS - 1
M1 - 317
ER -