TY  - JOUR
EP  - 11
PB  - BioMed Central; Springer
A1  - Nissen, Johanna C.
A1  - Hummel, Margit
A1  - Brade, Joachim
A1  - Kruth, Jens
A1  - Hofmann, Wolf-Karsten
A1  - Buchheidt, Dieter
A1  - Reinwald, Mark
UR  - https://archiv.ub.uni-heidelberg.de/volltextserver/20811/
IS  - 364
CY  - London; Berlin; Heidelberg
VL  - 14
ID  - heidok20811
JF  - BMC Infectious Diseases
TI  - The risk of infections in hematologic patients treated with rituximab is not influenced by cumulative rituximab dosage - a single center experience
Y1  - 2014///
AV  - public
SN  - 1471-2334
N2  - Background: Rituximab, a monoclonal antibody directed against CD20, is approved for the treatment of CD20-positive B-cell Non-Hodgkin?s lymphoma and rheumatologic disorders. Due to its potent activity in depleting CD20-positive lymphocytes, the influence on opportunistic infections is still under discussion. Thus, we analyzed the impact of rituximab either as monotherapy or in combination with other chemotherapeutic regimens to elucidate its role in contributing to infectious complications.   Methods: The records of consecutive patients (n?=?125, 141 treatment episodes) treated with rituximab alone or in combination with chemotherapy and corticosteroids were analyzed retrospectively for the incidence, spectrum and outcome of infections during treatment and 6 months after the last course of rituximab. Univariate analysis of cofactors such as steroid medication, antiinfective prophylaxis, underlying disease and remission status were performed.   Results: Altogether 80 therapy episodes were associated with infections, the median number of infections per patient being 1 (range 1?7). The number of infectious complications was significantly higher in patients receiving a combination of rituximab and chemotherapy compared to rituximab monotherapy (p?<?0.001). There was no statistically significant difference regarding number of rituximab courses or cumulative rituximab dosage between episodes with and without infections, respectively.Mean cumulative prednisone dosage between the cohort with infections and the one without infections showed a trend towards higher dosage of prednisone in the patients with infections (mean difference 441 mg, p?>?0.14).   Conclusions: Rituximab in induction treatment, either as monotherapy or combined with chemotherapy by itself does not increase the incidence or change the spectrum of infections in hematologic patients. However the possible influence of higher dosages of concomitant steroid medication on frequency of infections suggests that a heightened awareness of the potential for infectious complications should be applied to patients receiving higher doses of glucocorticoids in combination with other therapeutic regimens.
SP  - 1
ER  -