| Literature DB >> 20919860 |
Kenji Hashimoto1, Yukio Kobayashi, Yoshitaka Asakura, Masakazu Mori, Teruhisa Azuma, Dai Maruyama, Sung-Won Kim, Takashi Watanabe, Kensei Tobinai.
Abstract
An increasing incidence of Pneumocystis jiroveci pneumonia (PCP) in patients with B-cell non-Hodgkin lymphoma (B-NHL) receiving rituximab treatment has been reported. We reviewed patients with B-NHL who underwent chemotherapy from 2004 to 2008 at our institution to identify risk factors for PCP development during and after chemotherapy. Among 297 patients with B-NHL, six developed PCP. Of 121 patients (41%) who received PCP prophylaxis with sulfamethoxazole–trimethoprim during chemotherapy, none developed PCP (0%), while among 176 patients (59%) who had no prophylaxis, six (3.4%) developed PCP at a median of 2 months (range: 1–3 months) after starting chemotherapy. Patients with CD4+ lymphocyte counts ≤200/mm3 before chemotherapy had a higher risk of developing PCP (p=0.045), while a history of rituximab treatment was not related to PCP. CD4+ lymphocyte counts ≤200/mm3 during and after chemotherapy were observed in 18.9% of patients.Entities:
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Year: 2010 PMID: 20919860 DOI: 10.3109/10428194.2010.506569
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022