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Updated: Jan 24, 2026

Isolation and Transplantation of Hematopoietic Stem Cells HSCs
Published on: February 25, 2007
Pneumocystis jirovecii infection in autologous hematopoietic stem cell transplantation
Yumiko Toda1, Shin-Ichiro Fujiwara1, Seina Honda1
1Division of Hematology, Department of Medicine, Jichi Medical University, Tochigi, Japan.
Abstract:
Pneumocystis jirovecii pneumonia (PJP) after autologous stem cell transplantation (ASCT) remains insufficiently characterized. We retrospectively analyzed 304 ASCT recipients (2005-2024) at a single center (B-cell lymphoma n = 138; plasma cell tumor n = 126). Fourteen patients (4.6%) developed PJP at a median of 143 days (86-286) post-ASCT; none were on prophylaxis at diagnosis. The 1-year cumulative incidence was 5.2% overall, and varied by disease: 24% in follicular lymphoma (FL), 5.9% in other B-cell lymphomas, 1.9% in plasma cell tumor, and 0% in T-cell lymphomas. Prior rituximab exposure (HR 6.75; 95% CI 1.50-30.2) and FL diagnosis (HR 7.26; 95% CI 2.51-20.9) were associated with higher risk; age, purine analogs, lymphocyte count, globulin/IgG, and conditioning were not. No death was directly attributable to PJP. These data suggest, diagnosis-dependent risk after ASCT; prophylaxis may be considered for rituximab-treated patients, especially FL, while the optimal duration warrants further study.
Insights
Pneumocystis jirovecii pneumonia (PJP) risk after autologous stem cell transplantation (ASCT) varies by diagnosis. Follicular lymphoma and rituximab use increase PJP risk, suggesting tailored prophylaxis may be beneficial.
Area of Science:
- Hematology
- Infectious Diseases
- Oncology
Background:
- Pneumocystis jirovecii pneumonia (PJP) is a significant opportunistic infection following autologous stem cell transplantation (ASCT).
- Characterizing PJP incidence and risk factors post-ASCT is crucial for optimizing patient management and prophylaxis strategies.
Purpose of the Study:
- To investigate the incidence and risk factors of PJP in patients undergoing ASCT.
- To identify specific patient subgroups at higher risk for PJP development after ASCT.
Main Methods:
- Retrospective analysis of 304 ASCT recipients from 2005-2024.
- Evaluation of PJP incidence, timing, and associated risk factors, including disease type and prior treatments.
Main Results:
- Fourteen patients (4.6%) developed PJP, with a 1-year cumulative incidence of 5.2%.
- Follicular lymphoma (24%) and prior rituximab exposure (HR 6.75) were significantly associated with increased PJP risk.
- No deaths were directly attributed to PJP.
Conclusions:
- PJP risk after ASCT is diagnosis-dependent, with follicular lymphoma patients and those exposed to rituximab being at higher risk.
- Current prophylaxis strategies may be insufficient for certain high-risk groups.
- Further research is needed to determine optimal PJP prophylaxis duration and strategies in ASCT recipients.
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