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Real-world infectious complications of CD3/CD20 bispecific antibodies in relapsed/refractory non-Hodgkin lymphoma.

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Leukemia & lymphoma 📖 저널 OA 8.7% 2022: 1/1 OA 2025: 2/55 OA 2026: 14/137 OA 2022~2026 2025 Vol.66(12) p. 2260-2268
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Xiao A, Chen L, Pak S, Lee B, Mei M, Budde E

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Infections occur in up to 44% of trial participants treated with CD3/CD20 bispecific antibodies (BsAb), but real-world data are limited.

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  • 95% CI 0.81-2.1

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APA Xiao A, Chen L, et al. (2025). Real-world infectious complications of CD3/CD20 bispecific antibodies in relapsed/refractory non-Hodgkin lymphoma.. Leukemia & lymphoma, 66(12), 2260-2268. https://doi.org/10.1080/10428194.2025.2540442
MLA Xiao A, et al.. "Real-world infectious complications of CD3/CD20 bispecific antibodies in relapsed/refractory non-Hodgkin lymphoma.." Leukemia & lymphoma, vol. 66, no. 12, 2025, pp. 2260-2268.
PMID 40765130 ↗

Abstract

Infections occur in up to 44% of trial participants treated with CD3/CD20 bispecific antibodies (BsAb), but real-world data are limited. In this study of 48 real-world R/R-NHL patients receiving commercial BsAbs, 50% and 23% experienced any-grade and grade ≥3 infections, respectively. The cumulative number of infections per patient at 12 months was 1.3 (95% CI: 0.81-2.1). Severe infections were mostly bacterial. Only 1 grade 5 event occurred, and no COVID-19-related deaths were observed. Severe neutropenia, lymphopenia, and hypogammaglobulinemia occurred in 39.6, 83.3, and 64.1% of patients, respectively. In exploratory univariate analyses, recent infection, aggressive histology, number of prior lines of therapy, CAR T exposure, and severe treatment-emergent lymphopenia and hypogammaglobulinemia were linked to increased infection risk. Moreover, infection was associated with decreased overall survival (HR 3.4,  = 0.0066) in the Cox proportional hazards model. These real-world findings reinforce the need for monitoring of infectious complications following BsAb therapy.

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