# Prognostic factors of patients with intravascular large B cell lymphoma: a multicenter study in China

**Authors:** Yan Guo, Yi Zhong, Lixia Zhu, Fengping Zhou, Xuanru Lin, Xian Li, Xiufeng Wang, Yan Huang, Sun Wu, Guoqing Lv, Jinghang Zhang, Yi Zhao, Wenjun Wu, Xiujin Ye, Hanjin Yang, Jin Zhang, Kang Yu, Yun Liang, Zhen Cai, Jingsong He

PMC · DOI: 10.3389/fonc.2025.1689028 · Frontiers in Oncology · 2025-12-19

## TL;DR

This study identifies key prognostic factors for intravascular large B-cell lymphoma in China, showing that certain subtypes and conditions are linked to worse survival.

## Contribution

The study is the first multicenter analysis in China to identify specific prognostic factors for IVLBCL, including CNS involvement and hemophagocytic variant subtype.

## Key findings

- Hemophagocytic variant patients had worse outcomes, including higher mortality and elevated inflammatory markers.
- The 2-year overall survival was significantly worse in hemophagocytic variant compared to classical variant (43.3% vs. 76.4%).
- CNS involvement and hemophagocytic variant were confirmed as significant poor prognostic factors in multivariate analysis.

## Abstract

Intravascular large B-cell lymphoma (IVLBCL) is a rare and highly aggressive lymphoma, but current knowledge is still inadequate. We retrospectively analyzed 50 IVLBCL patients from five Chinese tertiary hospitals in China between 2017 and 2024. Hemophagocytic variant (HV) patients showed worse performance status, universal B symptoms, more bone marrow infiltration, higher mortality, pancytopenia, elevated inflammatory markers (CRP, LDH, ferritin), hypoglobulinemia and hypogammaglobulinemia. Among 46 treated patients, CR/CRu rate was 71% (27/38). The 2-year OS was 65.5%, significantly worse in HV vs. classical variant (CV) (43.3% vs. 76.4%, P = 0.007). Multivariate analysis identified CNS involvement (HR = 10.86, P < 0.001), HV subtype (HR = 1.91, P = 0.018), and nodal organs involvement (HR = 5.26, P = 0.052) as poor prognostic factors. IVLBCL exhibits marked heterogeneity, with HV and CNS involvement conferring dismal outcomes. This study provides key diagnostic/therapeutic insights for IVLBCL in China, warranting prospective trials to validate prognostic models and optimize therapies.

## Linked entities

- **Diseases:** intravascular large B-cell lymphoma (MONDO:0020324), pancytopenia (MONDO:0001529)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** Hemophagocytic (MESH:D051359), pancytopenia (MESH:D010198), bone marrow infiltration (MESH:D001855), lymphoma (MESH:D008223), hypoglobulinemia (MESH:C565765), inflammatory (MESH:D007249), hypogammaglobulinemia (MESH:D000361), IVLBCL (MESH:D016393)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12757299/full.md

## References

29 references — full list in the complete paper: https://tomesphere.com/paper/PMC12757299/full.md

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Source: https://tomesphere.com/paper/PMC12757299