# Real world outcomes and prognostic factors in Chinese patients with primary mediastinal B cell lymphoma: A single center experience and the Surveillance, Epidemiology, and End Results validation

**Authors:** Boya Wang, Ruize Chen, Huanhuan Wang, Tonglu Qiu, Zihan Liang, Lei Cao, Huayuan Zhu, Wei Xu, Lei Fan, Jianyong Li, Yi Miao, Yi Xia

PMC · DOI: 10.1007/s00277-026-06914-4 · Annals of Hematology · 2026-02-28

## TL;DR

This study examines the treatment and survival outcomes of Chinese patients with primary mediastinal B-cell lymphoma, finding that older age is linked to worse survival.

## Contribution

The study provides real-world validation of treatment efficacy and identifies age as a novel prognostic factor in PMBCL.

## Key findings

- Chinese PMBCL patients had high response rates to R-DA-EPOCH therapy.
- Age over 40 years was associated with worse overall survival.
- Consolidative radiotherapy did not improve survival outcomes.

## Abstract

This study aimed to characterize the clinical characteristics, treatment patterns, survival outcomes, and prognostic factors of Chinese patients with primary mediastinal B-cell lymphoma (PMBCL). We retrospectively reviewed 69 consecutive patients with PMBCL treated at our center between 2010 and 2025. External validation was performed using data from the Surveillance, Epidemiology, and End Results (SEER) database (n = 1,460). The median age at diagnosis was 33 years (range, 18–62), with a female predominance (female-to-male ratio, 2.1:1). Most patients (92.8%, 64/69) received R-DA-EPOCH as frontline therapy, and 29.0% (20/69) additionally underwent consolidative radiotherapy (RT). Among 51 evaluable patients, the objective response rate was 90.2%, with a complete response rate of 74.5%. After a median follow-up of 74 months (range, 2–166), the estimated 5-year progression-free survival (PFS) and overall survival (OS) rates in whole cohort were 88.7% and 94.8%, respectively. Hematologic toxicity, predominantly febrile neutropenia, was the most common adverse event; nevertheless, 60.4% of patients maintained a relative dose intensity ≥ 100%. Consolidative RT did not confer a survival advantage, whereas age > 40 years emerged as an adverse prognostic factor for OS, a finding further validated in the SEER cohort. Chinese patients with PMBCL generally have favorable outcomes in the modern treatment era. However, older age (> 40 years) is associated with inferior survival. The R-DA-EPOCH regimen demonstrated high efficacy in this real-world setting, whereas additionally consolidative RT failed to provide a significant survival benefit.

The online version contains supplementary material available at 10.1007/s00277-026-06914-4.

## Full-text entities

- **Genes:** PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, TNFRSF8 (TNF receptor superfamily member 8) [NCBI Gene 943] {aka CD30, D1S166E, Ki-1}
- **Diseases:** infection (MESH:D007239), dyspnea (MESH:D004417), Cancer (MESH:D009369), hematologic adverse events (MESH:D064420), Tumors of Haematopoietic and Lymphoid Tissues (MESH:D018442), nodal (MESH:D013611), superior vena cava syndrome (MESH:D013479), chest discomfort (MESH:D013898), II disease (MESH:D004194), death (MESH:D003643), neutropenia (MESH:D009503), Hematologic toxicity (MESH:D006402), Stage I (MESH:D062706), cardiac toxicity (MESH:D066126), diffuse large B-cell lymphoma (MESH:D016403), MDS (MESH:D009190), pericardial effusion (MESH:D010490), febrile neutropenia (MESH:D064147), hematologic and infectious toxicities (MESH:D003141), lymphoma (MESH:D008223), pleural effusion (MESH:D010996), PMBCL (MESH:D016393), pneumonia (MESH:D011014), non-Hodgkin lymphoma (MESH:D008228)
- **Chemicals:** Dexamethasone (MESH:D003907), Rituximab (MESH:D000069283), DA (MESH:C025953), COMP (MESH:C037238), EPOCH (MESH:C079446), Brentuximab vedotin (MESH:D000079963), R (MESH:D001120), CHOP21 (-), cisplatin (MESH:D002945), doxorubicin (MESH:D004317), anthracycline (MESH:D018943), Gemcitabine (MESH:D000093542), acyclovir (MESH:D000212), Oxaliplatin (MESH:D000077150), cyclophosphamide (MESH:D003520), GemOx (MESH:C508870), cytarabine (MESH:D003561), trimethoprim-sulfamethoxazole (MESH:D015662)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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## References

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Source: https://tomesphere.com/paper/PMC12950073