Evidence map›Paper›PMID 41182357›Full record

ArticleAnnals of hematology2025

Treatment outcomes of zanubrutinib-based regimen in newly diagnosed patients with MYC/BCL2 double-expressor diffuse large B-cell lymphoma: a retrospective multicenter real-world study.

Bo Lu, Ying Wang, Mengdi Jin, Jingwei Zhang, Xiaojun Xu, Yunxin Zeng, Lina Zhao, Hua Wang

Abstract readMulticenter Study
In one paragraph

Article in Annals of hematology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Bo Lu *Department of Hematology, The Seventh Affiliated Hospital, Sun Yat - Sen University, Shenzhen, 518107, China.
Ying Wang *Department of Hematology, The Seventh Affiliated Hospital, Sun Yat - Sen University, Shenzhen, 518107, China.
Mengdi Jin *Department of Hematology, Affiliated Nanshan Hospital of Shenzhen University, Shenzhen, China.
Jingwei ZhangSchool of Medicine, Sun Yat - sen University, Shenzhen, China.
Xiaojun XuDepartment of Hematology, The Seventh Affiliated Hospital, Sun Yat - Sen University, Shenzhen, 518107, China.
Yunxin ZengDepartment of Hematology, The Seventh Affiliated Hospital, Sun Yat - Sen University, Shenzhen, 518107, China. zeng_0714@163.com.
Lina ZhaoDepartment of Hematology, Harbin Medical University Cancer Hospital, Harbin, Heilongiiang Province, 150081, China. 1601@hrbmu.edu.cn.
Hua WangHematologic Oncology Department,State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center for Cancer, Sun Yat-Sen University Cancer Center, Guangzhou, 510060, China. wanghua@sysucc.org.cn.

Funding

Shenzhen Science and Technology Basic Research Project JCYJ20190809172403604the Sanming Project of Medicine in Shenzhen SZSM202411022
6 · The paper itself

Abstract

Diffuse large B-cell lymphoma (DLBCL) patients with co-expression of MYC (≥ 40%) and BCL2 (≥ 50%), classified as double-expressor DLBCL (DE-DLBCL), consistently exhibit poor prognosis with traditional first-line therapies. In order to address the unmet therapeutic needs in this high-risk population, this real-world study retrospectively reviewd 46 newly diagnosed DE-DLBCL patients from two centers to evaluate the efficacy and safety of zanubrutinib-based regimens. Key outcomes included complete response rate (CRR), objective response rates (ORR), progression-free survival (PFS), overall survival (OS) and adverse events. Univariate analysis was conducted to evaluate the impact of various prognostic factors on complete response. The median age was 57.8 years (range:20-81), with 45.65% of patients over 60 years old and 17.39% over 75 years old. Advanced-stage (III/IV) disease was present in 60.87% of patients at diagnosis, 78.26% had a non-germinal center B-cell (non-GCB) subtype, and 41.3% exhibited an International Prognostic Index score ≥ 3. The best CRR was 73.90% (95% CI, 58.90%-85.70%), and the best ORR was 95.70% (95% CI, 85.20%-99.50%). At a median follow-up of 15.7 months, the 3-year PFS and OS was 86.27% (95% CI, 75.37%-98.75%) and 89.79% (95% CI, 78.40%-100%) respectively. Multivariate analysis revealed that zanubrutinib-based chemotherapy regimen significantly improved CRR. Significant differences in PFS were observed across age, bulky disease, IPI score, and extranodal involvement stratification. Adverse events were mainly hematologic toxicities and fatigue. These findings suggest that zanubrutinib may serve as an effective component of first-line therapy for this population, with favorable tolerability.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsLymphoma, Large B-Cell, DiffusePiperidinesProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-mycPyrazolesPyrimidinesAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedRetrospective StudiesTreatment OutcomeBCL2 protein, humanMYC protein, humanPiperidinesProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-mycPyrazolesPyrimidineszanubrutinibDiffuse large b-cell lymphomaDouble-expressorZanubrutinib

Identifiers

PMID41182357
PMCPMC12619722

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.