Evidence map›Paper›PMID 40317419›Full record

Trial reportAdvances in therapy2025

Indirect Comparisons of Efficacy of Zanubrutinib Versus Orelabrutinib in Patients with R/R MCL: An Extended Follow-up Analysis.

Lijuan Deng, Yuqin Song, Keshu Zhou, Dengju Li, Jianda Hu, Dehui Zou, Sujun Gao, Haiyan Yang, Huilai Zhang, Jie Ji and 7 more

Abstract readClinical Trial, Phase IIComparative StudyMulticenter Study
In one paragraph

Trial report in Advances in therapy, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Lijuan Deng *Department of Lymphoma, Peking University Cancer Hospital & Institute (Beijing Cancer Hospital), No. 52 Fucheng Road, Haidian District, Beijing, 100142, China.
Yuqin Song *Department of Lymphoma, Peking University Cancer Hospital & Institute (Beijing Cancer Hospital), No. 52 Fucheng Road, Haidian District, Beijing, 100142, China.
Keshu ZhouDepartment of Hematology, Affiliated Cancer Hospital of Zhengzhou University, Henan Cancer Hospital, Zhengzhou, China.
Dengju LiDepartment of Hematology, Tongji Hospital, Tongji Medical College, Wuhan, China.
Jianda HuFujian Provincial Key Laboratory on Hematology, Fujian Institute of Hematology, Fujian Medical University Union Hospital, Fuzhou, China.
Dehui ZouState Key Laboratory of Experimental Hematology, Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
Sujun GaoDepartment of Hematology of Cancer Center, The First Hospital of Jilin University, Changchun, China.
Haiyan YangDepartment of Oncology, Zhejiang Cancer Hospital, Hangzhou, China.
Huilai ZhangDepartment of Lymphoma, National Clinical Research Center for Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin's Clinical Research Center for Cancer, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China.
Jie JiDepartment of Hematology, West China Hospital of Sichuan University, Chengdu, China.
Wei XuDepartment of Hematology, The First Affiliated Hospital of Nanjing Medical University, Jiangsu Province Hospital, Nanjing, China.
Ru FengDepartment of Hematology, Nanfang Hospital of Southern Medical University, Guangzhou, China.
Jie JinDepartment of Hematology, The First Affiliated Hospital, Zhejiang University College of Medicine, Hangzhou, China.
Fangfang LvDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Cheng FangBeiGene (Shanghai) Co., Ltd., Shanghai, China.
Sheng XuBeiGene (Shanghai) Co., Ltd., Shanghai, China.
Jun ZhuDepartment of Lymphoma, Peking University Cancer Hospital & Institute (Beijing Cancer Hospital), No. 52 Fucheng Road, Haidian District, Beijing, 100142, China. zhu-jun2017@outlook.com.ORCID http://orcid.org/0000-0003-3479-2547

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionOur previous study has suggested a favorable progression-free survival (PFS) with zanubrutinib over orelabrutinib in patients with relapsed or refractory mantle cell lymphoma (R/R MCL). Here, we conducted an updated analysis to indirectly compare the long-term efficacy between zanubrutinib and orelabrutinib in patients with R/R MCL.

methodsIndividual patient data from the zanubrutinib study were adjusted to match the patient population profile of the orelabrutinib study. An unanchored matching-adjusted indirect comparison (MAIC) was performed to adjust for effect modifiers and prognostic variables. The efficacy outcomes included investigator-assessed PFS, overall survival (OS), and overall response rate (ORR). Response evaluations were only computed tomography (CT)-based assessments in the orelabrutinib study, while positron emission tomography (PET)- and CT-based assessment were both performed in the zanubrutinib study. The comparison of PFS assessed by CT between zanubrutinib and orelabrutinib was the primary result.

resultsAfter matching, the baseline characteristics were balanced between zanubrutinib and orelabrutinib, with an effective sample size of 70 in the zanubrutinib study. PFS assessed by CT was significantly longer in the zanubrutinib study vs. the orelabrutinib study (median PFS, not reached vs. 22.0 months; hazard ratio [HR] 0.54, 95% confidence interval [CI] 0.34-0.86; P = 0.009). With longer follow-up, OS continued to trend favorably for zanubrutinib, with OS rate at 24 months numerically higher (83.7% vs. 74.3%); no statistical difference was observed (HR 0.68, 95% CI 0.36-1.27; P = 0.223). ORR was numerically higher in the zanubrutinib study (85.5% vs. 82.1%; odds ratio 1.28, 95% CI 0.56-2.94; P = 0.556).

conclusionMAIC results demonstrated that zanubrutinib had significantly longer PFS compared with orelabrutinib in the treatment of patients with R/R MCL.

Indexed as

Antineoplastic AgentsBenzamidesLymphoma, Mantle-CellPiperidinesPyrazinesPyrazolesPyrimidinesAgedFemaleFollow-Up StudiesHumansMaleMiddle AgedProgression-Free SurvivalPyridinesTreatment OutcomeAntineoplastic AgentsBenzamidesorelabrutinibPiperidinesPyrazinesPyrazolesPyridinesPyrimidineszanubrutinibMatching-adjusted indirect comparisonOrelabrutinibProgression-free survivalRelapsed or refractory mantle cell lymphomaZanubrutinib

Identifiers

PMID40317419
PMCPMC12085368

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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.