Evidence map›Paper›PMID 36505470›Full record

ArticleFrontiers in immunology2022

Zanubrutinib plus salvage chemotherapy for relapsed or refractory diffuse large B-cell lymphoma.

Xianggui Yuan, Xian Li, Yurong Huang, Xueli Jin, Hui Liu, Aiqi Zhao, Weiping Zhang, Wenbin Qian, Yun Liang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 18% of its field
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

7 citing papers in PubMed, 11 citations in OpenAlex.

  1. Trial
  2. Trial
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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

9 authors at 3 institutions in 1 country.

Xianggui YuanDepartment of Hematology, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Xian LiDepartment of Hematology, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Yurong HuangDepartment of Hematology, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Xueli JinDepartment of Hematology, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Hui LiuDepartment of Hematology, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Aiqi ZhaoDepartment of Hematology, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Weiping ZhangDepartment of Oncology, The Third Affiliated Hospital of Zhejiang Chinese Medical University, Hangzhou, China.
Wenbin QianDepartment of Hematology, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Yun LiangDepartment of Hematology, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Second Affiliated Hospital of Zhejiang University · CNFirst Affiliated Hospital of Soochow University · CNThe Third Affiliated Hospital of Zhejiang Chinese Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Relapsed or refractory diffuse large B-cell lymphoma (R/R DLBCL) has poor clinical outcomes when treated with conventional salvage chemotherapy. Monotherapy using zanubrutinib, a selective Bruton's tyrosine kinase (BTK) inhibitor, has achieved modest antitumor effect in R/R DLBCL. Here we aimed to evaluate the efficacy and safety of zanubrutinib plus salvage chemotherapy in R/R DLBCL patients. Methods: We retrospectively reviewed R/R DLBCL patients who were administered with zanubrutinib plus salvage chemotherapy in our center between January, 2019 and December, 2021. Targeted panel sequencing of 11 lymphoma-related genes was performed on 8 patients with poor responses to zanubrutinib-based chemotherapy. Results: 27 R/R DLBCL patients were enrolled. Median age at this study was 59 years (range, 15-72). The best overall response rate (ORR) was 74.1% and complete remission rate was 33.3%. With a median follow-up of 11 months (range, 1-17), the median progression-free survival (PFS) was 8.1 months, and the overall survival (OS) was not achieved. The most common grade-3/4 adverse events were neutropenia (70.4%), thrombocytopenia (66.7%), and febrile neutropenia (33.3%). In multivariate analysis, early treatment and overall response after chemotherapy were independent favorable prognostic factors for PFS. Overall response after chemotherapy was an independent favorable factor for OS. Among the 8 patients with poor response to zanubrutinib-based treatment, the majority of patients had Conclusion: With high efficacy and manageable tolerability, zanubrutinib plus salvage chemotherapy may be a potential treatment option for R/R DLBCL. CAR-T cell therapy may be a priority strategy for these poor responders to BTKi-based treatment.

Indexed as

Lymphoma, Large B-Cell, DiffuseLymphoma, Non-HodgkinNeutropeniaAdolescentAdultAgedHumansMiddle AgedProgression-Free SurvivalRetrospective StudiesYoung AdultBruton’s tyrosine kinase inhibitorchimeric antigen receptor T-cell (CAR-T)combination chemotherapyrelapsed or refractory diffuse large B-cell lymphomaTP53zanubrutinib

Identifiers

PMID36505470
PMCPMC9729240
OpenAlexW4309842506

What OpenQuestion holds

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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.