Evidence map›Paper›PMID 38457222›Full record

ArticleCancer medicine2024

A single-centre, real-world study of BTK inhibitors for the initial treatment of MYD88

Ting Deng, Shiyuan Zhang, Min Xiao, Jia Gu, Liang Huang, Xiaoxi Zhou

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 4% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Molecular Insights and Novel Therapies for Lymphoproliferative Disorders.International journal of molecular sciences · 2026
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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

6 authors at 2 institutions in 1 country.

Ting DengDepartment of Hematology, Chongqing Fifth People's Hospital, Chongqing, PR China.ORCID 0000-0002-8399-5220
Shiyuan ZhangDepartment of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, PR China.
Min XiaoDepartment of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, PR China.ORCID 0000-0001-9421-6344
Jia GuDepartment of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, PR China.
Liang HuangDepartment of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, PR China.ORCID 0000-0002-8370-3232
Xiaoxi ZhouDepartment of Hematology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, PR China.ORCID 0000-0001-9790-859X
Tongji Hospital · CNFirst People's Hospital of Chongqing · CN

Funding

National Natural Science Foundation of China 82170167
6 · The paper itself

Abstract

backgroundMCD (MYD88

aimsThis study aimed to analyse the efficacy and safety of Bruton's tyrosine kinase inhibitor (BTKi) (zanubrutinib or orelabrutinib) therapy for newly diagnosed DLBCL patients with MYD88 MATERIALS AND

methodsTwenty-three newly diagnosed DLBCL patients with MYD88

resultsThe main clinical features were a high International Prognostic Index (IPI) score (≥3, 22/40, 55%) and a high rate of extranodal involvement (27/40,67.5%). Among the 23 DLBCL patients, 18 received BTKi + R-CHOP, and five elderly DLBCL patients were treated with BTKi + R DISCUSSION: The efficacy of BTKi combined with R-CHOP was similar to previous reports, which was significantly better than R-CHOP alone. It is necessary to fully consider that 14 patients in the BTKi + R-CHOP group received a BTKi as maintenance therapy when evaluating efficacy. Meanwhile, the addition of a BTKi may improve the prognosis of non-GCB, DEL or high-IPI-score DLBCL patients with MYD88

conclusionThis study suggests that newly diagnosed DLBCL patients with MYD88

Indexed as

Lymphoma, Large B-Cell, DiffuseMyeloid Differentiation Factor 88PiperidinesPyridinesAgedAntineoplastic Combined Chemotherapy ProtocolsCD79 AntigensCyclophosphamideDisease-Free SurvivalDoxorubicinHumansPrednisoneRetrospective StudiesRituximabVincristineCD79 AntigensCD79B protein, humanCyclophosphamideDoxorubicinMyeloid Differentiation Factor 88orelabrutinibPiperidinesPrednisonePyridinesRituximabVincristineBruton's tyrosine kinase inhibitorCD79Bmutdiffuse large B-cell lymphomaMCD subtypeMYD88mut

Identifiers

PMID38457222
PMCPMC10923040
OpenAlexW4392605362

What OpenQuestion holds

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LicenceCC BY
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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.