Evidence map›Paper›PMID 41102901›Full record

ArticleJournal of cellular and molecular medicine2025

Daratumumab for CD20

ZeTong Hong, ZhaoYang Hong, YaXian Ma, Qing Yin, Min Liu, Wei Huang, KuangGuo Zhou, Dan Li, TongJuan Li, Miao Zheng

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Daratumumab for CD20Journal of cellular and molecular medicine · 2025
    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

10 authors.

ZeTong HongDepartment of Hematology, Tongji Medical College, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.
ZhaoYang HongTongji Medical College, Huazhong University of Science and Technology, Wuhan, China.ORCID 0009-0006-7607-9183
YaXian MaDepartment of Hematology, Tongji Medical College, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.ORCID 0000-0002-4412-5564
Qing YinDepartment of Hematology, Tongji Medical College, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.
Min LiuDepartment of Hematology, Tongji Medical College, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.
Wei HuangDepartment of Hematology, Tongji Medical College, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.ORCID 0000-0001-6959-7077
KuangGuo ZhouDepartment of Hematology, Tongji Medical College, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.
Dan LiDepartment of Hematology, Tongji Medical College, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.
TongJuan LiDepartment of Hematology, Tongji Medical College, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.
Miao ZhengDepartment of Hematology, Tongji Medical College, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.

Funding

Beijing Xisike Clinical Oncology Research Foundation Y-SYBLD2022MS-0055National Natural Science Foundation of China 81974005National Natural Science Foundation of China 82100211Natural Science Foundation of Hubei Province 2025AFD777
6 · The paper itself

Abstract

Patients with R/R DLBCL (relapsed/refractory diffuse large B-cell lymphoma) treated with rituximab-based regimens often have a reduction in the expression level of CD20. Replacement of target proteins for new targeted chemotherapy has become a popular direction for the treatment of R/R DLBCL. To investigate whether Daratumumab can be an effective alternative to targeted agents as monotherapy or combination chemotherapy in patients with CD20-CD38+ R/R DLBCL who have failed to respond to CD20 monoclonal antibody treatment and its adjuvant effect on subsequent CAR-T (chimeric antigen receptor T-cell immunotherapy). A total of four CD20-CD38+ R/R DLBCL patients treated with multiple lines of Daratumumab-based combination chemotherapy were retrospectively collected. For eligible patients, CAR-T therapy was used afterwards. Also, the authors successfully constructed allografted tumour models in mice. Relevant evaluation showed that four patients who received Daratumumab combination chemotherapy had varying degrees of remission after treatment, including 2 CR, 1 PR and 1 SD. The 1-year OS rate was 75%, the 1-year PFS rate was 50% and mOS was 12 months. Adverse effects were moderate and reversible, and no treatment-related deaths occurred. Daratumumab therapy led to a successful transition to CAR-T in two patients. Among them, grade 1 CRS occurred. These cases demonstrated that Daratumumab combination therapy has a good application prospect in the treatment of CD20-CD38+ R/R DLBCL and is helpful for the bridge of CAR-T therapy.

Indexed as

ADP-ribosyl Cyclase 1Antibodies, MonoclonalAntigens, CD20Lymphoma, Large B-Cell, DiffuseMembrane GlycoproteinsAdultAgedAnimalsAntineoplastic Combined Chemotherapy ProtocolsFemaleHumansImmunotherapy, AdoptiveMaleMiceMiddle AgedRetrospective StudiesADP-ribosyl Cyclase 1Antibodies, MonoclonalAntigens, CD20CD38 protein, humandaratumumabMembrane GlycoproteinsCAR‐T therapyCD20CD38chemotherapyimmunotherapy

Identifiers

PMID41102901
PMCPMC12530957

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.