Evidence map›Paper›PMID 40078989›Full record

ArticleFrontiers in immunology2025

Combination autologous stem cell transplantation with chimeric antigen receptor T-cell therapy for refractory/relapsed B-cell lymphoma: a single-arm clinical study.

Danyang Li, Rui Liu, Zhonghua Fu, Fan Yang, Lixia Ma, Yuelu Guo, Miaomiao Cao, Yang Lei, Yimeng Dou, Xuenan Zhang and 5 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

15 authors.

Danyang LiDepartment of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China.
Rui LiuDepartment of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China.
Zhonghua FuDepartment of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China.
Fan YangDepartment of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China.
Lixia MaDepartment of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China.
Yuelu GuoDepartment of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China.
Miaomiao CaoDepartment of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China.
Yang LeiDepartment of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China.
Yimeng DouDepartment of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China.
Xuenan ZhangDepartment of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China.
Yan GaoDepartment of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China.
Bian WeiDepartment of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China.
Biping DengDepartment of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China.
Xiaoyan KeDepartment of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China.
Kai HuDepartment of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autologous stem cell transplantation (ASCT) and chimeric antigen receptor T-cells (CAR-T) have been used as consolidation therapies for patients with refractory/relapsed B cell non-Hodgkin's lymphoma (R/R B-NHL) in remission after second-line chemotherapy or salvage therapy. However, patients with different pathological subtypes and remission states may benefit differently from ASCT or CAR-T cell therapy. Furthermore, consolidation treatment involving ASCT or CAR-T cells still poses a significant risk of disease relapse. We conducted a retrospective, single-arm study of 47 patients with R/R B-NHL, and found that the combination of ASCT and CAR-T therapy improved the 3-year progression-free survival (PFS) and overall survival (OS) rates to 66.04% (95%CI: 48.311-78.928) and 72.442% (95%CI: 53.46-84.708) respectively. Furthermore, the combination therapy has no serious adverse events. Thus, ASCT combined with CAR-T cell therapy is effective against multiple subtypes of R/R B-NHL, and can effectively prolong the long-term survival of patients.

Indexed as

Hematopoietic Stem Cell TransplantationImmunotherapy, AdoptiveLymphoma, B-CellReceptors, Chimeric AntigenAdultAgedCombined Modality TherapyFemaleHumansMaleMiddle AgedRetrospective StudiesTransplantation, AutologousTreatment OutcomeYoung AdultReceptors, Chimeric AntigenASCTB-NHLCAR-Tcombination therapyrefractory/relapsed B-cell lymphoma

Identifiers

PMID40078989
PMCPMC11897563

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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.