Evidence map›Paper›PMID 33363008›Full record

ArticleFrontiers in oncology2020

Altered T-Lymphocyte Biology Following High-Dose Melphalan and Autologous Stem Cell Transplantation With Implications for Adoptive T-Cell Therapy.

Thomas Mika, Swetlana Ladigan-Badura, Abdelouahid Maghnouj, Bakr Mustafa, Susanne Klein-Scory, Alexander Baraniskin, Sascha Döhring, Ilka Fuchs, Stephan Ehl, Stephan A Hahn and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

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  3. Advancing CAR-T cell therapy: Insights into patient biology, leukapheresis, and cryopreservation.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
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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

11 authors at 2 institutions in 1 country.

Thomas MikaDepartment of Medicine, Hematology and Oncology, Ruhr-University Bochum, Bochum, Germany.
Swetlana Ladigan-BaduraDepartment of Medicine, Hematology and Oncology, Ruhr-University Bochum, Bochum, Germany.
Abdelouahid MaghnoujDepartment of Molecular Gastrointestinal Oncology, Ruhr-University Bochum, Bochum, Germany.
Bakr MustafaDepartment of Molecular Gastrointestinal Oncology, Ruhr-University Bochum, Bochum, Germany.
Susanne Klein-ScoryDepartment of Medicine, Hematology and Oncology, Ruhr-University Bochum, Bochum, Germany.
Alexander BaraniskinDepartment of Medicine, Hematology and Oncology, Ruhr-University Bochum, Bochum, Germany.
Sascha DöhringDepartment of Molecular Gastrointestinal Oncology, Ruhr-University Bochum, Bochum, Germany.
Ilka FuchsCenter for Chronic Immunodeficiency, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Stephan EhlCenter for Chronic Immunodeficiency, Faculty of Medicine, University of Freiburg, Freiburg im Breisgau, Germany.
Stephan A HahnDepartment of Molecular Gastrointestinal Oncology, Ruhr-University Bochum, Bochum, Germany.
Roland SchroersDepartment of Medicine, Hematology and Oncology, Ruhr-University Bochum, Bochum, Germany.
Ruhr University Bochum · DEUniversity of Freiburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In relapsed and refractory multiple myeloma (MM), adoptive cell therapies (ACT) including CAR-T-cells are under clinical investigation. However, relapse due to T-cell exhaustion or limited persistence is an obstacle. Before ACT are considered in MM, high-dose (HD) melphalan followed by autologous stem-cell transplantation (autoSCT) has been administered in most clinical situations. Yet, the impact of HD chemotherapy on T-cells in MM with respect to ACT is unclear. In this study, T-lymphocytes' phenotypes, expansion properties, lentiviral transduction efficacy, and gene expression were examined with special respect to patients following HD melphalan. Significant impairment of T-cells' expansion and transduction rates could be demonstrated. Expansion was diminished due to inherent disadvantages of the predominant T-cell phenotype but restored over time. The quantitative fraction of CD27

Indexed as

chimeric antigen receptorgene expressionlentiviral transductionlymphocyte proliferationmelphalanmultiple myelomaT-cell biology

Identifiers

PMID33363008
PMCPMC7759611
OpenAlexW3110864187

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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.