Evidence map›Paper›PMID 37040425›Full record

Observational studyCancer immunology research2023

Influence of Adipose Tissue Distribution, Sarcopenia, and Nutritional Status on Clinical Outcomes After CD19 CAR T-cell Therapy.

Kai Rejeski, David M Cordas Dos Santos, Nathan H Parker, Veit L Bücklein, Michael Winkelmann, Khushali S Jhaveri, Lian Liu, Paul Trinkner, Sophie Günther, Philipp Karschnia and 7 more

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Cancer immunology research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 3 pooled it
9.7field-weighted citation impact, top 2% 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

35 citing papers in PubMed, 3 syntheses or guidelines pooled it, 42 citations in OpenAlex.

  1. Pooled it
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  18. Observational
  19. Sarcopenia and Skeletal Muscle Loss after CAR T-cell Therapy in Diffuse Large B-cell Lymphoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 4 institutions in 2 countries.

Kai Rejeski *Department of Medicine III, University Hospital, Ludwig Maximilian University (LMU) Munich, Munich, Germany.ORCID 0000-0003-3905-0251
David M Cordas Dos Santos *Department of Medicine III, University Hospital, Ludwig Maximilian University (LMU) Munich, Munich, Germany.ORCID 0000-0002-9198-8338
Nathan H ParkerDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, Florida.ORCID 0000-0002-8947-7942
Veit L BückleinDepartment of Medicine III, University Hospital, Ludwig Maximilian University (LMU) Munich, Munich, Germany.ORCID 0000-0001-7391-7280
Michael WinkelmannDepartment of Radiology, University Hospital, LMU Munich, Munich, Germany.ORCID 0000-0003-4655-7341
Khushali S JhaveriDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, Florida.ORCID 0000-0002-0232-3896
Lian LiuComprehensive Cancer Center Munich, LMU Munich, Munich, Germany.ORCID 0000-0002-4021-552X
Paul TrinknerDepartment of Medicine III, University Hospital, Ludwig Maximilian University (LMU) Munich, Munich, Germany.ORCID 0000-0001-9586-5362
Sophie GüntherDepartment of Medicine III, University Hospital, Ludwig Maximilian University (LMU) Munich, Munich, Germany.ORCID 0000-0002-5392-8158
Philipp KarschniaDepartment of Neurosurgery, University Hospital, LMU Munich, Munich, Germany.ORCID 0000-0002-1254-5310
Viktoria BlumenbergDepartment of Medicine III, University Hospital, Ludwig Maximilian University (LMU) Munich, Munich, Germany.ORCID 0000-0003-1379-0876
Christian SchmidtDepartment of Medicine III, University Hospital, Ludwig Maximilian University (LMU) Munich, Munich, Germany.ORCID 0000-0002-3653-0615
Wolfgang G KunzDepartment of Radiology, University Hospital, LMU Munich, Munich, Germany.ORCID 0000-0002-5021-1952
Michael von Bergwelt-BaildonDepartment of Medicine III, University Hospital, Ludwig Maximilian University (LMU) Munich, Munich, Germany.ORCID 0000-0002-1952-052X
Michael D JainDepartment of Blood and Marrow Transplant and Cellular Immunotherapy, Moffitt Cancer Center, Tampa, Florida.ORCID 0000-0002-7789-1257
Sebastian Theurich *Department of Medicine III, University Hospital, Ludwig Maximilian University (LMU) Munich, Munich, Germany.ORCID 0000-0001-5706-8258
Marion Subklewe *Department of Medicine III, University Hospital, Ludwig Maximilian University (LMU) Munich, Munich, Germany.ORCID 0000-0001-9154-9469
German Cancer Research Center · DELMU Klinikum · DEMoffitt Cancer Center · USLudwig-Maximilians-Universität München · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although CD19-directed chimeric antigen receptor T-cell therapy (CD19.CAR-T) has proven clinical efficacy for multiple refractory B-cell malignancies, over 50% of patients ultimately relapse. Recent evidence has underlined the critical role of the host in determining treatment responses. In this retrospective observational study of 106 patients with relapsed/refractory large B-cell lymphoma receiving standard-of-care CD19.CAR-T, we analyzed the impact of immunometabolic host features and detailed body composition measurements on post-CAR T clinical outcomes. We extracted muscle and adipose tissue distributions from prelymphodepletion CT images and assessed laboratory-based immuno-nutritional scores. Early responders displayed increased total abdominal adipose tissue deposits (TAT: 336 mm3 vs. 266 mm3, P = 0.008) and favorable immuno-nutritional scores compared to nonresponding patients. On univariate Cox regression analysis, visceral fat distribution, sarcopenia, and nutritional indices significantly impacted both progression-free (PFS) and overall survival (OS). Patients with a low skeletal muscle index (SMI; e.g.<34.5), a sarcopenia indicator, exhibited poor clinical outcomes (mOS 3.0 months vs. 17.6 months, log-rank P = 0.0026). Prognostically adverse immuno-nutritional scores were linked to inferior survival [low PNI: HROS, 6.31; 95% confidence interval (CI), 3.35-11.90; P < 0.001]. In a multivariable analysis adjusting for baseline Eastern Cooperative Oncology Group performance status, C-reactive protein, and lactate dehydrogenase, increased TAT was independently associated with improved clinical outcomes (adjusted HROS, 0.27; 95% CI, 0.08-0.90; P = 0.03). We noted particularly favorable treatment outcomes in patients with both increased abdominal fat and muscle mass (TAThigh/SMIhigh: 1-year PFS 50%, 1-year OS 83%). These real-world data provide evidence for a role of body composition and immuno-nutritional status in the context of CD19.CAR-T and suggest that the obesity paradox may extend to modern T cell-based immunotherapies. See related Spotlight by Nawas and Scordo, p. 704.

Indexed as

Lymphoma, B-CellReceptors, Chimeric AntigenSarcopeniaAntigens, CD19HumansImmunotherapy, AdoptiveNeoplasm Recurrence, LocalTissue DistributionAntigens, CD19Receptors, Chimeric Antigen

Identifiers

PMID37040425
PMCPMC10236147
OpenAlexW4364351852

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.