Evidence map›Paper›PMID 42140929›Full record

ArticleNature communications2026

Naïve CD4

Michael Schneider, Luca Paruzzo, Federico Stella, Julia Han Noll, Matthew Ho, Victor Babatunde, Bianca Ho, Pooja Devi, Elise A Chong, Stefan K Barta and 21 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

31 authors.

Michael Schneider *Division of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Luca Paruzzo *Division of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0002-6505-0194
Federico Stella *Center for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0003-3401-1309
Julia Han NollCenter for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0003-3066-7378
Matthew HoDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0001-7937-1557
Victor BabatundeDivision of Nuclear Medicine Imaging and Therapy, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Bianca HoDivision of Nuclear Medicine Imaging and Therapy, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Pooja DeviDepartment of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Elise A ChongDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0001-8895-1625
Stefan K BartaDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Sunita D NastaDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Jakub SvobodaDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Jordan CarterDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Michael R CookDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Nasheed M HossainDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Colin J ThomasDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Vrutti PatelDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Vitor B de SouzaCenter for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, PA, USA.
Mohannad H AlkhatibCenter for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, PA, USA.
Ziyu LiCenter for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, PA, USA.
Melody TanCenter for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, PA, USA.
Peter MichenerDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Puneeth GuruprasadDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Antonio ImparatoCenter for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, PA, USA.
Alberto CarturanDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Patrizia PorazziDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.ORCID http://orcid.org/0000-0002-1372-7482
Joseph A FraiettaCenter for Cellular Immunotherapies, University of Pennsylvania, Philadelphia, PA, USA.
Stephen J SchusterDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Ivan MaillardDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Marco RuellaDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA. mruella@upenn.edu.ORCID http://orcid.org/0000-0003-4301-5811
Daniel J LandsburgDivision of Hematology-Oncology, Hospital of the University of Pennsylvania, Philadelphia, PA, USA. daniel.landsburg@pennmedicine.upenn.edu.ORCID http://orcid.org/0000-0002-5077-4181

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Elisa de Stanchina · 1985 to 2026
$347.4M
Project 3: Combinatorial and gene-editing approaches to enhance the efficacy of CAR T cell therapy of multiple myeloma.P01CA214278 · NCI · UNIVERSITY OF PENNSYLVANIA · PI CARL H. JUNE · 2017 to 2026
$26.8M
MODULATION OF CD5 SIGNALING TO ENHANCE ADOPTIVE T-CELL THERAPIES FOR CANCERR37CA262362 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Marco Ruella · 2022 to 2026
$2.6M
NCI NIH HHS P01 CA214278NCI NIH HHS P30 CA008748NCI NIH HHS R37 CA262362
6 · The paper itself

Abstract

Axicabtagene ciloleucel (axi-cel) and lisocabtagene maraleucel (liso-cel) are standard-of-care second-line therapies for relapsed or refractory large B-cell lymphomas, yet clinical and immunological predictors of durable benefit remain poorly defined. Here, we retrospectively analyze 64 patients treated with second-line commercial axi-cel (n = 35) or liso-cel (n = 29). Overall (66%) and complete (55%) response rates are similar between CART products. The 24-month progression-free survival (PFS) and overall survival rates are 46% and 76%, respectively. Primary refractory disease and progressive disease at infusion are associated with inferior response rates on multivariate analysis. Importantly, toxicity rate is relatively low, with 3% of patients experiencing Grade 3-4 cytokine release syndrome (CRS) and immune effector cell-associated neurotoxicity syndrome (ICANS). Furthermore, lower CD4

Indexed as

CD4-Positive T-LymphocytesImmunotherapy, AdoptiveLymphoma, Large B-Cell, DiffuseAdultAgedBiological ProductsCytokine Release SyndromeFemaleHumansMaleMiddle AgedProgression-Free SurvivalReceptors, Chimeric AntigenRetrospective StudiesTreatment Outcomeaxicabtagene ciloleucelBiological ProductsReceptors, Chimeric Antigen

Identifiers

PMID42140929
PMCPMC13376360

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.