Evidence map›Paper›PMID 35259043›Full record

ArticleLeukemia & lymphoma2022

Lenalidomide enhances CD23.CAR T cell therapy in chronic lymphocytic leukemia.

Sarah Tettamanti, Maria Caterina Rotiroti, Greta Maria Paola Giordano Attianese, Silvia Arcangeli, Ronghua Zhang, Priyanka Banerjee, Giovanni Galletti, Sheighlah McManus, Massimiliano Mazza, Fabio Nicolini and 14 more

Open access · greenAbstract read
In one paragraph

Article in Leukemia & lymphoma, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.4field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 23 citations in OpenAlex.

  1. Advancing Immunotherapy in Chronic Lymphocytic Leukemia.International journal of molecular sciences · 2026
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  16. The magic of small-molecule drugs duringFrontiers in immunology · 2023
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  17. Chimeric Antigen Receptor T-Cell Therapy: What We Expect Soon.International journal of molecular sciences · 2022
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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

24 authors at 8 institutions in 3 countries.

Sarah TettamantiCentro Ricerca Tettamanti, Clinica Pediatrica, Università Milano Bicocca, Osp. San Gerardo/Fondazione MBBM, Monza, Italy.ORCID 0000-0002-7327-418X
Maria Caterina RotirotiCentro Ricerca Tettamanti, Clinica Pediatrica, Università Milano Bicocca, Osp. San Gerardo/Fondazione MBBM, Monza, Italy.
Greta Maria Paola Giordano AttianeseCentro Ricerca Tettamanti, Clinica Pediatrica, Università Milano Bicocca, Osp. San Gerardo/Fondazione MBBM, Monza, Italy.
Silvia ArcangeliCentro Ricerca Tettamanti, Clinica Pediatrica, Università Milano Bicocca, Osp. San Gerardo/Fondazione MBBM, Monza, Italy.
Ronghua ZhangDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Priyanka BanerjeeDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Giovanni GallettiDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Sheighlah McManusDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Massimiliano MazzaImmunotherapy, Cell Therapy and Biobank (ITCB), IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori, Meldola, Italy.
Fabio NicoliniImmunotherapy, Cell Therapy and Biobank (ITCB), IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori, Meldola, Italy.
Giovanni MartinelliImmunotherapy, Cell Therapy and Biobank (ITCB), IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori, Meldola, Italy.
Cristina IvanDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0002-4848-0168
Tania Veliz RodriguezDivision of Experimental Oncology, IRCCS San Raffaele Hospital, Milan, Italy.
Federica BarbaglioDivision of Experimental Oncology, IRCCS San Raffaele Hospital, Milan, Italy.
Lydia ScarfòDivision of Experimental Oncology, IRCCS San Raffaele Hospital, Milan, Italy.
Maurilio PonzoniUniversità Vita-Salute San Raffaele, Milan, Italy.
William WierdaDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Varsha GandhiDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Michael KeatingDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Andrea BiondiCentro Ricerca Tettamanti, Clinica Pediatrica, Università Milano Bicocca, Osp. San Gerardo/Fondazione MBBM, Monza, Italy.ORCID 0000-0002-6757-6173
Federico Caligaris-CappioDivision of Experimental Oncology, IRCCS San Raffaele Hospital, Milan, Italy.
Ettore BiagiCentro Ricerca Tettamanti, Clinica Pediatrica, Università Milano Bicocca, Osp. San Gerardo/Fondazione MBBM, Monza, Italy.
Paolo GhiaDivision of Experimental Oncology, IRCCS San Raffaele Hospital, Milan, Italy.
Maria Teresa Sabrina BertilaccioDepartment of Experimental Therapeutics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0002-2304-4618
The University of Texas MD Anderson Cancer Center · USVita-Salute San Raffaele University · ITUniversity of Milano-Bicocca · ITIstituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori · ITBristol-Myers Squibb (Switzerland) · CHHumanitas University · ITLudwig Cancer Research · CHTexas A&M Health Science Center · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
NCI NIH HHS P30 CA016672
6 · The paper itself

Abstract

Chimeric antigen receptors (CAR)-modified T cells are an emerging therapeutic tool for chronic lymphocytic leukemia (CLL). However, in patients with CLL, well-known T-cell defects and the inhibitory properties of the tumor microenvironment (TME) hinder the efficacy of CAR T cells. We explored a novel approach combining CARs with lenalidomide, an immunomodulatory drug that tempers the immunosuppressive activity of the CLL TME. T cells from patients with CLL were engineered to express a CAR specific for CD23, a promising target antigen. Lenalidomide maintained the in vitro effector functions of CD23.CAR

Indexed as

Immunotherapy, AdoptiveLeukemia, Lymphocytic, Chronic, B-CellHumansInterleukin Receptor Common gamma SubunitLenalidomideT-LymphocytesTumor MicroenvironmentInterleukin Receptor Common gamma SubunitLenalidomideCAR T cellsCD23Chronic lymphocytic leukemiaimmunomodulationimmunotherapylenalidomide

Identifiers

PMID35259043
PMCPMC9828187
OpenAlexW4220688343

What OpenQuestion holds

Textmetadata
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Read underepoch 390

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.