Evidence map›Paper›PMID 32900797›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2020

CSPG4-Specific CAR.CIK Lymphocytes as a Novel Therapy for the Treatment of Multiple Soft-Tissue Sarcoma Histotypes.

Valeria Leuci, Chiara Donini, Giovanni Grignani, Ramona Rotolo, Giulia Mesiano, Erika Fiorino, Loretta Gammaitoni, Lorenzo D'Ambrosio, Alessandra Merlini, Elisa Landoni and 14 more

Abstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article
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.

Valeria Leuci *Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.ORCID 0000-0003-3592-9779
Chiara Donini *Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.ORCID 0000-0003-1988-9762
Giovanni GrignaniCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.
Ramona RotoloCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.ORCID 0000-0002-8544-115X
Giulia MesianoCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.ORCID 0000-0001-8950-9054
Erika FiorinoCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.ORCID 0000-0002-8662-9525
Loretta GammaitoniCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.ORCID 0000-0003-2251-9578
Lorenzo D'AmbrosioCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.ORCID 0000-0003-3294-8819
Alessandra MerliniCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.
Elisa LandoniLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Enzo MedicoCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.
Sonia CapelleroCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.ORCID 0000-0001-9043-9014
Lidia GiraudoCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.ORCID 0000-0002-0931-8352
Giulia CattaneoCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.
Ilenia IaiaCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.ORCID 0000-0001-9698-1402
Ymera PignochinoCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.ORCID 0000-0001-5073-8618
Marco BasiricòCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.ORCID 0000-0002-3059-7501
Elisa VignaCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.ORCID 0000-0001-9787-5732
Alberto PisacaneCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.
Franca FagioliPediatric Onco-Hematology, Division of Stem Cell Transplantation and Cellular Therapy, Regina Margherita Children's Hospital, University of Turin, Turin, Italy.ORCID 0000-0002-9257-900X
Soldano FerroneDivision of Surgical Oncology, Department of Surgery, Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts.ORCID 0000-0003-2900-8834
Massimo AgliettaCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.
Gianpietro DottiLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
Dario SangioloCandiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy. dario.sangiolo@ircc.it.ORCID 0000-0002-7163-7071

Funding

T cell plasticity, fusion proteins and CAR T cell-based immunotherapy of head and neck cancerR01DE028172 · NIDCR · MASSACHUSETTS GENERAL HOSPITAL · PI WANG, XINHUI · 2018 to 2022
$1.9M
IL-15 TRiKES-based specific immunotherapy of TNBC; resistance mechanismsR03CA216114 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI FERRONE, SOLDANO, VALLERA, DANIEL A · 2018 to 2019
$177k
Safety and anti-tumor activity of B7-H3 CAR T cells in TNBCR03CA223886 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI DOTTI, GIANPIETRO, FERRONE, SOLDANO · 2018 to 2019
$176k
Adaptive immunotherapy of anaplastic thyroid cancerR03CA239193 · NCI · MASSACHUSETTS GENERAL HOSPITAL · PI PARANGI, SAREH · 2019 to 2020
$165k
NCI NIH HHS R03 CA216114NCI NIH HHS R03 CA223886NCI NIH HHS R03 CA239193NIDCR NIH HHS R01 DE028172
6 · The paper itself

Abstract

purposeNo effective therapy is available for unresectable soft-tissue sarcomas (STS). This unmet clinical need prompted us to test whether chondroitin sulfate proteoglycan 4 (CSPG4)-specific chimeric antigen receptor (CAR)-redirected cytokine-induced killer lymphocytes (CAR.CIK) are effective in eliminating tumor cells derived from multiple STS histotypes EXPERIMENTAL

designThe experimental platform included patient-derived CAR.CIK and cell lines established from multiple STS histotypes. CAR.CIK were transduced with a retroviral vector encoding second-generation CSPG4-specific CAR (CSPG4-CAR) with 4-1BB costimulation. The functional activity of CSPG4-CAR.CIK was explored

resultsCSPG4-CAR.CIK were efficiently generated from patients with STS. CSPG4 was highly expressed in multiple STS histotypes by

conclusionsThis study has shown that CSPG4-CAR.CIK effectively targets multiple STS histotypes

Indexed as

AnimalsApoptosisCell ProliferationChondroitin Sulfate Proteoglycan 4Chondroitin Sulfate ProteoglycansCytokine-Induced Killer CellsFemaleHumansImmunotherapy, AdoptiveInterleukin-2LymphocytesMembrane ProteinsMiceMice, Inbred NODMice, SCIDReceptors, Chimeric AntigenChondroitin Sulfate Proteoglycan 4Chondroitin Sulfate ProteoglycansCSPG4 protein, humanInterleukin-2Membrane ProteinsReceptors, Chimeric Antigen

Identifiers

PMID32900797
PMCPMC7710537

What OpenQuestion holds

Textmetadata
LicenceTDM
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.