Evidence map›Paper›PMID 36075914›Full record

ArticleNature communications2022

Biomarker correlates with response to NY-ESO-1 TCR T cells in patients with synovial sarcoma.

Alexandra Gyurdieva, Stefan Zajic, Ya-Fang Chang, E Andres Houseman, Shan Zhong, Jaegil Kim, Michael Nathenson, Thomas Faitg, Mary Woessner, David C Turner and 12 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Nature communications, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01343043 (A Pilot Study of Genetically Engineered NY-ESO-1 Specific NY-ESO-1ᶜ²⁵⁹T in HLA-A2+ Patients With Synovial Sarcoma), which is not on this map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
4.8field-weighted citation impact, top 4% 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.

NCT01343043 phase1completednot on this map

A Pilot Study of Genetically Engineered NY-ESO-1 Specific NY-ESO-1ᶜ²⁵⁹T in HLA-A2+ Patients With Synovial Sarcoma

TypeinterventionalSponsorGlaxoSmithKlineRan2012 to 2019Enrolled50ConditionsNeoplasmsArmsNY-ESO-1(c259)T Cells, Fludarabine, Cyclophosphamide
3 · Its place in the literature

Who cites it

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
  2. Letetresgene Autoleucel in Advanced/Metastatic Myxoid/Round Cell Liposarcoma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2025
    Trial
  3. Safety and Tolerability of Letetresgene Autoleucel (GSK3377794): Pilot Studies in Patients with Advanced Non-Small Cell Lung Cancer.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Trial
  4. Trial
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. Review
  20. Immunotherapy in Breast Cancer: Beyond Immune Checkpoint Inhibitors.International journal of molecular sciences · 2025
    Review
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

22 authors at 9 institutions in 1 country.

Alexandra GyurdievaGlaxoSmithKline, Collegeville, PA, USA.
Stefan ZajicGlaxoSmithKline, Collegeville, PA, USA.
Ya-Fang ChangGlaxoSmithKline, Collegeville, PA, USA.
E Andres HousemanGlaxoSmithKline, Collegeville, PA, USA.
Shan ZhongGlaxoSmithKline, Collegeville, PA, USA.ORCID 0000-0001-5871-3634
Jaegil KimGlaxoSmithKline, Collegeville, PA, USA.
Michael NathensonGlaxoSmithKline, Collegeville, PA, USA.
Thomas FaitgGlaxoSmithKline, Collegeville, PA, USA.
Mary WoessnerGlaxoSmithKline, Collegeville, PA, USA.
David C TurnerGlaxoSmithKline, Collegeville, PA, USA.
Aisha N HasanGlaxoSmithKline, Collegeville, PA, USA.
John GlodNational Cancer Institute, Bethesda, MD, USA.
Rosandra N KaplanNational Cancer Institute, Bethesda, MD, USA.ORCID 0000-0002-8580-0001
Sandra P D'AngeloMemorial Sloan Kettering Cancer Center, New York, NY, USA.ORCID 0000-0002-3736-3783
Dejka M AraujoUniversity of Texas/MD Anderson Cancer Center, Houston, TX, USA.
Warren A ChowCity of Hope Comprehensive Cancer Center, Duarte, CA, USA.
Mihaela DrutaH. Lee Moffitt Cancer Center, Tampa, FL, USA.
George D DemetriDana-Farber Cancer Institute and Ludwig Center at Harvard, Boston, MA, USA.
Brian A Van TineWashington University in St. Louis School of Medicine, St. Louis, MO, USA.ORCID 0000-0003-4572-6668
Stephan A GruppKelly Center for Cancer Immunotherapy, Division of Oncology, Children's Hospital of Philadelphia and University of Pennsylvania, Philadelphia, PA, USA.ORCID 0000-0001-8030-7595
Gregg D FineGlaxoSmithKline, Collegeville, PA, USA.
Ioanna EleftheriadouGlaxoSmithKline, Collegeville, PA, USA. ioanna.x.eleftheriadou@gsk.com.ORCID 0000-0002-0278-1061
GlaxoSmithKline (United States) · USNational Cancer Institute · USChildren's Hospital of Philadelphia · USCity of Hope · USDana-Farber Cancer Institute · USMemorial Sloan Kettering Cancer Center · USMoffitt Cancer Center · USThe University of Texas MD Anderson Cancer Center · USWashington University in St. Louis · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
NCI NIH HHS P30 CA008748
6 · The paper itself

Abstract

Autologous T cells transduced to express a high affinity T-cell receptor specific to NY-ESO-1 (letetresgene autoleucel, lete-cel) show promise in the treatment of metastatic synovial sarcoma, with 50% overall response rate. The efficacy of lete-cel treatment in 45 synovial sarcoma patients (NCT01343043) has been previously reported, however, biomarkers predictive of response and resistance remain to be better defined. This post-hoc analysis identifies associations of response to lete-cel with lymphodepleting chemotherapy regimen (LDR), product attributes, cell expansion, cytokines, and tumor gene expression. Responders have higher IL-15 levels pre-infusion (p = 0.011) and receive a higher number of transduced effector memory (CD45RA- CCR7-) CD8 + cells per kg (p = 0.039). Post-infusion, responders have increased IFNγ, IL-6, and peak cell expansion (p < 0.01, p < 0.01, and p = 0.016, respectively). Analysis of tumor samples post-treatment illustrates lete-cel infiltration and a decrease in expression of macrophage genes, suggesting remodeling of the tumor microenvironment. Here we report potential predictive and pharmacodynamic markers of lete-cel response that may inform LDR, cell dose, and strategies to enhance anticancer efficacy.

Indexed as

Sarcoma, SynovialAntigens, NeoplasmBiomarkersCD8-Positive T-LymphocytesHumansMembrane ProteinsReceptors, Antigen, T-CellTumor MicroenvironmentAntigens, NeoplasmBiomarkersMembrane ProteinsReceptors, Antigen, T-Cell

Identifiers

PMID36075914
PMCPMC9458750
OpenAlexW4294958151

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.