Evidence map›Paper›PMID 37261361›Full record

ArticleFrontiers in immunology2023

Prognostic impact of the post-treatment T cell composition and spatial organization in soft tissue sarcoma patients treated with neoadjuvant hyperthermic radio(chemo)therapy.

Luise Rupp, Antonia Resag, Vlatko Potkrajcic, Verena Warm, Rebekka Wehner, Korinna Jöhrens, Hans Bösmüller, Franziska Eckert, Marc Schmitz

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

8 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Type I conventional dendritic cells and CD8Frontiers in immunology · 2024
    Article
  7. Article
  8. 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

9 authors at 4 institutions in 2 countries.

Luise RuppInstitute of Immunology, Faculty of Medicine Carl Gustav Carus, Technische Universität (TU) Dresden, Dresden, Germany.
Antonia ResagInstitute of Immunology, Faculty of Medicine Carl Gustav Carus, Technische Universität (TU) Dresden, Dresden, Germany.
Vlatko PotkrajcicDepartment of Radiation Oncology, University Hospital Tuebingen, Tuebingen, Germany.
Verena WarmInstitute of Pathology, University Hospital Tuebingen, Tuebingen, Germany.
Rebekka WehnerInstitute of Immunology, Faculty of Medicine Carl Gustav Carus, Technische Universität (TU) Dresden, Dresden, Germany.
Korinna JöhrensNational Center for Tumor Diseases (NCT), Partner Site Dresden, Dresden, Germany.
Hans BösmüllerInstitute of Pathology, University Hospital Tuebingen, Tuebingen, Germany.
Franziska EckertDepartment of Radiation Oncology, University Hospital Tuebingen, Tuebingen, Germany.
Marc SchmitzInstitute of Immunology, Faculty of Medicine Carl Gustav Carus, Technische Universität (TU) Dresden, Dresden, Germany.
Technische Universität Dresden · DEUniversity of Tübingen · DEGerman Cancer Research Center · DEMedical University of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Soft tissue sarcomas (STS) form a heterogeneous group of tumors sharing a mesenchymal origin. Despite good local control of the disease, the occurrence of distant metastases often limits survival of STS patients with localized, high-risk tumors of the extremities. Accumulating evidence suggests a central role for the tumor immune microenvironment in determining the clinical outcome and response to therapy. Thus, it has been reported that STS patients with a high immune signature and especially presence of B cells and tertiary lymphoid structures display improved overall survival and response to checkpoint inhibitor treatment. Here, we explored the effect of curative multimodal therapy on the T cell landscape of STS using multiplex immunohistochemistry. We analyzed the phenotype, frequency, and spatial distribution of STS-infiltrating CD8

Indexed as

Hyperthermia, InducedSarcomaSoft Tissue NeoplasmsCD8-Positive T-LymphocytesHumansKi-67 AntigenNeoadjuvant TherapyProgrammed Cell Death 1 ReceptorTumor MicroenvironmentKi-67 AntigenProgrammed Cell Death 1 Receptorchemotherapyhyperthermiaimmune microenvironmentimmune modulationradiotherapysoft tissue sarcomaT cells

Identifiers

PMID37261361
PMCPMC10228739
OpenAlexW4376956046

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.