Evidence map›Paper›PMID 36905579›Full record

ArticleThe oncologist2023

Emerging Trends in Immunotherapy for Adult Sarcomas.

Marium Husain, Luxi Chen, David Liebner, Joal Beane, Mark Rubinstein, Raphael Pollock, Claire Verschraegen, Gabriel Tinoco

Open access · goldAbstract read
In one paragraph

Article in The oncologist, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 21% 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

5 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. 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

8 authors at 1 institution in 1 country.

Marium HusainDepartment of Internal Medicine, Division of Medical Oncology, The Ohio State University Comprehensive Cancer Center, Division of Medical Oncology, Columbus, OH, USA.
Luxi ChenThe Ohio State University, Columbus, OH, USA.
David LiebnerDepartment of Internal Medicine, Division of Medical Oncology, The Ohio State University Comprehensive Cancer Center, Division of Medical Oncology, Columbus, OH, USA.
Joal BeaneDepartment of Surgery, Division of Surgical Oncology, The Ohio State University Comprehensive Cancer Center, Division of Surgical Oncology, Columbus, OH, USA.
Mark RubinsteinThe Ohio State University Comprehensive Cancer Center, Pelotonia Institute for Immuno-Oncology, Columbus, OH, USA.
Raphael PollockDepartment of Surgery, Division of Surgical Oncology, The Ohio State University Comprehensive Cancer Center, Division of Surgical Oncology, Columbus, OH, USA.
Claire VerschraegenDepartment of Internal Medicine, Division of Medical Oncology, The Ohio State University Comprehensive Cancer Center, Division of Medical Oncology, Columbus, OH, USA.
Gabriel TinocoDepartment of Internal Medicine, Division of Medical Oncology, The Ohio State University Comprehensive Cancer Center, Division of Medical Oncology, Columbus, OH, USA.ORCID 0000-0002-2565-6124
The Ohio State University · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Daniel G. Stover · 1985 to 2026
$132.3M
NIH HHS P30CA016058
6 · The paper itself

Abstract

Soft-tissue sarcomas (STS) are a rare and heterogeneous group of malignant tumors that arise from the oncogenic transformation of mesenchymal tissue. There are over 100 distinct STS histological and molecular subtypes with unique clinical, therapeutic, and prognostic features with variable responses to therapy regimens. Given the quality-of-life concerns and limited efficacy with current regimens, including cytotoxic chemotherapy, there is a need for novel therapies and regimens to treat advanced STS. Although immune checkpoint inhibitors have demonstrated significant improvements in survival outcomes in other cancer types, there remains ambiguous data on the impact of immunotherapy in sarcoma. Biomarkers like PD-1/PD-L1 are not always predictive of outcomes. Therefore, researching emerging novel therapies, such as CAR-T and adoptive cell therapies, is critical to understanding STS biology, STS tumor immune microenvironment immunomodulatory strategies that improve immune response, and survival outcomes. We discuss the underlying biology of the STS tumor immune microenvironment, immunomodulatory strategies that augment pre-existing immune responses, and novel approaches to develop sarcoma-specific antigen-based therapies.

Indexed as

SarcomaSoft Tissue NeoplasmsAdultCombined Modality TherapyHumansImmunotherapyPrognosisTumor Microenvironmentadoptive cellular therapyimmune checkpoint inhibitorssarcoma

Identifiers

PMID36905579
PMCPMC10166169
OpenAlexW4323920668

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.