Evidence map›Paper›PMID 26423769›Full record

ReviewCurrent oncology reports2015

Immunotherapy in Sarcoma: Future Horizons.

Melissa Burgess, Vikram Gorantla, Kurt Weiss, Hussein Tawbi

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current oncology reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Sarcoma · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Clinical and prognostic significance of PD-1 and PD-L1 expression in sarcomas.Medical oncology (Northwood, London, England) · 2016
    Article
  11. Review
  12. 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

4 authors at 3 institutions in 2 countries.

Melissa BurgessDivision of Hematology/Oncology, Department of Medicine, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA. burgessma@upmc.edu.
Vikram GorantlaMedical Oncology, American Oncology Institute, Serilingampally, Hyderabad, TS, India.
Kurt WeissDivision of Musculoskeletal Oncology, Department of Orthopedic Surgery, University of Pittsburgh, Pittsburgh, PA, USA.
Hussein TawbiDivision of Hematology/Oncology, Department of Medicine, School of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Cancer Hospital and Research Institute · INUniversity of Pittsburgh · USUPMC Hillman Cancer Center · US

Funding

Exploring Sarcoma Metastatic PotentialK08CA177927 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WEISS, KURT RICHARD · 2013 to 2017
$827k
NCI NIH HHS K08 CA177927
6 · The paper itself

Abstract

Immunologic approaches to cancer are over a century old. Over the years, the strategy has been fine-tuned from inciting infections in subjects to inhibiting negative regulatory signals from the innate immune system. Sarcomas are among the first tumors to be considered for immune interventions. From Coley's toxin to cytokine-based therapies to adoptive cell therapy, there have been numerous immunotherapeutic investigations in this patient population. A promising strategy includes adoptive T cell therapy which has been studied in small cohorts of synovial sarcoma, a subtype that is known to widely express the cancer testis antigen, NY-ESO-1. Additionally, recent data in metastatic melanoma and renal cell carcinoma demonstrate the utility and tremendous efficacy of immune checkpoint blockade with increased rates of durable responses compared to standard therapies. Responses in traditionally "non-immunogenic" tumors, such as lung and bladder cancers, provide ample rationale for the study of immune checkpoint inhibitors in sarcoma. While immunotherapy has induced some responses in sarcomas, further research will help clarify optimal patient selection for future clinical trials and new combinatorial immunotherapeutic strategies.

Indexed as

Antigens, NeoplasmHumansImmunotherapy, AdoptiveMolecular Targeted TherapyNeoplasm Recurrence, LocalPatient SelectionPractice Guidelines as TopicProgrammed Cell Death 1 ReceptorSarcomaAntigens, NeoplasmProgrammed Cell Death 1 ReceptorImmune checkpoint blockadeImmunosurveillanceImmunotherapyProgrammed death-1 (PD-1)Soft tissue sarcomaTumor-infiltrating lymphocyte (TIL)

Identifiers

PMID26423769
OpenAlexW1873340436

What OpenQuestion holds

Textmetadata
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.