Evidence map›Paper›PMID 36178573›Full record

ReviewCurrent treatment options in oncology2022

Regorafenib for the Treatment of Sarcoma.

Jean-Yves Blay, Florence Duffaud, Suzanne George, Robert G Maki, Nicolas Penel

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current treatment options in oncology, 2022. 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
2.0field-weighted citation impact, top 12% 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, 13 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Systemic Therapy for Solitary Fibrous Tumor.Current treatment options in oncology · 2026
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Neoadjuvant Chemotherapy for Adults with Osteogenic Sarcoma.Current treatment options in oncology · 2024
    Review
  12. NOTCH Signaling in Osteosarcoma.Current issues in molecular biology · 2023
    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

5 authors at 5 institutions in 2 countries.

Jean-Yves BlayDepartment of Medicine, Léon Bérard Center, Lyon, France. jean-yves.blay@lyon.unicancer.fr.ORCID 0000-0001-7190-120X
Florence DuffaudMedical Oncology Unit, La Timone University Hospital, Marseille, France.
Suzanne GeorgeDana-Farber Cancer Institute, Harvard Medical School, Cambridge, MA, USA.
Robert G MakiPerelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Nicolas PenelMedical Oncology Department, Oscar Lambret Cancer Center and Lille University, Lille, France.
Aix-Marseille Université · FRCentre Léon Bérard · FRCentre Oscar Lambret · FRHarvard University · USUniversity of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

opinion statementSarcomas are a rare group of tumors with many subtypes, conventionally classified into soft-tissue sarcomas and bone sarcomas. Chemotherapeutic regimens form the mainstay of systemic therapy but are not well defined beyond the first-line setting and clinical outcomes are variable. Tyrosine kinase inhibitors (TKIs), with a broad inhibition profile which have been shown to target tumor angiogenesis, have an established role in the treatment of sarcomas without characteristic driver alterations. One such TKI, regorafenib, has been evaluated in sarcomas and clinical data are discussed in this review. An overview of regorafenib data from five phase 2 and one phase 1b clinical trials in over 10 sarcoma subtypes (both soft-tissue and bone) in adult and pediatric patients is reviewed. Regorafenib demonstrated clinical benefit in patients with non-adipocytic soft-tissue sarcomas, osteosarcoma and Ewing sarcoma who had progressed on prior therapy. Patients with otherwise limited treatment options may therefore benefit from regorafenib therapy.

Indexed as

Bone NeoplasmsOsteosarcomaSarcomaSoft Tissue NeoplasmsAdultChildHumansPhenylurea CompoundsProtein Kinase InhibitorsPyridinesPhenylurea CompoundsProtein Kinase InhibitorsPyridinesregorafenibBone sarcomaNon-adipocytic sarcomaRegorafenibSoft-tissue sarcomaTyrosine kinase inhibitors

Identifiers

PMID36178573
OpenAlexW4298086480

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.