Evidence map›Paper›PMID 29931504›Full record

ReviewTargeted oncology2018

Growing Role of Regorafenib in the Treatment of Patients with Sarcoma.

Mark Agulnik, Steven Attia

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Targeted oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05395741 (Evaluation of the Efficacy and Safety of Regorafenib in Patients With Refractory Primary Bone Tumors), which is not on this map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

NCT05395741 phase1 / phase2completednot on this mapstarted 2022, after this paper: background citation

Evaluation of the Efficacy and Safety of Regorafenib in Patients With Refractory Primary Bone Tumors

TypeinterventionalSponsorInstitute of Mother and Child, Warsaw, PolandRan2022 to 2026Enrolled30ConditionsOsteosarcoma, Ewing Sarcoma of BoneArmsRegorafenib
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. 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

2 authors.

Mark AgulnikDivision of Hematology/Oncology, Northwestern University, Feinberg School of Medicine, NMH/Arkes Family Pavilion Suite 850, 676 N Saint Clair, Chicago, IL, USA. Mark.Agulnik@nm.org.
Steven AttiaDivision of Hematology/Oncology, Mayo Clinic in Florida, Jacksonville, FL, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sarcomas encompass a group of rare solid tumors responsible for approximately 1% of all cancer-related deaths in the United States each year. Subtypes include, but are not limited to, soft tissue sarcomas (STS) such as leiomyosarcoma, liposarcoma, pleomorphic sarcoma, and gastrointestinal stromal tumor (GIST). Treatment options for patients with STS vary depending on, among other factors, histological subtype. Data from a mix of phase 2 and phase 3 trials have suggested that the orally available multikinase inhibitor regorafenib may have efficacy in patients with STS who have progressed on previous lines of systemic therapy. Some clinical benefit of regorafenib has been shown in patients with leiomyosarcoma, synovial sarcoma, GIST, Ewing's sarcoma, and other sarcoma subtypes, suggesting a broad spectrum of potential activity in this population. Studies have also shown that the safety profile of regorafenib is acceptable in these patients, with adverse events that can be managed through dose reductions and/or interruptions as well as other supportive measures.

Indexed as

HumansPhenylurea CompoundsPyridinesSarcomaPhenylurea CompoundsPyridinesregorafenib

Identifiers

What OpenQuestion holds

Textmetadata
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.