Evidence map›Paper›PMID 27319943›Full record

ReviewCurrent oncology reports2016

An Unusual Case of Central Retinal Vein Occlusion and Review of the Toxicity Profile of Regorafenib in GIST Patients.

Gustavo Schvartsman, Michael J Wagner, Chrystia M Zobniw, Van Anh Trinh, Shreyaskumar Patel, Neeta Somaiah

Abstract readCase ReportsReview
PubMed Publisher
In one paragraph

Review in Current oncology reports, 2016. 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
0.5field-weighted citation impact, top 31% 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, 10 citations in OpenAlex.

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

6 authors at 1 institution in 1 country.

Gustavo SchvartsmanDivision of Cancer Medicine, University of Texas M.D. Anderson Cancer Center, 1400 Holcombe Boulevard, unit 463, Houston, TX, 77030, USA.
Michael J WagnerDivision of Cancer Medicine, University of Texas M.D. Anderson Cancer Center, 1400 Holcombe Boulevard, unit 463, Houston, TX, 77030, USA.
Chrystia M ZobniwDepartment of Pharmacy Clinical Programs, University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX, 77030, USA.
Van Anh TrinhDepartment of Pharmacy Clinical Programs, University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX, 77030, USA.
Shreyaskumar PatelDepartment of Sarcoma Medical Oncology, University of Texas M.D. Anderson Cancer Center, 1400 Holcombe Boulevard, unit 450, Houston, TX, 77030, USA.
Neeta SomaiahDepartment of Sarcoma Medical Oncology, University of Texas M.D. Anderson Cancer Center, 1400 Holcombe Boulevard, unit 450, Houston, TX, 77030, USA. nsomaiah@mdanderson.org.
The University of Texas MD Anderson Cancer Center · US

Funding

TRAINING FOR ACADEMIC ONCOLOGY/HEMATOLOGYT32CA009666 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Michael Davies, Courtney DiNardo · 1994 to 2026
$9.8M
NCI NIH HHS T32 CA009666
6 · The paper itself

Abstract

Gastrointestinal stromal tumor (GIST) is the most common sarcoma of the gastrointestinal tract with around 5000 new cases per year. Outcomes for patients with GIST dramatically improved after the development of tyrosine kinase inhibitors targeted against the aberrant signaling pathways that drive GIST oncogenesis. Majority of patients derive benefit from first-line imatinib, and the type of driver mutation is predictive of response. However, almost half of the patients eventually develop resistance to initial targeted therapy and further lines of treatment do not have the same impact. Regorafenib is an oral multi-kinase inhibitor approved as a third-line therapy for advanced GIST and though its efficacy is limited in comparison to imatinib, it has activity across the various driver mutation categories in GIST even in the setting of imatinib resistance. Herein, we describe a case of central retinal vein occlusion (CRVO) secondary to regorafenib and review regorafenib's efficacy and toxicity profile.

Indexed as

AgedFatal OutcomeGastrointestinal NeoplasmsGastrointestinal Stromal TumorsHumansImatinib MesylatePhenylurea CompoundsProtein Kinase InhibitorsProto-Oncogene Proteins c-kitPyridinesRetinal Vein OcclusionImatinib MesylatePhenylurea CompoundsProtein Kinase InhibitorsProto-Oncogene Proteins c-kitPyridinesregorafenibCentral retinal vein occlusionGastrointestinal stromal tumorGISTKITRegorafenibTyrosine kinase inhibitors

Identifiers

PMID27319943
OpenAlexW2437735439

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.