Evidence map›Paper›PMID 22805326›Full record

Trial reportBritish journal of cancer2012

Cytokine and angiogenic factors associated with efficacy and toxicity of pazopanib in advanced soft-tissue sarcoma: an EORTC-STBSG study.

S Sleijfer, T Gorlia, C Lamers, H Burger, J-Y Blay, A Le Cesne, M Scurr, F Collin, L Pandite, S Marreaud and 1 more

Registry-linked trialOpen access · hybridAbstract readClinical Trial, Phase II
In one paragraph

Trial report in British journal of cancer, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00297258 (Phase II Study of GW786034 in Patients With Relapsed or Refractory Soft Tissue Sarcoma), which is not on this map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.9field-weighted citation impact, top 9% 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.

NCT00297258 phase2completednot on this map

Phase II Study of GW786034 in Patients With Relapsed or Refractory Soft Tissue Sarcoma

TypeinterventionalSponsorGlaxoSmithKlineRan2005 to 2014Enrolled148ConditionsSarcoma, Soft TissueArmspazopanib
3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 49 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
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  7. Article
  8. Regorafenib for the Treatment of Sarcoma.Current treatment options in oncology · 2022
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Sarcoma Tumor Microenvironment.Advances in experimental medicine and biology · 2020
    Article
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Targeted therapy for soft tissue sarcomas in adolescents and young adults.Adolescent health, medicine and therapeutics · 2017
    Review
  20. 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

11 authors at 8 institutions in 6 countries.

S SleijferDepartment of Medical Oncology, Erasmus University Medical Center, Daniel den Hoed Cancer Center, Groene Hilledijk 301, 3075 EA Rotterdam, The Netherlands. s.sleijfer@erasmusmc.nl
T Gorlia
C Lamers
H Burger
J-Y Blay
A Le Cesne
M Scurr
F Collin
L Pandite
S Marreaud
P Hohenberger
Erasmus MC · NLEuropean Organisation for Research and Treatment of Cancer · BECentre Georges François Leclerc · FRCentre Léon Bérard · FRHeidelberg University · DEInstitut Gustave Roussy · FRResearch Triangle Park Foundation · USRoyal Marsden NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPazopanib has activity in relapsed non-adipocytic soft-tissue sarcomas (STS). A series of serum cytokines and angiogenic factors (CAFs) at baseline and changes in soluble vascular endothelial growth factor receptor-2 (sVEGFR2) or placental-derived growth factor (PlGF) levels during treatment were explored for their association with outcome.

methodsTwenty-three baseline CAFs, and sVEGFR2 and PlGF changes were measured in 85 and 32 patients, respectively. Associations between baseline CAF levels and efficacy parameters, plus between-week 12 sVEGFR2 and PlGF levels and pazopanib-specific toxicities were investigated.

resultsAt baseline, low interleukin (IL)-12 p40 subunit and MPC3 levels were associated with better progression-free survival (PFS) at 12 weeks (PFS(12wks)), low basic nerve growth factor and hepatocyte growth factor with a better PFS, and low inter-cellular adhesion molecule-1 and IL-2 receptor alpha with prolonged overall survival (OS; all P<0.05). Pazopanib decreased sVEGFR2 and increased PlGF levels. Low sVEGFR2 and high PlGF levels at week 12 were associated with higher-grade hypertension, with TSH elevations and with poorer PFS(12wks), and OS (both P<0.05).

conclusionSeveral baseline CAFs were related to outcome parameters. Low sVEGFR2 and high PlGF at week 12 associate with several pazopanib-specific toxicities and poorer efficacy. If confirmed, these factors may be used as early markers for response to and toxicity from pazopanib, enabling further individualisation of STS treatment.

Indexed as

AdolescentAdultAgedAngiogenesis InhibitorsAntineoplastic AgentsCytokinesDisease-Free SurvivalFemaleHumansIndazolesInterleukin-12 Subunit p40MaleMembrane ProteinsMiddle AgedPlacenta Growth FactorPolycomb-Group ProteinsAngiogenesis InhibitorsAntineoplastic AgentsCytokinesIndazolesInterleukin-12 Subunit p40Membrane ProteinspazopanibPGF protein, humanPIGF protein, humanPlacenta Growth FactorPolycomb-Group ProteinsPregnancy ProteinsPyrimidinesRepressor ProteinsSulfonamidesVascular Endothelial Growth Factor Receptor-2

Identifiers

PMID22805326
PMCPMC3419967
OpenAlexW2029717031

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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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.