Evidence map›Paper›PMID 28619014›Full record

ArticleBMC cancer2017

Prognostic impact of blood and urinary angiogenic factor levels at diagnosis and during treatment in patients with osteosarcoma: a prospective study.

Marie-Dominique Tabone, Laurence Brugières, Sophie Piperno-Neumann, Marie-Ange Selva, Perrine Marec-Bérard, Hélène Pacquement, Cyril Lervat, Nadège Corradini, Jean-Claude Gentet, Rémy Couderc and 5 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in BMC cancer, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00470223 (OS2006), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 42% 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.

NCT00470223 phase3active not recruitingnot on this map

OS2006 : Protocole de Traitement Des ostéosarcomes de l'Enfant, de l'Adolescent et de l'Adulte Comportant

TypeinterventionalSponsorUNICANCERRan2007 to 2026Enrolled318ConditionsSarcomaArmscisplatin, doxorubicin hydrochloride, etoposide, ifosfamide, methotrexate
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 7 citations in OpenAlex.

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

15 authors at 9 institutions in 1 country.

Marie-Dominique TaboneDepartment of Paediatric Onco-Haematology, Armand Trousseau Hospital, 26 avenue du Dr A. Netter, 75571, Paris cedex12, France. marie-dominique.tabone@aphp.fr.
Laurence BrugièresDepartment of Children and adolescents Oncology, Gustave Roussy Cancer campus, 114 rue E. Vaillant, 94805, Villejuif, France.
Sophie Piperno-NeumannDepartment of Medical Oncology, Curie Institute, 26 rue d'Ulm, 75005, Paris, France.
Marie-Ange SelvaDepartment of Biochemistry, Armand Trousseau Hospital, 26 avenue du Dr A. Netter, 75571, Paris cedex12, France.
Perrine Marec-BérardInstitute for Paediatric Haematology and Oncology, Léon Bérard Cancer Centre, 28 rue Laennec, 69008, Lyon, France.
Hélène PacquementDepartment of Paediatric Oncology, Curie Institute, 26 rue d'Ulm, 75005, Paris, France.
Cyril LervatDepartment of Paediatric Oncology, Oscar Lambret Cancer Centre, 3 rue Frédéric Combemale, 59020, Lille cedex, France.
Nadège CorradiniDepartment of Paediatric Haemato-Oncology, Mother and Child Hospital, 7 quai Moncousu, 44093, Nantes, France.
Jean-Claude GentetDepartment of Paediatric Oncology, La Timone Hospital, 264 rue Saint Pierre, 13385, Marseille cedex 5, France.
Rémy CoudercDepartment of Biochemistry, Armand Trousseau Hospital, 26 avenue du Dr A. Netter, 75571, Paris cedex12, France.
Aurélie ChevanceBiostatistics and Epidemiology unit, Gustave Roussy Cancer Campus, 114 rue E. Vaillant, 94805, Villejuif, France.
Céline Mahier-Ait OukhatarDepartment of Clinical Studies, Unicancer, 101 rue de Tolbiac, 75654, 13, Paris cedex, France.
Natacha Entz-WerleDepartment of Paediatric Oncology, Hautepierre Hospital, 1 avenue Molière, 67100, Strasbourg, France.
Jean-Yves BlayDepartment of Medical Oncology, Léon Bérard Cancer Centre, 28 rue Laennec, 69008, Lyon, France.
Marie-Cecile Le DeleyBiostatistics and Epidemiology unit, Gustave Roussy Cancer Campus, 114 rue E. Vaillant, 94805, Villejuif, France.
Institut Gustave Roussy · FRSorbonne Université · FRInstitut Curie · FRCentre Oscar Lambret · FRHôpital de la Timone · FRHôpital d'Hautepierre · FRHôpital Mère-Enfant · FRUniCancer Group · FRUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAngiogenesis is essential for the progression and metastatic spread of solid tumours. Expression of vascular endothelial growth factor (VEGF) has been linked to poor survival among osteosarcoma patients but the clinical relevance of monitoring blood and urine angiogenic factors is uncertain. The aim of this study was to determine the prognostic significance of blood VEGF and blood and urinary basic fibroblast growth factor (bFGF) levels in osteosarcoma patients, both at diagnosis and during treatment.

methodsPatients with localised or metastatic osteosarcoma enrolled in OS2005 and OS2006 studies between 2005 and 2011 were prospectively included in this study. VEGF and bFGF levels in serum and plasma and bFGF levels in urine were measured by ELISA at diagnosis, before surgery, and at the end of treatment. Endpoints considered for the prognostic analysis were histological response, progression-free and overall survival. Kruskal-Wallis tests were used to compare the distribution of baseline biomarker values across the different subgroups, and paired sample Wilcoxon rank tests were used to analyze changes over time. Association between biomarker levels and outcomes were assessed in multivariable models (logistic regression for histologic response, and Cox models for survival).

resultsSamples were available at diagnosis for 269 patients (54% males; age ≤ 18 years: 73%; localised disease in 68%, doubtful lung lesions in 17%, and metastases in 15%). High serum VEGF and bFGF levels were observed in respectively 61% and 51% of patients. Serum and plasma VEGF values were not strongly correlated with one another (r = 0.53). High serum and plasma VEGF levels were significantly more frequent in patients with large tumours (≥10 cm; p = 0.003 and p = 0.02, respectively). VEGF levels fell significantly during pre-operative chemotherapy (p < 0.0001). No significant correlation was found between this variation and either the histological response, progression-free survival or overall survival (p = 0.26, p = 0.67, and p = 0.87, respectively). No significant association was found between blood or urinary bFGF levels and clinical characteristics, histological response, or survival.

conclusionsLevels of VEGF and bFGF angiogenic factors are high in most osteosarcoma patients, but have no significant impact on response to chemotherapy or outcome in this large prospective series. OS 2006 TRIAL REGISTRATION NUMBER: clinicaltrials.gov NCT00470223; date of registration: May 3th 2007.

Indexed as

BiomarkersAdolescentAngiogenesis Inducing AgentsBone NeoplasmsChildFemaleFibroblast Growth Factor 2HumansMaleNeoplasm StagingOsteosarcomaPrognosisProspective StudiesSurvival AnalysisTumor BurdenVascular Endothelial Growth FactorsAngiogenesis Inducing AgentsBiomarkersFibroblast Growth Factor 2Vascular Endothelial Growth FactorsAngiogenic factorsBasic fibroblast growth factorOsteosarcomaVascular endothelial growth factor

Identifiers

PMID28619014
PMCPMC5473001
OpenAlexW2625278111

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.