Evidence map›Paper›PMID 30305054›Full record

Trial reportBMC cancer2018

Prognostic and predictive factors for angiosarcoma patients receiving paclitaxel once weekly plus or minus bevacizumab: an ancillary study derived from a randomized clinical trial.

Loïc Lebellec, François Bertucci, Emmanuelle Tresch-Bruneel, Isabelle Ray-Coquard, Axel Le Cesne, Emmanuelle Bompas, Jean-Yves Blay, Antoine Italiano, Olivier Mir, Thomas Ryckewaert and 5 more

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in BMC cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01303497 (Phase II Study, Multicenter, Randomized, Stratified, Evaluating the Efficacity of Weekly Paclitaxel, With or Without Bevacizumab in the Treatment of Metastatic or Locally Advanced Angiosarcomas Not Accessible to Surgery Treatment.), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.8field-weighted citation impact, top 24% 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.

NCT01303497 phase2completednot on this map

Phase II Study, Multicenter, Randomized, Stratified, Evaluating the Efficacity of Weekly Paclitaxel, With or Without Bevacizumab in the Treatment of Metastatic or Locally Advanced Angiosarcomas Not Accessible to Surgery Treatment.

TypeinterventionalSponsorCentre Oscar LambretRan2010 to 2019Enrolled70ConditionsAngiosarcomaArmsPaclitaxel, Bevacizumab
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Hypoxia-driven angiogenesis and metabolic reprogramming in vascular tumors.Frontiers in cell and developmental biology · 2025
    Review
  5. Article
  6. Observational
  7. Review
  8. Article
  9. Article
  10. Management of Cutaneous Angiosarcoma: an Update Review.Current treatment options in oncology · 2022
    Review
  11. Review
  12. Article
  13. The vascular landscape of human cancer.The Journal of clinical investigation · 2021
    Article
  14. Review
  15. Angiosarcoma: a review of diagnosis and current treatment.American journal of cancer research · 2019
    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

15 authors at 8 institutions in 1 country.

Loïc LebellecLille University Hospital and Medical School, 59045, Lille cedex, France.
François BertucciDepartment of Medical Oncology, Institut Paoli-Calmettes, 232 Boulevard de Sainte-Marguerite, 13009, Marseille, France.
Emmanuelle Tresch-BruneelDirection of Research and Innovation, Centre Oscar Lambret, 3 rue Combemale, 59020, Lille cedex, France.
Isabelle Ray-CoquardDepartment of Medical Oncology, Centre Léon Bérard, 28 Prom. Léa et Napoléon Bullukian, 69008, Lyon, France.
Axel Le CesneDepartment of Medical Oncology, Gustave Roussy Institute, 114 Rue Edouard Vaillant, 94800, Villejuif, France.
Emmanuelle BompasDepartment of Medical Oncology, Centre René Gauducheau, Boulevard Professeur Jacques Monod, 44805, Saint-Herblain, France.
Jean-Yves BlayDepartment of Medical Oncology, Centre Léon Bérard, 28 Prom. Léa et Napoléon Bullukian, 69008, Lyon, France.
Antoine ItalianoDepartment of Medical Oncology, Institut Bergonié, 229 Cours de l'Argonne, 33000, Bordeaux, France.
Olivier MirDepartment of Medical Oncology, Gustave Roussy Institute, 114 Rue Edouard Vaillant, 94800, Villejuif, France.
Thomas RyckewaertDepartment of Medical Oncology, Institut Bergonié, 229 Cours de l'Argonne, 33000, Bordeaux, France.
Yves ToironDepartment of Molecular Pharmacology, Institute Paoli-Calmettes, 232 Boulevard de Sainte-Marguerite, 13009, Marseille, France.
Luc CamoinDepartment of Molecular Pharmacology, Institute Paoli-Calmettes, 232 Boulevard de Sainte-Marguerite, 13009, Marseille, France.
Anthony GoncalvesDepartment of Medical Oncology, Institut Paoli-Calmettes, 232 Boulevard de Sainte-Marguerite, 13009, Marseille, France.
Nicolas PenelLille University Hospital and Medical School, 59045, Lille cedex, France. n-penel@o-lambret.fr.ORCID http://orcid.org/0000-0001-5243-1548
Marie-Cécile Le DeleyDirection of Research and Innovation, Centre Oscar Lambret, 3 rue Combemale, 59020, Lille cedex, France.
Institut Paoli-Calmettes · FRCentre Léon Bérard · FRInstitut Bergonié · FRInstitut Gustave Roussy · FRUniversité de Lille · FRCentre Oscar Lambret · FRInstitut Génétique Nantes Atlantique · FRUniversité Paris-Sud · FR

Funding

Institut National Du Cancer PHRC 2010Roche 0906-EPPA153667-G
6 · The paper itself

Abstract

backgroundWe report here a correlation analysis conducted along with a phase II trial assessing bevacizumab in combination with weekly paclitaxel.

methodsCirculating pro/anti-angiogenic factors were assessed on day 1 (D1) and day 8 (D8). The prognostic value for progression-free survival (PFS) was evaluated using a Cox model with biomarkers as continuous variables.

resultsAmong the 51 patients enrolled and treated in this trial, biomarker analysis was performed for 42: 18 in Arm A (single-agent) and 24 in Arm B (combination). With a median follow-up of 46 months, PFS was 5.5 versus 5.7 months, respectively (p = 0.75). According to univariate analysis, factors associated with a poor PFS were as follows: visceral angiosarcoma, de novo angiosarcoma, and high PlGF and low VEGF-C baseline values. In multivariate analysis, de novo angiosarcoma (HR = 2.5; p = 0.024) and baseline VEGF-C value (HR = 0.7; p = 0.003) were significant prognostic factors. We observed a significant increase in circulating PlGF (< 0.001) and a decrease in VEGF (< 0.001) during bevacizumab treatment. An increase in FGF was associated with a poor outcome.

conclusionsDe novo angiosarcoma and a low baseline level of VEGF-C were found to be associated with a poor prognosis. Addition of bevacizumab induces major changes in circulating biomarkers (VEGF and PlGF) in a short timeframe without impacting PFS.

trial registrationRetrospectively registered on EudraCT N° 2009-017020-59 and NCT01303497 (February 24, 2011).

Indexed as

Biomarkers, TumorAdultAgedAged, 80 and overAntineoplastic Agents, PhytogenicBevacizumabFemaleHemangiosarcomaHumansMiddle AgedPaclitaxelPlacenta Growth FactorPrognosisVascular Endothelial Growth Factor AAntineoplastic Agents, PhytogenicBevacizumabBiomarkers, TumorPaclitaxelPGF protein, humanPlacenta Growth FactorVascular Endothelial Growth Factor AVEGFA protein, humanAngiosarcomaBevacizumabBiomarkersRadiation-induced angiosarcomaWeekly paclitaxel

Identifiers

PMID30305054
PMCPMC6180490
OpenAlexW2895960861

What OpenQuestion holds

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LicenceCC BY
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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.