Evidence map›Paper›PMID 26921265›Full record

Trial reportOncotarget2016

MMP2 and MMP9 serum levels are associated with favorable outcome in patients with inflammatory breast cancer treated with bevacizumab-based neoadjuvant chemotherapy in the BEVERLY-2 study.

Emeline Tabouret, François Bertucci, Jean-Yves Pierga, Thierry Petit, Christelle Levy, Jean-Marc Ferrero, Mario Campone, Joseph Gligorov, Florence Lerebours, Henri Roché and 10 more

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

Trial report in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03185039 (Study of the Predictive Impact of MMP2 and MMP9 Levels for Patients With Metastatic Kidney Cancer Treated With Anti-angiogenic Agents Compared to Patients Not Treated With Antiangiogenic), which is not on this map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.5field-weighted citation impact, top 7% 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.

NCT03185039 naactive not recruitingnot on this mapstarted 2017, after this paper: background citation

Study of the Predictive Impact of MMP2 and MMP9 Levels for Patients With Metastatic Kidney Cancer Treated With Anti-angiogenic Agents Compared to Patients Not Treated With Antiangiogenic (Localized Kidney Cancer and Oligometastatic)

TypeinterventionalSponsorInstitut Paoli-CalmettesRan2017 to 2026Enrolled50ConditionsKidney CancerArmsBlood and tumor samples
3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 41 citations in OpenAlex.

  1. Trial
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  13. Secretome analysis of oral keratinocytes chronically exposed to shisha.Cancer biomarkers : section A of Disease markers · 2019
    Article
  14. Cancer-Associated Fibroblasts Build and Secure the Tumor Microenvironment.Frontiers in cell and developmental biology · 2019
    Review
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  20. Propofol Suppresses Esophageal Squamous Cell Carcinoma Cell Migration and Invasion by Down-Regulation of Sex-Determining Region Y-box 4 (SOX4).Medical science monitor : international medical journal of experimental and clinical research · 2017
    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

20 authors at 14 institutions in 3 countries.

Emeline TabouretInstitut Paoli-Calmettes, Medical Oncology Department, Marseille, France.
François BertucciInstitut Paoli-Calmettes, Medical Oncology Department, Marseille, France.
Jean-Yves PiergaInstitut Curie & Université Paris Descartes, Medical Oncology Department, Paris, France.
Thierry PetitCentre Paul Strauss, Medical Oncology Department, Strasbourg, France.
Christelle LevyCentre François Baclesse, Medical Oncology Department, Caen, France.
Jean-Marc FerreroCentre Antoine Lacassagne, Medical Oncology Department, Nice, France.
Mario CamponeCentre René Gauducheau, Medical Oncology Department, Saint-Herblin, France.
Joseph GligorovAPHP-Tenon, APREC, Paris, France.
Florence LereboursHopital Rene Huguenin-Institut Curie, Medical Oncology Department, Saint-Cloud, France.
Henri RochéInstitut Claudius Regaud, Medical Oncology Department, Toulouse, France.
Thomas BachelotInstitut Leon Berard, Medical Oncology Department, Lyon, France.
Steven van LaereTranslational Cancer Research Unit, GZA Hospitals Sint-Augustinus, Wilrijk, Belgium.
Naoto T UenoThe University of Texas MD Anderson Cancer Center, Morgan Welch Inflammatory Breast Cancer Research Program and Clinic, Houston, TX, USA.
Yves ToironCentre de Recherche en Cancérologie de Marseille, Inserm, Marseille, France.
Pascal FinettiCentre de Recherche en Cancérologie de Marseille, Inserm, Marseille, France.
Daniel BirnbaumCentre de Recherche en Cancérologie de Marseille, Inserm, Marseille, France.
Jean-Paul BorgCentre de Recherche en Cancérologie de Marseille, Inserm, Marseille, France.
Patrice ViensInstitut Paoli-Calmettes, Medical Oncology Department, Marseille, France.
Olivier ChinotCRO2, Neuro-Oncology Department, UMRS_911, Marseille, France.
Anthony GonçalvesInstitut Paoli-Calmettes, Medical Oncology Department, Marseille, France.
Centre National de la Recherche Scientifique · FRInserm · FRAix-Marseille Université · FRCentre Antoine Lacassagne · FRCentre François Baclesse · FRCentre Hospitalier René-Dubos · FRCentre Léon Bérard · FRHôpital René Huguenin · FRInstitut Claudius Regaud · FRInstitut Paoli-Calmettes · FRKU Leuven · BESorbonne Université · FRThe University of Texas MD Anderson Cancer Center · USUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAddition of bevacizumab to trastuzumab-based neoadjuvant chemotherapy in HER2-positive inflammatory breast cancer (IBC) was associated with favorable outcome in the BEVERLY-2 phase II trial. Circulating levels of matrix metalloproteinases (MMP) 2 and 9 were correlated to high response rate and prolonged survival in high-grade glioma treated with bevacizumab. We examined the prognostic impact of MMP2 and MMP9 serum levels in BEVERLY-2 patients. EXPERIMENTAL

designMMP2 and MMP9 serum levels were assessed using ELISA at baseline and before surgery in 45/52 available samples. Correlations were tested with pathological complete response (pCR), disease-free survival (DFS) and overall survival (OS).

resultsBaseline (b) MMP2 and MMP9 serum levels were independent from patient characteristics and circulating tumor or endothelial cells, and were not correlated to pCR. High bMMP2 was correlated to better DFS (p=0.001) and OS (p=0.032), while low bMMP9 was correlated to better OS (p=0.022) and tended to be associated with longer DFS (p=0.071). In multivariate analyses, bMMP2 (p=0.003, Hazard Ratio [HR]: 0.115) and bMMP9 (p=0.041, HR: 3.511) remained correlated to DFS. As continuous variables, bMMP2 was associated with relapse (p=0.002) and death (p=0.049), while bMMP9 was associated with death (p=0.035). During treatment, significant increase in MMP2 and decrease in MMP9 levels (p<0.001 for both) were observed in 100% and 87% of patients respectively.

conclusionsHigh bMMP2 and low bMMP9 serum levels were associated with better survival in HER2-positive IBC patients treated with bevacizumab- and trastuzumab-based neoadjuvant chemotherapy. Their predictive value of bevacizumab benefit should be evaluated in a randomized trial.

Indexed as

AdultAgedAngiogenesis InhibitorsAntineoplastic Combined Chemotherapy ProtocolsBevacizumabChemotherapy, AdjuvantFemaleHumansInflammatory Breast NeoplasmsMatrix Metalloproteinase 2Matrix Metalloproteinase 9Middle AgedNeoadjuvant TherapyTreatment OutcomeAngiogenesis InhibitorsBevacizumabMatrix Metalloproteinase 2Matrix Metalloproteinase 9MMP2 protein, humanMMP9 protein, humanbevacizumabbiomarkerinflammatory breast cancermatrix metalloproteinase 2matrix metalloproteinase 9

Identifiers

PMID26921265
PMCPMC4951307
OpenAlexW2312600030

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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.