Evidence map›Paper›PMID 31064127›Full record

ArticleJournal of clinical medicine2019

Stem Cells Inhibition by Bevacizumab in Combination with Neoadjuvant Chemotherapy for Breast Cancer.

Renaud Sabatier, Emmanuelle Charafe-Jauffret, Jean-Yves Pierga, Hervé Curé, Eric Lambaudie, Dominique Genre, Gilles Houvenaeghel, Patrice Viens, Christophe Ginestier, François Bertucci and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 35% 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

6 citing papers in PubMed, 1 synthesis or guideline pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Protein Marker-Dependent Drug Discovery Targeting Breast Cancer Stem Cells.International journal of molecular sciences · 2025
    Review
  3. Review
  4. Review
  5. Review
  6. 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

13 authors at 4 institutions in 1 country.

Renaud SabatierDepartment of Medical Oncology, Institut Paoli-Calmettes, 13009 Marseille, France. sabatierr@ipc.unicancer.fr.ORCID 0000-0002-5821-682X
Emmanuelle Charafe-JauffretAix Marseille Univ, CNRS U7258, INSERM U1068, Institut Paoli-Calmettes, CRCM, 13009 Marseille, France. jauffrete@ipc.unicancer.fr.
Jean-Yves PiergaDepartment of Medical Oncology, Institut Curie, Paris & St Cloud, Université Paris Descartes, 75005 Paris, France. jean-yves.pierga@curie.fr.
Hervé CuréDepartment of Medical Oncology, Institut Jean Godinot, 51100 Reims, France. hcure@chu-grenoble.fr.
Eric LambaudieAix Marseille Univ, CNRS U7258, INSERM U1068, Institut Paoli-Calmettes, CRCM, 13009 Marseille, France. lambaudiee@ipc.unicancer.fr.
Dominique GenreDepartment of Clinical Research and Innovation, Institut Paoli-Calmettes, 13009 Marseille, France. genred@ipc.unicancer.fr.
Gilles HouvenaeghelAix Marseille Univ, CNRS U7258, INSERM U1068, Institut Paoli-Calmettes, CRCM, 13009 Marseille, France. houvenaeghelg@ipc.unicancer.fr.ORCID 0000-0002-4384-6255
Patrice ViensDepartment of Medical Oncology, Institut Paoli-Calmettes, 13009 Marseille, France. viensp@ipc.unicancer.fr.ORCID 0000-0003-1511-1048
Christophe GinestierAix Marseille Univ, CNRS U7258, INSERM U1068, Institut Paoli-Calmettes, CRCM, 13009 Marseille, France. CHristophe.ginestier@inserm.fr.
François BertucciDepartment of Medical Oncology, Institut Paoli-Calmettes, 13009 Marseille, France. bertuccif@ipc.unicancer.fr.
Patrick SfumatoDepartment of Clinical Research and Innovation, Biostatistics unit, Institut Paoli-Calmettes, 13009 Marseille, France. sfumatop@ipc.unicancer.fr.
Jean-Marc ExtraDepartment of Medical Oncology, Institut Paoli-Calmettes, 13009 Marseille, France. extrajm@ipc.unicancer.fr.
Anthony GonçalvesDepartment of Medical Oncology, Institut Paoli-Calmettes, 13009 Marseille, France. goncalvesa@ipc.unicancer.fr.ORCID 0000-0001-7570-7439
Centre National de la Recherche Scientifique · FRInstitut Paoli-Calmettes · FRInstitut Jean Godinot · FRUniversité Paris Cité · FR

Funding

Institut National Du Cancer PHRC 2009, réf. n°24-005Roche NA
6 · The paper itself

Abstract

Preclinical works have suggested cytotoxic chemotherapies may increase the number of cancer stem cells (CSC) whereas angiogenesis inhibition may decrease CSC proliferation. We developed a proof of concept clinical trial to explore bevacizumab activity on breast CSC. Breast cancer patients requiring preoperative chemotherapy were included in this open-label, randomized, prospective, multicenter phase II trial. All received FEC-docetaxel combination, and patients randomized in the experimental arm received concomitant bevacizumab. The primary endpoint was to describe ALDH1 (Aldehyde dehydrogenase 1) positive tumor cells rate before treatment and after the fourth cycle. Secondary objectives included safety, pathological complete response (pCR) rate, disease-free survival (DFS), relapse-free survival (RFS), and overall survival (OS). Seventy-five patients were included. ALDH1+ cells rate increase was below the predefined 5% threshold in both arms for the 32 patients with two time points available. Grade 3 or 4 adverse events rates were similar in both arms. A non-significant increase in pCR was observed in the bevacizumab arm (42.6% vs. 18.2%,

Indexed as

ALDH1bevacizumabcancer stem cellsearly breast cancerneoadjuvant chemotherapy

Identifiers

PMID31064127
PMCPMC6572380
OpenAlexW2943583661

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.