Evidence map›Paper›PMID 34504096›Full record

ArticleNPJ breast cancer2021

Multimodal liquid biopsy for early monitoring and outcome prediction of chemotherapy in metastatic breast cancer.

Amanda Bortolini Silveira, François-Clément Bidard, Marie-Laure Tanguy, Elodie Girard, Olivier Trédan, Coraline Dubot, William Jacot, Anthony Goncalves, Marc Debled, Christelle Levy and 15 more

Registry-linked trialAbstract read
In one paragraph

Article in NPJ breast cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01745757 (Cohort Study of Prospective Validation of Predictive Factors and Biological Imaging of Response to Bevacizumab), which is not on this map. Cited by 50 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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.

NCT01745757 completednot on this map

Cohort Study of Prospective Validation of Predictive Factors and Biological Imaging of Response to Bevacizumab (AVASTIN ®) in Combination With Weekly Paclitaxel Chemotherapy in First Line Treatment Patients With Metastatic Breast Cancer

TypeobservationalSponsorUNICANCERRan2012 to 2022Enrolled510ConditionsMetastatic, Breast CancerArmsBevacizumab, paclitaxel
3 · Its place in the literature

Who cites it

50 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Trial
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  14. Article
  15. Precision Oncology Framework Using Circulating Tumor Cells.International journal of molecular sciences · 2025
    Review
  16. Article
  17. Article
  18. Liquid Biopsy: The Challenges of a Revolutionary Approach in Oncology.International journal of molecular sciences · 2025
    Review
  19. Article
  20. Noninvasive Multicancer Detection Using DNA Hypomethylation of LINE-1 Retrotransposons.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    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

25 authors.

Amanda Bortolini Silveira *Circulating Tumor Biomarkers laboratory, INSERM CIC BT-1428, Institut Curie, Paris, France.
François-Clément Bidard *Circulating Tumor Biomarkers laboratory, INSERM CIC BT-1428, Institut Curie, Paris, France.
Marie-Laure TanguyDepartment of Biostatistics, Institut Curie, Paris, France.
Elodie GirardINSERM U900, Institut Curie, Mines ParisTech, PSL Research University, Paris, France.
Olivier TrédanDepartment of Medical Oncology, Centre Léon Bérard, Lyon, France.
Coraline DubotDepartment of Medical Oncology, Institut Curie, Paris and Saint Cloud, Paris, France.
William JacotDepartment of Medical Oncology, Institut du Cancer de Montpellier, Montpellier University, IRCM INSERM, Montpellier, France.ORCID http://orcid.org/0000-0001-7834-061X
Anthony GoncalvesDepartment of Medical Oncology, Aix-Marseille Univ, INSERM U1068, CNRS UMR7258, Institut Paoli-Calmettes, CRCM, Marseille, France.
Marc DebledDepartment of Medical Oncology, Institut Bergonié, Bordeaux, France.
Christelle LevyDepartment of Medical Oncology, Centre François Baclesse, Caen, France.
Jean-Marc FerreroDepartment of Medical Oncology, Centre Antoine Lacassagne, Nice, France.
Christelle JouannaudDepartment of Medical Oncology, Institut Jean Godinot, Reims, France.
Maria RiosDepartment of Medical Oncology, Institut de Cancérologie de Lorraine, Vandoeuvre-Lès-Nancy, France.
Marie-Ange Mouret-ReynierDepartment of Medical Oncology, Centre Jean Perrin, Clermont-Ferrand, France.
Florence DalencDepartment of Medical Oncology, Institut Claudius Regaud, IUCT-Oncopole, Toulouse, France.
Caroline HegoCirculating Tumor Biomarkers laboratory, INSERM CIC BT-1428, Institut Curie, Paris, France.
Aurore RampanouCirculating Tumor Biomarkers laboratory, INSERM CIC BT-1428, Institut Curie, Paris, France.
Benoit AlbaudICGex Next-Generation Sequencing Platform, Institut Curie, Paris, France.
Sylvain BaulandeICGex Next-Generation Sequencing Platform, Institut Curie, Paris, France.
Frédérique BergerDepartment of Biostatistics, Institut Curie, Paris, France.ORCID http://orcid.org/0000-0002-3251-4060
Jérôme LemonnierR&D UNICANCER, UCBG, Paris, France.
Shufang RenaultCirculating Tumor Biomarkers laboratory, INSERM CIC BT-1428, Institut Curie, Paris, France.
Isabelle DesmoulinsDepartment of Medical Oncology, Centre Georges-François Leclerc, Dijon, France.
Charlotte Proudhon *Circulating Tumor Biomarkers laboratory, INSERM CIC BT-1428, Institut Curie, Paris, France.ORCID http://orcid.org/0000-0002-4649-4574
Jean-Yves Pierga *Circulating Tumor Biomarkers laboratory, INSERM CIC BT-1428, Institut Curie, Paris, France. jean-yves.pierga@curie.fr.ORCID http://orcid.org/0000-0002-2863-9995

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-10-EQPX-03
6 · The paper itself

Abstract

Circulating tumor cells (CTCs) and circulating tumor DNA (ctDNA) are two cancer-derived blood biomarkers that inform on patient prognosis and treatment efficacy in breast cancer. We prospectively evaluated the clinical validity of quantifying both CTCs (CellSearch) and ctDNA (targeted next-generation sequencing). Their combined value as prognostic and early monitoring markers was assessed in 198 HER2-negative metastatic breast cancer patients. All patients were included in the prospective multicenter UCBG study COMET (NCT01745757) and treated by first-line chemotherapy with weekly paclitaxel and bevacizumab. Blood samples were obtained at baseline and before the second cycle of chemotherapy. At baseline, CTCs and ctDNA were respectively detected in 72 and 74% of patients and were moderately correlated (Kendall's τ = 0.3). Only 26 (13%) patients had neither detectable ctDNA nor CTCs. Variants were most frequently observed in TP53 and PIK3CA genes. KMT2C/MLL3 variants detected in ctDNA were significantly associated with a lower CTC count, while the opposite trend was seen with GATA3 alterations. Both CTC and ctDNA levels at baseline and after four weeks of treatment were correlated with survival. For progression-free and overall survival, the best multivariate prognostic model included tumor subtype (triple negative vs other), grade (grade 3 vs other), ctDNA variant allele frequency (VAF) at baseline (per 10% increase), and CTC count at four weeks (≥5CTC/7.5 mL). Overall, this study demonstrates that CTCs and ctDNA have nonoverlapping detection profiles and complementary prognostic values in metastatic breast cancer patients. A comprehensive liquid-biopsy approach may involve simultaneous detection of ctDNA and CTCs.

Identifiers

PMID34504096
PMCPMC8429692

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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.