Evidence map›Paper›PMID 29791503›Full record

ArticlePloS one2018

[18F]FDG and [18F]FLT PET for the evaluation of response to neo-adjuvant chemotherapy in a model of triple negative breast cancer.

Isabella Raccagni, Sara Belloli, Silvia Valtorta, Alessandro Stefano, Luca Presotto, Claudio Pascali, Anna Bogni, Monica Tortoreto, Nadia Zaffaroni, Maria Grazia Daidone and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
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  14. Radiolabelled Aptamers for Theranostic Treatment of Cancer.Pharmaceuticals (Basel, Switzerland) · 2018
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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.

Isabella RaccagniInstitute of Molecular Bioimaging and Physiology (IBFM), CNR, Segrate, Italy.
Sara BelloliInstitute of Molecular Bioimaging and Physiology (IBFM), CNR, Segrate, Italy.
Silvia ValtortaInstitute of Molecular Bioimaging and Physiology (IBFM), CNR, Segrate, Italy.
Alessandro StefanoInstitute of Molecular Bioimaging and Physiology (IBFM), CNR, Segrate, Italy.
Luca PresottoNuclear Medicine Unit, IRCCS San Raffaele Scientific Institute, Milano, Italy.
Claudio PascaliNuclear Medicine Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Anna BogniNuclear Medicine Unit, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Monica TortoretoMolecular Pharmacology Unit, Experimental Oncology and Molecular Medicine Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Nadia ZaffaroniMolecular Pharmacology Unit, Experimental Oncology and Molecular Medicine Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Maria Grazia DaidoneBiomarkers Unit, Experimental Oncology and Molecular Medicine Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.
Giorgio RussoInstitute of Molecular Bioimaging and Physiology (IBFM), CNR, Segrate, Italy.
Emilio BombardieriNuclear Medicine Department, Humanitas Gavazzeni, Bergamo, Italy.
Rosa Maria MorescoInstitute of Molecular Bioimaging and Physiology (IBFM), CNR, Segrate, Italy.ORCID 0000-0002-2771-9387
Fondazione IRCCS Istituto Nazionale dei Tumori · ITVita-Salute San Raffaele University · ITInstitute of Molecular Bioimaging and Physiology · ITHumanitas Gavazzeni · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

rationalePathological response to neo-adjuvant chemotherapy (NAC) represents a commonly used predictor of survival in triple negative breast cancer (TNBC) and the need to identify markers that predict response to NAC is constantly increasing. Aim of this study was to evaluate the potential usefulness of PET imaging with [18F]FDG and [18F]FLT for the discrimination of TNBC responders to Paclitaxel (PTX) therapy compared to the response assessed by an adapted Response Evaluation Criteria In Solid Tumors (RECIST) criteria based on tumor volume (Tumor Volume Response).

methodsNu/nu mice bearing TNBC lesions of different size were evaluated with [18F]FDG and [18F]FLT PET before and after PTX treatment. SUVmax, Metabolic Tumor Volume (MTV) and Total Lesion Glycolysis (TLG) and Proliferation (TLP) were assessed using a graph-based random walk algorithm.

resultsWe found that in our TNBC model the variation of [18F]FDG and [18F]FLT SUVmax similarly defined tumor response to therapy and that SUVmax variation represented the most accurate parameter. Response evaluation using Tumor Volume Response (TVR) showed that the effectiveness of NAC with PTX was completely independent from lesions size at baseline.

conclusionsOur study provided interesting results in terms of sensitivity and specificity of PET in TNBC, revealing the similar performances of [18F]FDG and [18F]FLT in the identification of responders to Paclitaxel.

Indexed as

Positron-Emission TomographyAnimalsAntineoplastic Agents, PhytogenicArea Under CurveCell Line, TumorFemaleFluorodeoxyglucose F18HumansKi-67 AntigenMiceMice, NudeMice, SCIDNeoadjuvant TherapyPaclitaxelRadiopharmaceuticalsROC CurveAntineoplastic Agents, PhytogenicFluorodeoxyglucose F18Ki-67 AntigenPaclitaxelRadiopharmaceuticalsThymidine

Identifiers

PMID29791503
PMCPMC5965848
OpenAlexW2804001592

What OpenQuestion holds

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LicenceCC BY
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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.