Evidence map›Paper›PMID 27043244›Full record

ArticleThe British journal of radiology2016

An alternative parameter for early forecasting clinical response in NSCLC patients during radiotherapy: proof of concept study.

Laetitia Padovani, Aurelie Baret, Joseph Ciccolini, David Taieb, Farman Bardia, Laetitia Teissonnier, Xavier Muracciole, Fabrice Barlesi, Dominique Barbolosi

Abstract readCase Reports
In one paragraph

Article in The British journal of radiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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.

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

1 citing paper in PubMed.

  1. 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

9 authors.

Laetitia Padovani1 SMARTc, INSERM, UMR 911 CRO2, Aix Marseille Université, Marseille, France.
Aurelie Baret2 Assistance Publique des Hôpitaux de Marseille, Radiotherapy Department, Marseille, France.
Joseph Ciccolini1 SMARTc, INSERM, UMR 911 CRO2, Aix Marseille Université, Marseille, France.
David Taieb3 Aix Marseille Université; Assistance Publique Hôpitaux de Marseille, Nuclear Medical Department, Marseille, France.
Farman Bardia3 Aix Marseille Université; Assistance Publique Hôpitaux de Marseille, Nuclear Medical Department, Marseille, France.
Laetitia Teissonnier3 Aix Marseille Université; Assistance Publique Hôpitaux de Marseille, Nuclear Medical Department, Marseille, France.
Xavier Muracciole1 SMARTc, INSERM, UMR 911 CRO2, Aix Marseille Université, Marseille, France.
Fabrice Barlesi1 SMARTc, INSERM, UMR 911 CRO2, Aix Marseille Université, Marseille, France.
Dominique Barbolosi1 SMARTc, INSERM, UMR 911 CRO2, Aix Marseille Université, Marseille, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivePositron emission tomography with (18)F fludeoxyglucose integrated with CT ((18)F-FDG PET/CT) is a recommended imaging procedure in the evaluation of non-small-cell lung cancers (NSCLCs). Radiochemotherapy (RCT) is a mainstay for treatment of locally advanced NSCLC, for which overall survival still remains poor. Early evaluation of treatment response may help in decision-making to complete radiotherapy (RT) or to switch to other treatment modalities. The present study aimed to evaluate the performance of new metabolic parameters based on a simplified kinetic analysis on a single time point (SKA-S)-derived mathematical method, as compared with standardized uptake value (SUV) measurement during RT.

methodsFour patients treated with RT or RCT for NSCLC were evaluated using (18)F-FDG PET/CT during RT and after treatment completion. Whole-body (18)F-FDG PET/CT was performed followed by four additional list-mode acquisitions centered over the target lesion. Response was evaluated at four times (i.e. PET1-PET4) by calculating standard SUV values and T80%, the time taken to reach 80% of (18)F-FDG metabolized fraction using a SKA-S-derived mathematical method.

resultsData from SUV and T80% calculations were found to be controversial. T80% was found to be more predictive of clinical outcome.

conclusionAlthough results from this pilot study should be further confirmed in a large prospective study, the data suggest that T80% is a promising metabolic biomarker for assessing early response to RT. ADVANCES IN KNOWLEDGE: In this proof of concept study, we show that T80% defined from a mathematic model taking into account the net influx rate constant and vascular volume could be consider as a promising biomarker as compared with the maximum SUV.

Indexed as

AdultAgedAged, 80 and overAlgorithmsCarcinoma, Non-Small-Cell LungFeasibility StudiesFemaleFluorodeoxyglucose F18HumansImage EnhancementImage Interpretation, Computer-AssistedLung NeoplasmsMaleMiddle AgedPilot ProjectsPositron Emission Tomography Computed TomographyFluorodeoxyglucose F18Radiopharmaceuticals

Identifiers

PMID27043244
PMCPMC5258176

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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.