Evidence map›Paper›PMID 35717429›Full record

ArticleLa Radiologia medica2022

CT-based radiomics for prediction of therapeutic response to Everolimus in metastatic neuroendocrine tumors.

Damiano Caruso, Michela Polici, Maria Rinzivillo, Marta Zerunian, Ilaria Nacci, Matteo Marasco, Ludovica Magi, Mariarita Tarallo, Simona Gargiulo, Elsa Iannicelli and 3 more

Open access · hybridAbstract read
In one paragraph

Article in La Radiologia medica, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 3 pooled it
7.6field-weighted citation impact, top 2% 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

43 citing papers in PubMed, 3 syntheses or guidelines pooled it, 50 citations in OpenAlex.

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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 3 institutions in 1 country.

Damiano CarusoDepartment of Medical Surgical Sciences and Translational Medicine, "Sapienza"-University of Rome, Sant'Andrea University Hospital, AOU Sant'Andrea, Via di Grottarossa, 1035-1039, 00189, Rome, Italy.
Michela PoliciDepartment of Medical Surgical Sciences and Translational Medicine, "Sapienza"-University of Rome, Sant'Andrea University Hospital, AOU Sant'Andrea, Via di Grottarossa, 1035-1039, 00189, Rome, Italy.
Maria RinzivilloDigestive Disease Unit, Sant'Andrea University Hospital, AOU Sant'Andrea, 00189, Rome, Italy.
Marta ZerunianDepartment of Medical Surgical Sciences and Translational Medicine, "Sapienza"-University of Rome, Sant'Andrea University Hospital, AOU Sant'Andrea, Via di Grottarossa, 1035-1039, 00189, Rome, Italy.
Ilaria NacciDepartment of Medical Surgical Sciences and Translational Medicine, "Sapienza"-University of Rome, Sant'Andrea University Hospital, AOU Sant'Andrea, Via di Grottarossa, 1035-1039, 00189, Rome, Italy.
Matteo MarascoDepartment of Medical Surgical Sciences and Translational Medicine, "Sapienza"-University of Rome, Sant'Andrea University Hospital, AOU Sant'Andrea, Via di Grottarossa, 1035-1039, 00189, Rome, Italy.
Ludovica MagiDepartment of Medical Surgical Sciences and Translational Medicine, "Sapienza"-University of Rome, Sant'Andrea University Hospital, AOU Sant'Andrea, Via di Grottarossa, 1035-1039, 00189, Rome, Italy.
Mariarita TaralloDepartment of Surgery "Pietro Valdoni", Sapienza University of Rome, 00161, Rome, Italy.
Simona GargiuloDepartment of Medical Surgical Sciences and Translational Medicine, "Sapienza"-University of Rome, Sant'Andrea University Hospital, AOU Sant'Andrea, Via di Grottarossa, 1035-1039, 00189, Rome, Italy.
Elsa IannicelliDepartment of Medical Surgical Sciences and Translational Medicine, "Sapienza"-University of Rome, Sant'Andrea University Hospital, AOU Sant'Andrea, Via di Grottarossa, 1035-1039, 00189, Rome, Italy.
Bruno AnnibaleDepartment of Medical Surgical Sciences and Translational Medicine, "Sapienza"-University of Rome, Sant'Andrea University Hospital, AOU Sant'Andrea, Via di Grottarossa, 1035-1039, 00189, Rome, Italy.
Andrea LaghiDepartment of Medical Surgical Sciences and Translational Medicine, "Sapienza"-University of Rome, Sant'Andrea University Hospital, AOU Sant'Andrea, Via di Grottarossa, 1035-1039, 00189, Rome, Italy. andrea.laghi@uniroma1.it.ORCID http://orcid.org/0000-0002-3091-7819
Francesco PanzutoDigestive Disease Unit, Sant'Andrea University Hospital, AOU Sant'Andrea, 00189, Rome, Italy.
CTO Andrea Alesini · ITAzienda Ospedaliera Sant'Andrea · ITSapienza University of Rome · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo test radiomic approach in patients with metastatic neuroendocrine tumors (NETs) treated with Everolimus, with the aim to predict progression-free survival (PFS) and death. MATERIALS AND

methodsTwenty-five patients with metastatic neuroendocrine tumors, 15/25 pancreatic (60%), 9/25 ileal (36%), 1/25 lung (4%), were retrospectively enrolled between August 2013 and December 2020. All patients underwent contrast-enhanced CT before starting Everolimus, histological diagnosis, tumor grading, PFS, overall survival (OS), death, and clinical data collected. Population was divided into two groups: responders (PFS ≤ 11 months) and non-responders (PFS > 11 months). 3D segmentation was performed on whole liver of naïve CT scans in arterial and venous phases, using a dedicated software (3DSlicer v4.10.2). A total of 107 radiomic features were extracted and compared between two groups (T test or Mann-Whitney), radiomics performance assessed with receiver operating characteristic curve, Kaplan-Meyer curves used for survival analysis, univariate and multivariate logistic regression performed to predict death, and interobserver variability assessed. All significant radiomic comparisons were validated by using a synthetic external cohort. P < 0.05 is considered significant.

results15/25 patients were classified as responders (median PFS 25 months and OS 29 months) and 10/25 as non-responders (median PFS 4.5 months and OS 23 months). Among radiomic parameters, Correlation and Imc1 showed significant differences between two groups (P < 0.05) with the best performance (internal cohort AUC 0.86-0.84, P < 0.0001; external cohort AUC 0.84-0.90; P < 0.0001). Correlation < 0.21 resulted correlated with death at Kaplan-Meyer analysis (P = 0.02). Univariate analysis showed three radiomic features independently correlated with death, and in multivariate analysis radiomic model showed good performance with AUC 0.87, sensitivity 100%, and specificity 66.7%. Three features achieved 0.77 ≤ ICC < 0.83 and one ICC = 0.92.

conclusionsIn patients affected by metastatic NETs eligible for Everolimus treatment, radiomics could be used as imaging biomarker able to predict PFS and death.

Indexed as

Neuroendocrine TumorsEverolimusHumansNeoplasm GradingRetrospective StudiesTomography, X-Ray ComputedEverolimusEverolimusNeuroendocrine tumorsRadiomicsResponse to treatment

Identifiers

PMID35717429
PMCPMC9308597
OpenAlexW4283071205

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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.