Evidence map›Paper›PMID 31855572›Full record

Observational studyRadiology and oncology2019

Scintigraphic load of bone disease evaluated by DASciS software as a survival predictor in metastatic castration-resistant prostate cancer patients candidates to 223RaCl treatment.

Viviana Frantellizzi, Arianna Pani, Maria Dea Ippoliti, Alessio Farcomeni, Irvin Aloise, Mirco Colosi, Claudia Polito, Roberto Pani, Giuseppe De Vincentis

Abstract readObservational Study
In one paragraph

Observational study in Radiology and oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 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.

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

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

  1. Pooled it
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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

9 authors.

Viviana FrantellizziDepartment of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Arianna PaniPostgraduate School of Clinical Pharmacology and Toxicology, University of Milan "Statale", Milan, Italy.
Maria Dea IppolitiDepartment of Radiological Sciences, Oncology and Anatomical Pathology , Sapienza University of Rome, Rome, Italy.
Alessio FarcomeniDepartment of Public Health and Infectious Diseases, "Sapienza" University of Rome, Rome, Italy.
Irvin AloiseDepartment of Computer, Control, and Management Engineering Antonio Ruberti, Sapienza University of Rome, Rome, Italy.
Mirco ColosiDepartment of Computer, Control, and Management Engineering Antonio Ruberti, Sapienza University of Rome, Rome, Italy.
Claudia PolitoSpecialty School in Medical Physics, Department of Medico-Surgical Sciences and Biotechnologies, University La Sapienza, Rome, Italy.
Roberto PaniSpecialty School in Medical Physics, Department of Medico-Surgical Sciences and Biotechnologies, University La Sapienza, Rome, Italy.
Giuseppe De VincentisDepartment of Radiological Sciences, Oncology and Anatomical Pathology , Sapienza University of Rome, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Aim of our study was to assess the load of bone disease at starting and during Ra-223 treatment as an overall survival (OS) predictor in metastatic castration-resistant prostate cancer (mCRPC) patients. Bone scan index (BSI) is defined as the percentage of total amount of bone metastasis on whole-body scintigraphic images. We present a specific software (DASciS) developed by an engineering team of "Sapienza" University of Rome for BSI calculation. Patients and methods 127 mCRPC patients bone scan images were processed with DASciS software, and BSI was tested as OS predictor. Results 546 bone scans were analyzed revealing that the extension of disease is a predictor of OS (0-3% = 28 months of median survival (MoMS]; 3%-5% = 11 MoMS, > 5% = 5 MoMS). BSI has been analyzed as a single parameter for OS, determining an 88% AUC. Moreover, the composition between the BSI and the 3-PS (3-variable prognostic score) determines a remarkable improvement of the AUC (91%), defining these two parameters as the best OS predictors. Conclusions This study suggests that OS is inversely correlated with the load of bone disease in mCRPC Ra-223-treated subjects. DASciS software appears a promising tool in identifying mCRPC patients that more likely take advantage from Ra-223 treatment. BSI is proposed as a predictive variable for OS and included to a multidimensional clinical evaluation permits to approach the patients' enrollment in a rational way, allowing to enhance the treatment effectiveness together with cost optimization.

Indexed as

SoftwareAgedAged, 80 and overBone NeoplasmsHumansImage Processing, Computer-AssistedMaleMiddle AgedProstatic Neoplasms, Castration-ResistantRadiumRetrospective StudiesSurvival AnalysisRadiumRadium-223bone diseasebone scan indexDASciS softwaremCRPCoverall survivalradium223 dichloride

Identifiers

PMID31855572
PMCPMC7087429

What OpenQuestion holds

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Registered trials

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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.