Evidence map›Paper›PMID 30654776›Full record

ArticleBMC medical informatics and decision making2019

Modelling cancer outcomes of bone metastatic patients: combining survival data with N-Telopeptide of type I collagen (NTX) dynamics through joint models.

Hugo Loureiro, Eunice Carrasquinha, Irina Alho, Arlindo R Ferreira, Luís Costa, Alexandra M Carvalho, Susana Vinga

Open access · goldAbstract read
In one paragraph

Article in BMC medical informatics and decision making, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
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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

7 authors at 3 institutions in 1 country.

Hugo LoureiroINESC-ID, Instituto Superior Técnico, Universidade de Lisboa, Rua Alves Redol, 9, Lisboa, 1000-029, Portugal.ORCID 0000-0002-1954-5487
Eunice CarrasquinhaINESC-ID, Instituto Superior Técnico, Universidade de Lisboa, Rua Alves Redol, 9, Lisboa, 1000-029, Portugal.
Irina AlhoInstituto de Medicina Molecular, Av. Professor Egas Moniz, Lisboa, 1649-028, Portugal.
Arlindo R FerreiraInstituto de Medicina Molecular, Av. Professor Egas Moniz, Lisboa, 1649-028, Portugal.
Luís CostaInstituto de Medicina Molecular, Av. Professor Egas Moniz, Lisboa, 1649-028, Portugal.
Alexandra M CarvalhoInstituto de Telecomunicações, Av. Rovisco Pais 1, Lisboa, 1049-001, Portugal.
Susana VingaINESC-ID, Instituto Superior Técnico, Universidade de Lisboa, Rua Alves Redol, 9, Lisboa, 1000-029, Portugal. susanavinga@tecnico.ulisboa.pt.
Hospital de Egas Moniz · PTInstituto de Engenharia de Sistemas e Computadores Investigação e Desenvolvimento · PTUniversity of Lisbon · PT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundJoint models (JM) have emerged as a promising statistical framework to concurrently analyse survival data and multiple longitudinal responses. This is particularly relevant in clinical studies where the goal is to estimate the association between time-to-event data and the biomarkers evolution. In the context of oncological data, JM can indeed provide interesting prognostic markers for the event under study and thus support clinical decisions and treatment choices. However, several problems arise when dealing with this type of data, such as the high-dimensionality of the covariates space, the lack of knowledge about the function structure of the time series and the presence of missing data, facts that may hamper the accurate estimation of the JM.

methodsWe propose to apply JM for the analysis of bone metastatic patients and infer the association of their survival with several covariates, in particular the N-Telopeptide of Type I Collagen (NTX) dynamics. This biomarker has been identified as a relevant prognostic factor in patients with metastatic cancer, but only using static information in some specific time points.

resultsWe extended this analysis using the full NTX time series for a larger cohort of patients with bone metastasis, and compared the results obtained by the JM and the extended Cox regression model. Imputation based on fuzzy clustering was used to deal with missing values and several functions for NTX evolution were compared, such as rational, exponential and cubic splines.

conclusionsThe JM obtained confirm the association between NTX values and patients' response, attesting the importance of this time series, and additionally provide a deep understanding of the key survival covariates.

Indexed as

Models, TheoreticalSurvival AnalysisBiomarkers, TumorBone NeoplasmsCollagen Type IHumansLongitudinal StudiesPeptidesBiomarkers, TumorCollagen Type Icollagen type I trimeric cross-linked peptidePeptidesBone metastasisCancer studiesFuzzy clusteringJoint modelsLongitudinal analysisSurvival analysis

Identifiers

PMID30654776
PMCPMC6337820
OpenAlexW2913585455

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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.