Evidence map›Paper›PMID 38200511›Full record

ArticleJournal of translational medicine2024

Multi-institutional prognostic modeling of survival outcomes in NSCLC patients treated with first-line immunotherapy using radiomics.

Sevinj Yolchuyeva, Leyla Ebrahimpour, Marion Tonneau, Fabien Lamaze, Michele Orain, François Coulombe, Julie Malo, Wiam Belkaid, Bertrand Routy, Philippe Joubert and 1 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Article
  7. [Advancements in Radiomics for Immunotherapy of Non-small Cell Lung Cancer].Zhongguo fei ai za zhi = Chinese journal of lung cancer · 2024
    Review
  8. Review
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

11 authors.

Sevinj YolchuyevaDepartment of Mathematics and Computer Science, Université du Québec à Trois Rivières, Trois-Rivières, Canada.
Leyla EbrahimpourQuebec Heart & Lung Institute Research Center, Québec , Canada.
Marion TonneauCentre de Recherche du Centre Hospitalier Universitaire de Montréal, Montreal, Canada.
Fabien LamazeQuebec Heart & Lung Institute Research Center, Québec , Canada.
Michele OrainQuebec Heart & Lung Institute Research Center, Québec , Canada.
François CoulombeQuebec Heart & Lung Institute Research Center, Québec , Canada.
Julie MaloCentre de Recherche du Centre Hospitalier Universitaire de Montréal, Montreal, Canada.
Wiam BelkaidCentre de Recherche du Centre Hospitalier Universitaire de Montréal, Montreal, Canada.
Bertrand RoutyCentre de Recherche du Centre Hospitalier Universitaire de Montréal, Montreal, Canada.
Philippe JoubertQuebec Heart & Lung Institute Research Center, Québec , Canada.
Venkata Sk ManemDepartment of Mathematics and Computer Science, Université du Québec à Trois Rivières, Trois-Rivières, Canada. venkata.manem@crchudequebec.ulaval.ca.

Funding

Fonds de Recherche du Québec - Santé Fonds de Recherche du Québec - SantéPulmonary Association of Quebec Pulmonary Association of QuebecQuebec Heart & Lung Institute Research Center foundation grant Quebec Heart & Lung Institute Research Center foundation grant
6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs) have emerged as one of the most promising first-line therapeutics in the management of non-small cell lung cancer (NSCLC). However, only a subset of these patients responds to ICIs, highlighting the clinical need to develop better predictive and prognostic biomarkers. This study will leverage pre-treatment imaging profiles to develop survival risk models for NSCLC patients treated with first-line immunotherapy.

methodsAdvanced NSCLC patients (n = 149) were retrospectively identified from two institutions who were treated with first-line ICIs. Radiomics features extracted from pretreatment imaging scans were used to build the predictive models for progression-free survival (PFS) and overall survival (OS). A compendium of five feature selection methods and seven machine learning approaches were utilized to build the survival risk models. The concordance index (C-index) was used to evaluate model performance.

resultsFrom our results, we found several combinations of machine learning algorithms and feature selection methods to achieve similar performance. K-nearest neighbourhood (KNN) with ReliefF (RL) feature selection was the best-performing model to predict PFS (C-index = 0.61 and 0.604 in discovery and validation cohorts), while XGBoost with Mutual Information (MI) feature selection was the best-performing model for OS (C-index = 0.7 and 0.655 in discovery and validation cohorts).

conclusionThe results of this study highlight the importance of implementing an appropriate feature selection method coupled with a machine learning strategy to develop robust survival models. With further validation of these models on external cohorts when available, this can have the potential to improve clinical decisions by systematically analyzing routine medical images.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsHumansImmunotherapyPrognosisRadiomicsRetrospective Studies

Identifiers

PMID38200511
PMCPMC10777540

What OpenQuestion holds

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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.