Evidence map›Paper›PMID 37738580›Full record

ReviewJNCI cancer spectrum2023

Overview of approaches to estimate real-world disease progression in lung cancer.

Rossybelle Amorrortu, Melany Garcia, Yayi Zhao, Issam El Naqa, Yoganand Balagurunathan, Dung-Tsa Chen, Thanh Thieu, Matthew B Schabath, Dana E Rollison

Open access · goldAbstract readReview
In one paragraph

Review in JNCI cancer spectrum, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 8 citations in OpenAlex.

  1. Observational
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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 at 1 institution in 1 country.

Rossybelle AmorrortuDepartment of Cancer Epidemiology, Moffitt Cancer Center, Tampa, FL, USA.ORCID 0000-0001-6851-0179
Melany GarciaDepartment of Cancer Epidemiology, Moffitt Cancer Center, Tampa, FL, USA.ORCID 0000-0001-7756-0514
Yayi ZhaoDepartment of Cancer Epidemiology, Moffitt Cancer Center, Tampa, FL, USA.ORCID 0000-0003-0806-823X
Issam El NaqaDepartment of Machine Learning, Moffitt Cancer Center, Tampa, FL, USA.ORCID 0000-0001-6023-1132
Yoganand BalagurunathanDepartment of Machine Learning, Moffitt Cancer Center, Tampa, FL, USA.ORCID 0000-0002-5598-4727
Dung-Tsa ChenDepartment of Biostatistics and Bionformatics, Moffitt Cancer Center, Tampa, FL, USA.ORCID 0000-0001-5026-415X
Thanh ThieuDepartment of Machine Learning, Moffitt Cancer Center, Tampa, FL, USA.ORCID 0000-0002-4926-9292
Matthew B SchabathDepartment of Cancer Epidemiology, Moffitt Cancer Center, Tampa, FL, USA.ORCID 0000-0003-3241-3216
Dana E RollisonDepartment of Cancer Epidemiology, Moffitt Cancer Center, Tampa, FL, USA.ORCID 0000-0002-3171-8045
Moffitt Cancer Center · US

Funding

TRANSLATIONAL RESEARCHP30CA076292 · NCI · UNIVERSITY OF SOUTH FLORIDA · PI Christine O'Connell · 1998 to 2026
$93.5M
NCI NIH HHS P30 CA076292
6 · The paper itself

Abstract

backgroundRandomized clinical trials of novel treatments for solid tumors normally measure disease progression using the Response Evaluation Criteria in Solid Tumors. However, novel, scalable approaches to estimate disease progression using real-world data are needed to advance cancer outcomes research. The purpose of this narrative review is to summarize examples from the existing literature on approaches to estimate real-world disease progression and their relative strengths and limitations, using lung cancer as a case study.

methodsA narrative literature review was conducted in PubMed to identify articles that used approaches to estimate real-world disease progression in lung cancer patients. Data abstracted included data source, approach used to estimate real-world progression, and comparison to a selected gold standard (if applicable).

resultsA total of 40 articles were identified from 2008 to 2022. Five approaches to estimate real-world disease progression were identified including manual abstraction of medical records, natural language processing of clinical notes and/or radiology reports, treatment-based algorithms, changes in tumor volume, and delta radiomics-based approaches. The accuracy of these progression approaches were assessed using different methods, including correlations between real-world endpoints and overall survival for manual abstraction (Spearman rank ρ = 0.61-0.84) and area under the curve for natural language processing approaches (area under the curve = 0.86-0.96).

conclusionsReal-world disease progression has been measured in several observational studies of lung cancer. However, comparing the accuracy of methods across studies is challenging, in part, because of the lack of a gold standard and the different methods used to evaluate accuracy. Concerted efforts are needed to define a gold standard and quality metrics for real-world data.

Indexed as

Lung NeoplasmsDisease ProgressionHumansOutcome Assessment, Health Care

Identifiers

PMID37738580
PMCPMC10637832
OpenAlexW4386949580

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.