Evidence map›Paper›PMID 38201657›Full record

ArticleCancers2024

Cachexia and Sarcopenia in Oligometastatic Non-Small Cell Lung Cancer: Making a Potential Curable Disease Incurable?

Valentina Bartolomeo, Mandy Jongbloed, Wouter R P H van de Worp, Ramon Langen, Juliette Degens, Lizza E L Hendriks, Dirk K M de Ruysscher

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Article
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 2 countries.

Valentina BartolomeoRadiation Oncology, Fondazione IRCCS Policlinico San Matteo, 27100 Pavia, Italy.ORCID 0009-0007-1493-7282
Mandy JongbloedDepartment of Pulmonary Diseases, GROW-School for Oncology and Reproduction, Maastricht University Medical Center, 6229 ER Maastricht, The Netherlands.ORCID 0000-0003-4686-9169
Wouter R P H van de WorpDepartment of Respiratory Medicine, NUTRIM Research Institute of Nutrition and Translational Research in Metabolism, Maastricht University Medical Center, 6229 ER Maastricht, The Netherlands.
Ramon LangenDepartment of Respiratory Medicine, NUTRIM Research Institute of Nutrition and Translational Research in Metabolism, Maastricht University Medical Center, 6229 ER Maastricht, The Netherlands.
Juliette DegensDepartment of Pulmonology, Zuyderland Medical Center, 6419 PC Heerlen, The Netherlands.
Lizza E L HendriksDepartment of Pulmonary Diseases, GROW-School for Oncology and Reproduction, Maastricht University Medical Center, 6229 ER Maastricht, The Netherlands.ORCID 0000-0002-3521-2535
Dirk K M de RuysscherDepartment of Radiation Oncology (Maastro Clinic), GROW-School for Oncology and Reproduction, Maastricht University Medical Center, 6229 ER Maastricht, The Netherlands.
Maastricht University · NLUniversity of Pavia · ITZuyderland Medisch Centrum · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Among patients with advanced NSCLC, there is a group of patients with synchronous oligometastatic disease (sOMD), defined as a limited number of metastases detected at the time of diagnosis. As cachexia and sarcopenia are linked to poor survival, incorporating this information could assist clinicians in determining whether a radical treatment should be administered. In a retrospective multicenter study, including all patients with adequately staged (FDG-PET, brain imaging) sOMD according to the EORTC definition, we aimed to assess the relationship between cachexia and/or sarcopenia and survival. Of the 439 patients that were identified between 2015 and 2021, 234 met the criteria for inclusion and were included. The median age of the cohort was 67, 52.6% were male, and the median number of metastasis was 1. Forty-six (19.7%) patients had cachexia, thirty-four (14.5%) had sarcopenia and twenty-one (9.0%) had both. With a median follow-up of 49.7 months, median PFS and OS were 8.6 and 17.3 months, respectively. Moreover, a trend toward longer PFS was found in patients without cachexia and sarcopenia compared to those with cachexia and/or sarcopenia. In multivariate analysis, cachexia and sarcopenia were not associated with an inferior survival, irrespective of receiving radical treatment. High CRP was associated with inferior survival and could be a prognostic factor, helping the decision of clinicians in selecting patients who may benefit from the addition of LRT. However, despite the homogeneous definition of oligometastatic disease and the adequate staging, our subgroups were small. Therefore, further studies are needed to better understand our hypothesis and generating findings.

Indexed as

cachexiaintention to treatNSCLCoverall survivalprogression-free survivalpsoas muscle indexsarcopeniasynchronous oligometastatic diseasetoxicity

Identifiers

PMID38201657
PMCPMC10777972
OpenAlexW4390582380

What Socratic 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 Socratic graph.