Evidence map›Paper›PMID 39289919›Full record

ArticleJournal of cachexia, sarcopenia and muscle2024

Frequency of weight and body composition increases in advanced non-small cell lung cancer patients during first line therapy.

Philip Bonomi, Hita Moudgalya, Sandra L Gomez, Palmi Shah, Sanjib Basu, Marta Batus, Levi B Martinka, Ahmed Abdelkader, Iphigenia Tzameli, Sonia Cobain and 6 more

Abstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

5 citing papers in PubMed.

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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

16 authors.

Philip BonomiDivision of Hematology/Oncology, Rush University Medical Center, Chicago, IL, USA.ORCID 0000-0002-6539-3111
Hita MoudgalyaDepartment of Anatomy and Cell Biology, Rush University Medical Center, Chicago, IL, USA.
Sandra L GomezDepartment of Clinical Nutrition, Rush University Medical Center, Chicago, IL, USA.
Palmi ShahDepartment of Radiology, Rush University Medical Center, Chicago, IL, USA.
Sanjib BasuBiostatistics, School of Public Health, University of Illinois Chicago, Chicago, IL, USA.
Marta BatusDivision of Hematology/Oncology, Rush University Medical Center, Chicago, IL, USA.
Levi B MartinkaDepartment of Anatomy and Cell Biology, Rush University Medical Center, Chicago, IL, USA.
Ahmed AbdelkaderDepartment of Anatomy and Cell Biology, Rush University Medical Center, Chicago, IL, USA.
Iphigenia TzameliInternal Medicine Research Unit, Pfizer Inc., Cambridge, MA, USA.
Sonia CobainGlobal Biometrics and Data Management, Pfizer R&D UK Ltd, Sandwich, UK.
Susie CollinsGlobal Biometrics and Data Management, Pfizer R&D UK Ltd, Sandwich, UK.
Edmund J KeliherEarly Clinical Development, Pfizer Inc., Cambridge, MA, USA.
Danna M BreenInternal Medicine Research Unit, Pfizer Inc., Cambridge, MA, USA.
Roberto A CalleInternal Medicine Research Unit, Pfizer Inc., Cambridge, MA, USA.
Mary Jo FidlerDivision of Hematology/Oncology, Rush University Medical Center, Chicago, IL, USA.
Jeffrey A BorgiaDepartment of Anatomy and Cell Biology, Rush University Medical Center, Chicago, IL, USA.ORCID 0000-0002-1520-7966

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe primary objective of this study was to assess the frequency of body composition increases and their relationships to changes in body weight in two cohorts of real world, treatment-naïve, advanced non-small cell lung cancer (NSCLC) patients. One cohort received the current standard of care (CSOC), which consisted of immunotherapy and newer chemotherapy regimens, and the other cohort was treated with the former standard of care (FSOC), consisting only of older platinum-containing regimens.

methodsCSOC (n = 106) and FSOC (n = 88) cohorts of advanced NSCLC patients were included in this study. Weights were collected at each clinical visit, and body composition analysis from routine chest computed tomography via automated segmentation software assessed at baseline and at 6 and 12 weeks. Standard statistical methods were used to calculate relationships between changes in weight and in body composition.

resultsThe CSOC cohort contained 106 stage IV NSCLC patients treated between 16/12/2014 and 22/10/2020 while the FSOC cohort contained 88 stage III/IV NSCLC patients treated between 16/6/2006 and 18/11/2014. While each cohort exhibited decreases in median weight, body mass index (BMI), mean skeletal muscle index (SMI) and subcutaneous adipose tissue index (SATI) at the 6 and 12 week time points, a subset of patients experienced increases in these parameters. Using a threshold of ≥2.5% increase for weight, BMI, SMI, and SATI at the 12 week time point, both cohorts showed similar (20.5% and 27.3%) increases in these parameters. With a cut point of ≥5% increase at 12 weeks follow-up, 8.0% to 25.0% of the patients gained ≥5% in weight, BMI, SMI and SATI. Comparing these results in each cohort showed no significant differences. Pearson coefficients for weight change related to changes in SMI and SATI at 6 and 12 weeks ranged from 0.31 to 0.58 with all P values <0.02. Pearson coefficients for weight change at 12 weeks related to changes in VATI and IMATI ranged from 0.26 to 0.47 with all P values <0.05. Comparison of Pearson coefficients for each cohort showed no significant differences.

conclusionsAlthough decreases in median weight, BMI, SMI and SATI were observed in both cohorts, similar percentage of patients in each cohort experienced increases in these parameters. These findings, plus the positive correlations between longitudinal measurements of weight, muscle mass and adipose tissue, indicate that weight gain in these patients involves increases in both muscle mass and adipose tissue. Upon validation, these findings could have implications for clinical trial design and for translational research in cancer cachexia.

Indexed as

Body CompositionCarcinoma, Non-Small-Cell LungLung NeoplasmsAgedBody Mass IndexBody WeightFemaleHumansMaleMiddle AgedNeoplasm Stagingbody compositionbody weightcancer cachexiachemotherapyimmunotherapynon‐small cell lung cancer

Identifiers

PMID39289919
PMCPMC11634467

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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.