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Body composition and lung cancer-associated cachexia in TRACERx.

Authors :
Al-Sawaf O
Weiss J
Skrzypski M
Lam JM
Karasaki T
Zambrana F
Kidd AC
Frankell AM
Watkins TBK
Martínez-Ruiz C
Puttick C
Black JRM
Huebner A
Bakir MA
Sokač M
Collins S
Veeriah S
Magno N
Naceur-Lombardelli C
Prymas P
Toncheva A
Ward S
Jayanth N
Salgado R
Bridge CP
Christiani DC
Mak RH
Bay C
Rosenthal M
Sattar N
Welsh P
Liu Y
Perrimon N
Popuri K
Beg MF
McGranahan N
Hackshaw A
Breen DM
O'Rahilly S
Birkbak NJ
Aerts HJWL
Jamal-Hanjani M
Swanton C
Source :
Nature medicine [Nat Med] 2023 Apr; Vol. 29 (4), pp. 846-858. Date of Electronic Publication: 2023 Apr 12.
Publication Year :
2023

Abstract

Cancer-associated cachexia (CAC) is a major contributor to morbidity and mortality in individuals with non-small cell lung cancer. Key features of CAC include alterations in body composition and body weight. Here, we explore the association between body composition and body weight with survival and delineate potential biological processes and mediators that contribute to the development of CAC. Computed tomography-based body composition analysis of 651 individuals in the TRACERx (TRAcking non-small cell lung Cancer Evolution through therapy (Rx)) study suggested that individuals in the bottom 20th percentile of the distribution of skeletal muscle or adipose tissue area at the time of lung cancer diagnosis, had significantly shorter lung cancer-specific survival and overall survival. This finding was validated in 420 individuals in the independent Boston Lung Cancer Study. Individuals classified as having developed CAC according to one or more features at relapse encompassing loss of adipose or muscle tissue, or body mass index-adjusted weight loss were found to have distinct tumor genomic and transcriptomic profiles compared with individuals who did not develop such features. Primary non-small cell lung cancers from individuals who developed CAC were characterized by enrichment of inflammatory signaling and epithelial-mesenchymal transitional pathways, and differentially expressed genes upregulated in these tumors included cancer-testis antigen MAGEA6 and matrix metalloproteinases, such as ADAMTS3. In an exploratory proteomic analysis of circulating putative mediators of cachexia performed in a subset of 110 individuals from TRACERx, a significant association between circulating GDF15 and loss of body weight, skeletal muscle and adipose tissue was identified at relapse, supporting the potential therapeutic relevance of targeting GDF15 in the management of CAC.<br /> (© 2023. The Author(s) under exclusive license to Springer Nature America, Inc.)

Details

Language :
English
ISSN :
1546-170X
Volume :
29
Issue :
4
Database :
MEDLINE
Journal :
Nature medicine
Publication Type :
Academic Journal
Accession number :
37045997
Full Text :
https://doi.org/10.1038/s41591-023-02232-8