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Poster Display session

513P - The prognostic value of baseline CT-based body composition, functional status, and systemic inflammation in older adults with metastatic gastrointestinal cancers: A pooled analysis of two prospective Nordic cohorts

Date

27 Jun 2024

Session

Poster Display session

Presenters

Gabor Liposits

Citation

Annals of Oncology (2024) 35 (suppl_1): S205-S215. 10.1016/annonc/annonc1483

Authors

G. Liposits1, K. Aasebø2, A.G. Aker3, L. Lähteenmäki3, D.T. Alavi3, E. Jespersen4, J. Ryg4, S. Möller5, S.B. Winther4, S.L. Krogh4, M. Harneshaug6, H.B. Eggesbø6, H. Sorbye2, P. Pfeiffer4

Author affiliations

  • 1 Regional Hospital West Jutland, Herning/DK
  • 2 Haukeland University Hospital, Bergen/NO
  • 3 University of Oslo, Oslo/NO
  • 4 Odense University Hospital, Odense/DK
  • 5 University of Southern Denmark, Odense/DK
  • 6 Oslo University Hospital, Oslo/NO

Resources

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Abstract 513P

Background

Proper patient selection for palliative systemic treatment is crucial in older adults with metastatic gastrointestinal cancers (mGIC). Information on CT-based body composition, physical function, and systemic inflammation obtained at the time of diagnosis has the potential to support prognostic understanding and shared decision-making ensuring tailored care in a population where frailty is common.

Methods

We investigated the prognostic value of CT-based body composition (abdominal muscle compartment (AMC) and adipose tissue, intramuscular (IMAT), visceral (VAT), and subcutaneous (SAT)), functional status (ECOG PS), and systemic inflammation (neutrophil/lymphocyte ratio (NLR), Glasgow Prognostic Score (GPS), and CRP) regarding overall survival (OS) in older adults with mGIC. We included patients in this analysis from two prospective cohorts enrolling adults ≥70 years with mGIC between 2015-2018. CT-scans, ECOG PS, and blood samples were collected at baseline. Descriptive statistics, survival analysis, and Cox regression were applied; moreover, C-statistics were estimated.

Results

337 patients (206 men) were eligible with a median age of 76 years (IQR: 72-79); 70% had colorectal cancer. While body composition parameters were significantly associated with body-mass index, CRP, GPS, and NLR were correlated with ECOG PS, weight loss, and se-LDH. In multivariable analyses for OS, patients with higher AMC had lower risk for death (HR=0.67, 95% CI: 0.48-0.92, p=0.013); patients presented with impaired functional status (ECOG PS 1-2) or systemic inflammation (CRP>10, GPS>0) had significant higher risk for shorter OS (Table). Table: 513P

Overall survival according to physical function, systemic inflammation, and body composition parameters: Multivariable analyses

Marker n Overall survival
Hazard ratio 95% CI p-value AUC
Body composition (cm2)
AMC
<123.4 149 1.00 0.013 0.65
≥123.4 180 0.67 0.48-0.92
IMAT
<11.88 149 1.00 0.075 0.61
≥11.88 180 1.26 0.98-1.61
VAT
<119.3 147 1.00 0.182 0.61
≥119.3 182 0.83 0.63-1.09
SAT
<155.1 145 1.00 0.364 0.60
≥155.1 184 0.88 0.68-1.15
Physical function
ECOG PS
0 84 1.00 NA 0.70
1 131 1.48 1.11-1.98 0.008
≥2 73 2.85 1.99-4.10 <0.001
Systemic inflammation
CRP (mg/L)
≤ 10 171 1.00 0.001 0.70
> 10 155 1.56 1.19-2.03
NLR
≤ 2.2 179 1.00 0.167 0.69
> 2.2 150 1.20 0.93-1.55
GPS
0 168 1.00 0.004 0.61
1-2 161 1.42 1.11-1.82

Conclusions

Increased muscle mass reduced the risk of early death in older adults with mGIC. ECOG PS and CRP are accessible in clinical practice; this important prognostic information should be included in shared decision-making.

Clinical trial identification

Danish Data Protection Agency: J. nr.16/8147; Danish Regional Ethical Comitte: J. nr. S-20162000-48; EudraCT 2014-000394-39.

Legal entity responsible for the study

Gabor Liposits.

Funding

Academy of Geriatric Cancer Research (AgeCare) and Dansih Cancer Society.

Disclosure

G. Liposits: Financial Interests, Personal, Other, Received funding for working in an expert panel.: Nutricia AS; Financial Interests, Personal, Invited Speaker, Workshop: Servier; Non-Financial Interests, Member: International Society of Geriatric Oncology (SIOG). All other authors have declared no conflicts of interest.

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