Prognostic implication of body composition changes in patients with borderline resectable/locally advanced pancreatic adenocarcinoma (PDAC) treated with mFOLFIRINOX.

J Jong Hyuk Lee H Hyehyun Jeong (Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea) Y Yousun Ko (Biomedical Research Center, Asan Institute for Life Sciences, Asan Medical Center, University of Ulsan, Seoul, South Korea) K Kyung Won Kim H Hyunseok Yoon (1Asan Medical Center, University of Ulsan College of Medicine, Department of Oncology, Seoul, Korea) K Kyu-pyo Kim (Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea) C Changhoon Yoo (Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea) T Tae Won Kim (Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea) S Sun Young Kim

Abstract

783 Background: Although cachexia is a known prognostic factor in patients with advanced cancer, individual body composition changes during chemotherapy and their association with survival in PDAC warrant further investigation. We aimed to analyze the prognostic implication of comprehensive body composition, including areas and attenuation of muscle mass, body fat area and its distribution, and body mass index (BMI) during mFOLFIRINOX in patients with PDAC. Methods: Patients with borderline resectable or locally advanced PDAC, who were not able to undergo curative surgery and received first-line mFOLFIRINOX between January 2017 and December 2020 from Asan Medical Center, Seoul, Korea, were included in this retrospective study if they had paired CT scans of the abdomen at baseline and after 12 weeks of mFOLFIRINOX. Body composition was measured using artificial intelligence software (AID-UTM, iAID Inc.) from the CT images, and their association with overall survival (OS) were analyzed. Results: A total of 377 patients were included. Median age was 63 (range, 56–69) and 214 patients (56.8%) were males and 163 patients (43.2%) were females. During the first 12 weeks, significant changes in the body composition occurred as follows (median changes and interquartile range): skeletal muscle area, -5.8% [-11.1%–0.6%]; normal attenuation muscle area/total attenuation muscle area, -2.8% [-8.7%–3.2%]; visceral fat area (VFA), -6.1% [-23.7%–18.6%]; skeletal fat area (SFA), -12.2% [-27.8%–77.1%]; and BMI, -2.2% [-6.8%–1.5%]. Furthermore, changes in the VFA and BMI was associated with tumor response (Kruskal-Wallis test, p = 0.012 for VFA; p = 0.054 for BMI). There was no significant relationship between body composition abnormalities including sarcopenia, myosteatosis, or obesity at baseline and OS. However, patients who experienced the greatest decrease in SFA and BMI after 12 weeks of mFOLFIRINOX had poorer OS (tertile 1 [greatest decrease] vs 3 [smallest decrease]: HR 0.67 [95% CI, 0.52–0.87] for SFA, p = 0.003; 0.68 [95% CI, 0.49–0.83] for BMI, p = 0.001). Conclusions: In patients with borderline resectable/locally advanced PDAC, body composition significantly changes during the first 12 weeks. Decrease in the body fat and BMI from baseline were associated with poorer tumor response and OS.

Article Details

Volume / Issue Vol. 43, Issue 4_suppl
Published February 01, 2025
Pages 783-783
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (9)

J

Jong Hyuk Lee

H

Hyehyun Jeong

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea

Y

Yousun Ko

Biomedical Research Center, Asan Institute for Life Sciences, Asan Medical Center, University of Ulsan, Seoul, South Korea

K

Kyung Won Kim

H

Hyunseok Yoon

1Asan Medical Center, University of Ulsan College of Medicine, Department of Oncology, Seoul, Korea

K

Kyu-pyo Kim

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea

C

Changhoon Yoo

Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea

T

Tae Won Kim

Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Korea

S

Sun Young Kim