Body composition measurements and overall survival in patients with resectable pancreatic adenocarcinoma receiving neoadjuvant chemotherapy: Analysis from SWOG S1505.

Authors

null

Davendra Sohal

University of Cincinnati, Cincinnati, OH

Davendra Sohal , Mai T. Duong , Robert Boutin , Leon Lenchik , Jiyoon Kim , Namita Gandhi , Muhammad Shaalan Beg , Andrea Wang-Gillam , James Lloyd Wade III, Katherine A Guthrie , Elena Gabriela Chiorean , Syed A. Ahmad , Andrew M. Lowy , Howard S. Hochster , Philip Agop Philip , Victor Tsu-Shih Chang

Organizations

University of Cincinnati, Cincinnati, OH, Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, Stanford University, Stanford, CA, Wake Forest University, Winston-Salem, NC, Cleveland Clinic, Cleveland, OH, University of Texas Southwestern Medical Center, Dallas, TX, Washington University School of Medicine in St. Louis, St. Louis, MO, Heartland Cancer Research NCORP, Decatur, IL, Fred Hutchinson Cancer Research Center, and SWOG Statistics and Data Management Center, Seattle, WA, University of Washington, Fred Hutchinson Cancer Research Center, Seattle, WA, University of Cincinnati Medical Center, Cincinnati, OH, UCSD Moores Cancer Center, La Jolla, CA, Rutgers Cancer Institute, New Brunswick, NJ, Karmanos Cancer Institute, Detroit, MI, Section of Hematology/Oncology, Veterans Administration New Jersey Health Care System, East Orange, NJ

Research Funding

U.S. National Institutes of Health
U.S. National Institutes of Health

Background: Sarcopenia and sarcopenic obesity have been associated with overall survival (OS) in patients (pts) with borderline resectable and advanced pancreatic ductal adenocarcinoma (PDA), but little is known about the effect of body composition on OS in pts with resectable PDA. We examined the relationship between skeletal muscle and adipose tissue measurements on baseline computed tomography (CT) and OS of pts with resectable PDA in a secondary analysis of SWOG S1505 (NCT02562716). Methods: SWOG S1505 enrolled pts with resectable PDA who were randomized to receive neoadjuvant FOLFIRINOX or gemcitabine-nab paclitaxel, followed by surgical resection. Baseline axial CT images at the L3 level were analyzed with externally validated software and measurements were recorded for skeletal muscle area (SMA), density (SMD) and index (SMI); visceral adipose tissue area (VATA) and density (VATD); and subcutaneous adipose tissue area (SATA) and density (SATD). Sarcopenia was defined as SMI < 52 cm2/m2 for men and < 39 cm2/m2 for women; sarcopenic obesity was defined as sarcopenia and a body mass index (BMI) >30 kg/m2. The relationships between CT metrics and OS were analyzed using Cox regression models, with 95% CI. Statistical significance was defined as p < 0.05. Results: Of 98 pts with available baseline abdominal CT, 8 were excluded for scan quality, resulting in 90 evaluable cases: 51 men (57%), 39 women (43%); mean age, 63.2 years, SD 8.5; mean BMI, 29.3 kg/m2, SD 6.4; 80 (89%) White, 6 (7%) Black, and 4 (4%) unknown. Sarcopenia was present in 32 (36%) and sarcopenic obesity in 10 (11%) patients. Univariable analyses for the variables of interest indicated VATA (HR 1.24; 0.97-1.60; p = 0.09) and SMD (HR 0.75; 0.57-0.98; p = 0.04) were associated with OS. Analyses adjusted for sex, race, age, BMI, performance score, contrast use, sarcopenia, and sarcopenic obesity showed VATA was associated with OS (HR 1.58; 1.0-2.51; p = 0.05). No significant difference in median OS was observed between pts with vs. without sarcopenia (OS 23.6 [19.3-NA] vs. 27.9 months [18.6-NA], respectively). Pts with vs. without sarcopenic obesity had lower median OS: 18.6 (14.7-NA) vs. 25.1 (10.5-46.0) months, respectively, but this difference was not statistically significant (HR 1.90, 95%CI 0.81-4.47, p = 0.14). Conclusions: This is one of the first studies to systematically evaluate body composition parameters in a prospective trial of patients with resectable PDA who received neoadjuvant chemotherapy. We found that visceral fat (VATA) is a prognostic marker in this population, but that sarcopenia may not be predictive in early PDA. Further studies to define the impact of longitudinal changes in body composition on individual outcomes may provide greater precision in predicting OS for subsets of pts with pancreatic cancer. Clinical trial information: NCT02562716

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Abstract Details

Meeting

2021 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Gastrointestinal Cancer—Gastroesophageal, Pancreatic, and Hepatobiliary

Track

Gastrointestinal Cancer—Gastroesophageal, Pancreatic, and Hepatobiliary

Sub Track

Pancreatic Cancer

Clinical Trial Registration Number

NCT02562716

Citation

J Clin Oncol 39, 2021 (suppl 15; abstr 4131)

DOI

10.1200/JCO.2021.39.15_suppl.4131

Abstract #

4131

Poster Bd #

Online Only

Abstract Disclosures