The Role of Computed Tomography-Determined Total Tumor Volume at Baseline in Predicting Outcomes of Patients with Locally Advanced Unresectable or Metastatic Pancreatic Ductal Adenocarcinoma

<b>Background:</b> Total tumor volume (TTV), derived from imaging data, has emerged as a potential prognostic biomarker in various cancers. This study aimed to evaluate the impact of TTV on outcomes in advanced pancreatic ductal adenocarcinoma (PDAC) and to validate a survival prediction model combining TTV with baseline clinico-biological markers. <b>Materials and Methods:</b> We conducted a retrospective analysis of 150 patients with locally advanced or metastatic PDAC treated with first-line FOLFIRINOX from 2010 to 2021. TTV was calculated by manually segmenting all visible lesions on baseline CT scans. Progression-free survival (PFS) and overall survival (OS) were the primary endpoints. A cut-off value for TTV predicting 6-month PFS was determined in 140 patients using AUC and Youden's Index and then applied to OS analysis. A multivariate Cox regression model incorporating TTV, CA 19-9, and neutrophil-to-lymphocyte ratio (NLR) was developed in 94 patients to establish a survival risk score. <b>Results:</b> 12,028 lesions were annotated. OS was slightly but significantly different between TTV above and below the median value of 69.60 cm<sup>3</sup> (12.4 vs. 13.5 months, <i>p</i> = 0.0269). A cut-off of 400 cm<sup>3</sup> distinguished two groups: patients with TTV > 400 cm<sup>3</sup> had significantly shorter OS (9.4 months) compared to those with TTV ≤ 400 cm<sup>3</sup> (13.0 months, <i>p</i> = 0.0056). A similar trend was observed for PFS, though not statistically significant (7.4 months for TTV > 400 cm<sup>3</sup> vs. 8.2 months for TTV ≤ 400 cm<sup>3</sup>, <i>p</i> = 0.0735). The combined model achieved a mean c-index of 0.62 for PFS and 0.64 for OS. Based on the risk score, high-risk patients had significantly worse median PFS (5.5 vs. 9.2 months, <i>p</i> = 0.0008) and median OS (7.2 vs. 13.5 months, <i>p</i> < 0.0001). <b>Conclusions:</b> TTV is a valuable prognostic marker in advanced PDAC. A model integrating TTV with biological markers enhances survival prediction and supports risk stratification in clinical practice.

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Journal
Cancers
Published
2025-12-20
DOI
https://doi.org/10.3390/cancers18010020
Primary Topic
Pancreatic and Hepatic Oncology Research
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article

The Role of Computed Tomography-Determined Total Tumor Volume at Baseline in Predicting Outcomes of Patients with Locally Advanced Unresectable or Metastatic Pancreatic Ductal Adenocarcinoma

Littisha Lawrance, Jules Dupont, M. Valery, N. Lassau et al.
Cancers
Pancreatic and Hepatic Oncology Research
article

The Role of Computed Tomography-Determined Total Tumor Volume at Baseline in Predicting Outcomes of Patients with Locally Advanced Unresectable or Metastatic Pancreatic Ductal Adenocarcinoma

Littisha Lawrance, Jules Dupont, M. Valery, N. Lassau, Samy Ammari, Nohad Masri, Michèle Kind, T. Pudlarz, Alice Boilève, Antoine Hollebecque, Géraldine M. Camilleri, Michel Ducreux, Caroline Su, G. Jardali, Cristina Smolenschi, Fiona Frau, Anamaria Bianca Mihele, Elissar Moujaes, Lama Dawi, Valérie Boige
article en

Abstract

<b>Background:</b> Total tumor volume (TTV), derived from imaging data, has emerged as a potential prognostic biomarker in various cancers. This study aimed to evaluate the impact of TTV on outcomes in advanced pancreatic ductal adenocarcinoma (PDAC) and to validate a survival prediction model combining TTV with baseline clinico-biological markers. <b>Materials and Methods:</b> We conducted a retrospective analysis of 150 patients with locally advanced or metastatic PDAC treated with first-line FOLFIRINOX from 2010 to 2021. TTV was calculated by manually segmenting all visible lesions on baseline CT scans. Progression-free survival (PFS) and overall survival (OS) were the primary endpoints. A cut-off value for TTV predicting 6-month PFS was determined in 140 patients using AUC and Youden's Index and then applied to OS analysis. A multivariate Cox regression model incorporating TTV, CA 19-9, and neutrophil-to-lymphocyte ratio (NLR) was developed in 94 patients to establish a survival risk score. <b>Results:</b> 12,028 lesions were annotated. OS was slightly but significantly different between TTV above and below the median value of 69.60 cm<sup>3</sup> (12.4 vs. 13.5 months, <i>p</i> = 0.0269). A cut-off of 400 cm<sup>3</sup> distinguished two groups: patients with TTV > 400 cm<sup>3</sup> had significantly shorter OS (9.4 months) compared to those with TTV ≤ 400 cm<sup>3</sup> (13.0 months, <i>p</i> = 0.0056). A similar trend was observed for PFS, though not statistically significant (7.4 months for TTV > 400 cm<sup>3</sup> vs. 8.2 months for TTV ≤ 400 cm<sup>3</sup>, <i>p</i> = 0.0735). The combined model achieved a mean c-index of 0.62 for PFS and 0.64 for OS. Based on the risk score, high-risk patients had significantly worse median PFS (5.5 vs. 9.2 months, <i>p</i> = 0.0008) and median OS (7.2 vs. 13.5 months, <i>p</i> < 0.0001). <b>Conclusions:</b> TTV is a valuable prognostic marker in advanced PDAC. A model integrating TTV with biological markers enhances survival prediction and supports risk stratification in clinical practice.

CancersVol. 18(1)
Guerbet (France) (FR), Centre National de la Recherche Scientifique (FR), Inserm (FR), Commissariat à l'Énergie Atomique et aux Énergies Alternatives (FR), Université Paris-Saclay (FR), Institut Gustave Roussy (FR), CEA Paris-Saclay (FR), Institut Bergonié (FR)
Good health and well-being
Openalex Percentile: Top 32%
Pancreatic and Hepatic Oncology Research
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