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.
Authors
- Littisha Lawrance (ORCID: https://orcid.org/0000-0002-0838-2053)
- Jules Dupont
- M. Valery
- N. Lassau
- Samy Ammari
- Nohad Masri
- Michèle Kind (ORCID: https://orcid.org/0000-0002-5444-2811)
- T. Pudlarz (ORCID: https://orcid.org/0009-0006-6591-2213)
- Alice Boilève (ORCID: https://orcid.org/0000-0003-3708-4909)
- Antoine Hollebecque (ORCID: https://orcid.org/0000-0003-2869-7551)
- Géraldine M. Camilleri
- Michel Ducreux (ORCID: https://orcid.org/0000-0001-8649-7449)
- Caroline Su
- G. Jardali
- Cristina Smolenschi
- Fiona Frau
- Anamaria Bianca Mihele
- Elissar Moujaes
- Lama Dawi
- Valérie Boige
Institutions
- 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)
Publication Details
- Journal
- Cancers
- Published
- 2025-12-20
- DOI
- https://doi.org/10.3390/cancers18010020
- Primary Topic
- Pancreatic and Hepatic Oncology Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00