ALTOPANC: Local ablative therapies in oligometastatic pancreatic adenocarcinoma—A bi-national French-Belgian retrospective study.

P Pauline Parent V Victoria Pacquement (Department of Medical Oncologie, CHU Lille, Lille, France) A Alice Boileve (Gustave Roussy, Villejuif, France) J Julie Henriques (Methodology and Quality of Life in Oncology Unit, Centre Hospitalier Universitaire de Besançon, Besançon, France) J Julie Navez (Hopital Erasme, Hôpital Universitaire de Bruxelles, Bruxelles, Belgium) A Alexandre Taillez (Department of Radiotherapy, Oscar Lambret Center, Lille, France) S Simon Pernot (Department of Medical Oncology, Institute Bergonié Cancer Center, Bordeaux, Nouvelle Aquitaine, France) L Louis de Mestier J Jean-Baptiste Bachet P Pascal Artru N Nicolas Bertrand (Department of Medical Oncology, Eugène Marquis Cancer Centre, Rennes, France) R Rami Rhaiem (CHU de Reims, Reims, France) J Jean-Frédéric Blanc E Emily Linda Alouani (Memorial Sloan Kettering Cancer Center, New York, NY) J Juliette Logeart (Curie Institute, Versaille-Saint Quentin University, Saint-Cloud, Saint-Cloud, France) T Thierry Lecomte S Sara El Kurdi (Lille University Hospital, Lille, France) P Pascal Hammel S Stephanie Truant (Lille University Hospital, Lille, France) A Anthony Turpin

Abstract

728 Background: Oligometastatic disease (OMD) in pancreatic ductal adenocarcinoma (PDAC) is an emerging clinical entity. The limited extension of the disease prompt to explore the role of metastases-directed therapies (MDT); however, their actual survival and clinical benefits remain uncertain. Additional studies with larger effectives are needed to clarify the role of MDT in clinical practice. Methods: We conducted a retrospective multicenter, observational French-Belgian study to evaluate the impact of MDT on event-free survival (EFS) and overall survival (OS) in patients with OMD-PDAC. OMD was defined as metastases (mets) involving no more than 2 organ and ≤5 mets (Leonhardt CS. ESMO Open 2023). Eligible patients were adults with histologically confirmed PDAC who underwent a resection of the primary tumor, with concurrent or subsequent MDT of MDT. OS was defined as the delay from MDT to death from any cause; EFS was calculated from the date of MDT until radiologically confirmed disease progression, recurrence or death. The ALTOPANC score—based on known prognostic factors (CA 19-9 >90 U/mL, > 1 met, and non-pulmonary mets)—was correlated with OS and EFS. Results: Between 01/2011 and 12/2024, 155 patients with OMD-PDAC were included; 138 had metachronous metastases. Sites of mets included liver (n=71, 45%), lung (n=61, 39%), periaortic lymph nodes (n=13, 8%) and peritoneum (n=5, 3%). At time of the met's diagnosis, 107 patients (71%) had a single met, and 25 (17%) patients had presented two mets. After a median follow-up of 4.42 years, median EFS and median OS in the entire population were of 0.8 and 3,4 years respectively. MDT modalities consisted in surgery (n=69, 45%), radiotherapy (n=50, 32%), and thermoablation (n=36, 23%). In the multivariate Cox model, higher CA 19-9 level (HR = 1.29, 95% CI: 1.13–1.48, p = 0.0002) and the presence of 2 (HR = 2.54, 95% CI: 1.32–4.88, p <0.0001) or ≥3 treated mets (HR = 4.39, 95% CI: 2.18–8.84, p <0.0001) were independent adverse prognostic factors for OS. Thermoablation was independently associated with an improved OS compared to other technics (HR=0.51, 95%CI: 0.27–0.96, p =0.0127). The ALTOPANC score was significantly associated with EFS :2-year EFS rates were 53.1%, 23.8%, 8.3%, and 0% in patients with scores of 0, 1, 2, and 3, respectively (p < 0.001). A similar trend was observed for OS. Conclusions: 1) This real-world, study shows promising results of MDT in patients with OMD-PDAC, particularly thermoablation ; 2) among patients with favorable prognostic profile (low ALTOPANC score) may have the higher benefit. A prospective randomized study is warranted to confirm these results.

Article Details

Volume / Issue Vol. 44, Issue 2_suppl
Published January 10, 2026
Pages 728-728
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (20)

P

Pauline Parent

V

Victoria Pacquement

Department of Medical Oncologie, CHU Lille, Lille, France

A

Alice Boileve

Gustave Roussy, Villejuif, France

J

Julie Henriques

Methodology and Quality of Life in Oncology Unit, Centre Hospitalier Universitaire de Besançon, Besançon, France

J

Julie Navez

Hopital Erasme, Hôpital Universitaire de Bruxelles, Bruxelles, Belgium

A

Alexandre Taillez

Department of Radiotherapy, Oscar Lambret Center, Lille, France

S

Simon Pernot

Department of Medical Oncology, Institute Bergonié Cancer Center, Bordeaux, Nouvelle Aquitaine, France

L

Louis de Mestier

J

Jean-Baptiste Bachet

P

Pascal Artru

N

Nicolas Bertrand

Department of Medical Oncology, Eugène Marquis Cancer Centre, Rennes, France

R

Rami Rhaiem

CHU de Reims, Reims, France

J

Jean-Frédéric Blanc

E

Emily Linda Alouani

Memorial Sloan Kettering Cancer Center, New York, NY

J

Juliette Logeart

Curie Institute, Versaille-Saint Quentin University, Saint-Cloud, Saint-Cloud, France

T

Thierry Lecomte

S

Sara El Kurdi

Lille University Hospital, Lille, France

P

Pascal Hammel

S

Stephanie Truant

Lille University Hospital, Lille, France

A

Anthony Turpin