Preliminary results of tumor-informed minimal residual disease detection in pancreatic cancer patients following curative resection and FOLFIRINOX adjuvant chemotherapy.

M Myung Ah Lee S Se Jun Park C Choong-kun Lee S Seok Jae Huh H Hyung Soon Park (St. Vincent's Hospital, The Catholic University of Korea, Suwon, South Korea) H Hongsik Kim (Department of Materials) D Dong-Hoe Koo J Ju Won Kim E Eun Mi Nam D Dae Young Zhang (Division of Hematology-Oncology, Department of Internal Medicine, Hallym University Medical Center, Hallym University College of Medicine, Anyang, South Korea) H Hong Jae Chon J Jin Won Kim S Sunghoon Heo Y Yongjun Cha

Abstract

753 Background: Circulating tumor DNA (ctDNA)–based minimal residual disease (MRD) testing has emerged as a powerful prognostic tool in solid tumors and may inform postoperative management. We evaluated the prognostic significance of ctDNA MRD monitoring in patients with pancreatic cancer (PC) undergoing curative resection followed by adjuvant FOLFIRINOX. Methods: Between Oct 2023 and Feb 2025, patients with resected PC receiving adjuvant FOLFIRINOX were prospectively enrolled from 11 hospitals in Korea. Whole blood (20 mL) was collected at up to seven postoperative time points [4 (P1), 12 (P12), 24 (P24), 40 (P40), 56 (P56), 72 (P72), and 88 (P88) weeks] and analyzed with a tumor-informed assay (CancerDetect, IMBdx). MRD positivity was defined as detection of ≥2 mutations. Results: Eighty-six of 92 enrolled patients were included (median age 68, range 42–82; 49% male). Pathologic stages were I (39.5%), II (46.5%), III (12.8%), and IV (1.1%). Postoperative MRD positivity at P1 was 31.3%, increasing with stage (15.2% I, 34.8% II, 54.5% III–IV; P for trend = 0.003). At a median follow-up of 13.0 months, 20 patients (23.3%) had recurred. While stage, T, and N classifications were not associated with disease-free survival (DFS), MRD positivity at P1 predicted inferior DFS [HR 5.31; 95% CI 2.1-13.4; P <0.001; 1-year DFS 56.0% vs. 92.8%]. Stage-stratified analysis showed prognostic significance for stage I (HR 8.90, P <0.001; 1-year DFS 40.0% vs. 92.9%) and stage II (HR 6.87, P = 0.02; 1-year DFS 64.3% vs. 95.6%), but not for stage III/IV (HR 2.02, P = 0.45). Longitudinally, MRD persisters had the worst outcomes (HR 21.17, P<0.001; 1-year DFS 25.0%), followed by positive converters (HR 4.30, P = 0.045; 1-year DFS 85.7%) and negative converters (HR 3.87, P = 0.033; 1-year DFS 73.7%), compared with negative persisters (1-year DFS 94.2%). Conclusions: Postoperative ctDNA MRD detection strongly predicted recurrence in resected PC treated with adjuvant FOLFIRINOX. Longitudinal MRD dynamics correlated with treatment response and recurrence risk, supporting the clinical utility of MRD to inform postoperative surveillance and therapeutic strategies.

Article Details

Volume / Issue Vol. 44, Issue 2_suppl
Published January 10, 2026
Pages 753-753
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (14)

M

Myung Ah Lee

S

Se Jun Park

C

Choong-kun Lee

S

Seok Jae Huh

H

Hyung Soon Park

St. Vincent's Hospital, The Catholic University of Korea, Suwon, South Korea

H

Hongsik Kim

Department of Materials

D

Dong-Hoe Koo

J

Ju Won Kim

E

Eun Mi Nam

D

Dae Young Zhang

Division of Hematology-Oncology, Department of Internal Medicine, Hallym University Medical Center, Hallym University College of Medicine, Anyang, South Korea

H

Hong Jae Chon

J

Jin Won Kim

S

Sunghoon Heo

Y

Yongjun Cha