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CA19-9 With Two-stage Resection Is Useful for Conversion Surgery in PDAC With Synchronous Oligometastases.

Authors :
Inoue K
Mizuma M
Motoi F
Kokumai T
Sato H
Kusaka A
Aoki S
Iseki M
Douchi D
Miura T
Maeda S
Ishida M
Ohtsuka H
Nakagawa K
Kamei T
Unno M
Source :
Anticancer research [Anticancer Res] 2023 Nov; Vol. 43 (11), pp. 5223-5234.
Publication Year :
2023

Abstract

Background/aim: Pancreatic adenocarcinoma (PDAC) with synchronous oligometastases may indicate a surgical benefit after chemotherapy. We investigated whether primary and metastatic resection of PDAC with oligometastases can improve the survival and then explored prognostic factors to identify indications for conversion surgery.<br />Patients and Methods: We reviewed 425 patients with PDAC who underwent pancreatic resection from 2005 to 2019. Clinical characteristics and outcomes were analyzed. Two-stage resection was defined as preceding metastasectomy and subsequent primary resection after chemotherapy.<br />Results: Fifteen patients (3.5%) had synchronous oligometastases. We evaluated the overall survival of the patients with oligometastases and those without metastases. The survival curves almost completely overlapped (median survival time: 35.9 vs. 32.1 months). The univariate Cox regression analysis revealed a normal level of preoperative CA19-9 (p=0.075), two-stage resection (p=0.072), and R0 resection (p=0.064) were likely promising prognostic factors. The combination of a normal level of preoperative CA19-9 with two-stage resection was a significant prognostic factor (p=0.038). In addition, patients with a normal preoperative CA19-9 level and two-stage resection had better survival (46.1 vs. 28.1 months, p=0.026).<br />Conclusion: The combination of normal preoperative CA19-9 with two-stage resection can be a useful way to identify patients with PDAC and oligometastases for surgical indication.<br /> (Copyright © 2023 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.)

Details

Language :
English
ISSN :
1791-7530
Volume :
43
Issue :
11
Database :
MEDLINE
Journal :
Anticancer research
Publication Type :
Academic Journal
Accession number :
37909951
Full Text :
https://doi.org/10.21873/anticanres.16724