Hepatic disease control in patients with intrahepatic cholangiocarcinoma correlates with overall survival.


Journal

Cancer medicine
ISSN: 2045-7634
Titre abrégé: Cancer Med
Pays: United States
ID NLM: 101595310

Informations de publication

Date de publication:
06 2023
Historique:
revised: 22 03 2023
received: 22 01 2023
accepted: 30 03 2023
medline: 20 6 2023
pubmed: 17 4 2023
entrez: 16 4 2023
Statut: ppublish

Résumé

The role of locoregional therapy compared to systemic chemotherapy (SYS) for unresectable intrahepatic cholangiocarcinoma (IHC) remains controversial. The importance of hepatic disease control, either as initial or salvage therapy, is also unclear. We compared overall survival (OS) in patients treated with resection, hepatic arterial infusion pump (HAIP) chemotherapy, or SYS as it relates to hepatic recurrence or progression. We also evaluated recurrence after resection to determine the efficacy of locoregional salvage therapy. In this single-institution retrospective analysis, patients with biopsy-proven IHC treated with either curative-intent resection, HAIP (with or without SYS), or SYS alone were analyzed. Propensity score matching (PSM) was used to compare patients with liver-limited, advanced disease treated with HAIP versus SYS. The impact of locoregional salvage therapies in patients with liver-limited recurrence was analyzed in the resection cohort. From 2000 to 2017, 714 patients with IHC were treated, 219 (30.7%) with resectable disease, 316 (44.3%) with locally advanced disease, and 179 (25.1%) with metastatic disease. Resected patients were less likely to recur or progress in the liver (hazard ratio [HR] 0.41, 95% CI 0.34-0.45) versus those that received HAIP or SYS (HR 0.58, 95% CI 0.50-0.65 vs. HR 0.63, 95% CI 0.57-0.69, respectively). In resected patients, 161 (64.4%) recurred, with 65 liver-only recurrences. Thirty of these patients received subsequent locoregional therapy. On multivariable analysis, locoregional therapy was associated with improved OS after isolated liver recurrence (HR 0.46, 95% CI 0.29-0.75; p = 0.002). In patients with locally advanced unresectable or multifocal liver disease (with or without distant organ metastases), PSM demonstrated improved hepatic progression-free survival in patients treated with HAIP versus SYS (HR 0.65; 95% CI 0.46-0.91; p = 0.01), which correlated with improved OS (HR 0.59, 95% CI 0.43-0.80; p < 0.001). In patients with liver-limited IHC, hepatic disease control is associated with improved OS, emphasizing the potential importance of liver-directed therapy.

Identifiants

pubmed: 37062071
doi: 10.1002/cam4.5925
pmc: PMC10278501
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

12272-12284

Subventions

Organisme : NCI NIH HHS
ID : U01 CA238444
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States

Informations de copyright

© 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

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Auteurs

Kevin C Soares (KC)

Department of Surgery, Hepatopancreatobiliary Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Joshua S Jolissaint (JS)

Department of Surgery, Hepatopancreatobiliary Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Department of Surgery, Brigham and Women's Hospital, Boston, Massachusetts, USA.

Sarah M McIntyre (SM)

Department of Surgery, Hepatopancreatobiliary Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Kenneth P Seier (KP)

Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Mithat Gönen (M)

Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Carlie Sigel (C)

Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Naaz Nasar (N)

Department of Surgery, Hepatopancreatobiliary Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Andrea Cercek (A)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

James J Harding (JJ)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Nancy E Kemeny (NE)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Louise C Connell (LC)

Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Bas Groot Koerkamp (BG)

Department of Surgery, Erasmus Medical Center, Rotterdam, The Netherlands.

Vinod P Balachandran (VP)

Department of Surgery, Hepatopancreatobiliary Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Michael I D'Angelica (MI)

Department of Surgery, Hepatopancreatobiliary Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Jeffrey A Drebin (JA)

Department of Surgery, Hepatopancreatobiliary Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

T Peter Kingham (TP)

Department of Surgery, Hepatopancreatobiliary Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

Alice C Wei (AC)

Department of Surgery, Hepatopancreatobiliary Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

William R Jarnagin (WR)

Department of Surgery, Hepatopancreatobiliary Service, Memorial Sloan Kettering Cancer Center, New York, New York, USA.

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