Impact of perioperative chemotherapy on survival in patients with cholangiocarcinoma undergoing curative resection.


Journal

European journal of surgical oncology : the journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology
ISSN: 1532-2157
Titre abrégé: Eur J Surg Oncol
Pays: England
ID NLM: 8504356

Informations de publication

Date de publication:
Nov 2023
Historique:
received: 09 10 2022
revised: 13 07 2023
accepted: 26 07 2023
medline: 13 11 2023
pubmed: 1 8 2023
entrez: 31 7 2023
Statut: ppublish

Résumé

Most patients with localized cholangiocarcinoma (CCA) endure cancer relapse after curative resection underscoring the importance of systemic therapy. The current study attempts to determine the impact of perioperative chemotherapy (PC) on survival in patients with CCA undergoing resection. Patients diagnosed with CCA undergoing curative-intent resection between January 1, 2000, and December 31, 2019, in a tertiary care center were included. Cox proportional hazard modeling was used to determine the impact of PC on disease-free survival (DFS) and overall survival (OS). In addition, a nomogram was constructed to estimate 3-year DFS. Among the 182 patients included in the analysis, 102 underwent surgery alone, and 80 received surgery plus PC. Forty-two patients received neoadjuvant therapy, and 38 patients received adjuvant therapy. On multivariate analysis, PC was significantly associated with an improved DFS (HR, 95% CI: 0.63, 0.41-0.98; p = 0.04) and OS (HR, 95% CI: 0.46, 0.27-0.78; p < 0.01). In the interaction analysis, the survival benefit was especially seen in patients with positive resection margins and tumor size > 5 cm. In patients with CCA undergoing curative resection, receipt of PC was associated with improved DFS and OS. The nomogram constructed from this database provides an estimate of 3-year DFS after surgical resection. Randomized trials are needed to define the optimal regimen and sequence.

Sections du résumé

BACKGROUND BACKGROUND
Most patients with localized cholangiocarcinoma (CCA) endure cancer relapse after curative resection underscoring the importance of systemic therapy. The current study attempts to determine the impact of perioperative chemotherapy (PC) on survival in patients with CCA undergoing resection.
METHODS METHODS
Patients diagnosed with CCA undergoing curative-intent resection between January 1, 2000, and December 31, 2019, in a tertiary care center were included. Cox proportional hazard modeling was used to determine the impact of PC on disease-free survival (DFS) and overall survival (OS). In addition, a nomogram was constructed to estimate 3-year DFS.
RESULTS RESULTS
Among the 182 patients included in the analysis, 102 underwent surgery alone, and 80 received surgery plus PC. Forty-two patients received neoadjuvant therapy, and 38 patients received adjuvant therapy. On multivariate analysis, PC was significantly associated with an improved DFS (HR, 95% CI: 0.63, 0.41-0.98; p = 0.04) and OS (HR, 95% CI: 0.46, 0.27-0.78; p < 0.01). In the interaction analysis, the survival benefit was especially seen in patients with positive resection margins and tumor size > 5 cm.
CONCLUSION CONCLUSIONS
In patients with CCA undergoing curative resection, receipt of PC was associated with improved DFS and OS. The nomogram constructed from this database provides an estimate of 3-year DFS after surgical resection. Randomized trials are needed to define the optimal regimen and sequence.

Identifiants

pubmed: 37524649
pii: S0748-7983(23)00620-0
doi: 10.1016/j.ejso.2023.106994
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106994

Informations de copyright

© 2023 Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of competing interest None.

Auteurs

Hind Hassan (H)

Department of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.

Sakti Chakrabarti (S)

Department of Oncology, University Hospitals Seidman Cancer Center and Case Western Reserve University, Cleveland, OH, USA.

Tyler Zemla (T)

Department of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, MN, USA.

Jun Yin (J)

Department of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, MN, USA.

Vanessa Wookey (V)

Mayo Clinic Comprehensive Cancer Center, Rochester, MN, USA.

Kritika Prasai (K)

Department of Pathology and Laboratory Medicine, Northshore University Health Care System, Evanston, IL, USA.

Amro Abdellatief (A)

Department of Internal Medicine, Harlem Hospital Center, Columbia University Medical Center, New York, NY, USA.

Renuka Katta (R)

Department of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.

Nguyen Tran (N)

Mayo Clinic Comprehensive Cancer Center, Rochester, MN, USA.

Zhaohui Jin (Z)

Mayo Clinic Comprehensive Cancer Center, Rochester, MN, USA.

Sean Cleary (S)

Mayo Clinic Comprehensive Cancer Center, Rochester, MN, USA.

Lewis Roberts (L)

Mayo Clinic Comprehensive Cancer Center, Rochester, MN, USA.

Amit Mahipal (A)

Department of Oncology, University Hospitals Seidman Cancer Center and Case Western Reserve University, Cleveland, OH, USA; Mayo Clinic Comprehensive Cancer Center, Rochester, MN, USA. Electronic address: amit.mahipal@uhhospitals.org.

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