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Liver oligometastatic disease in synchronous metastatic gastric cancer patients : a nationwide population-based cohort study. / Kroese, Tiuri E.; Takahashi, Yuko; Lordick, Florian et al.

In: European Journal of Cancer, Vol. 179, 01.01.2023, p. 65-75.

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Kroese TE, Takahashi Y, Lordick F, van Rossum PSN, Ruurda JP, Lagarde SM et al. Liver oligometastatic disease in synchronous metastatic gastric cancer patients: a nationwide population-based cohort study. European Journal of Cancer. 2023 Jan 1;179:65-75. doi: 10.1016/j.ejca.2022.11.011

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Kroese, Tiuri E. ; Takahashi, Yuko ; Lordick, Florian et al. / Liver oligometastatic disease in synchronous metastatic gastric cancer patients : a nationwide population-based cohort study. In: European Journal of Cancer. 2023 ; Vol. 179. pp. 65-75.

BibTeX

@article{e6ef2d11b829431c8f0d6aa85d538417,
title = "Liver oligometastatic disease in synchronous metastatic gastric cancer patients: a nationwide population-based cohort study",
abstract = "Introduction: This population-based cohort study analysed treatment, overall survival (OS), and independent prognostic factors for OS in gastric cancer patients with liver metastases. Methods: Between 2015 and 2017, patients with synchronous metastatic gastric or gastroesophageal junction adenocarcinoma limited to the liver were included from the prospectively maintained population-based Netherlands Cancer Registry. Liver oligometastatic disease (OMD) was defined as ≤3 liver metastases. The primary outcome was OS. Independent prognostic factors for OS were analysed using multivariable Cox regression analysis. Results: A total 295 patients with metastases limited to the liver were included. The primary tumour was resected in four patients (1.4%). Treatment for liver metastases consisted of chemotherapy alone (28.1%), trastuzumab plus chemotherapy (4.7%), surgery (1.0%), or best supportive care (67.5%). Median OS across all included patients was 4.0 months (95% confidence interval [CI]: 3.1–4.5). Liver OMD was detected in 77 patients (26%). Treatment for liver OMD consisted of chemotherapy alone (24.6%), trastuzumab plus chemotherapy (5.2%), surgery (3.9%), or best supportive care (67.5%). Median OS among patients with liver OMD was 5.7 months (95% CI: 4.8–7.5). Across all patients, better OS was independently associated with liver OMD (hazard ratio [HR] 0.66, 95% CI: 0.50–0.87), trastuzumab (HR 0.41, 95% CI: 0.23–0.72) but not with triplet compared with doublet chemotherapy (HR 0.94, 95% CI: 0.57–2.87). Worse OS was independently associated with unknown nodal stage versus cN0 (HR 1.74, 95% CI: 1.17–2.60), diffuse-type versus intestinal-type adenocarcinoma (HR 2.06, 95% CI: 1.32–3.20), and monotherapy or best supportive care versus doublet chemotherapy (HR 1.72, 95% CI: 1.03–2.87, and HR 3.61, 95% CI: 2.55–5.10, respectively). Conclusion: In this population-based cohort study, liver OMD was detected in 26% of patients. Liver OMD and trastuzumab treatment were independently associated with better OS while triplet as compared with doublet chemotherapy was not. OS among patients with liver OMD nevertheless remained poor. The concept of OMD and the benefit of resection of liver OMD may still have been relatively unknown in this disease type during the study inclusion years.",
keywords = "Gastric cancer, Liver metastases, Metastasectomy, Oligometastases, Radiofrequency ablation, Systemic therapy",
author = "Kroese, {Tiuri E.} and Yuko Takahashi and Florian Lordick and {van Rossum}, {Peter S. N.} and Ruurda, {Jelle P.} and Lagarde, {Sjoerd M.} and {van Hillegersberg}, Richard and Verhoeven, {Rob H. A.} and {van Laarhoven}, {Hanneke W. M.}",
note = "Funding Information: The data collection for this study was supported by the European Organisation for Research and Treatment of Cancer (EORTC) Gastrointestinal Tract Cancer Trials Group. The funding group had a role in the study design, while conduct and management of the study, analysis, and interpretation of the data, preparation, review, or approval of the manuscript and decision to submit the manuscript for publication was independent of the funding group. Publisher Copyright: {\textcopyright} 2022 The Authors",
year = "2023",
month = jan,
day = "1",
doi = "10.1016/j.ejca.2022.11.011",
language = "English",
volume = "179",
pages = "65--75",
journal = "European journal of cancer (Oxford, England",
issn = "0959-8049",
publisher = "Elsevier Limited",

}

RIS

TY - JOUR

T1 - Liver oligometastatic disease in synchronous metastatic gastric cancer patients

T2 - a nationwide population-based cohort study

AU - Kroese, Tiuri E.

AU - Takahashi, Yuko

AU - Lordick, Florian

AU - van Rossum, Peter S. N.

AU - Ruurda, Jelle P.

AU - Lagarde, Sjoerd M.

AU - van Hillegersberg, Richard

AU - Verhoeven, Rob H. A.

AU - van Laarhoven, Hanneke W. M.

N1 - Funding Information: The data collection for this study was supported by the European Organisation for Research and Treatment of Cancer (EORTC) Gastrointestinal Tract Cancer Trials Group. The funding group had a role in the study design, while conduct and management of the study, analysis, and interpretation of the data, preparation, review, or approval of the manuscript and decision to submit the manuscript for publication was independent of the funding group. Publisher Copyright: © 2022 The Authors

PY - 2023/1/1

Y1 - 2023/1/1

N2 - Introduction: This population-based cohort study analysed treatment, overall survival (OS), and independent prognostic factors for OS in gastric cancer patients with liver metastases. Methods: Between 2015 and 2017, patients with synchronous metastatic gastric or gastroesophageal junction adenocarcinoma limited to the liver were included from the prospectively maintained population-based Netherlands Cancer Registry. Liver oligometastatic disease (OMD) was defined as ≤3 liver metastases. The primary outcome was OS. Independent prognostic factors for OS were analysed using multivariable Cox regression analysis. Results: A total 295 patients with metastases limited to the liver were included. The primary tumour was resected in four patients (1.4%). Treatment for liver metastases consisted of chemotherapy alone (28.1%), trastuzumab plus chemotherapy (4.7%), surgery (1.0%), or best supportive care (67.5%). Median OS across all included patients was 4.0 months (95% confidence interval [CI]: 3.1–4.5). Liver OMD was detected in 77 patients (26%). Treatment for liver OMD consisted of chemotherapy alone (24.6%), trastuzumab plus chemotherapy (5.2%), surgery (3.9%), or best supportive care (67.5%). Median OS among patients with liver OMD was 5.7 months (95% CI: 4.8–7.5). Across all patients, better OS was independently associated with liver OMD (hazard ratio [HR] 0.66, 95% CI: 0.50–0.87), trastuzumab (HR 0.41, 95% CI: 0.23–0.72) but not with triplet compared with doublet chemotherapy (HR 0.94, 95% CI: 0.57–2.87). Worse OS was independently associated with unknown nodal stage versus cN0 (HR 1.74, 95% CI: 1.17–2.60), diffuse-type versus intestinal-type adenocarcinoma (HR 2.06, 95% CI: 1.32–3.20), and monotherapy or best supportive care versus doublet chemotherapy (HR 1.72, 95% CI: 1.03–2.87, and HR 3.61, 95% CI: 2.55–5.10, respectively). Conclusion: In this population-based cohort study, liver OMD was detected in 26% of patients. Liver OMD and trastuzumab treatment were independently associated with better OS while triplet as compared with doublet chemotherapy was not. OS among patients with liver OMD nevertheless remained poor. The concept of OMD and the benefit of resection of liver OMD may still have been relatively unknown in this disease type during the study inclusion years.

AB - Introduction: This population-based cohort study analysed treatment, overall survival (OS), and independent prognostic factors for OS in gastric cancer patients with liver metastases. Methods: Between 2015 and 2017, patients with synchronous metastatic gastric or gastroesophageal junction adenocarcinoma limited to the liver were included from the prospectively maintained population-based Netherlands Cancer Registry. Liver oligometastatic disease (OMD) was defined as ≤3 liver metastases. The primary outcome was OS. Independent prognostic factors for OS were analysed using multivariable Cox regression analysis. Results: A total 295 patients with metastases limited to the liver were included. The primary tumour was resected in four patients (1.4%). Treatment for liver metastases consisted of chemotherapy alone (28.1%), trastuzumab plus chemotherapy (4.7%), surgery (1.0%), or best supportive care (67.5%). Median OS across all included patients was 4.0 months (95% confidence interval [CI]: 3.1–4.5). Liver OMD was detected in 77 patients (26%). Treatment for liver OMD consisted of chemotherapy alone (24.6%), trastuzumab plus chemotherapy (5.2%), surgery (3.9%), or best supportive care (67.5%). Median OS among patients with liver OMD was 5.7 months (95% CI: 4.8–7.5). Across all patients, better OS was independently associated with liver OMD (hazard ratio [HR] 0.66, 95% CI: 0.50–0.87), trastuzumab (HR 0.41, 95% CI: 0.23–0.72) but not with triplet compared with doublet chemotherapy (HR 0.94, 95% CI: 0.57–2.87). Worse OS was independently associated with unknown nodal stage versus cN0 (HR 1.74, 95% CI: 1.17–2.60), diffuse-type versus intestinal-type adenocarcinoma (HR 2.06, 95% CI: 1.32–3.20), and monotherapy or best supportive care versus doublet chemotherapy (HR 1.72, 95% CI: 1.03–2.87, and HR 3.61, 95% CI: 2.55–5.10, respectively). Conclusion: In this population-based cohort study, liver OMD was detected in 26% of patients. Liver OMD and trastuzumab treatment were independently associated with better OS while triplet as compared with doublet chemotherapy was not. OS among patients with liver OMD nevertheless remained poor. The concept of OMD and the benefit of resection of liver OMD may still have been relatively unknown in this disease type during the study inclusion years.

KW - Gastric cancer

KW - Liver metastases

KW - Metastasectomy

KW - Oligometastases

KW - Radiofrequency ablation

KW - Systemic therapy

UR - http://www.scopus.com/inward/record.url?scp=85143985352&partnerID=8YFLogxK

U2 - 10.1016/j.ejca.2022.11.011

DO - 10.1016/j.ejca.2022.11.011

M3 - Article

C2 - 36509000

VL - 179

SP - 65

EP - 75

JO - European journal of cancer (Oxford, England

JF - European journal of cancer (Oxford, England

SN - 0959-8049

ER -

ID: 29709541