Evaluation of Systemic Inflammatory Response and Nutritional Biomarkers as Predictive Factors in Patients with Recurrent Gastric Cancer.


Journal

Oncology
ISSN: 1423-0232
Titre abrégé: Oncology
Pays: Switzerland
ID NLM: 0135054

Informations de publication

Date de publication:
2020
Historique:
received: 18 12 2019
accepted: 16 01 2020
pubmed: 18 3 2020
medline: 16 7 2020
entrez: 18 3 2020
Statut: ppublish

Résumé

The present study sought to evaluate host-related factors as predictors in patients receiving chemotherapy for recurrent advanced gastric cancer. Sixty-three patients were enrolled in the study and received chemotherapy for recurrent gastric cancer at the Kochi Medical School from 2008 to 2015. Clinicopathological information and systemic inflammatory response data were obtained retrospectively to investigate associations between baseline cancer-related prognostic variables and survival outcomes. The median survival time was significantly higher for patients with a Glasgow prognostic score (GPS) of 0 compared to a GPS of 1 or 2 (18.2 vs. 7.1 months; p = 0.006), and for patients in the normal range for carbohydrate antigen-125 (CA125) compared to higher levels (17.9 vs. 4.1 months; p = 0.003). There was no significant influence on overall survival by age, gender, disease status, metastatic site, time to recurrence, carcinoembryonic antigen level, CA19-9 level, prognostic nutrition index, or neutrophil to lymphocyte ratio according to the results of the univariate log-rank tests. Multivariate survival analysis identified a GPS of 1 or 2 (hazard ratio, 3.520; 95% confidence interval, 1.343-9.227; p = 0.010) and a high CA125 level (hazard ratio, 3.135; 95% confidence interval, 1.276-7.697; p = 0.013) as significant independent predictors associated with a poorer prognosis in the studied group of cancer patients. A GPS of 1 or 2 and a high level of CA125 are independent predictors of a poorer prognosis in patients receiving chemotherapy for recurrent gastric cancer.

Sections du résumé

BACKGROUND BACKGROUND
The present study sought to evaluate host-related factors as predictors in patients receiving chemotherapy for recurrent advanced gastric cancer.
METHODS METHODS
Sixty-three patients were enrolled in the study and received chemotherapy for recurrent gastric cancer at the Kochi Medical School from 2008 to 2015. Clinicopathological information and systemic inflammatory response data were obtained retrospectively to investigate associations between baseline cancer-related prognostic variables and survival outcomes.
RESULTS RESULTS
The median survival time was significantly higher for patients with a Glasgow prognostic score (GPS) of 0 compared to a GPS of 1 or 2 (18.2 vs. 7.1 months; p = 0.006), and for patients in the normal range for carbohydrate antigen-125 (CA125) compared to higher levels (17.9 vs. 4.1 months; p = 0.003). There was no significant influence on overall survival by age, gender, disease status, metastatic site, time to recurrence, carcinoembryonic antigen level, CA19-9 level, prognostic nutrition index, or neutrophil to lymphocyte ratio according to the results of the univariate log-rank tests. Multivariate survival analysis identified a GPS of 1 or 2 (hazard ratio, 3.520; 95% confidence interval, 1.343-9.227; p = 0.010) and a high CA125 level (hazard ratio, 3.135; 95% confidence interval, 1.276-7.697; p = 0.013) as significant independent predictors associated with a poorer prognosis in the studied group of cancer patients.
CONCLUSIONS CONCLUSIONS
A GPS of 1 or 2 and a high level of CA125 are independent predictors of a poorer prognosis in patients receiving chemotherapy for recurrent gastric cancer.

Identifiants

pubmed: 32182616
pii: 000505973
doi: 10.1159/000505973
doi:

Substances chimiques

Antigens, Tumor-Associated, Carbohydrate 0
CA-125 Antigen 0
Carcinoembryonic Antigen 0
carbohydrate antigen 199, human 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

452-459

Informations de copyright

© 2020 S. Karger AG, Basel.

Auteurs

Tsutomu Namikawa (T)

Department of Surgery, Kochi Medical School, Kochi, Japan, tsutomun@kochi-u.ac.jp.

Keiichiro Yokota (K)

Department of Surgery, Kochi Medical School, Kochi, Japan.

Sachi Yamaguchi (S)

Department of Surgery, Kochi Medical School, Kochi, Japan.

Jun Iwabu (J)

Department of Surgery, Kochi Medical School, Kochi, Japan.

Masaya Munekage (M)

Department of Surgery, Kochi Medical School, Kochi, Japan.

Sunao Uemura (S)

Department of Surgery, Kochi Medical School, Kochi, Japan.

Shigehiro Tsujii (S)

Department of Surgery, Kochi Medical School, Kochi, Japan.

Hiromichi Maeda (H)

Department of Surgery, Kochi Medical School, Kochi, Japan.

Hiroyuki Kitagawa (H)

Department of Surgery, Kochi Medical School, Kochi, Japan.

Masamitsu Kumon (M)

Department of Surgery, Noichi Central Hospital, Kochi, Japan.

Michiya Kobayashi (M)

Department of Human Health and Medical Sciences, Kochi Medical School, Kochi, Japan.

Kazuhiro Hanazaki (K)

Department of Surgery, Kochi Medical School, Kochi, Japan.

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