Tumor deposit serves as a prognostic marker in gastric cancer: A propensity score‐matched analysis comparing survival outcomes
Background Gastric cancer (GC) treatment is determined by accurate tumor staging. The value of tumor deposit (TD) in prognostic prediction staging system is not yet determined. Methods We retrospectively analyzed clinical information on GC patients who underwent gastrectomy at the Department of Gene...
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Published in | Cancer medicine (Malden, MA) Vol. 9; no. 10; pp. 3268 - 3277 |
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Main Authors | , , , , , , , , , , , , , , |
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John Wiley & Sons, Inc
01.05.2020
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Abstract | Background
Gastric cancer (GC) treatment is determined by accurate tumor staging. The value of tumor deposit (TD) in prognostic prediction staging system is not yet determined.
Methods
We retrospectively analyzed clinical information on GC patients who underwent gastrectomy at the Department of General Surgery of the Chinese PLA General Hospital from July 2014 to June 2016. Propensity score matching (PSM) was performed to reduce the possibility of selection bias according to the presence of TD.
Results
Of the 1034 GC patients, 240 (23.21%) presented with TD, which was associated with younger age and larger tumor size (all P < .05). TD‐positive patients had a worse survival than TD‐negative patients before (P < .001) and after (P = .017) matching. Multivariable analysis showed that mortality risk of patients with TD increased by 58%, 62%, 37%, and 40% in the crude (HR = 1.58, 95% CI 1.32‐1.89, P < .001), adjusted I (HR = 1.62, 95% CI 1.35‐1.94, P < .001), adjusted II (HR = 1.37, 95% CI 1.13‐1.66, P = .001), and adjusted III (HR = 1.40, 95% CI 1.16‐1.68, P < .001) models before matching. Similarly, in the PSM cohort patients with TD had worse prognosis in the crude (HR = 1.32, 95% CI 1.07‐1.63, P = .011), adjusted I (HR = 1.35, 95% CI 1.09‐1.67, P = .005), adjusted II (HR = 1.26, 95% CI 1.00‐1.58, P = .049), and adjusted III (HR = 1.33, 95% CI 1.07‐1.65, P = .010) models. TD had a similar value range between N1 and N2 stages among different models.
Conclusions
Among GC patients, TD is associated with survival and may have a role in the staging of patients.
Kaplan‐Meier curves for TD negative and positive gastric patients before and after propensity score matching. |
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AbstractList | Gastric cancer (GC) treatment is determined by accurate tumor staging. The value of tumor deposit (TD) in prognostic prediction staging system is not yet determined.
We retrospectively analyzed clinical information on GC patients who underwent gastrectomy at the Department of General Surgery of the Chinese PLA General Hospital from July 2014 to June 2016. Propensity score matching (PSM) was performed to reduce the possibility of selection bias according to the presence of TD.
Of the 1034 GC patients, 240 (23.21%) presented with TD, which was associated with younger age and larger tumor size (all P < .05). TD-positive patients had a worse survival than TD-negative patients before (P < .001) and after (P = .017) matching. Multivariable analysis showed that mortality risk of patients with TD increased by 58%, 62%, 37%, and 40% in the crude (HR = 1.58, 95% CI 1.32-1.89, P < .001), adjusted I (HR = 1.62, 95% CI 1.35-1.94, P < .001), adjusted II (HR = 1.37, 95% CI 1.13-1.66, P = .001), and adjusted III (HR = 1.40, 95% CI 1.16-1.68, P < .001) models before matching. Similarly, in the PSM cohort patients with TD had worse prognosis in the crude (HR = 1.32, 95% CI 1.07-1.63, P = .011), adjusted I (HR = 1.35, 95% CI 1.09-1.67, P = .005), adjusted II (HR = 1.26, 95% CI 1.00-1.58, P = .049), and adjusted III (HR = 1.33, 95% CI 1.07-1.65, P = .010) models. TD had a similar value range between N1 and N2 stages among different models.
Among GC patients, TD is associated with survival and may have a role in the staging of patients. Kaplan‐Meier curves for TD negative and positive gastric patients before and after propensity score matching. BACKGROUNDGastric cancer (GC) treatment is determined by accurate tumor staging. The value of tumor deposit (TD) in prognostic prediction staging system is not yet determined. METHODSWe retrospectively analyzed clinical information on GC patients who underwent gastrectomy at the Department of General Surgery of the Chinese PLA General Hospital from July 2014 to June 2016. Propensity score matching (PSM) was performed to reduce the possibility of selection bias according to the presence of TD. RESULTSOf the 1034 GC patients, 240 (23.21%) presented with TD, which was associated with younger age and larger tumor size (all P < .05). TD-positive patients had a worse survival than TD-negative patients before (P < .001) and after (P = .017) matching. Multivariable analysis showed that mortality risk of patients with TD increased by 58%, 62%, 37%, and 40% in the crude (HR = 1.58, 95% CI 1.32-1.89, P < .001), adjusted I (HR = 1.62, 95% CI 1.35-1.94, P < .001), adjusted II (HR = 1.37, 95% CI 1.13-1.66, P = .001), and adjusted III (HR = 1.40, 95% CI 1.16-1.68, P < .001) models before matching. Similarly, in the PSM cohort patients with TD had worse prognosis in the crude (HR = 1.32, 95% CI 1.07-1.63, P = .011), adjusted I (HR = 1.35, 95% CI 1.09-1.67, P = .005), adjusted II (HR = 1.26, 95% CI 1.00-1.58, P = .049), and adjusted III (HR = 1.33, 95% CI 1.07-1.65, P = .010) models. TD had a similar value range between N1 and N2 stages among different models. CONCLUSIONSAmong GC patients, TD is associated with survival and may have a role in the staging of patients. Abstract Background Gastric cancer (GC) treatment is determined by accurate tumor staging. The value of tumor deposit (TD) in prognostic prediction staging system is not yet determined. Methods We retrospectively analyzed clinical information on GC patients who underwent gastrectomy at the Department of General Surgery of the Chinese PLA General Hospital from July 2014 to June 2016. Propensity score matching (PSM) was performed to reduce the possibility of selection bias according to the presence of TD. Results Of the 1034 GC patients, 240 (23.21%) presented with TD, which was associated with younger age and larger tumor size (all P < .05). TD‐positive patients had a worse survival than TD‐negative patients before (P < .001) and after (P = .017) matching. Multivariable analysis showed that mortality risk of patients with TD increased by 58%, 62%, 37%, and 40% in the crude (HR = 1.58, 95% CI 1.32‐1.89, P < .001), adjusted I (HR = 1.62, 95% CI 1.35‐1.94, P < .001), adjusted II (HR = 1.37, 95% CI 1.13‐1.66, P = .001), and adjusted III (HR = 1.40, 95% CI 1.16‐1.68, P < .001) models before matching. Similarly, in the PSM cohort patients with TD had worse prognosis in the crude (HR = 1.32, 95% CI 1.07‐1.63, P = .011), adjusted I (HR = 1.35, 95% CI 1.09‐1.67, P = .005), adjusted II (HR = 1.26, 95% CI 1.00‐1.58, P = .049), and adjusted III (HR = 1.33, 95% CI 1.07‐1.65, P = .010) models. TD had a similar value range between N1 and N2 stages among different models. Conclusions Among GC patients, TD is associated with survival and may have a role in the staging of patients. Abstract Background Gastric cancer (GC) treatment is determined by accurate tumor staging. The value of tumor deposit (TD) in prognostic prediction staging system is not yet determined. Methods We retrospectively analyzed clinical information on GC patients who underwent gastrectomy at the Department of General Surgery of the Chinese PLA General Hospital from July 2014 to June 2016. Propensity score matching (PSM) was performed to reduce the possibility of selection bias according to the presence of TD. Results Of the 1034 GC patients, 240 (23.21%) presented with TD, which was associated with younger age and larger tumor size (all P < .05). TD‐positive patients had a worse survival than TD‐negative patients before ( P < .001) and after ( P = .017) matching. Multivariable analysis showed that mortality risk of patients with TD increased by 58%, 62%, 37%, and 40% in the crude (HR = 1.58, 95% CI 1.32‐1.89, P < .001), adjusted I (HR = 1.62, 95% CI 1.35‐1.94, P < .001), adjusted II (HR = 1.37, 95% CI 1.13‐1.66, P = .001), and adjusted III (HR = 1.40, 95% CI 1.16‐1.68, P < .001) models before matching. Similarly, in the PSM cohort patients with TD had worse prognosis in the crude (HR = 1.32, 95% CI 1.07‐1.63, P = .011), adjusted I (HR = 1.35, 95% CI 1.09‐1.67, P = .005), adjusted II (HR = 1.26, 95% CI 1.00‐1.58, P = .049), and adjusted III (HR = 1.33, 95% CI 1.07‐1.65, P = .010) models. TD had a similar value range between N1 and N2 stages among different models. Conclusions Among GC patients, TD is associated with survival and may have a role in the staging of patients. Background Gastric cancer (GC) treatment is determined by accurate tumor staging. The value of tumor deposit (TD) in prognostic prediction staging system is not yet determined. Methods We retrospectively analyzed clinical information on GC patients who underwent gastrectomy at the Department of General Surgery of the Chinese PLA General Hospital from July 2014 to June 2016. Propensity score matching (PSM) was performed to reduce the possibility of selection bias according to the presence of TD. Results Of the 1034 GC patients, 240 (23.21%) presented with TD, which was associated with younger age and larger tumor size (all P < .05). TD‐positive patients had a worse survival than TD‐negative patients before (P < .001) and after (P = .017) matching. Multivariable analysis showed that mortality risk of patients with TD increased by 58%, 62%, 37%, and 40% in the crude (HR = 1.58, 95% CI 1.32‐1.89, P < .001), adjusted I (HR = 1.62, 95% CI 1.35‐1.94, P < .001), adjusted II (HR = 1.37, 95% CI 1.13‐1.66, P = .001), and adjusted III (HR = 1.40, 95% CI 1.16‐1.68, P < .001) models before matching. Similarly, in the PSM cohort patients with TD had worse prognosis in the crude (HR = 1.32, 95% CI 1.07‐1.63, P = .011), adjusted I (HR = 1.35, 95% CI 1.09‐1.67, P = .005), adjusted II (HR = 1.26, 95% CI 1.00‐1.58, P = .049), and adjusted III (HR = 1.33, 95% CI 1.07‐1.65, P = .010) models. TD had a similar value range between N1 and N2 stages among different models. Conclusions Among GC patients, TD is associated with survival and may have a role in the staging of patients. Kaplan‐Meier curves for TD negative and positive gastric patients before and after propensity score matching. |
Author | Lin, Chen Zhi, Qiao Yixun, Lu Yi, Liu Shen, Qiao Yuhua, Liu Hongqing, Xi Kecheng, Zhang Wang, Zhang Shaoqing, Li Jiyang, Li Wanguo, Xue Jianxin, Cui Wenquan, Liang Yunhe, Gao |
AuthorAffiliation | 4 Medical Big Data Center Chinese People’s Liberation Army General Hospital Beijing China 1 Department of General Surgery & Institute of General Surgery Chinese PLA General Hospital Beijing China 3 Institute of Army Hospital Management Chinese People’s Liberation Army General Hospital Beijing China 2 Medical School of Chinese PLA Beijing China |
AuthorAffiliation_xml | – name: 4 Medical Big Data Center Chinese People’s Liberation Army General Hospital Beijing China – name: 1 Department of General Surgery & Institute of General Surgery Chinese PLA General Hospital Beijing China – name: 2 Medical School of Chinese PLA Beijing China – name: 3 Institute of Army Hospital Management Chinese People’s Liberation Army General Hospital Beijing China |
Author_xml | – sequence: 1 givenname: Liang orcidid: 0000-0001-5211-8148 surname: Wenquan fullname: Wenquan, Liang organization: Medical School of Chinese PLA – sequence: 2 givenname: Liu surname: Yuhua fullname: Yuhua, Liu organization: Chinese People’s Liberation Army General Hospital – sequence: 3 givenname: Cui surname: Jianxin fullname: Jianxin, Cui organization: Chinese PLA General Hospital – sequence: 4 givenname: Xi surname: Hongqing fullname: Hongqing, Xi organization: Chinese PLA General Hospital – sequence: 5 givenname: Zhang surname: Kecheng fullname: Kecheng, Zhang organization: Chinese PLA General Hospital – sequence: 6 givenname: Li surname: Jiyang fullname: Jiyang, Li organization: Chinese PLA General Hospital – sequence: 7 givenname: Gao surname: Yunhe fullname: Yunhe, Gao organization: Medical School of Chinese PLA – sequence: 8 givenname: Liu surname: Yi fullname: Yi, Liu organization: Medical School of Chinese PLA – sequence: 9 givenname: Zhang surname: Wang fullname: Wang, Zhang organization: Medical School of Chinese PLA – sequence: 10 givenname: Li surname: Shaoqing fullname: Shaoqing, Li organization: Medical School of Chinese PLA – sequence: 11 givenname: Lu surname: Yixun fullname: Yixun, Lu organization: Medical School of Chinese PLA – sequence: 12 givenname: Qiao surname: Shen fullname: Shen, Qiao organization: Chinese People’s Liberation Army General Hospital – sequence: 13 givenname: Xue surname: Wanguo fullname: Wanguo, Xue email: drqiaozhi@126.com organization: Chinese People’s Liberation Army General Hospital – sequence: 14 givenname: Qiao orcidid: 0000-0002-2158-4901 surname: Zhi fullname: Zhi, Qiao organization: Chinese PLA General Hospital – sequence: 15 givenname: Chen orcidid: 0000-0001-6935-1552 surname: Lin fullname: Lin, Chen email: chenlin@301hospital.com.cn organization: Chinese PLA General Hospital |
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CitedBy_id | crossref_primary_10_1007_s11605_023_05668_y crossref_primary_10_1186_s12957_022_02507_3 crossref_primary_10_1016_j_heliyon_2021_e07185 crossref_primary_10_1186_s12957_022_02773_1 crossref_primary_10_1016_j_medp_2024_100025 crossref_primary_10_1016_j_surg_2023_09_039 |
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Keywords | tumor deposit gastric cancer staging survival |
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Notes | Funding information This study was supported by the National Nature Science Foundation of China (No. 81672319, 81602507, 81773135, and 81972790) and National Key Research and Development Project (2017YFC0908305). ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Liang Wenquan, Liu Yuhua and Cui Jianxin contributed equally to this work. |
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Snippet | Background
Gastric cancer (GC) treatment is determined by accurate tumor staging. The value of tumor deposit (TD) in prognostic prediction staging system is... Gastric cancer (GC) treatment is determined by accurate tumor staging. The value of tumor deposit (TD) in prognostic prediction staging system is not yet... Abstract Background Gastric cancer (GC) treatment is determined by accurate tumor staging. The value of tumor deposit (TD) in prognostic prediction staging... BackgroundGastric cancer (GC) treatment is determined by accurate tumor staging. The value of tumor deposit (TD) in prognostic prediction staging system is not... BACKGROUNDGastric cancer (GC) treatment is determined by accurate tumor staging. The value of tumor deposit (TD) in prognostic prediction staging system is not... Kaplan‐Meier curves for TD negative and positive gastric patients before and after propensity score matching. Abstract Background Gastric cancer (GC) treatment is determined by accurate tumor staging. The value of tumor deposit (TD) in prognostic prediction staging... |
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SubjectTerms | Age Clinical Cancer Research Colorectal cancer Gastrectomy Gastric cancer Hospitals Laparoscopy Lymphatic system Medical prognosis Medical records Metastasis Original Research Patients staging Statistical analysis Studies Surgery Survival Survival analysis tumor deposit |
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Title | Tumor deposit serves as a prognostic marker in gastric cancer: A propensity score‐matched analysis comparing survival outcomes |
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