The Clinicopathological Features and Overall Survival of Patients With Gastric Neuroendocrine Carcinoma
Objectives: Gastric neuroendocrine carcinoma (GNEC) is a class of rare histological subtypes in gastric cancer (GC). This retrospective case-control study aimed to explore the clinicopathological features and overall survival (OS) of patients with GNEC. Methods: A large population of GNEC and intest...
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2021
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oai:doaj.org-article:7b52e8d6ac874ed79d7f8192ab4e28ab2021-11-21T02:04:31ZThe Clinicopathological Features and Overall Survival of Patients With Gastric Neuroendocrine Carcinoma1533-033810.1177/15330338211055340https://doaj.org/article/7b52e8d6ac874ed79d7f8192ab4e28ab2021-11-01T00:00:00Zhttps://doi.org/10.1177/15330338211055340https://doaj.org/toc/1533-0338Objectives: Gastric neuroendocrine carcinoma (GNEC) is a class of rare histological subtypes in gastric cancer (GC). This retrospective case-control study aimed to explore the clinicopathological features and overall survival (OS) of patients with GNEC. Methods: A large population of GNEC and intestinal-type GC (IGC) patients were extracted from the Surveillance, Epidemiology, and End Results (SEER) database. The 1:1 propensity score matching (PSM) analysis was initiated to adjust the confounders between GNEC and IGC cohorts. Kaplan-Meier (KM) plots with log-rank tests were used to compare the survival differences in GNEC versus IGC. Additionally, Cox proportional hazard regression models were adopted to characterize the prognostic factors relevant to OS of the GNEC patients. Results: An entity of 4596 patients were collected, including 3943 (85.8%) IGC patients and 653 (14.2%) GNEC patients. The PSM analysis well-balanced all confounders in GNEC versus IGC (all P > .05). The KM plots showed that GNEC had significantly superior OS to IGC both before and after PSM analysis. Before PSM, the median OS was 52 (33.6-70.4) months in GNEC versus 32 (29.3-34.7) months in IGC ( P = .0015). After PSM, the median OS was 26 (18.3-33.7) months in GNEC versus 21 (17.7-24.3) months in IGC ( P = .0039). Stratified analysis indicated that GNEC had superior survivals to IGC in early stage patients and those who received surgery. In Cox regression analysis, age ≥ 60, tumor size > 50 mm, stage II-IV, T2, and N3 were independent risk factors for the GNEC patients (hazard ratio [HR]>1, P < .05). By contrast, year 2010 to 2015, female, and surgery were independent protective factors for these patients (HR < 1, P < .05). Conclusions: GNEC has unique clinicopathological features quite different from IGC and may have a superior survival to IGC in early stage patients. The prognostic factors identified here may assist the clinicians to more individually treat these patients.Bin Xu MDYuxin Chu MDQinyong Hu MDQibin Song MDSAGE PublishingarticleNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENTechnology in Cancer Research & Treatment, Vol 20 (2021) |
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Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 |
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Neoplasms. Tumors. Oncology. Including cancer and carcinogens RC254-282 Bin Xu MD Yuxin Chu MD Qinyong Hu MD Qibin Song MD The Clinicopathological Features and Overall Survival of Patients With Gastric Neuroendocrine Carcinoma |
description |
Objectives: Gastric neuroendocrine carcinoma (GNEC) is a class of rare histological subtypes in gastric cancer (GC). This retrospective case-control study aimed to explore the clinicopathological features and overall survival (OS) of patients with GNEC. Methods: A large population of GNEC and intestinal-type GC (IGC) patients were extracted from the Surveillance, Epidemiology, and End Results (SEER) database. The 1:1 propensity score matching (PSM) analysis was initiated to adjust the confounders between GNEC and IGC cohorts. Kaplan-Meier (KM) plots with log-rank tests were used to compare the survival differences in GNEC versus IGC. Additionally, Cox proportional hazard regression models were adopted to characterize the prognostic factors relevant to OS of the GNEC patients. Results: An entity of 4596 patients were collected, including 3943 (85.8%) IGC patients and 653 (14.2%) GNEC patients. The PSM analysis well-balanced all confounders in GNEC versus IGC (all P > .05). The KM plots showed that GNEC had significantly superior OS to IGC both before and after PSM analysis. Before PSM, the median OS was 52 (33.6-70.4) months in GNEC versus 32 (29.3-34.7) months in IGC ( P = .0015). After PSM, the median OS was 26 (18.3-33.7) months in GNEC versus 21 (17.7-24.3) months in IGC ( P = .0039). Stratified analysis indicated that GNEC had superior survivals to IGC in early stage patients and those who received surgery. In Cox regression analysis, age ≥ 60, tumor size > 50 mm, stage II-IV, T2, and N3 were independent risk factors for the GNEC patients (hazard ratio [HR]>1, P < .05). By contrast, year 2010 to 2015, female, and surgery were independent protective factors for these patients (HR < 1, P < .05). Conclusions: GNEC has unique clinicopathological features quite different from IGC and may have a superior survival to IGC in early stage patients. The prognostic factors identified here may assist the clinicians to more individually treat these patients. |
format |
article |
author |
Bin Xu MD Yuxin Chu MD Qinyong Hu MD Qibin Song MD |
author_facet |
Bin Xu MD Yuxin Chu MD Qinyong Hu MD Qibin Song MD |
author_sort |
Bin Xu MD |
title |
The Clinicopathological Features and Overall Survival of Patients With Gastric Neuroendocrine Carcinoma |
title_short |
The Clinicopathological Features and Overall Survival of Patients With Gastric Neuroendocrine Carcinoma |
title_full |
The Clinicopathological Features and Overall Survival of Patients With Gastric Neuroendocrine Carcinoma |
title_fullStr |
The Clinicopathological Features and Overall Survival of Patients With Gastric Neuroendocrine Carcinoma |
title_full_unstemmed |
The Clinicopathological Features and Overall Survival of Patients With Gastric Neuroendocrine Carcinoma |
title_sort |
clinicopathological features and overall survival of patients with gastric neuroendocrine carcinoma |
publisher |
SAGE Publishing |
publishDate |
2021 |
url |
https://doaj.org/article/7b52e8d6ac874ed79d7f8192ab4e28ab |
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