Evidence map›Paper›PMID 37735712›Full record

ArticleEuropean journal of medical research2023

Development and validation of a competitive risk model in patients with rectal cancer: based on SEER database.

Ruobing Hu, Xiuling Li, Xiaomin Zhou, Songze Ding

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Article in European journal of medical research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ruobing HuDepartment of Gastroenterology and Hepatology, People's Hospital of Zhengzhou University, No.7 Weiwu Road, Zhengzhou, 450003, Henan, China.
Xiuling LiDepartment of Gastroenterology and Hepatology, People's Hospital of Zhengzhou University, No.7 Weiwu Road, Zhengzhou, 450003, Henan, China.
Xiaomin ZhouDepartment of Infection Disease, Shanghai Jinshan District Tinglin Hospital, Shanghai, 201505, China.
Songze DingDepartment of Gastroenterology and Hepatology, People's Hospital of Zhengzhou University, No.7 Weiwu Road, Zhengzhou, 450003, Henan, China. dingsongze@hotmail.com.

Funding

Henan Provincial Government-Health and Family Planning Commission Research Science Innovative Talents Project 51282
6 · The paper itself

Abstract

backgroundRectal cancer is one of the most common malignancies. To predict the specific mortality risk of rectal cancer patients, we constructed a predictive nomogram based on a competing risk model.

methodsThe information on rectal cancer patients was extracted from the SEER database. Traditional survival analysis and specific death analysis were performed separately on the data.

resultsThe present study included 23,680 patients, with 16,580 in the training set and 7100 in the validation set. The specific mortality rate calculated by the competing risk model was lower than that of the traditional survival analysis. Age, Marriage, Race, Sex, ICD-O-3Hist/Behav, Grade, AJCC stage, T stage, N stage, Surgery, Examined LN, RX SUMM-SURG OTH, Chemotherapy, CEA, Deposits, Regional nodes positive, Brain, Bone, Liver, Lung, Tumor size, and Malignant were independent influencing factors of specific death. The overall C statistic of the model in the training set was 0.821 (Se = 0.001), and the areas under the ROC curve for cancer-specific survival (CSS) at 1, 3, and 5 years were 0.842, 0.830, and 0.812, respectively. The overall C statistic of the model in the validation set was 0.829 (Se = 0.002), and the areas under the ROC curve for CSS at 1, 3, and 5 years were 0.851, 0.836, and 0.813, respectively.

conclusionsThe predictive nomogram based on a competing risk model for time-specific mortality in patients with rectal cancer has very desirable accuracy. Thus, the application of the predictive nomogram in clinical practice can help physicians make clinical decisions and follow-up strategies.

Indexed as

PhysiciansRectal NeoplasmsBrainHumansLiverNomogramsCompetitive risk modelRectal cancerSEER databaseValidation

Identifiers

PMID37735712
PMCPMC10515244

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