Evidence map›Paper›PMID 39587468›Full record

ArticleBMC gastroenterology2024

Developing and validation a prognostic model for predicting prognosis among synchronous colorectal cancers patients using combined log odds ratio of positive lymph nodes: a SEER database study.

Yue Ma, Bangquan Chen, Yayan Fu, Jun Ren, Daorong Wang

Abstract readValidation Study
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Article in BMC gastroenterology, 2024. 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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5 · Who and what money

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5 authors.

Yue MaDepartment of Gastrointestinal Surgery, Northern Jiangsu People's Hospital, Clinical Teaching Medical School of Nanjing University, No.98 Nantong West Road, Yangzhou, Jiangsu Province, 225001, China.
Bangquan ChenMedical College of Yangzhou University, Yangzhou, 225001, China.
Yayan FuMedical College of Yangzhou University, Yangzhou, 225001, China.
Jun RenNorthern Jiangsu People's Hospital Affiliated to Yangzhou University, Yangzhou, 225001, China.
Daorong WangDepartment of Gastrointestinal Surgery, Northern Jiangsu People's Hospital, Clinical Teaching Medical School of Nanjing University, No.98 Nantong West Road, Yangzhou, Jiangsu Province, 225001, China. wdaorong666@sina.com.

Funding

The research was sponsored by Key Laboratory of Basic and Clinical Transformation of Digestive /Metabolic Diseases of Yangzhou City No.YZ2020159
6 · The paper itself

Abstract

purposeThe aim of the study is to identify risk factors for the prognosis and survival of synchronous colorectal cancer and to create and validate a functional Nomogram for predicting cancer-specific survival in patients with synchronous colorectal cancer.

methodsSynchronous colorectal cancers cases were retrieved from the Surveillance, Epidemiology, and End Results database retrospectively, then they were randomly divided into training (n = 3371) and internal validation (n = 1440) sets, and a set of 100 patients from our group was used as external validation. Risk factors for synchronous colorectal cancer were determined using univariate and multivariate Cox regression analyses, and two Nomograms were established to forecast the overall survival and cancer-specific survival, respectively. We assessed the Nomogram performance in terms of discrimination and calibration. Bootstrap resampling was used as an internal verification method, and we select external data from our hospital as independent validation sets.

resultsTwo Nomograms are established to predict the overall survival and cancer-specific survival. In OS Nomogram, sex, age, marital status, ttumor pathological grade, AJCC TNM stage, preoperative serum CEA level, LODDS, radiotherapy and chemotherapy were determined as prognostic factors. In CSS Nomogram, age and marital status, AJCC TNM stage, tumor pathological grade, preoperative serum CEA level, LODDS, radiotherapy and chemotherapy were determined as prognostic factors.The C-indexes for the forecast of overall survival were 0.70, and the C-index was 0.68 for the training and internal validation cohort, respectively. The C-indexes for the forecast of cancer-specific survival were 0.75, and the C-index was 0.74 for the training and internal validation cohort, respectively. The Nomogram calibration curves showed no significant deviation from the reference line, indicating a good level of calibration. Both C-index and calibration curves indicated noticeable performance of newly established Nomograms.

conclusionsThose Nomograms with risk rating system can identify high risk patients who require more aggressive therapeutic intervention and longer and more frequent follow-up scheme, demonstrated prognostic efficiency.

Indexed as

Colorectal NeoplasmsNeoplasms, Multiple PrimaryNeoplasm StagingNomogramsSEER ProgramAdultAgedCarcinoembryonic AntigenFemaleHumansLymphatic MetastasisLymph NodesMaleMiddle AgedOdds RatioPrognosisCarcinoembryonic AntigenCancer-specific survivalNomogramOverall survivalSEERSynchronous colorectal cancers

Identifiers

PMID39587468
PMCPMC11587701

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.