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Supplementary research table presenting clinicopathological variables and statistical comparison between ISGHIGH and ISGLOW patient subgroups within the Rotterdam cohort in relation to age, tumor features, and response to first-line tamoxifen.
Document type: Supplementary table
Study cohort: Rotterdam cohort
Topic: Clinicopathological characteristics and treatment response
Medical field: Oncology
Variables described: Age, tumor characteristics, response to first-line tamoxifen
Subgroups: ISGHIGH, ISGLOW
Statistical analysis: Statistical tests for subgroup differences indicated for each variable
Treatment referenced: First-line tamoxifen
Population: Patients included in the Rotterdam cohort
Section: Supplementary material
Table number: 2
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Supplementary table 1. Correlation between CAC grade and clinicopathological characteristics in validation cohort.
Year: 2023
Region: Global
Topic: Medical research
Document type: Research table
Institution: Not specified
Author: Not specified
Target audience: Medical professionals, researchers
Duration: Not specified
Approval date: Not specified
Modification date: Not specified
Note: Contextual description
Supplemental Figures and Tables on Survival Outcomes and Clinicopathological Characteristics in WUH and SEER Cohorts
Document type: Supplemental digital content
Content components: Figures and tables
Subject area: Oncology
Research focus: Survival analysis and clinicopathological characteristics
Clinical variables: Retrieved lymph nodes, chemoradiotherapy, adjuvant therapy, tumor stage and size
Patient groups: N0 and N1 patients
Data sources: WUH cohort and SEER cohort
Institutions / databases: Wuhan Union Hospital; Surveillance, Epidemiology, and End Results program
Measured outcomes: Overall survival and prognostic differences
Clinical treatments analyzed: Chemotherapy, radiotherapy, chemoradiotherapy
Population characteristics: Age, sex, BMI, tumor grade, tumor stage, tumor size, nerve invasion, vascular invasion
Tables included: Clinicopathological features before and after propensity score matching
Figures included: Survival curves and cutoff value analyses for retrieved lymph nodes
Association between DNM3OS Expression and Clinicopathological Characteristics of Gastric GIST Patients
Source section: Table 3
Disease: Gastric gastrointestinal stromal tumor (GIST)
Biomarker: DNM3OS expression
Variables analyzed: Gender; Age; Tumor size; Mitotic count; NIH risk classification; Mutational status; Prior TKI treatment
Sample size: 251 patients
Low expression group: n=143
High expression group: n=108
Mutation analysis subset: n=130
Statistical methods: P value comparison; Fisher exact test
Genetic markers: KIT exon 9/11; PDGFRA exon 18; WT
Clinical parameters: Tumor size (cm); Mitotic count per 50 HPFs; NIH risk classification categories
Therapeutic variable: Prior tyrosine kinase inhibitor (TKI) treatment
Field of study: Oncology; Molecular pathology
Clinicopathological and Demographics Data of Non-Metastatic Rectal Cancer Cohort by Treatment
Year: 2026
Study Type: Supplementary Table
Cohort Size: 76 patients
Treatment Groups: CRT, I+CRT, Unfront surgery
Parameters Measured: Age, Gender, Tumor Stage, EMVI, CRM, Lateral Lymph Nodes, CEA, CA19.9, NPS score, Histology, MMR status, CDX2 expression, HER2/Neu expression, CD3-CD8 TILs density, PD-L1 expression, Perineural invasion, Vascular invasion, pEMVI, pCRM
Data Source: Clinical records and histopathological analysis
Statistical Significance: p-values provided for each parameter
Topics: ISGHIGH ISGLOW clinicopathological