Signet Ring Cell Carcinoma and Risk of Multiple Gastrointestinal Cancers
Data Collection
Collected from past medical records and data - RetrospectiveAdenocarcinoma+14
+ Carcinoma
+ Colonic Diseases
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Summary
Study start date: January 1, 2000
Actual date on which the first participant was enrolled.This study focuses on a rare and aggressive type of colorectal cancer known as signet ring cell carcinoma (SRCC) and its link to the development of additional cancers in the gastrointestinal tract. By examining data from the SEER database, covering the years 2000 to 2021, researchers aim to understand the risk of developing new gastrointestinal cancers shortly after an initial SRCC diagnosis. This research is vital as it seeks to uncover patterns that could improve monitoring and treatment strategies for those affected by this aggressive cancer type, potentially leading to better outcomes and survival rates. The study is observational and involves analyzing historical data rather than testing new treatments. It calculates something called the standardized incidence ratio, which helps to compare the number of new cancer cases in patients with SRCC to what would be expected in the general population. The focus is on identifying new cancers in different parts of the gastrointestinal tract, such as the stomach, liver, or pancreas, within a specific timeframe after the initial cancer diagnosis. This approach helps to pinpoint any increased risk of secondary cancers in these patients, potentially guiding future screenings or preventive measures.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.8171 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Inclusion Criteria: * Patients diagnosed with primary colorectal SRCC between 2000 and 2021 * Latency exclusion period of two months Exclusion Criteria: * patients with unknown age data
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Study Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location