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ACCORD-CRC: Australian Comprehensive Cancer Outcomes and Research Database: COLORECTAL

ABSTRACT: Interventions: Data collected will include: •Patient demographics and characteristics •Disease clinicopathological and molecular features •Treatment history •Outcomes and survival •Follow-up data at 3 to 6-montly intervals until death There is no participant contact for clinical data collection as a waiver of consent is in place. Participants will be asked to consent to any removed cancer samples being stored in tissue bank. Primary outcome(s): Clinical data collection target of 10,000 colorectal cancer (CRC) patients as assessed by CRC registry data. This outcome is assessed by the use of statistical analytics software SAS to analyse the data and prepare regular reports on the target numbers. [10 years] Study Design: Purpose: Natural history;Duration: Longitudinal;Selection: Defined population;Timing: Both

DISEASE(S): Colorectal Cancer,Cancer-bowel-back Passage (rectum) Or Large Bowel (colon)

PROVIDER: 2470027 | ecrin-mdr-crc |

REPOSITORIES: ECRIN MDR

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