Skip to content

Metastatic Colorectal Cancer. Real-World Data Analysis.

The Treatment Choices, Duration and Outcomes in Patients With Ras Wild Type (RAS WT) Metastatic Colorectal Cancer (mCRC). Retrospective, Multi-Center, Real-World Data Analysis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04757311
Acronym
RWD-mCRC-001
Enrollment
1750
Registered
2021-02-17
Start date
2020-08-01
Completion date
2021-10-01
Last updated
2021-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metastatic Colorectal Cancer

Brief summary

The Treatment Choices, Duration and Outcomes in Patients with Ras Wild Type (RAS WT) Metastatic Colorectal Cancer (mCRC). Retrospective, Multi-Center, Real-World Data Analysis

Detailed description

In this study, with the given rationale is to reveal treatment approaches, survival data, side effect profile and their management in our country in RAS WT mCRC patients by means of the real-world data collection.

Interventions

None listed

Sponsors

Istanbul Medeniyet University
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

1. Patients who have been histologically diagnosed with mCRC 2. Patients over the age of 18 3. Patients receiving at least a cycle systemic treatment for metastatic disease 4. RAS wild type patients 5. Patients who has demographic, histopathological and clinical information

Exclusion criteria

1. Patients diagnosed as mCRC but only referred to BSC 2. Patients with RAS mutation 3. Patients who were included in any clinical trial except standard treatments during their treatment

Design outcomes

Primary

MeasureTime frameDescription
Percentage of use anti-EGFR agentsthroughout of treatment, 3 yearsThe anti-EGFR agent selection
Progression Free Survival (PFS)3 years treatmentPFS three years after initiation of treatment with anti-EGFR agents

Secondary

MeasureTime frameDescription
Advers eventsthroughout of treatment, 3 yearsAdvers event of anti EGFR is defined as any untoward or unfavourable medical occurrence, including any abnormal sign, symptom, or disease, temporally associated with the patient's participation. The CTCAE v.4.0 will use in this research.

Other

MeasureTime frameDescription
Percentage of use biologics in right side tumors.throughout of treatment, 3 yearsTreatment selection in right side tumors.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026