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Screening Platform for Clinical Trials in Advanced Colorectal Cancer

Screening Platform of the EORTC for Clinical Trials in Advanced Colorectal Cancer SPECTAcolor

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01723969
Acronym
SPECTAcolor
Enrollment
668
Registered
2012-11-08
Start date
2013-09-30
Completion date
2020-03-10
Last updated
2022-07-07

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

Conditions

Advanced Colorectal Cancer, Colorectal Cancer

Brief summary

The EORTC GastroIntestinal Tract Cancer Group and the EORTC HeadQuarters wish to set up a European screening platform for advanced colo-rectal cancer (CRC) patients. The goal of this screening platform is to provide quick access to new drugs to patients by offering a new structure for clinical trials. Currently some of the most challenging clinical questions arise from the molecular sub-division of CRC that would theoretically allow to inhibit the specific, altered pathways in the patients. A major problem for trials in this personalized medicine is that the low frequency of the different mutations requires a high effort for screening and identifying the patients. The EORTC CRC screening platform will hopefully offer a feasible and efficient way to characterize the patients on the molecular basis of their tumors and allow to offer them rapid and preferential participation in clinical studies with new drugs targeted to their specific pathway alterations.

Interventions

Tumour markers testing in patients advanced or metastatic colo-rectal cancer.

Sponsors

European Organisation for Research and Treatment of Cancer - EORTC
Lead SponsorNETWORK

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Colo-rectal cancer (advanced or metastatic) * Before patient registration, written informed consent must be given according to ICH/GCP, and national/local regulations.

Exclusion criteria

* Absence of patient's consent

Design outcomes

Primary

MeasureTime frameDescription
Tumour markers assessmentWithin 1 week after patient registrationFive basic tumour markers will be tested: Kras, nras, braf, MSI and PKI3

Countries

Belgium, Cyprus, France, Germany, Greece, Italy, Poland, Portugal, Spain, Sweden, Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026