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Completed

NCT Number: NCT01212718

Response Prediction in Metastasized Colorectal Cancer Using Intratumoral Thymidylate Synthase

The aim of the study was to evaluate the feasibility of TS determination in a multicenter trial setting using a central facility for measurement and confirm its role as predictive factor for 5-FU treatment in MCRC.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Department of General, Visceral, and Transplantations Surgery, Univeristy of Ulm

Ulm, Germany

About this study

Eligible were patients with non-resectable metastasized or recurrent histologically proven CRC with the presence of a reference lesion two-dimensional measurable and accessible for a biopsy.The biopsy was taken from the reference lesion either by surgery during primary tumor resection, by trans-cutaneous true-cut needle biopsy or by trans-anal approach. Intratumoral relative TS mRNA expression levels were determined using samples shipped in RNA-preserving solution or as glass slides after microdissection of tumor cells. An independent company stratified the patients according to ther relative TS mRNA expression level in TS low and TS high followed by randomization to receive either FUFA of Folfiri. Response to chemotherapy was evaluated and documented according to the RECIST criteria after every therapy cycle.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patients (>= 18 years) with non-resectable metastasized or recurrent histologically proven CRC with the presence of a reference lesion two-dimensional measurable and accessible for a biopsy
  • a performance status WHO 0-2 (Karnofsky >= 60%)
  • an estimated life expectancy of at least 3 months
  • written informed consent

Exclusion criteria

  • patients older than 75 years not fulfilling these criteria
  • brain metastases or a secondary cane
  • a history of a systemic palliative chemotherapy
  • and an adjuvant chemotherapy (within 6 months)
  • pregnant or nursing women
  • a known allergy toward irinotecanhydroclorid or of any ingredients of Campto or other severe medical
  • laboratory and social conditions not allowing chemotherapy and follow-up

Treatment and study plan

FUFA

Drug

2600/500 mg/m2 i.v. 24 h via port, 1 time weekly for six weeks, than have a break for 2 weeks (=8 weeks for 1 cycle)

systemic chemotherapy

Drug

CPT-11, 80 mg/m2 for 90 minutes and 5 FU/FA 2000/500 mg/m2 iv. 24h via port; 1 time weekly for six weeks, than have a break for 2 weeks

Primary outcomes

  1. Best response to first-line chemotherapy (recist)

    Time frame: 1 year

    Response to chemotherapy was evaluated and documented according to the RECIST criteria after every therapy cycle (every two months).

Secondary outcomes

  1. overall survival, toxicity, treatment related complications, time to progression

    Time frame: 3-year

    See above.

Sponsors and collaborators

Lead sponsor

University of Ulm

Other

Collaborators

  • Medac, Hamburg, Germany
  • Pfizer, Berlin Germany
  • Study Group Oncology of Gastrointestinal Tumors (FOGT)

Registry information

Official study title

Stratified and Randomized Multi-center Phase II - to Determine Potential Benefit of Treating Patients With Advanced Colorectal Cancer According to the Intratumoral TS RNA Levels

Acronym: FOGT5

Important dates

Study start
2001
Primary completion
2010
Study completion
2010
First posted
Oct 1, 2010
Registry last updated
Oct 1, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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