Detection of CF-DNA in Patients With Gastrointestinal Stromal Tumors (GIST)

Gastrointestinal Stromal Tumors Clinical Trial

Official title:

Prospective, Explorative Trial for the Detection of Circulating Cell-free Tumor DNA in the Plasma of Patients With Gastrointestinal Stromal Tumors (GIST)Harboring Activating Mutations of CKIT or PDGFRA Pre/Post Surgery or Pre/Under Treatment With a Tyrosine Kinase Inhibitor or Progressive Disease Irrespective of Current or Planned Treatment. An Open-label, Non-randomized, Multicenter Phase IIIb Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01462994
• Other study ID #: CSTI571BDE78T
• Status: Completed
• Phase: Phase 3
• First received: October 25, 2011
• Last updated: March 16, 2016
• Start date: November 2011
• Est. completion date: March 2016

Study information

• Verified date: March 2016
• Source: Technische Universität München
• Contact: n/a
• Is FDA regulated: No
• Health authority: Germany: Federal Institute for Drugs and Medical Devices
• Study type: Interventional

Clinical Trial Summary

Activating mutations of the kinases CKIT or PDGFRA can be detected in 90% of cases by DNA sequence analysis of a pathological specimen. These mutated genomic DNA fragments are highly specific for the tumor and are released by the tumor into the circulation. Allele-specific PCR can be used to specifically amplify and quantify mutated CKIT and PDGFR DNA fragments.

The current trial aims to evaluate whether tumor DNA carrying mutations for CKIT and PDGFRA can be detected and quantified in the plasma of patients with active GIST, and whether detection can be correlated with the clinical course of disease either under therapy or in progressive disease irrespective of current therapy.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 25
• Est. completion date: March 2016
• Est. primary completion date: December 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Signed written informed consent

• Male or female patients aged >= 18 years

• Histologically confirmed GIST

• Known activating mutation of CKIT or PDGFRA and tissue sample can be provided for central mutation analysis or mutation status unknown and tissue sample can be provided for central mutation analysis at baseline

• Routinely planned follow-up visits in no longer than three months intervals (+ 14 days) including local standard of care diagnostic imaging (CT, PET- CT, or MRI)

• At least one GIST lesion that can be measured by CT, PET-CT, or MRI

• Planned surgery of one or more disease manifestations or planned TKI treatment (such as imatinib or sunitinib) in neoadjuvant or palliative intention or disease progression irrespective of current/planned treatment

• Life expectancy of at least three months

Exclusion Criteria:

• Wild type sequence for CKIT exon 9, 11, 13, 14, 17, 18 and PDGFRA exon 18

• Tissue sample can not be provided for central mutation analysis

• Surgery of primary or progressive lesions already completed and currently no evidence of progressive lesions

• Patients currently receiving adjuvant TKI treatment after surgery and no evidence of progressive lesions

• Patients currently receiving palliative TKI treatment and no evidence of progressive lesions

• Planned follow-up intervals including CT, PET-CT or MRI at more than three months intervals (+ 14 days)

• Coexisting medical condition or treatment that could interfere with the ability of the patient to comply with planned treatment interventions (surgery or TKI treatment) or regular follow-up visits

• Patients unwilling to or unable to comply with the planned therapeutic intervention (surgery or TKI treatment) or to comply with the regular follow-up visits including blood sample collection

• Pregnancy and lactation

• Presence of chronic inflammatory diseases, autoimmune diseases, or liver cirrhosis

• Known HIV and/or hepatitis B or C infection

• Other malignancies within the past 3 years except for adequately treated carcinoma of the cervix and basal or squamous cell carcinoma of the skin

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

• Gastrointestinal Stromal Tumors

Intervention

Other:
• Blood will be withdrawn at baseline and in intervals of 3 months for a total period of 2 years

Locations

Country	Name	City	State
Germany	Klinikum rechts der Isar - III. Medizinische Klinik und Poliklinik	Munic	Bavaria

Sponsors (1)

Lead Sponsor	Collaborator
Technische Universität München

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percentage of patients with histologically proven GIST, measurable lesion in imaging and activating CKIT and PDGFRA mutation, where detection of tumor specific DNA encoding for mutated CKIT or PDGFA is possible in the plasma at least at one timepoint			No