Circulating Cell-free Tumor DNA in the Plasma of Patients With Gastrointestinal Stromal Tumors (GIST)

Sponsor
Fondazione del Piemonte per l'Oncologia (Other)
Overall Status
Unknown status
CT.gov ID
NCT02443948
Collaborator
(none)
60
1
48
1.3

Study Details

Study Description

Brief Summary

This observational study is proposed to evaluate if the trend in the levels of cf-DNA evaluated on a sample of peripheral blood may be related to different clinical behaviors of the disease monitored by radiological investigations conducted.

Condition or Disease Intervention/Treatment Phase
  • Other: Vena puncture for blood collection

Detailed Description

Demetri and colleagues presented, at the AACR and ASCO Annual Meeting 2013, an exploratory analysis to assess GIST genotypes on patients in the GRID study. Mutations in the KIT gene were detected in 58 percent of the blood samples compared with 66 percent of the tumor tissue samples (31). However, when focusing their analysis on secondary KIT mutations, which are the mutations that drive resistance to targeted therapies like imatinib and sunitinib, the researchers found mutations in 47 percent of blood samples compared with only 12 percent of tissue samples. In addition, nearly half of blood samples in which secondary KIT mutations were found, harbored multiple secondary mutations. Therefore, cf-DNA may become an efficient marker of mutational GIST status and disease itself.

On this basis, this trial aims to evaluate whether tumor DNA carrying mutations (for KIT, PDGFRα, BRAF, RAS, SDH) can be detected and quantified in the plasma of patients with GISTs, either with active disease or during follow-up, and whether detection can be correlated with the disease status.

Study Design

Study Type:
Observational
Anticipated Enrollment :
60 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Circulating Cell-free Tumor DNA in the Plasma of Patients With Gastrointestinal Stromal Tumors (GIST): Detection and Correlation With Disease Status Assessed by Conventional Technique. Prospective Observational Study
Study Start Date :
Jun 1, 2014
Anticipated Primary Completion Date :
Dec 1, 2017
Anticipated Study Completion Date :
Jun 1, 2018

Arms and Interventions

Arm Intervention/Treatment
adjuvant/follow up setting

Other: Vena puncture for blood collection
Cf-DNA blood samples will be collected in EDTA tubes (20 ml) during the routine blood test

neo-adjuvant setting

Other: Vena puncture for blood collection
Cf-DNA blood samples will be collected in EDTA tubes (20 ml) during the routine blood test

advanced disease

Other: Vena puncture for blood collection
Cf-DNA blood samples will be collected in EDTA tubes (20 ml) during the routine blood test

Outcome Measures

Primary Outcome Measures

  1. Correlation of change in cf-DNA levels with disease status in GIST patients harboring specific DNA mutations [baseline, every 12 weeks, up to 2 years]

    To assess the correlation of change in cf-DNA levels with disease status evaluated according to RECIST criteria v 1.1

Secondary Outcome Measures

  1. Clearance of cf-DNA levels after surgery in GIST patients harboring specific DNA mutations [the day before surgery, every 12 weeks, up to 2 years]

    To evaluate the time (half-life esteem) of cf-DNA levels clearance after definitive surgery

  2. Detection of secondary mutations in KIT, PDGFRα and/or other genes [baseline, every 12 weeks, up to 2 years]

    To evaluate the possibility to detect secondary mutations in KIT, PDGFRα and/or other genes

  3. Correlation of cf-DNA levels with overall survival (OS) [baseline and up to 2 years]

    To evaluate the correlation between cf-DNA levels and overall survival (time from the date of enrollment to date of death or to the date being censored at two years, whichever occurs first)

  4. Correlation of detection of secondary mutations in KIT, PDGFRα and/or other genes with radiological disease progression [baseline, every 12 weeks, up to 2 years]

    To correlate the detection of secondary mutations in KIT, PDGFRα and/or other genes with radiological disease progression according to RECIST criteria v 1.1

  5. Correlation of the level of cf-DNA related to disease status in GIST patients harboring specific DNA mutations [baseline, every 12 weeks, up to 2 years]

    To assess if the cf-DNA levels are related to disease status detected according to Choi criteria.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
  • Male or female patients aged >= 18 years

  • Histologically confirmed diagnosis of GIST of any anatomical location either by biopsy or surgical specimen

  • Available archival tumor tissue

  • Signed informed consent form

Exclusion Criteria:
  • Impossibility to ensure adequate clinical and serum sample follow-up

  • Serious psychiatric disease that precludes informed consent or limits compliance

Contacts and Locations

Locations

Site City State Country Postal Code
1 Fondazione del Piemonte per l'Oncologia Candiolo TO Italy 10060

Sponsors and Collaborators

  • Fondazione del Piemonte per l'Oncologia

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Fondazione del Piemonte per l'Oncologia
ClinicalTrials.gov Identifier:
NCT02443948
Other Study ID Numbers:
  • cf-DNA GIST
First Posted:
May 14, 2015
Last Update Posted:
Feb 14, 2017
Last Verified:
Feb 1, 2017
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 14, 2017