Official Title
Next Generation pErsonalized tX(Therapy) With Plasma DNA Trial-2 in Refractory Solid Tumors (The NEXT-2 Trial)
Brief Title
Next Generation pErsonalized tX(Therapy) With Plasma DNA Trial-2 in Refractory Solid Tumors (The NEXT-2 Trial)
Protocol ID
NCT02140463
Lead Sponsor
Samsung Medical Center
Brief Summary
Analysis of cell free DNA(cfDNA), unlike tissue biopsy, presents a new tool for the
monitoring and treatment of cancer. The investigators have developed a differentiated
sequencing assay, Digital Sequencing Technology (DST) that enables detection of rare
genomic abnormalities with ultra high-specificity and sensitivity. The investigators
assay is able to eliminate the error and distortion created by sample-prep and sequencing
processes in standard NGS(next-generation sequencing ) workflows and produce near-perfect
representations of all rare variants.
The investigators have shown that in sequencing a comprehensive cancer panel of 80kbp in
0.1% cancer cell line titration samples, standard Illumina SBS(sequencing by synthesis )
generates many high-quality false positive variant calls in the range of 0.05-5%, while
the investigators assay resulted in highly sensitive and completely error-free variant
calls across the entire panel.
This work indicates the remarkable potential of using the investigators assay in deep
analysis of cfDNA, thereby allowing researchers and clinicians to comprehensively and
non-invasively monitor the genetic dimension of cancer throughout the body.
Detailed Description
Same as above
Enrollment Count
229 participants
Eligibility Criteria
Inclusion Criteria:
- Patients older than 20 years
- Patients with histologically confirmed metastatic gastrointestinal cancer, rare
cancer, lung cancer
- Patients with histologically confirmed metastatic cancer, who do not have sufficient
biopsy material to undergo mutational testing of their tumor, or do not have
feasible biopsy sites; melanoma/lung cancer and any solid tumor cancer types will be
eligible for the study.
- Written informed consent form
Exclusion Criteria:
- Concurrent disease or condition that would make the subject inappropriate for study
participation or any serious medical condition that would interfere with the
subject's safety.
- Double primary cancer (except for any cancer in remission for > 5 years, cervix
cancer in situ, basal cell cancer in situ, any in situ cancers that are resected)
Filters
Metastatic Gastrointestinal Cancer
Genitourinary Cancer
COMPLETED
ADULT
OLDER_ADULT