Assessing Systemic Treatment and ctDNA Monitoring Efficacy in Metastatic Cancer Patients Using K4Care Testing.

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeNot listed
SponsorGene Solutions

About this trial

The goal of this observational study is to investigate the real-world treatment landscape of patients with metastatic cancer and determine the role of ctDNA in monitoring treatment response in patients with metastatic cancer who have undergone K4Care testing

Eligibility criteria

Qualifiers

Pathological and imaging confirmation of metastatic or progressive stage IV cancer.

Consent to the use of their clinical data.

Diagnosis of one of the following common solid tumor types: lung, colorectal, breast, gastric, or cancer of unknown primary origin.

Prior K4Care testing to identify tumor tissue (FFPE) mutations and consent to the use of their sequencing data.

Disqualifiers

Refusal to participate in the study.

Absence of prior K4Care testing.

Diagnosis of early-stage cancer or hematologic malignancy.

Refusal to provide clinical information or blood samples.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed

Sponsors and collaborators

Gene Solutions

Lead sponsor

The Medical Genetics Institute (MGI) of HCMC

Collaborator