Skip to content

Circulating Tumor Cells (CTC) in Cancer

Circulating Tumor Cells (CTC) in Cancer

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04520672
Enrollment
3000
Registered
2020-08-20
Start date
2020-10-01
Completion date
2030-08-31
Last updated
2025-03-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Keywords

circulating tumor cells (CTCs), CTC clusters, Molecular analysis of CTCs, CTC culture, overall survival (OS), progression free survival (PFS)

Brief summary

This observational study with circulating tumor cells (CTC) count, isolation and analysis at several time points during disease progression is to investigate the role and biology of CTCs and clusters of CTCs in different cancer types. It also evaluates the role of CTCs as biomarkers, and aims at the identification of key signaling networks that are active in CTCs.

Interventions

OTHERBlood samples

Blood samples (3 ethylenediaminetetraacetic acid (EDTA) tubes with a volume of 7.5 ml blood each) will be processed for CTC isolation and characterization, ranging from molecular analysis to culture and drug screen.

OTHERSamples from tumor draining vessels

In case of tumor resection, 3 EDTA tubes (5 ml) will be withdrawn from the tumor draining vessels for CTC isolation and characterization, ranging from molecular analysis to culture and drug screen.

Sponsors

University Hospital, Basel, Switzerland
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult cancer patients * All patients with histology-based proved diagnosis of cancer, all stages and subtypes can be included. Precancerous lesions cannot be included. * All patients with the diagnosis of a solid tumor including adenocarcinoma, squamous cell carcinoma, neuroendocrine carcinoma, sarcoma * Written pathology report must be available. * Written informed consent.

Exclusion criteria

* No written informed consent. * No proved diagnosis of malignancy by pathology report. * Patients with the diagnosis of blood cancer

Design outcomes

Primary

MeasureTime frameDescription
Overall survival (OS) in heterogeneous cancer populationScreening (Visit 1) until the date of death (assessed up to 240 months)overall survival (OS) in heterogeneous cancer population
Change in total number of isolated CTCsThrough study completion, an average of 20 yearsChange in total number of isolated CTCs

Secondary

MeasureTime frameDescription
Progression free survival (PFS)Through study completion, an average of 20 yearsprogression free survival (PFS) in the different cancer cohorts with different treatment regimes

Other

MeasureTime frameDescription
Change in circulating tumor DNA (ctDNA) from blood samplesThrough study completion, an average of 20 yearsChange in circulating tumor DNA (ctDNA) from blood samples

Countries

Switzerland

Contacts

Primary ContactMarcus Vetter, PD Dr. med.
marcus.vetter@ksbl.ch+41 61 925 27 15
Backup ContactNicola Aceto, Prof. Dr. med.
nicola.aceto@biol.ethz.ch+41 44 633 40 23

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026