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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01573494
Other study ID # 11-AOI-04
Secondary ID
Status Completed
Phase N/A
First received March 23, 2012
Last updated June 25, 2014
Start date May 2012
Est. completion date June 2014

Study information

Verified date June 2014
Source Centre Hospitalier Universitaire de Nice
Contact n/a
Is FDA regulated No
Health authority France: Committee for the Protection of PersonnesFrance: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Interventional

Clinical Trial Summary

Circulating tumor cells (CTC) are the subject of increasing interest in clinical oncology as a prognostic factor and predictor of therapeutic response. The detection of CTC by immunomagnetic method has proved its reliability and its usefulness for monitoring breast cancer, colon and prostate in the metastatic and immunomagnetic detection system (CellSearch, Veridex LLC) was approved by the FDA in these indications. However, to date there is no reliable method to detect CTCs in melanoma (CMC). Studies based on PCR amplification of mRNA by reverse specific melanoma is disappointing. Recently, a new detection system of CMC immunomagnetic was presented (CellSearch, Veridex LLC, United States). This system has the advantage of combining immunomagnetic selection step and a step of identifying by immunofluorescence. A preclinical study on serial dilutions of melanoma cells has shown encouraging results. The investigators propose a prospective study of the CellSearch system in patients with melanoma.

Primary objective: To determine the effect of treatment on the number of circulating melanoma cells in patients with metastatic melanoma.

Secondary objectives:

- determine the percentage of patients with metastatic melanoma with melanoma cells circulating

- seek a relationship between the number of circulating melanoma cells and prognosis in patients with metastatic melanoma

- seek a relationship between the change in the number of circulating melanoma cells before / after treatment and tumor response in patients with metastatic melanoma


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date June 2014
Est. primary completion date November 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients > or = 18 years

- Patients with advanced melanoma stage IIIC (unresectable) or stage IV

- Patient not treated or not responding to chemotherapy with chemotherapy session last> 1 month

- Patients who signed informed consent

- Patients presenting no socio-economic, psychological, familial or geographical allow proper understanding of the information leaflet of the protocol or the regular monitoring in the department of dermatology

- Patients with a life expectancy greater than 3 months

- Patients with melanoma measurable by RECIST version 1.1

- Patients with venous good for venipuncture

Exclusion Criteria:

- Patients with contraindication for treatment with chemotherapy or V600E BRAF inhibitor or ipilimumab or have conditions concomitant heavy may interfere with the treatment of metastatic melanoma

- Pregnant women or nursing

- People vulnerable detainees, adults under guardianship or curatorship, minors.

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms


Intervention

Other:
Sampling of blood
7,5 ml of blood

Locations

Country Name City State
France CHU de Nice Nice

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Nice

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Measuring the number of circulating melanoma cells/ml in blood Measuring the number of circulating melanoma cells/ml in the peripheral blood by the test before and after treatment CellSearch. baseline and 3 months No
Secondary number of patients who test positive detection of circulating melanoma cells measured in peripheral blood with the CellSearch test Calculating the number of patients who test positive detection of circulating melanoma cells measured in peripheral blood with the CellSearch test before and after treatment. 3 months No
Secondary Difference in survival Difference in survival between patients depending on the number of circulating melanoma cells/ml before treatment, according to Kaplan-Meier method. baseline and 6 months No
Secondary Difference in tumor response Difference in tumor response between patients according to the variation of circulating melanoma cells/ml before and after treatment. 6 months No
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