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Analysis of Circulating MYCN DNA in Serum Samples Obtained From Patients With Neuroblastoma


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Open (Enrolling)
Both
Neuroblastoma

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Trial Information

Analysis of Circulating MYCN DNA in Serum Samples Obtained From Patients With Neuroblastoma


OBJECTIVES:

- Perform in a blind study a multicentric study by analyzing serum from patients at
diagnosis (with a known tumour MYCN status determined in the COG reference lab), in
order to confirm our previous data and to define the most appropriate MYCN/control
ratio cutoff capable of determining positive and negative cases.

- Define the limits of the procedure in non-metastatic patients and in those with reduced
tumor burden (INSS stage 1 and 2).

OUTLINE: Circulating DNA is extracted from serum. PCR amplification of MYCN is performed and
analyzed by agarose gel electrophoresis. Real-time quantitative PCR is also performed.

Inclusion Criteria


DISEASE CHARACTERISTICS:

- Serum samples from neuroblastoma patients obtained through the COG (and legacy
CCG/POG Biology Studies)

- Stage 4S, 4, 1, or 2 disease

- MYCN status of corresponding tumors previously determined using standard techniques

PATIENT CHARACTERISTICS:

- See Disease Characteristics

PRIOR CONCURRENT THERAPY:

- Not specified

Type of Study:

Observational

Study Design:

N/A

Outcome Measure:

Most appropriate MYCN/control ratio cutoff capable of determining positive and negative cases of neuroblastoma

Safety Issue:

No

Principal Investigator

Michael D. Hogarty, MD

Investigator Role:

Study Chair

Investigator Affiliation:

Children's Hospital of Philadelphia

Authority:

United States: Federal Government

Study ID:

CDR0000554566

NCT ID:

NCT00898391

Start Date:

June 2007

Completion Date:

Related Keywords:

  • Neuroblastoma
  • recurrent neuroblastoma
  • stage 4S neuroblastoma
  • localized resectable neuroblastoma
  • localized unresectable neuroblastoma
  • regional neuroblastoma
  • disseminated neuroblastoma
  • Neuroblastoma

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