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Peripheral Blood and/or Bone Marrow, Including Detection of Occult Metastases, in Patients With Melanoma

Completed
Conditions
Melanoma
Registration Number
NCT00588198
Lead Sponsor
Memorial Sloan Kettering Cancer Center
Brief Summary

The purpose of this study is to determine if tumor cells can be detected in the peripheral blood and/or bone marrow of patients with melanoma.

Detailed Description

Patients with melanoma can succumb to subclinical metastatic disease, not detectable at presentation by conventional physical examination, hematologic and biochemical screening, or radiologic evaluation. More intensive radiologic evaluation with CT or radioisotope scanning has not proven to be useful. What may be useful is a more sensitive method of staging melanoma patients at presentation, specifically evaluating them for subclinical systemic disease.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
754
Inclusion Criteria

MSK Patients with histologically confirmed melanoma of any site and at least one of the following:

  • Primary tumor > 4.0 mm thick (AJCC Stage IIB)
  • Clinically or histologically positive regional nodes (AJCC Stage III)
  • Any in transit disease (AJCC Stage III)
  • Any systemic metastases (AJCC Stage IV)
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Exclusion Criteria

Not provided

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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Assess the sensitivity of RT-PCR to detect evidence of melanoma cells in bone marrow and/or peripheral blood and estimate sensitivity separately for each of the different stage groupings for melanoma2 years
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Memorial Sloan Kettering Cancer Center

🇺🇸

New York, New York, United States

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