Spontaneous Regression in Metastatic Melanoma and Renal Cell Carcinoma



Status:Recruiting
Conditions:Skin Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:11/4/2018
Start Date:February 24, 2003
End Date:March 1, 2021
Contact:Theodore Logan, MD
Email:tlogan@iu.edu
Phone:317-948-7576

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Blood Drawing for Study of Peripheral Blood T-lymphocytes and Other Parameters in Patients With Metastatic Melanoma and Renal Cell Cancer With Spontaneous Regression

The purpose of this study is to collect blood and clinical data from patients with metastatic
melanoma and renal cell cancer who have experienced spontaneous regression for studies of
immune response and other factors that may influence these occurrences.

Spontaneous regression in patients with metastatic cancer is an incredibly rare event. It has
been described after infection in cancer patients and also rarely in patients with renal cell
cancer (usually after resection of the renal primary) and, less commonly, in patients with
metastatic melanoma.

Primary Objective To collect peripheral blood from patients with metastatic melanoma and
renal cell cancer and spontaneous regression for studies of immune response and other
studies.

Secondary Objective To collect clinical data from subjects registered to this study. Clinical
data collection will include demographics and cancer characteristics, history and treatment.

Inclusion Criteria

1. ≥ 18 years old at the time of informed consent

2. Ability to provide written informed consent and HIPAA authorization

3. Patients must have metastatic melanoma or renal cell cancer with spontaneous
regression.

4. Willingness to undergo phlebotomy for research blood samples

Exclusion Criteria

1. Concurrent disease or condition that would make the patient inappropriate for study
participation or any serious medical or psychiatric disorder that would interfere with
the subject's safety

2. Dementia, altered mental status, or any psychiatric condition that would prohibit the
understanding or rendering of informed consent
We found this trial at
1
site
Indianapolis, Indiana 46202
Principal Investigator: Theodore Logan, MD
Phone: 317-278-4191
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mi
from
Indianapolis, IN
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