Laboratory Assay in Determining Cancer Resistance in Patients With Metastatic Cancer and in Healthy Participants

NCT00899496CompletedOBSERVATIONAL

Summary

Key Facts

Lead Sponsor

Wake Forest University Health Sciences

Enrollment

54

Start Date

2005-09-01

Completion Date

2009-10-23

Study Type

OBSERVATIONAL

Official Title

Pilot Study of Cancer Resistance in Humans

Interventions

immunological diagnostic methodphysiologic testing

Conditions

Cancer

Eligibility

Sex

ALL

Inclusion Criteria:

-Meets 1 of the following criteria:

* Diagnosis of metastatic cancer including, but not limited to, any of the following:

  * Stage IV non-small cell lung cancer
  * Extensive-stage small cell lung cancer
  * Metastatic testicular cancer
  * Stage IV breast carcinoma
  * Stage III or IV ovarian carcinoma
  * Stage IV endometrial carcinoma
  * Stage IV prostate carcinoma
  * Stage IV colorectal or pancreatic cancer
  * Stage IV renal cancer
  * Stage III or IV non-Hodgkin's lymphoma
  * Stage IV bladder cancer
  * Stage III multiple myeloma (Salmon-Durie staging)
  * Metastatic melanoma
  * Metastatic sarcoma
* Healthy participant, meeting the following criteria:

  * No prior cancer
  * Over 50 years of age

Exclusion Criteria:

* Serious medical or psychiatric condition that would preclude study compliance
* Chemotherapy or radiotherapy within the past 3 months (patient)
* Prior immunosuppressive therapy or radiotherapy for any disease (healthy participant)

Outcome Measures

Primary Outcomes

Cell killing ability (positive or negative)

Time frame: Day 180

Percentage of cells killed

Time frame: Day 180

Locations

Wake Forest University Comprehensive Cancer Center, Winston-Salem, United States

Laboratory Assay in Determining Cancer Resistance in Patients With Metastatic Cancer and in Healthy Participants