Breast Cancer Clinical Trial
Official title:
Clinical Study on Anti-tumor Effect Induced by Activated Primary Natural Killer(NK)Cells
This study will analyze and evaluate the following items:
1. The safety of natural killer(NK) cells for treatment of subjects with solid tumors.
Forty patients will be enrolled for each of the five cancers (in total 200 patients will
be enrolled).
2. The effectiveness of natural killer(NK)cell therapy alone or with chemotherapy or
targeted drugs.
Subjects from 18 to 75 years of age who are diagnosed with a solid tumor including pancreatic
cancer, lung cancer, breast cancer, ovarian cancer and colon cancer, and for whom standard
treatments are not effective, may be eligible for this study. Participants undergo the
following procedures:
Peripheral blood will be collected from a vein of arm. Peripheral blood mononuclear
cells(PBMC) will be isolated and purified for NK manufacturing. After 14~21 days cultivation,
activated NK will be harvested and formulated for clinical administration.
Subjects will receive NK cell treatment by intravenous infusion. The frequency is once every
3 or 4 weeks for the first 3 months. Participants who respond well after 3 months may be
eligible to continue NK cell therapy; and those not may receive NK therapy combined with
chemotherapy and/or targeted drugs, or chemotherapy/targeted drugs alone.
Evaluations during therapy including:
1. Clinical assessment, and history of medications;
2. Blood draws for routine and research tests, including but not limited to: lymphocyte
population and circulating tumor cell analysis in peripheral blood;
3. CT scan, bone scan and positron emission tomography(PET )scan, if indicated, for disease
evaluation;
4. Pharmacokinetics study after NK infusion. For this test, the number of NK cells in the
blood is measured over time at indicated time-points.
n/a
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