The purpose of this study is to determine safety and feasibility of Chemo-Immunotherapy using cyclophosphamide, docetaxel, OK-432, and autologous immature dendritic cells for patients with relapsed and refractory head and neck squamous cell carcinoma.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
10
Cyclophosphamide 50mg/day, day1-7 and 22-28 Docetaxel 30mg/m2, day6 and 27 OK-432 5KE/day, day7,14,28,35
Umiversity of Yamanashi Hospital
Chūō, Yamanashi, Japan
RECRUITINGThe safety and feasibility of chemo-immunotherapy
Time frame: 1 year
The number and function of immune effector cells in treated patients
Time frame: 1 year
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