Recurrence Clinical Trial
Official title:
The Clinical Relevance of Immune Cells and Circulating Tumor Cells in Patients With Head and Neck Cancer
Verified date | April 2017 |
Source | Chang Gung Memorial Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
Head and neck squamous cell carcinomas (HNSCCs) are mainly caused by tobacco, alcohol
consumption and betel nut chewing and the sixth most common cancer in the world. Despite
significant advances in the treatment modalities involving surgery, radiotherapy, and
concomitant chemoradiotherapy, the 5-year survival rate remained below 50% for the past 30
years.
The worse prognosis of these cancers must certainly be linked to the fact that HNSCCs
strongly influence the host immune system. During this process, mesenchymal tumor-like cells
are highly mobile and enter quickly adjacent structure (intravasation), from where they
travel through lymphatic and blood vessels as circulating tumor cells (CTC), which are single
cells with malignant potential detected in the peripheral bloodstream and essential for
establishing metastasis.
Programmed death 1 (PD-1) and its ligand (PD-L1) play pivotal roles in regulating host immune
responses. Substantial evidence has demonstrated that PD-L1 can deliver an inhibitory signal
to PD-1 expressing T cells, leading to suppression of the immune response by inducing
apoptosis, energy, unresponsiveness and functional exhaustion of T cells. However, the
inhibitory effects of this pathway on the function of cytotoxic T lymphocytes, the main
effector cells in HNSCC patients, are not well defined.
In this study aims to solve two main problems: one is to improve and try to optimize current
protocols of CTC isolations based on the investigator previous work, which is one of most
challenging problems in CTC field to date; the other is to understand the status of immune
system in HNSCC patients, especially focusing on PD-1-PD-L1 pathway and its expressions.
After series basic experiments of immune cell analysis and conditional adjustment of CTC
isolation protocols, the investigator are willing to isolate CTCs and immune cells at a
single blood drawing at the same time. A prospective trial will be conducted to elucidate the
roles of PD-1 expression lymphocytes and CTC numbers on the clinical outcomes of HNSCC
patients.
Status | Recruiting |
Enrollment | 300 |
Est. completion date | December 2018 |
Est. primary completion date | December 2017 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 20 Years and older |
Eligibility |
Inclusion Criteria: 1. Established head and neck squamous cell carcinoma. 2. Age >=20 years old with clear consciousness, decided by free wills. Ability to sign informed consent Exclusion Criteria: 1. Patient's refusal 2. Poor compliance, cannot draw blood for CTCs isolation as time schedule or clinical treatment or follow-up 3. Difficult blood sampling 4. No more needs for CTCs evaluation, decided by clinicians. Inability to comply with study and/or follow-up procedures. |
Country | Name | City | State |
---|---|---|---|
Taiwan | Chang Gung Memorial Hospital | Taoyuan |
Lead Sponsor | Collaborator |
---|---|
Chang Gung Memorial Hospital |
Taiwan,
Hsieh JC, Lin HC, Huang CY, Hsu HL, Wu TM, Lee CL, Chen MC, Wang HM, Tseng CP. Prognostic value of circulating tumor cells with podoplanin expression in patients with locally advanced or metastatic head and neck squamous cell carcinoma. Head Neck. 2015 Oc — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The correlation among CTC numbers, PD-1 expressions and the prognosis of patients. | The CTCs will be isolated and then the number of CTCs will be measured. PD-1 expression from locally advanced or metastatic HNSCC patients will be validated. Measure response or progression events via all available imaging studies, including Chest-Xray, CT scans, or MRI, PET study. The relationship between CTCs number, PD1 expression and time from CTCs checkpoint to disease progression will be analyzed. | one year | |
Secondary | Overall survival | All causes of death would be documented and the relationship between CTCs number and time from CTCs checkpoint to death will be analyzed. | one year |
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