[c09aa8]: / clusters / final9knumclusters / clust_668.txt

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Patient must be able to provide study-specific informed consent prior to study entry
Patient must be able to provide study specific informed consent prior to study entry
Patients must provide study-specific informed consent prior to step 1 registration
Patient must provide study specific informed consent prior to study entry, including the mandatory pre-treatment plasma EBV DNA assay
Patients must provide study specific informed consent prior to study entry, including consent for mandatory tissue submission for central review
Patient must provide study-specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
Patients must provide study specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry
Patient must provide study-specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry
Patient must sign study specific informed consent prior to study entry
Patients must sign a study-specific informed consent prior to study entry
Patient must provide study-specific informed consent prior to study entry
All patients must sign study specific informed consent prior to study entry
Patient must sign study specific informed consent prior to study entry
Patients must sign a study-specific informed consent form prior to study entry
The patient must provide study-specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry; no durable power of attorney or next of kin can provide initial consent
Patients must provide study specific informed consent prior to study entry
Patient must capable of, and provide, study specific informed consent prior to study entry
All patients must sign study specific informed consent prior to study entry or within 1 week of first treatment, provided other criteria were met
Patient signs study specific informed consent prior to study enrollment
Did the patient provide study-specific informed consent prior to study entry
Patient must be able to provide study specific informed consent prior to study entry
Patient must be able to provide study specific informed consent prior to study entry
Patient must sign study specific informed consent prior to study entry
Patient must be able to provide study-specific informed consent prior to study entry
Patient must provide study-specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
Subject must sign a study specific informed consent prior to study entry
Patient must be able to provide study-specific informed consent prior to study entry
Patients must give study specific informed consent prior to enrollment
Patient must sign study specific informed consent prior to study entry
Patient must have provided study specific informed consent prior to study entry
Patient must be able to provide study-specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry, including consent for mandatory submission of tissue for required, central p16 review
Patient must provide study specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry
Patient must provide study-specific informed consent prior to study registration
The patient must provide study specific informed consent prior to study entry
Patients must sign a study-specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
Patients must sign study specific informed consent prior to study entry
Patients must provide study specific informed consent prior to study entry, including consent for mandatory tissue submission for EGFR and for oropharyngeal patients, HPV analyses
Patients must sign a study-specific consent form prior to study entry
The patient must provide study-specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
Patient must capable of and provide study specific informed consent prior to study entry
Patient must be able to provide study-specific informed consent prior to study entry
Patient must be able to provide study-specific informed consent prior to study entry
Patient must be able to provide study-specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry
Must provide study-specific informed consent prior to study entry
The subject must provide study-specific informed consent prior to study entry
Patient must be able to provide study-specific informed consent prior to study entry
Patients must provide study-specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry, including consent for mandatory screening of tissue
Patients must provide study-specific informed consent prior to study entry
Patients must sign a study-specific informed consent form prior to study entry
The patient must sign specific informed consent prior to study entry
The patient must provide study specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry
The patient must provide study-specific informed consent prior to study entry/screening
Patient must provide study specific informed consent prior to study entry.
Subject must sign a study specific informed consent prior to study entry
Patients must provide study specific informed consent prior to study entry
Patients must sign a study-specific informed consent prior to study entry
Patients must provide study-specific informed consent prior to registration
Patients must provide study specific informed consent prior to study entry
Patients must provide study-specific informed consent prior to study entry
Patient must be capable to read and speak English and provide study specific informed consent prior to study entry
SPECIFIC TO STUDY PART #1
SPECIFIC TO STUDY PART #2
Patient must sign study-specific informed consent prior to study entry
Patient must sign study-specific informed consent prior to study entry
Subject must sign a study specific informed consent prior to study entry
The patient must have capacity to be able to sign a study-specific informed consent prior to study entry
Patients must be capable to read and speak English and provide study specific informed consent prior to study entry
Patient must provide study specific informed consent prior to study entry