Patients must NOT suffer from medical or psychiatric conditions that would interfere with protocol compliance, the ability to provide informed consent, or assessment of response or anticipated toxicities; this includes uncontrolled intercurrent illness including, but not limited to ongoing or active infection
Patients with known serious concurrent infection or medical illness, including psychiatric disorders
Psychiatric illness, which would prevent the patient from giving informed consent or adhering to the study protocol.
Patients who have any debilitating medical or psychiatric illness that would preclude their giving informed consent or their receiving optimal treatment and follow up
Any major medical, addictive or psychiatric illnesses which would affect the consent process, completion of treatment and/or interfere with follow-up. Consent by legal authorized representative is not permitted in this study.
Individuals with major medical or psychiatric illness which would prevent the completion of study treatment and/or interfere with follow up are excluded from this study
Uncontrolled serious medical or psychiatric illness
Patients with an active psychiatric or mental illness making informed consent or careful clinical follow-up unlikely are excluded
Major medical, addictive or psychiatric illness which in the investigator's opinion, will prevent the consent process, completion of the treatment and/or interfere with follow-up. (Consent by legal authorized representative is not permitted for this study).
Patients should have NO significant medical or psychiatric illness that would interfere with compliance and ability to tolerate treatment as outlined in the protocol
Major medical, addictive or psychiatric illness which in the investigators opinion, will prevent the consent process, completion of the treatment and/or interfere with follow-up. (Consent by legal authorized representative is not permitted for this study)
Patients must not have a serious medical or psychiatric illness that would, in the opinion of the treating physician prevent informed consent or completion of protocol treatment, and/or follow-up visits
History of current or past medical or psychiatric illness that would make participation difficult or not feasible at the discretion of the principal investigator or co-investigators
Evidence of significant medical illness, abnormal laboratory finding, or psychiatric illness/social situations that could, in the investigators judgment, make the patient inappropriate for this study
Severe psychiatric illness or mental deficiency making compliance to treatment unlikely and/or informed consent impossible
DONOR: Severe psychiatric illness or mental deficiency making compliance with donation unlikely and/or informed consent impossible
A major psychiatric illness which would limit understanding of the proposed protocol treatment and consent process
Patients with severe co-extensive comorbidities or significant psychiatric illness
Evidence of significant medical illness, abnormal laboratory finding, or psychiatric illness/social situations that would, in the Investigators judgment, make the patient inappropriate for this study
Any serious medical illness, other than that treated by this study, which would limit survival to less than  month or psychiatric illness which would limit informed consent
Serious medical or psychiatric illness/condition likely in the judgment of the Investigator to interfere with compliance to protocol treatment/research
Any serious medical illness, other than treated by this study, which would limit survival to less than  month or psychiatric illness which would limit informed consent
Patients with a mental disorder, psychiatric illness/social or concussion which would inhibit their ability to provide informed consent or prevent compliance with follow-up
Patients should not have a history of significant psychiatric illness
If history of depression or psychiatric illness, has to be well controlled with antidepressants and/or under psychiatrist/ psychologist care
Significant underlying medical or psychiatric illness
Have additional uncontrolled serious medical or psychiatric illness.
Other serious medical illness other than that treated by this study which would limit survival to < years or psychiatric conditions which would prevent informed consent or compliance with treatment.
Any major medical psychiatric or neurologic illness, which in the investigators' opinions would interfere with either completion of therapy or with full and complete understanding of the risks and potential complications of the therapy
Patients must not have a serious medical or psychiatric illness which prevents informed consent or compliance with treatment
Psychiatric illness which may make compliance to the clinical protocol unmanageable or which may compromise the ability of the patient to give informed consent
Psychiatric disturbance
Significant underlying medical or psychiatric illness.
All patients must be consented prior to chemotherapy; the patient should not have any serious medical or psychiatric illness that would prevent either the giving of informed consent or the receipt of treatment
Patients should not have a history of significant psychiatric illness
Patients who have any debilitating medical or psychiatric illness that would preclude their giving informed consent or their receiving optimal treatment and follow-up
Significant underlying medical or psychiatric illness
Significant underlying medical or psychiatric illness
Patients who have any debilitating medical or psychiatric illness that would preclude their giving informed consent or their receiving optimal treatment and follow-up
Major psychiatric illness, which would prevent completion of treatment or interfere with follow up
Psychiatric illness that may affect the patient's compliance with the treatment.
Have psychiatric or other medical illness, or any other condition that in the opinion of the investigator prevents compliance with the study procedures or ability to provide valid informed consent.
Psychiatric, other medical illness or other condition that in the opinion of the principal investigator (PI) prevents compliance with study procedures or ability to provide valid informed consent.
No serious medical or psychiatric illness which prevents informed consent or intensive treatment is allowed
Psychiatric, other medical illness or other condition that in the opinion of the PI prevents compliance with study procedures or ability to provide valid informed consent
Evidence of significant medical illness, abnormal laboratory finding, or psychiatric illness/social situations that could, in the Investigator's judgment, make the patient inappropriate for this study
Serious intercurrent medical or psychiatric illness that will prevent participation or compliance with study procedures, including serious active infection
Psychiatric, other medical illness or other condition that in the opinion of the PI prevents compliance with study procedures or ability to provide valid informed consent.
Psychiatric, other medical illness or other condition that in the opinion of the PI prevents compliance with study procedures or ability to provide valid informed consent
No debilitating medical or psychiatric illness that would preclude giving informed consent or receiving optimal treatment and follow-up
Have additional uncontrolled serious medical or psychiatric illness that in the point of view of the investigator can render the patient unable to receive therapy or make it unsafe to receive therapy.
uncontrolled psychiatric illness;
Significant psychiatric illness
Evidence of significant medical illness, abnormal laboratory finding or psychiatric illness/social situations that would, in the investigators judgment, makes the patient inappropriate for this study
Significant comorbidity (cirrhosis, severe coronary artery disease, significant psychiatric illness, or other that may compromise the ability to safely administer the therapy at the discretion of the primary investigator)
Subjects who have a history of significant psychiatric illness
Have no active cardiac, neurologic, or psychiatric illness, and
No significant co-morbid medical or psychiatric illness that would significantly compromise the patients clinical care and chances of survival
Patients must not have a severe psychiatric illness, including major depression or any previous suicide attempts
Patient has a debilitating medical or psychiatric illness that would preclude giving informed consent or receiving optimal treatment or follow up.
Hospitalized for psychiatric illness within the past two years
Patient has a serious medical or psychiatric illness which prevents informed consent or adherence with treatment
Psychiatric illness that may make compliance to the clinical protocol unmanageable or may compromise the ability of the patient to give informed consent
Any serious medical or psychiatric illness that would prevent either the giving of informed consent or the receipt of treatment
Serious medical or psychiatric illness that would in the opinion of the investigator interfere with the prescribed treatment
Severe concomitant medical or psychiatric illness
Major medical or psychiatric illness, which in the investigator's opinion would interfere with either completion of therapy and follow-up or with full and complete understanding of the risks and potential complications of the therapy
Any debilitating medical or psychiatric illness that would preclude ability to give informed consent or receive optimal treatment and follow-up
DONOR: Untreatable/unstable psychiatric illness
No serious medical or psychiatric illness which prevents informed consent or intensive treatment
Any serious illness or medical condition that would not permit the patient to be managed according to the protocol, including, but not to limited, any the following:\r\n* History of significant neurologic or psychiatric disorder (e.g., uncontrolled psychiatric disorders) that would impair the ability to obtain consent or limit compliance with study requirement\r\n* Active uncontrolled or serious infection\r\n* Active peptic ulcer disease
Patients may not have any debilitating medical or psychiatric illness that would preclude giving informed consent or receiving optimal treatment and follow-up
Patients should have no significant psychiatric illness or medical illness that would preclude the ability to comply with the protocol
Patients should have no significant psychiatric illness or medical illness that would preclude the ability to comply with the protocol
Any serious medical or psychiatric illness
Comorbid systemic illness or psychiatric illness that could interfere with study completion
Any serious medical or psychiatric illness
Significant medical co-morbidity that would preclude safe administration of cytotoxic therapy, including but not limited to: a.Cardiac disease i. Unstable angina ii. Myocardial infarction <  months prior to study initiation b. Ongoing serious infection i. Bacteremia or sepsis requiring intravenous antibiotics ii. HIV with AIDS defining illness c.Inadequate oral nutritional intake i. Requirement for daily intravenous fluids or total parenteral nutrition. d. Psychiatric illness/social situations that would limit compliance with study requirement
History of clinically significant psychiatric illness that would prevent the patient from providing a valid ICF and complying with protocol requirements
Have additional uncontrolled serious medical or psychiatric illness.
Severe concomitant medical or psychiatric illness
Patients who have active or uncontrolled infection or serious medical or psychiatric illness preventing informed consent or on intensive treatment
Major psychiatric illness, which would prevent completion of treatment or interfere with follow-up
Must be cognitively intact and free of serious psychiatric illness (as determined by study recruiter at intake)
Significant psychiatric history
Patients with any medical illness or concurrent psychiatric illness which, in the investigators opinion, cannot be adequately controlled with appropriate therapy
Major psychiatric illness or co-morbid conditions prohibiting compliance with study procedures
History of hospitalization for psychiatric illness
Have a diagnosis of psychiatric illness or other major illness in addition to PCa, such as other cancers, uncontrolled hypertension, lung disease, liver disease or heart disease
Patients must not have a serious medical or psychiatric illness that would, in the opinion of the investigator, prevent informed consent or completion of protocol treatment, and/or follow-up visits
Received treatment for serious psychiatric illness (e.g., schizophrenia, severe depression) in the past  months
Major psychiatric disease
No history of prior inpatient psychiatric treatment for severe mental illness within  year (e.g., psychosis)
History of prior inpatient psychiatric treatment for severe mental illness within the past year (e.g., psychosis),
No debilitating medical or psychiatric illness that would preclude giving informed consent or receiving optimal treatment and follow-up
Participants who exhibit confusion, disorientation, or have a history of major psychiatric illness which may impair their understanding of the informed consent
Serious medical or psychiatric illness that in the opinion of the site Investigator will interfere with the ability of the subject to give informed consent or adhere to the protocol
Severe psychiatric illness
No serious associated psychiatric illnesses
Severe psychiatric illness
No serious medical or psychiatric illnesses that would prevent informed consent
No uncontrolled serious medical or psychiatric illness
No serious associated psychiatric illnesses
Patients with a known history of psychiatric issues
Any serious or active medical or psychiatric illness which, in the opinion of the investigator, would interfere with subject treatment, assessment, or compliance
Have been hospitalized for treatment of a major psychiatric illness within the last five years