CTC Immune Checkpoint

Patients will be eligible for inclusion in this study only if all of the following criteria apply:

Histologically confirmed diagnosis of adenocarcinoma of the prostate. Small cell or neuroendocrine tumors of the prostate are also permitted.
Clinical or radiographic evidence of progressive metastatic disease, with progression defined as a rising PSA, new metastatic lesions (bone or soft tissue), or radiographic evidence of tumor growth on CT or MRI.
Age ≥ 18 years.
Ability to understand and the willingness to sign a written informed consent document.

In addition to meeting all of the above criteria, patients must meet all of the criteria for one of the following groups:

A) mCRPC starting sipuleucel-T (Provenge) with or without abiraterone acetate or enzalutamide

For patients with adenocarcinoma of the prostate (not applicable for patients with small cell or neuroendocrine tumors of the prostate, or those receiving ADT therapy): Castrate levels of testosterone (≤ 50 ng/dl)
Patient planning to start sipuleucel-T.
Enrollment prior to the initiation of sipuleucel-T.

B) mCRPC with visceral or high risk disease pre-abiraterone/enzalutamide

For patients with adenocarcinoma of the prostate (not applicable for patients with small cell or neuroendocrine tumors of the prostate, or those receiving ADT therapy): Castrate levels of testosterone (≤ 50 ng/dl)

Visceral OR high risk disease - must meet one of the following categories:

Visceral disease: Radiographic evidence of liver, adrenal, pulmonary, or brain metastases

High risk disease: Presence of at least 2 of the following factors:

Bone pain requiring opioids
Anemia (Hgb <13 g/dL)
Bone scan progression at baseline
>2 sites of metastatic disease
Karnofsky Performance Status (KPS) ≤ 70
PSA doubling time <3 months
Patient planning to start abiraterone acetate or enzalutamide.
Enrollment prior to the initiation of abiraterone acetate or enzalutamide.

C) Newly diagnosed metastatic castration sensitive prostate cancer (mCSPC) starting androgen deprivation therapy

Evidence of metastatic disease on radiographic imaging
Enrollment within 2 weeks of initiation of androgen deprivation therapy (ADT).
Lack of history of hypogonadism

D) Enzalutamide or abiraterone acetate resistant mCRPC

For patients with adenocarcinoma of the prostate (not applicable for patients with small cell or neuroendocrine tumors of the prostate, or those receiving ADT therapy): Castrate levels of testosterone (≤ 50 ng/dl)

Evidence of disease progression on or following enzalutamide or abiraterone acetate, as defined by one of the following:

Radiographic evidence of disease progression as defined by new bone scan lesions or growth of existing soft tissue/visceral/lymph node/bone metastases as determined by the investigator
Clinical progression of disease with cutaneous lesions or palpable lesions in absence of radiographic progression

Exclusion Criteria:

History of intercurrent or past medical or psychiatric illness that would make participation in a blood drawing protocol difficult or not feasible at the discretion of the principal investigator or co-investigator(s).
Treatment with an anthracycline (including mitoxantrone) within 1 week of CTC collection, as anthracyclines cause auto-fluorescence of cells.