ADT
Androgen deprivation therapy. LHRH agonists, antagonists, or orchiectomy. In BAT it stays on so the only testosterone is the injected pulse.
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Androgen deprivation therapy. LHRH agonists, antagonists, or orchiectomy. In BAT it stays on so the only testosterone is the injected pulse.
The protein cells use to read testosterone and DHT. CRPC cells often overexpress it — the liability BAT tries to exploit.
Enzalutamide, apalutamide, darolutamide, abiraterone. BAT is often used after one fails, and sometimes to resensitize to the next.
Splice variant missing the ligand-binding domain. Marker studied in BAT trials, not a standalone rule-out.
Rapid cycling between supraphysiologic and near-castrate testosterone, usually 400 mg cypionate IM every 28 days on ADT. “Bipolar” names the poles, not bipolar disorder.
Adaptive BAT: cycle length, pulse width, and partners change with ecosystem type instead of a fixed 28-day CRPC calendar.
Usually T <50 ng/dL (some labs <20). BAT troughs are often 100–200 ng/dL just before the next shot.
Disease that grows despite castrate testosterone. Setting with the most BAT evidence.
Disease that still responds to testosterone suppression. BAT here is experimental (BATMAN, SPIDERMAN).
Red-cell fraction. Testosterone can raise it. A standard reason to pause.
Olaparib and kin. Combined with BAT in phase II because SPA can induce DNA damage.
Rules for reading bone scans. Needed because BAT can flare a scan without true progression.
Androgen-driven protein. A bump on BAT is not automatic failure. PSA50 is a ≥50% drop — convenient, not the same as living longer.
After BAT, a previously failing ARPI often works again. TRANSFORMER’s 77.8% crossover PSA50 is the quoted number.
Supraphysiologic androgen / testosterone. The high pole, typically 1,000–3,000 ng/dL after injection.
Long-acting IM ester. Standard Hopkins BAT dose 400 mg gluteal every 28 days. Off-label for prostate cancer.