Blocking androgen signaling has been the focus of treatment for advanced and metastatic
prostate cancer (PC) for the past 70 years (1). First-line androgen deprivation therapy
(ADT), either through surgical or medical castration (luteinizing hormone-releasing
hormone agonists and antiandrogens), holds promise for PC patients; however, the disease
inevitably progresses to castration resistance (2). Second-generation ADT, abiraterone
acetate (AA), and enzalutamide (ENZ), have been effective for a subset of patients
with castration-resistant PC (CRPC) with relatively short median survival benefits
(~3–5 months) (3–5). Concerted effort in the field, including evidence from our group,
clearly demonstrates a sustained AR activity in the CRPC tumors including (1) amplification
of AR, (2) AR mutations, (3) expression of AR splice variants that are constitutively
active, (4) altered milieu of AR coactivators and corepressors, and (5) intracrine
synthesis of androgens to support CRPC progression (6, 7).
The addiction of PC to the AR signaling paradoxically creates a therapeutic vulnerability
that has recently attracted increasing attention. While ADT causes regression of PC,
high level of androgen can also inhibit PC progression. The concept of cancer suppression
using excessive hormone therapy was introduced by earlier work from Huggins in 1940:
“malignant cells can regress from too little or too much hormone” (8). In relation
to PC, AR regulates proliferation as well as differentiation of prostate epithelial
and cancer cells but it has not been established what conditions support one over
the other. Interestingly activation of AR with excessive hormone (i.e., supraphysiological
levels of testosterone; SPT) was shown to inhibit growth of CRPC in vitro by negative
effects on proliferation and increased expression of some of the AR-regulated genes
that are expressed in differentiated luminal epithelium, e.g., prostate-specific antigen.
Multiple preclinical studies demonstrated that SPT inhibits growth of PC cells that
express AR (9–21), with evidence suggesting that higher levels of AR might lead to
more pronounced SPT effects in certain phenotypes of CRPC [reviewed in Ref. (22)].
However, AR by itself is not necessarily sufficient for the SPT-induced growth inhibition;
cellular context (23) and AR-regulated transcriptome in its entirety will need to
be assessed to delineate the molecular effect of SPT (24). Mechanistically, SPT-induced
cell growth inhibition involves (1) cell-cycle arrest, (2) disruption of AR-mediated
DNA licensing, (3) DNA damage, (4) transcriptional repression of AR and its variants,
(5) transcriptional reprogramming, (6) cellular quiescence or senescence, and (7)
induction of apoptosis [reviewed in Ref. (22)]. However, these effects were demonstrated
exclusively in cell line models, and whether they play a significant biological role
in SPT-induced tumor inhibition in patients remains to be determined.
Clinical use of testosterone (T) supplementation in PC has been limited and provided
controversial results. Two older National Prostatic Cancer Project trials that used
T-supplementation to normal levels with a goal to enhance the effectiveness of chemotherapy
reported disappointing results (25, 26). Additional two phase I trials, which did
not achieve consistent supraphysiological T levels, showed minimally reduced disease
progression (27, 28). In contrast, several other studies showed that T-supplementation
to normal-supraphysiological range (303−2637 ng/dl), specifically in symptomatic hypogonadal
PC patients, provided prolonged disease control (as measured by sustainably low-PSA
level) (29–31). In our opinion, the lack of favorable response in some of the clinical
trials is, at least in part, due to the absence of a supraphysiological level of T
as well as the unselected patient population.
With advanced understanding of the biology and AR involvement in CRPC progression,
leveraging the active AR signaling to explore therapeutic opportunity has recently
received renewed attention in clinical settings. Dr. Denmeade’s group at John Hopkins
University pioneered a therapy termed “bipolar androgen therapy” (BAT) as a treatment
for PC patients. With BAT treatment, PC patients receive intermittent T injections
at doses shown to produce a spike in serum T to supraphysiological levels, followed
by a decline to below normal at the end of a 28-day treatment cycle (32). This cycling
strategy was developed based on the most common molecular hallmark of CRPC–overexpression
of AR (33) and the potential growth inhibitory effect of SPT in AR-overexpressing
PC. Rapidly cycling of T from SPT (~1,500 ng/dl) to below normal T levels (~150 ng/dl)
was expected to blunt the adaptive changes in AR expression, thereby delaying the
emergence of resistance. In these proof-of-principle BAT trials, one in CRPC showed
radiographic response rates of ~50% in men (32), and one in hormone-sensitive PC showed
favorable PSA responses (34). Promising results of these trials led to a new clinical
trial, in which asymptomatic CRPC patients that progressed on AA or ENZ receive BAT,
and after progression on BAT the patients are re-challenged with AA or ENZ. This trial
aims to evaluate the efficacy of BAT in patients who progressed on secondary ADT and
assess whether BAT re-sensitizes CRPC to secondary ADT. Recent data from this trial
showed a PSA50 response in 9/30 ENZ-resistant patients on BAT, and, importantly, 15/21
patients who progressed on BAT showed a PSA50 response upon ENZ re-challenge (35).
These results are encouraging. However, additional analyses and larger number of patients
are needed to correlate tumor/radiographic vs. PSA responses in individual patients.
One of the reasons is that PSA changes do not necessarily associate with tumor regression
in advanced CRPC. PSA, an AR-regulated gene, is highly sensitive to AR activation/inhibition
and can rise upon SPT and decline upon ADT. PSA response might not faithfully reflect
radiographic responses in advanced CRPC which growth often does not rely solely on
AR signaling [e.g., FGF signaling (36)].
Bipolar androgen therapy shows great clinical promise in a subset of patients. However,
universal to all cancer treatment modalities, not all patients respond to this treatment
and resistance to BAT develops. Therefore, there is an opportunity to improve this
therapy. It is notable that a critical step in drug development, determining the optimal
dosing schedule, was bypassed in the clinical development of BAT. Despite the clinical
efficacy of BAT, there were by far no clinical data to support the hypotheses that
cycling SPT (i.e., BAT) mitigates the development of resistance or that BAT represents
the optimal mode for administering SPT. Notably, several preclinical studies have
consistently demonstrated that SPT delivered on a continuous basis inhibits the growth
of PC cells (13, 20, 21). While several small clinical trials of continuous T administration
in men with CRPC have been carried out, they did not achieve SPT levels.
Cycling or not cycling—that is the question. While we currently do not have sufficient
evidence whether BAT results in better clinical outcome than continuous SPT, it is
possible that long-term continuous SPT and BAT could alter AR signaling differently.
One would anticipate that continuous SPT might trigger more pronounced differentiation,
potentially causing a change from a “low-T” oncogenic AR transcriptome to that of
a more differentiating SPT transcriptome (24). Meanwhile, BAT might provide better
efficacy if cell-cycle relicensing effects and DNA damage are the critical mechanism
of action (37, 38). While BAT was associated with improved quality of life (34, 35),
this effect diminished over the course of a cycle of BAT, presumably due to T levels
falling below normal range. It is possible that quality of life metrics will be better
with continuous SPT but there also might be increase in negative side effects. While
T therapy has been reported to be generally safe, with a small subset of patients
experiencing severe cardiovascular-related complications (27–32, 39–42), continuous
SPT has not been tested and monitoring will be essential. Careful evaluation of effects
of BAT vs. continuous SPT on tumor progression, as well as any potential health benefits
or side effects will be required to make final decision.
Interestingly, cycling of ADT, intermittent ADT, has been evaluated in PC extensively
since its introduction in mid-1980s. However, intermittent ADT was not found to be
inferior to continuous ADT with respect to the overall survival but it was shown to
improve patients’ quality of life, and therefore it is thought to be a viable option
for patients who experience significant adverse effects of continuous ADT [for review
see Ref. (43, 44)]. In addition, intermittent AA therapy has been recently shown to
delay the development of resistance from 16.5 (continuous treatment) to 27 months
(45). Whether the intermittent therapy diversifies the residual tumor clones or re-sensitize
the residual clones to a therapy that formerly failed remains scientifically and clinically
important.
In summary, we will need to seek answers to multiple important questions before unleashing
the full potential of SPT therapy in CRPC: (1) which mode of SPT, BAT or continuous
SPT, represents the optimal administration regimen for tumor growth inhibition; (2)
what population of patients will benefit from SPT therapy; (3) is there a way to prolong
the treatment response; and (4) what are the mechanisms of resistance, as these will
be diverse in different tumor phenotypes. To address these questions, systematic preclinical
trials will need to be performed, and pre-treatment and on-treatment clinical specimens
will be essential to identify mechanisms of SPT action and biomarkers that predict
SPT response.
Author Contributions
H-ML and EC jointly conceptualized and wrote the manuscript.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial
or financial relationships that could be construed as a potential conflict of interest.