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. 2009 Feb 17;100(5):671–675. doi: 10.1038/sj.bjc.6604904

CYP17 blockade by abiraterone: further evidence for frequent continued hormone-dependence in castration-resistant prostate cancer

J E Ang 1, D Olmos 1,2, J S de Bono 1,2,*
PMCID: PMC2653756  PMID: 19223900

Abstract

The limited prognosis of patients with castration-resistant prostate cancer (CRPC) on existing hormonal manipulation therapies calls out for the urgent need for new management strategies. The novel, orally available, small-molecule compound, abiraterone acetate, is undergoing evaluation in early clinical trials and emerging data have shown that the selective, irreversible and continuous inhibition of CYP17 is safe with durable responses in CRPC. Importantly, these efficacy data along with strong preclinical evidence indicate that a significant proportion of CRPC remains dependant on ligand-activated androgen receptor (AR) signalling. Coupled with the use of innovative biological molecular techniques, including the characterisation of circulating tumour cells and ETS gene fusion analyses, we have gained insights into the molecular basis of CRPC. We envision that a better understanding of the mechanisms underlying resistance to abiraterone acetate, as well as the development of validated predictive and intermediate endpoint biomarkers to aid both patient selection and monitor response to treatment, will improve the outcome of CRPC patients.

Keywords: abiraterone; castration-refractory prostate cancer; androgen synthesis; CYP450c17; 17α-hydroxylase/C17,20-lyase

AR-signalling pathway as a therapeutic target

Although the majority of patients diagnosed with prostate cancer are cured with definitive primary treatment, prostate cancer remains the second leading cause of male cancer-related death in the western world (Ferlay et al, 2007). Despite major advances made in the management of advanced prostate cancer, attributable mainly to the introduction of androgen-deprivation therapy (ADT) with most remissions lasting 2–3 years at best, many patients will eventually succumb due to the emergence of castration resistance (Pienta and Bradley, 2006). The centrality of androgens and the androgen receptor (AR) in castration-resistant prostate cancer (CRPC) is, paradoxically, echoed by the common, albeit erroneous, use of the terms ‘hormone resistant’ and ‘androgen independent’. Indeed, the progression of prostate cancer despite the administration of ADT is more a reflection of the ineffectiveness of current treatments than the disease gaining genuine autonomy from AR-signalling pathways.

The recognition that the state of androgen resistance is relative is certainly not new. Clinical experience in the management of breast and prostate cancers have clearly illustrated that repeated hormonal manipulations can be used successfully (Raghavan and Klein, 2008). Moreover, the importance of non-gonadal sources of androgens (adrenal and intracrine de novo synthesis) has long been recognised. In fact, contemporaneous ADT does not eliminate androgen synthesis within prostate cancer cells. On the contrary, intraprostatic (in situ and metastatic) levels of DHT and testosterone have been shown to remain elevated despite castrate serum levels (Titus et al, 2005). Additionally, not only is there autonomous overexpression of enzymes key to the synthesis of androgenic steroids (Stanbrough et al, 2006), AR-signalling pathways have also been shown to be persistently activated (Titus et al, 2005). All these point to the de novo intratumoural synthesis of androgens that could be critical to driving the progression of castration-resistant tumours. This may be compounded by the emergence of a hypersensitive phenotype (likely though AR mutation, amplification, and/or AR modulation by signalling pathways) that renders these cells exquisitely sensitive to extremely low levels of exogenous androgens (Taplin, 2007). Furthermore, currently approved antiandrogens, such as bicalutamide, hydroxyflutamide and nilutamide, have weak agonistic effects in prostate cancers with mutated or overexpressed AR (Chen et al, 2004), and this provides a mechanistic explanation for the treatment failure using these agents as well as the clinical phenomenon of the ‘androgen withdrawal response’. Overall, these data supported the study of a systemic CYP17 inhibitor to rationally deplete intratumoural and other extragonadal sources of steroid ligands to AR and ERα (androgenic and oestrogenic) that may impact CRPC biology.

Inhibition of CYP17 using abiraterone acetate

CYP17 in androgenic steroidogenesis

The CYP17 enzyme localises to the endoplasmic reticulum of Leydig cells in the testis, theca interna region of the ovaries, and zona fasciculata and reticularis in the adrenal glands. It is a key enzyme in the generation of androgens and oestrogens in the adrenal glands and tumour tissue, and works by the catalysis of two independently regulated steroid reactions, involving 17α-hydroxylase and C17, 20-lyase, in the biosynthesis pathway, as illustrated in Figure 1 (Miller et al, 1997). The 17α-hydroxylase activity converts pregnenolone to 17α-hydroxypregnenolone and progesterone to 17α-hydroxyprogesterone, whereas C17,20-lyase converts 17α-hydroxypregnenolone to dehydroepiandrosterone (DHEA) and 17α-hydroxyprogesterone to androstenedione (Miller et al, 1997; Auchus, 2004).

Figure 1.

Figure 1

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Androgen biosynthesis pathway. The physiological effects of abiraterone acetate on steroidogenesis are indicated by arrows next to each steroid precursor. Abiraterone acetate inhibits 17α-hydroxylase (blunt arrow), causing a decline in serum cortisol and a consequent rise in adrenocorticotrophic hormone (ACTH) (broken arrow). This, in turn, results in the rise of deoxycorticosterone and corticosterone by approximately 10- and 40-fold, respectively. The elevated deoxycorticosterone levels result in the expected toxicities of secondary mineralocorticoid syndrome. Abiraterone acetate also inhibits C17,20-lyase (blunt arrow) resulting in significant declines in dehydroepiandrostenedione (DHEA), androstenedione and testosterone. Aldosterone levels fall due to suppression of the renin–angiotensin pathway by high levels of deoxycorticosterone. However, there is a four-fold increase in 11-deoxycortisol, which may be due to the increased ACTH levels driving the partial reversal of the activity of 17α-hydroxylase but not C17,20-lyase.

Rationale for the safe inhibition of CYP17

In congenital CYP17 deficiencies, the production of cortisol, androgens and oestrogens is impaired, leading to the lack of sexual development (Auchus, 2004). Nonetheless, the synthesis of corticosterone, a weaker glucocorticoid, is preserved. Hence, patients do not develop symptoms of adrenal insufficiency. However, higher levels of adrenocorticotrophic hormone (ACTH) are required before a new steady state is reached, as corticosterone is a weaker glucocorticoid than cortisol. Raised levels of ACTH result in a syndrome of secondary mineralocorticoid excess characterised by fluid overload, hypertension and hypokalaemia (Figure 1). Fortuitously, this syndrome may be managed effectively with mineralocorticoid antagonists, with or without low dose glucocorticoids to suppress ACTH generation. ACTH suppression, in turn, leads to normalisation of mineralocorticoid levels, and thence, serum potassium levels and blood pressure.

Prior experience with ketoconazole

Ketoconazole, an antifungal with weak and non-specific CYP17 inhibitory properties, has been extensively used for the ‘off-label’ treatment of advanced CRPC. The effective inhibition of the 14α-demethylase enzyme (that is responsible for its antifungal properties) occurs at low doses of ketoconazole, whereas much higher doses are required for the non-specific inhibition of CYP17 (De Coster et al, 1986) and 11β-hydroxylase (Loose et al, 1983), but this results in neurological, respiratory and hepatic toxicities which are common and severe, with up to 20% of patients discontinuing treatment.

Efficacy data from phase II trials have shown that the response rate by prostate specific antigen (PSA) working group (PSAWG) criteria (Bubley et al, 1999) with ketoconazole range between 40–62% with a median duration of up to 7 months (Small et al, 1997; Millikan et al, 2001; Figg et al, 2005; Ryan et al, 2007). The CALGB 9583 phase III study compared antiandrogen withdrawal alone vs antiandrogen withdrawal plus ketoconazole 400 mg thrice daily, resulting in response rates by PSAWG of 11% vs 27%, respectively, but no difference in overall survival; the latter observation was thought to be attributable, at least in part, to a high crossover rate of 82% to the ketoconazole arm (Small et al, 2004). It was also noted that resistance to ketoconazole can develop rapidly due to the loss of CYP17 inhibitory effect (Small et al, 2004). In addition, most prospective studies incorporate the use of corticosteroids; this does not seem to reduce toxicities from high-dose ketoconazole and has additionally complicated the interpretation of the endocrine and antitumoural effects.

Overall ketoconazole has antitumoural activity in prostate cancer. Although its specific role in prostate cancer therapeutics remains debatable, results from studies using it argued for the potentially important role of more selective and irreversible CYP17 inhibitors.

Preclinical development of abiraterone acetate

The pregnenolone-derived compound, abiraterone (CB7598), was developed as part of a series of potent, inhibitory 17-(3-pyridyl) steroids at The Institute of Cancer Research, UK (Barrie et al, 1994; Potter et al, 1995; Rowlands et al, 1995). The features which set it apart from the other candidate small molecular inhibitors of the CYP17 enzyme included a 3-pyridyl substituent and a double-bond between positions 16 and 17 of the steroidal skeleton, as illustrated in Figure 2; these render both potency and selectivity in CYP17 inhibition to this compound with a Kiapp of <1 nM. The acetate prodrug, CB7630, was recommended for oral dosing due to its improved bioavailability and favourable pharmacokinetic profile.

Figure 2.

Figure 2

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Chemical structures of abiraterone acetate and abiraterone.

In preclinical toxicology studies, abiraterone reduced the weights of androgen-dependent organs (prostate, seminal vesicles and testes) with minimal side effects in other organs when administered daily.

Phase I studies of abiraterone acetate

First-in-man phase I studies reported that abiraterone acetate was safe when administered daily for 12 days to men with non-progressing prostate cancer, and resulted in >50% suppression of baseline testosterone in non-castrate patients (O’Donnell et al, 2004). However, this effect was transient and was negated by a compensatory rise in luteinizing hormone levels within 3 days. Hence, concomitant castration was maintained in subsequent studies to prevent this.

On the background of the need for an improved means of depleting androgens, coupled with the presence of a sound rationale for the safety of continuous inhibition of CYP17, alongside preliminary evidence for the favourable pharmacokinetic and endocrine profiles of abiraterone acetate, we performed a phase I clinical trial that has been recently reported (Attard et al, 2008). This involved the continuous, once-daily dosing of abiraterone acetate to castrate, chemotherapy-naïve patients with CRPC, escalating through five pre-planned dose levels of 250, 500, 750, 1000 and 2000 mg using three-patient cohorts. This was the first study to show that selective and continuous inhibition of CYP17 is safe with an associated durable suppression of serum androgens and oestrogens, as well as durable antitumour activity. This study was not designed to compare the antitumour activity of different dose-levels; as no treatment-related grade 3 or 4 toxicities were encountered and clinical responses were reported at all dose levels tested, the recommended phase II dose of 1000 mg was selected on the basis of the observation that the rise of upstream steroids reached a plateau at doses above 750 mg.

The toxicities observed in this study were predominantly due to secondary mineralocorticoid excess and were controlled with the mineralocorticoid receptor antagonist, eplerenone; spironolactone was not used as it has been previously reported to activate AR (Luthy et al, 1988). In keeping with the described congenital syndromes of CYP17 deficiency, no patient developed clinically significant adrenocortical insufficiency. Circulating testosterone levels in all patients were in the castrate range at baseline and rapidly became undetectable on treatment at all dose-levels. Indeed, downstream C-21 androgenic steroids were suppressed to levels below the lower limit of detection by conventional assays on treatment.

Overall, 66% of the CRPC patients treated in this study had a ⩾30% fall in PSA. Declines in PSA were frequently associated with symptomatic improvement, reduction in serum alkaline phosphatase levels, normalisation of elevated lactate dehydrogenase levels and partial responses by RECIST, with several patients reducing or discontinuing analgesic (including opiate) use. Significantly, tumour responses to abiraterone acetate were observed in castrate patients who had failed several prior lines of AR-targeting therapy (median of three prior hormonal therapies). Subsequent phase I/II studies in the UK and US have treated more than 100 patients and provide additional support to the efficacy of this agent. These preliminary efficacy data compare favourably with established second-line ADT and novel molecularly targeting agents, and mandate further evaluation of this agent in randomised studies.

Phase II/III studies of abiraterone acetate

The results of the phase I studies have led to the phase II evaluation of abiraterone acetate in CRPC patients in the UK and US (Danila et al, 2008; de Bono et al, 2008; Reid et al, 2008). Specifically, the efficacy of abiraterone in the settings of both taxane-naïve and taxane-resistant CRPC have been examined, the results of which will soon be fully reported. We have hypothesised that the antitumour activity of abiraterone acetate will not be significantly affected by previous treatment with docetaxel and that abiraterone acetate could be an efficacious treatment in docetaxel-resistant disease. Indeed, preliminary analyses suggest that this is likely to be true.

A placebo-controlled randomised phase III study with the aim of securing FDA licensing approval in the post-docetaxel setting is now open to accrual; 1180 patients will be randomised 2 : 1 for abiraterone acetate plus prednisolone (or prednisone) vs prednisolone (or prednisone) plus placebo, with a primary endpoint of overall survival. The combination of steroids and abiraterone acetate should potentially prevent the syndrome of secondary mineralocorticoid excess and maximise efficacy.

Roles of steroids upstream of CYP17 and abiraterone resistance

The antitumour activity reported with abiraterone acetate could be explained, at least in part, by the durable and profound suppression of serum androstenedione and DHEA, in addition to that of testosterone and oestradiol (Attard et al, 2008). In keeping with earlier reports regarding ketoconazole, these data from the phase I study suggest that higher baseline androstenedione and DHEA levels are present in patients who responded to abiraterone acetate. However, unlike ketoconazole, no rise in steroids downstream of CYP450c17 was observed at disease progression while on abiraterone acetate, indicating ongoing, irreversible CYP450c17 inhibition.

We hypothesised, a priori, that acquired resistance to abiraterone acetate could be reversed by suppressing the production of steroids upstream of CYP17 and this could be achieved by decreasing ACTH using low dose steroids replacement. Indeed, 4 out of 15 patients (26%) with two of these patients having had progressive disease earlier on the same dose of dexamethasone, were successfully salvaged using this approach (Attard et al, 2008) in the phase I study. Hence, it is possible that elevated levels of steroids upstream of CYP450c17 could drive the signalling of a promiscuous, possibly mutated, AR.

Other mechanisms that allow for constitutive AR signalling include mutated AR; ligandless activation of AR signalling, which could occur secondary to AR amplification or following phosphatase and tensin homologue (PTEN) loss; and/or activation of translocated ETS gene promoter elements by other steroid receptors, such as the oestrogen receptor (ER)-α (Taplin, 2007). In fact, oestradiol activate ER-α binding sites on the TMPRSS2 promoter and the suppression of its production could, in part, explain the antitumour activity observed with abiraterone acetate (Ellem and Risbridger, 2007). Translational studies are ongoing to test these hypotheses.

Robust biomarkers as predictive and intermediate endpoints

To maximise benefit to patients and accelerate drug approval by regulatory authorities, the evaluation of robust biomarkers that can serve as predictive and intermediate end-points is urgently required in CRPC therapeutic studies. We describe the preliminary experience we have of the two of the most promising biomarkers that are emerging in this field; the results of their prospective verification in larger cohorts of subjects are eagerly awaited.

Fusion of the androgen-regulated gene, TMPRSS2, with ERG occurs in up to 60% of prostate cancers and is likely to account for the majority of ETS oncogene rearrangements in prostate cancer (Attard et al, 2008). We therefore hypothesised that the presence of a TMPRSS2–ERG fusion gene could indicate dependance on AR signalling and consequently define a tumour sub-group that is responsive to abiraterone acetate. In preliminary studies, PSA decline rate appears to be higher in patients with an ERG rearrangement in archival trans-rectal biopsy of prostate (TRBP) samples (five out of six patients in the published phase I study with an ERG gene rearrangement had a decline in PSA ⩾50%). However, due to ETS gene rearrangement heterogeneity within a single prostate, the use of single TRBP cores may miss areas with ERG rearrangements and fusion of other ETS genes with androgen-regulated partners can also occur.

We have also recently shown that the presence of ⩾5 circulating tumour cells at baseline is associated with a poor outcome and that a fall in CTC count to <5 following treatment is associated with an improved prognosis (Olmos et al, 2009). Significantly, five patients in the phase I study had baseline CTC counts ⩾5 and three of these patients had their CTC counts reduced to <5 after 12 weeks of treatment. The aforementioned phase III study is therefore incorporating the prospective evaluation of whether changes in CTC counts post treatment can serve as a robust intermediate endpoint for overall survival to accelerate drug development for CRPC.

Other agents directly targeting the AR-signalling pathway

In addition to abiraterone and ketoconazole, there are other CYP17 inhibitors that are at various stages of development. VN/124-1, currently in preclinical development and recently licensed to Tokai Pharmaceuticals Inc. (Boston, NY, USA), is a 17-benzoimidazole that has direct inhibitory properties against CYP17 and AR (Handratta et al, 2005). It has potent antitumour effects in vitro with the ability to effectively inhibit proliferation of a bicalutamide-resistant prostate cancer cell lines, which had increased AR expression. Interestingly, the combination of VN/124-1 with either everolimus or gefitinib in vitro was also superior to that achieved with the addition of bicalutamide to either agent, and the VN/124-1 combination effects were synergistic compared with either agent alone (Schayowitz et al, 2008). It is expected that this agent will be evaluated in the clinical setting soon.

The novel small molecule AR antagonist, MDV3100, was rationally designed for its ability to overcome resistance to conventional bicalutamide in the setting of increased AR expression (Sawyers et al, 2007). Unlike bicalutamide, MDV3100 inhibits AR function by blocking nuclear translocation and has no agonist activity when AR is overexpressed. A first-in-man, multi-center phase I/II dose-escalation study has been reported with over 50 patients having enrolled when last reported (Scher et al, 2008). In all, MDV3100 has been well tolerated to date with no significant adverse events. Significantly, it has resulted in PSA reductions in a high proportion of evaluable patients and appears to be a promising candidate for the treatment of progressive CRPC. This trial is currently ongoing.

To summarise, these agents work directly to reduce or inhibit AR-mediated signalling by ligand depletion and/or receptor antagonism. Overall, these data provide further mechanistic and clinical evidence of the importance and relevance of AR-mediated signalling pathway in CRPC therapeutics.

Future directions

The promising efficacy of abiraterone acetate stemming from these early clinical trials in CRPC setting attests to our renewed recognition of the importance of the AR-signalling pathway in CRPC biology. It is sobering to realise that up to 70% of patients who had disease progression on previous lines of hormonal therapies, are still hormone dependant. Indeed, the recent revision of misnomers, such as ‘androgen independence’ and ‘hormone resistance’, by the Prostate Cancer Clinical Trials Working Group is a reflection of this. The successful reversal of resistance to abiraterone acetate using low-dose dexamethasone in some patients also points to the likely importance of steroids upstream of CYP17, and indicate that AR, although likely mutated and promiscuous, remains key in this process.

Although the numbers of subjects and biological specimens involved are small, the evidence from the translational studies involving ETS gene fusion products and CTCs provide further, albeit preliminary, molecular biological corroboration of the importance of AR-mediated signalling mechanisms. These novel molecular platforms may have additional utility in improving our ability to select patients more likely to benefit from abiraterone acetate treatment.

There are numerous questions emerging from the use of this compound. For instance, how are the intratumoural androgenic steroid levels affected by abiraterone acetate? What are the mechanisms of resistance to it? In what clinical settings ought the drug be used? With which agents, cytotoxic and novel, should abiraterone acetate be used? What about the role of abiraterone acetate in other hormonally driven malignancies?

Overall, these data support the development of further novel inhibitors of AR signalling. However, sceptics will trumpet the acknowledgement that we have been in similar positions before with other ADT modalities. We argue that these new clinical and translational seeds are being sowed in research soil more fertile than ever before, enriched by an improved understanding of the pathways of treatment resistance and the availability of new technologies in the evaluation of tumour biology. Hence, not only do we have more effective compounds, there are unparalleled opportunities for these to be combined with emerging novel biological agents, supported by the presence of new molecular and imaging methodologies.

Acknowledgments

The Drug Development Unit is based in the Royal Marsden Hospital NHS Foundation Trust and The Institute of Cancer Research Section of Medicine. We acknowledge support from the Department of Health through the Medical Research Council, Biomedicine Research Centre and Experimental Cancer Medicine Centre (ECMC) grants, and from Cancer Research UK through programme and ECMC grants.

Footnotes

Conflict of interest

Abiraterone acetate was discovered at The Institute of Cancer Research, which therefore has a commercial interest in the development of this agent. Dr de Bono has served as an unpaid consultant for Cougar Biotechnology that owns the rights to development of abiraterone acetate.

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