Vincenzo Adamo* Laura Noto Tindara Franchina Giuseppe Chiofalo Maria Picciotto Giuseppe Toscano Nicola Caristi
- Integrated Therapies in Oncology Unit, Department of Human Pathology, University of Messina, Messina, Italy
Until recently, few therapeutic options were available for patients with castration-resistant prostate cancer (CRPC). Since 2010, four new molecules with a demonstrated benefit (sipuleucel-T, cabazitaxel, abiraterone, and denosumab) have been approved in this setting, and to-date several other agents are under investigation in clinical trials. The purpose of this review is to present an update of targeted therapies for CRPC. Presented data are obtained from literature and congress reports updated until December 2011. Targeted therapies in advanced phases of clinical development include novel androgen signaling inhibitors, inhibitors of alternative signaling pathways, anti-angiogenic agents, inhibitors that target the bone microenvironment, and immunotherapeutic agents. Radium-223 and MDV3100 demonstrated a survival advantage in phase III trials and the road for their introduction in clinical practice is rapidly ongoing. Results are also awaited for phase III studies currently underway or planned with new drugs given as monotherapy (TAK-700, cabozantinib, tasquinimod, PROSTVAC-VF, ipilimumab) or in combination with docetaxel (custirsen, aflibercept, dasatinib, zibotentan). The optimal timing, combination, and sequencing of emerging therapies remain unknown and require further investigation. Additionally, the identification of novel markers of response and resistance to these therapies may better individualize treatment for patients with CRPC.
Introduction
Prostate cancer (PC) is a major public health problem worldwide. In recent years an increasing incidence has been reported, mainly due to both population aging and improvement of diagnostic screening. In United States it represents the most common cancer type and the second cause of cancer death among men, with about 240,000 estimated new cases and 33,000 estimated deaths in 2011 (Siegel et al., 2011). Different therapeutic approaches, including surgery, radiation therapy, and androgen deprivation therapy (ADT) with luteinizing hormone-releasing hormone (LHRH) analogs and/or antiandrogens, have become the gold standard treatment for hormone-dependent PC. Chemotherapy represents, instead, the main therapeutic option in the occurrence of castration-resistant PC (CRPC), defined as disease progressing even in the presence of castration levels of circulating androgens. In this case, docetaxel 75 mg/m2 every 3 weeks plus prednisone 5 mg twice daily (BID) represents the standard first-line treatment since 2004, when two phase III trials (Petrylak et al., 2004; Tannock et al., 2004) showed a prolongation of overall survival (OS) compared with mitoxantrone. Until 2010, there has been no standard second-line treatment for patients progressing on docetaxel-based therapy. The expanding knowledge of the important molecular pathways involved in PC progression has provided the opportunity to investigate specific therapeutics for these patients. Therefore, new therapeutic options have been very recently introduced into clinical practice, while other emerging molecules have shown hopeful results. The aim of this review is to summarize the most important new findings for metastatic CRPC (mCRPC) according to the different molecular pathways and to discuss their potential influence on future management of this disease.
New Approved Treatment Options for mCRPC
Thanks to the approval of four innovative molecules by Food and Drug Administration (FDA) and European Medicines Agency (EMA), the latest 2 years have marked the beginning of a new and exciting era for the treatment of mCRPC. Based on phase III clinical trials (De Bono et al., 2010, 2011; Kantoff et al., 2010a; Fizazi et al., 2011) cabazitaxel, abiraterone acetate, sipuleucel-T, and denosumab represent available therapeutic options in this setting. Cabazitaxel is a tubulin binding agent with weak affinity for P-glycoprotein (Bouchet and Galmarini, 2010). Following data from the TROPIC trial, which showed an OS benefit in patients treated with cabazitaxel 25 mg/m2 every 3 weeks versus standard mitoxantrone after docetaxel failure (De Bono et al., 2010), FDA on June 2010 and EMA on January 2011 approved this treatment for mCRPC. Two ongoing trials (FIRSTANA and PROSELICA), are now being evaluated two different doses (20 and 25 mg/m2) in pre- and post-docetaxel settings to assess if dose reduction, often required because of myelotoxicity, could affect therapeutic response. The mechanism of action of taxanes seems to involve not only microtubule stabilization and tubulin function, but also both androgen receptor (AR) nuclear localization and signaling inhibition (Gan et al., 2009; Jiang and Huang, 2010). This interaction may lead to a more complex and successful inhibition of cell growth, as it has been demonstrated that AR signaling is maintained in CRPC and is implicated in its progression (Attar et al., 2009). Evidence of persistent hormone dependence in mCRPC has opened the way to the development of new antiandrogens able to block testosterone synthesis not only by testes, but also by adrenal glands and prostate tumor tissue. Abiraterone acetate is an oral, selective, and irreversible inhibitor of CYP17, a critical enzyme in androgen biosynthesis, which blocks non-gonadal androgen production. Abiraterone at a dose of 1000 mg/day in combination with prednisone 10 mg/day was approved by FDA on April 2011 and by EMA on July 2011 for the treatment of mCRPC after a docetaxel chemotherapy following the results of the COU-AA-301 trial, which demonstrated a survival benefit for the experimental arm compared with placebo (De Bono et al., 2011). A similar placebo-controlled phase III trial (COU-AA-302) evaluating abiraterone in docetaxel-naïve patients progressing after ADT has completed accrual and will provide data about the use of this drug before chemotherapy.
Sipuleucel-T is obtained by activating patient’s leukapheresed antigen-presenting cells (APCs), including dendritic cells, with a recombinant fusion protein consisting of prostatic acid phosphatase (PAP) antigen and granulocyte-macrophage colony-stimulating factor (GM-CSF), an immune-cell activator. This cellular immunotherapy produced an advantage in terms of OS in the IMPACT study, a placebo-controlled phase III trial that led, on April 2010, to the FDA approval in patients with asymptomatic or minimally symptomatic mCRPC (Kantoff et al., 2010a). It will be important to evaluate the rational combination and proper sequencing of sipuleucel-T with these newly approved, as well as emerging (MDV3100, TAK-700, ipilimumab) agents (Sonpavde et al., 2012).
Finally, denosumab, a human monoclonal antibody against receptor activator of nuclear factor-kappa ligand (RANK-L), showed superiority in preventing skeletal-related events (SREs) versus zoledronic acid in patients with bone metastases from CRPC (Fizazi et al., 2011) and breast cancer (Stopeck et al., 2010), and non-inferiority in patients with other solid tumors, excluding multiple myeloma (Henry et al., 2011). It has therefore been approved by FDA and EMA for the prevention of SREs in patients with metastatic bone disease. In addition, denosumab was demonstrated to delay the time to first bone metastasis and to increase bone-metastasis-free survival (BMFS) in men with non-mCRPC at high risk of bone metastasis (Smith et al., 2012), confirming its potential clinical role.
Targeting the Androgen Receptor Pathway
Specific CYP17 Inhibitor: TAK-700
TAK-700 (orteronel) is an oral, selective, reversible, non-steroidal androgen synthesis inhibitor of the 17.20 lyase activity, one of two enzymatic reactions catalyzed by CYP17. Due to its low inhibition of 17-hydroxylase activity, administration does not require concomitant steroid replacement (Ryan and Tindall, 2011). This compound showed activity and good tolerability in a phase I/II clinical trial on chemotherapy naïve patients (Agus et al., 2011; Mortimer et al., 2011). Phase I patients received TAK-700 escalating doses (100–600 mg BID), while phase II ones were given TAK-700 300 mg BID, 600 mg once daily (QD), or two dose levels (400 or 600 mg BID) plus prednisone 5 mg BID. In the phase II portion, 97 patients received TAK-700. Most common adverse events (AEs) were fatigue (72%), nausea (44%), and constipation (31%), with fatigue (9%) and diarrhea (3%) as most common grade ≥3 AEs. TAK-700 resulted in reduced circulating testosterone and adrenal androgen dehydroepiandrosterone sulfate (DHEA-S) concentrations. Of 43 RECIST-evaluable patients, 6 had a partial response (PR), 23 had stable disease (SD), and 9 had progression disease (PD). PSA response rates (≥50% decrease) at 12 weeks were similar across treatment groups, with an overall response rate (ORR) of 53%. Researchers concluded that, in patients with mCRPC, oral TAK-700 (with/without prednisone) at doses of ≥300 mg BID was active and well tolerated. Based on these positive findings, two randomized, phase III, placebo-controlled multicenter studies are currently being investigated efficacy and safety of TAK-700 400 mg BID plus prednisone 5 mg BID versus placebo plus prednisone in chemotherapy naïve and docetaxel-pre-treated mCRPC patients.
New AR Antagonists
Ligand-independent continued activation of ARs is one of the mechanisms that allow PC cells to survive and grow in the presence of castrate androgen levels. Receptor mutations (Taplin et al., 2003), alternative splicing with synthesis of AR splice variants (Sun et al., 2010), AR encoding gene amplification (Liu et al., 2009) as well as co-activators dysregulation have been described as potential escape mechanisms implicated in CRPC progression. First-generation AR antagonists, such as bicalutamide or flutamide, represent the standard of care for advanced PC since the eighties. However, they bind reversibly to ARs and may have androgen-agonist properties, as demonstrated in cells engineered to over-express higher AR amounts (Tran et al., 2009), limiting therapeutic activity. This has raised the need to develop more potent and efficacious molecules. In such a perspective, new antiandrogens with improved binding properties have been produced. One of these agents, MDV3100, is an oral AR antagonist small molecule that binds to ARs with higher affinity than bicalutamide, blocking AR nuclear translocation, co-activators recruitment, and DNA binding without agonist activity when AR is overexpressed (Tran et al., 2009). Unlike bicalutamide, MDV3100 do not induce expression of the AR target genes PSA and transmembrane serine protease 2 (TMPRSS2) in a pre-clinical model, indicating the absence of agonist activity in a castration-resistant setting (Tran et al., 2009). MDV3100 has demonstrated a promising clinical activity in CRPC in a phase I/II trial (Scher et al., 2010) evaluating drug escalating doses (from 30 to 600 mg/day) on 140 patients, 65 chemotherapy naïve and 75 previously treated with docetaxel. A recent update (Higano et al., 2011) after a long-term follow-up on time to PSA and radiographic progression, confirmed a durable anti-tumor activity of MDV3100. The median time to PSA progression, defined per-protocol as a ≥25% increase in PSA from baseline, was not met for naïve patients and was 8 months for post-chemotherapy patients. The median time to radiographic progression was 13 months for naïve and 6 months for post-chemotherapy group. MDV3100 was generally well tolerated, with fatigue as most frequently reported AE (Scher et al., 2010). Based on these interesting results, MDV3100 is currently being evaluated in two phase III studies, in pre- (PREVAIL) and post-docetaxel (AFFIRM) settings. AFFIRM is a randomized, placebo-controlled, double-blind, multi-national trial evaluating MDV3100 160 mg/day in mCRPC men previously treated with docetaxel-based chemotherapy. The primary endpoint is OS, secondary endpoints include progression-free survival (PFS), safety, and tolerability. On November 2011, the results of a planned interim analysis performed by the Independent Data Monitoring Committee (IDMC) showed that MDV3100 produced a 4.8-month advantage in median OS compared to placebo (18.4 months for MDV3100 versus 13.6 for placebo), with a 37% (HR = 0.631) reduction in the risk of death in the treated population. Consequently, IDMC recommended AFFIRM early stop, and men given placebo were offered MDV3100. A full analysis of the results from AFFIRM including safety data will be soon presented. ARN-509 is a novel small molecule AR antagonist with a mechanism of action similar to that of MDV3100, which showed powerful anti-cancer activity and induced durable remission in advanced CRPC mouse models. It seems to produce higher rates and longer duration of responses than MDV3100. An ongoing phase I/II clinical trial of continuous oral ARN-509 in patients with progressive CRPC with and without prior chemotherapy was started in July 2010 (Rathkopf et al., 2011a). Finally, AZD3514, a selective AR degrading and down-regulating agent, orally available, given on a daily continuous schedule, is now being tested in a phase I clinical trial, with an estimated completion date of 2013.
Dual CYP17 Inhibitor and AR Antagonist: TOK-001
Some of the CYP17 inhibitors are of particular interest as they are also AR antagonists and cause receptor down-regulation. TOK-001 (VN/124-1) is the first compound to show superior efficacy compared with castration in PC xenograft models (Handratta et al., 2005). It also inhibits the proliferation of hormone-resistant PC cell lines (HP-LNCaP), which are no longer sensitive to bicalutamide and have an increased AR expression (Schayowitz et al., 2008). These impressive pre-clinical data led to the development of this compound in the clinical setting. The results of the phase I/II clinical trial ARMOR1, conducted in treatment-naïve CRPC patients progressing on ADT, are awaited after its completion in July 2012.
Targeting Non-Hormonal Intracellular Molecular Pathways
Signal Transduction Pathways Inhibitors
There is growing evidence indicating the presence of signaling mechanisms and cross-talk between growth factor receptor pathways and AR in androgen-dependent and hormone-resistant PC cell lines (Schayowitz et al., 2008), that lead to AR regulation by signal transduction pathways and vice versa (Traish and Morgentaler, 2009). Cross-talk between AR and growth factor pathways may represent a key factor during PC progression, conferring a survival, and invasion advantage to tumor cells, together with a resistance to hormonal therapy. This mutual relationship involves epidermal growth factor receptors (EGFR and HER-2), insulin-like growth factor receptor (IGFR), fibroblast growth factor receptor (FGFR), vascular endothelial growth factor (VEGF) receptor (VEGFR), transforming growth factor-β (TGFβ), phosphoinositide 3-kinase (PI3-K), Akt, and mammalian target of rapamycin (mTOR) pathways (Wen et al., 2000; Manin et al., 2002; Zhu and Kyprianou, 2008) and represents a potential target to overcome endocrine resistance. Drugs targeting EGFR and/or HER-2 did not produce significant results in CRPC (Boccardo et al., 2008; Nabhan et al., 2009; Slovin et al., 2009a; Whang et al., 2011), while mTOR inhibitors seemed to have some activity. In particular, in pre-clinical studies on cellular (Schayowitz et al., 2008; Wedel et al., 2011) and xenograft models (Morgan et al., 2008; Schayowitz et al., 2010) everolimus demonstrated positive results in combination with TOK-001 (Schayowitz et al., 2008, 2010), AEE788 (a dual VEGFR/EGFR inhibitor; Wedel et al., 2011), and docetaxel plus zoledronic acid (Morgan et al., 2008). A phase II study (Templeton et al., 2011) investigating the activity of everolimus 10 mg/daily as first-line treatment in patients with mCRPC has been recently presented. Among 37 enrolled patients, 12 (32%) remained progression-free at 12 weeks. Other phase II studies of everolimus, alone or in combination with bicalutamide, bevacizumab, or chemotherapy, as well as trials testing other mTOR inhibitors such as temsirolimus and ridaforolimus, are currently recruiting patients. IGF-1R inhibitors are also being evaluated in CRPC. Among these, cixutumumab (IMC-A12), a monoclonal antibody, is under study in a phase I/II trial in combination with temsirolimus in chemo-naïve mCRPC patients. The study has completed phase I accrual and early results have shown good tolerability (Rathkopf et al., 2011b).
Inhibitors of Survival Factors
Overexpression of proteins belonging to inhibitor of apoptosis (IAP) family, like Bcl-2, Bcl-X, survivin, and Mcl-1 (Raffo et al., 1995; Krajewska et al., 1996; Zhang et al., 2005), or of the stress-induced cytoprotective chaperone protein clusterin (Shiota et al., 2011) in PC cells is associated with disease progression, cell survival advantage, and resistance to ADT and chemotherapy-mediated apoptosis. Oblimersen, an anti-Bcl-2 antisense oligonucleotide (Sternberg et al., 2009), and AT-101, a small molecule inhibitor of the Bcl-2 family (Sonpavde et al., 2011), were studied as first-line treatment for CRPC in combination with docetaxel. However, clinical results were both negative in terms of PSA response and OS. Similarly, YM155, a small molecule suppressor of survivin, showed modest activity in taxane-pre-treated CRPC patients (Tolcher et al., 2012).
Custirsen (OGX-011) is an antisense oligonucleotide complementary to clusterin mRNA that inhibits its translation. In a randomized phase II trial (Chi et al., 2010) custirsen 640 mg intravenously weekly plus standard docetaxel as first-line treatment improved median OS in CRPC patients compared with docetaxel alone (23.8 versus 16.9 months), even if PSA and tumor response rates were similar. Another phase II trial tested custirsen in combination with mitoxantrone or docetaxel treatment as second-line therapy after progression during or within 6 months of initial docetaxel therapy (Saad et al., 2011). Pain relief was observed in 46 and 77% of patients, respectively. These rates were higher than expected, with interesting correlations between serum clusterin and survival. Two phase III studies are ongoing: SYNERGY, planned to enroll 800 patients, which will confirm whether adding custirsen to standard first-line docetaxel treatment slows tumor progression and enhances survival compared to chemotherapy alone, and SATURN, investigating custirsen in association with docetaxel as second-line retreatment.
Dual c-MET/VEGFR2 Inhibitor: Cabozantinib
As known, the hepatocyte growth factor/scatter factor (HGF/SF) and its receptor, the tyrosine kinase c-MET, promote tumor growth, invasion, and metastasis in several malignancies (Birchmeier et al., 2003). In PC, c-MET expression was demonstrated to be repressed by AR (Verras et al., 2007), with a consequent enhanced synthesis during ADT and in the hormone-independent state. Moreover, c-MET pathway activation is associated with progression to bone (Knudsen et al., 2002), and seems to induce a stem-like phenotype (Van Leenders et al., 2011) conferring a high invasive capacity, especially in the perimeter of prostate tumor, where this proto-oncogene is more expressed.
Cabozantinib (XL184) is an oral small molecule inhibitor of multiple kinase signaling pathways including c-MET and VEGFR2. An interim analysis of a phase II study, designed as a “randomized discontinuation” trial in patients with mCRPC, was recently presented (Hussain et al., 2011). After 12 weeks of treatment, patients with PR continued open-label cabozantinib, those with SD were blindly randomized to cabozantinib versus placebo, and those with PD discontinued treatment. Cabozantinib 100 mg/day led to improvement of bone parameters, especially bone scan and markers, as early as week 6. At this time, among bone evaluable patients, 86% complete or partial resolution of bone metastases and 12% stabilizations were reported. Prolonged PFS (21 versus 6 weeks) was registered in the cohort of patients undergone randomization. At week 12 disease control rate (PR + SD) was 71% with fatigue, hypertension, and hand-foot syndrome as major AEs. Based on this early clinical activity, two phase III trials are planned to test cabozantinib 60 mg/daily in patients with mCRPC after treatment with docetaxel and abiraterone: the 306 trial with mitoxantrone/prednisone as control arm and relief of bone pain as primary endpoint, and the 307 trial, comparing cabozantinib versus prednisone with OS as primary endpoint.
Targeting Angiogenesis
Angiogenesis and VEGFR pathway play a key role in CRPC progression and metastasis (Sweeney et al., 2002; Tomic et al., 2012), as in the majority of cancers and thus several anti-angiogenic drugs are currently studied in this setting. Bevacizumab, a humanized monoclonal antibody against VEGF, was evaluated in various phase II clinical trials in combination with docetaxel, either monotherapy or associated with other agents such as thalidomide, estramustine (Di Lorenzo et al., 2008; Ning et al., 2010; Picus et al., 2011), or lenalidomide (Huang et al., 2011), showing anti-tumor activity. Nevertheless, the phase III CALGB 90401 study (Kelly et al., 2010) failed to obtain OS advantage, and important morbidity and mortality rates were seen.
Lenalidomide is an angiogenesis inhibitor similar to thalidomide with immune-modulatory effects, which was tested in the MAINSAIL, a pivotal double-blinded phase III trial designed to evaluate the efficacy and safety of docetaxel and prednisone with or without lenalidomide in CRPC patients. In November 2011, Celgene International Sàrl announced study discontinuation, since the combination treatment would not demonstrate a statistically significant effect.
Aflibercept is a promising anti-VEGF agent, also called VEGF-trap (Lockhart et al., 2010). It is a recombinant protein consisting of the Fc portion of human IgG1 combined with the extracellular ligand-binding domains 2 and 3 of the human VEGFR 1 and 2, now under investigation in the phase III VENICE trial. This study, testing aflibercept in combination with first-line docetaxel, has completed accrual and results are awaited.
Tasquinimod is an oral quinoline-3 carboxamide derivative with a new anti-angiogenic and anti-tumor activity. It binds to S100A9 (Björk et al., 2009), an immune-modulatory protein expressed on myeloid-derived suppressor cells (MDSCs), important tumor microenvironment mediators of angiogenesis and tumor growth (Schmid and Varner, 2010). In a randomized pre-chemotherapy placebo-controlled phase II trial, an improved PFS (7.6 versus 3.3 months) was seen in patients in tasquinimod arm (Pili et al., 2011). Most frequent AEs recorded in tasquinimod group included gastrointestinal disorders, fatigue, musculoskeletal pains, and elevations of pancreatic and inflammatory biomarkers. A phase III placebo-controlled study is ongoing in a larger pre-docetaxel mCRPC population.
Given encouraging results in several phase II trials (Dror Michaelson et al., 2009; Sonpavde et al., 2010; Zurita et al., 2012), the multi-tyrosine kinase inhibitor and anti-angiogenic small molecule sunitinib was investigated in a phase III trial (SUN1120) with OS as primary endpoint in patients with progressive mCRPC after docetaxel-based chemotherapy (Michaelson et al., 2011). Nevertheless, the study was stopped for futility at the second interim analysis on September 2010. Many other drugs targeting angiogenesis are in clinical development for CRPC, including the multi-kinase inhibitor sorafenib active against c-raf, BRAF, VEGFR, platelet-derived growth factor receptor, Flt-3, c-KIT, and RET. Sorafenib showed contrasting results in phase II studies, due to discordant imaging and PSA responses (Steinbild et al., 2007; Chi et al., 2008; Aragon-Ching et al., 2009), therefore further evaluations are needed.
Targeting the Bone Microenvironment
Src-Family Kinases Inhibitors
Src and Src-family kinases (SFKs) are a family of intracellular tyrosine kinases that mediate transduction of several molecular pathways implicated in PC growth, invasion, and progression (Tatarov et al., 2009). Src signaling is also involved in the development of bone metastasis, as it regulates different osteoclast functions including bone resorption (Miyazaki et al., 2004). Dasatinib is a SFK and Abl kinase inhibitor able to suppress PC cells-induced osteoclast differentiation and activity in pre-clinical models (Araujo et al., 2009; Vandyke et al., 2010). It was studied in a phase II trial (Yu et al., 2009) conducted in 47 chemotherapy naïve men with CRPC and biochemical progression. Patients were given dasatinib 100 or 70 mg BID. Both these schedules demonstrated biologic activity, especially on bone turnover markers, but remarkable AEs including diarrhea (62% of patients), pleural (51%), and pericardial (23%) effusions were recorded. The trial was amended because of toxicity and an expansion cohort of 48 patients was treated with dasatinib 100 mg once daily (Yu et al., 2011). At this dose the drug confirmed a good clinical activity and had a better tolerability profile with lesser grade 3/4 AEs (13% versus 32%), particularly 19% versus 51% pleural effusions, compared with the BID dosage. Dasatinib in combination with docetaxel has been studied in a recently published phase I/II trial (Araujo et al., 2012). Of 46 treated patients, 37 (80%) had any PSA decrease, including 26 (57%) who had a confirmed PSA response. Among RECIST-evaluable patients, 18 of 30 (60%) had PR with a 77% of overall disease control rate (PR + SD). Parallel bone scan improvements and urinary bone resorption markers decline were also observed. The combination was well tolerated, with a decreased frequency of pleural effusion (15%), probably due to the concomitant prednisone administration. READY, a phase III trial of docetaxel with or without dasatinib as first-line treatment of mCRPC is now ongoing. Another SFK inhibitor in clinical development for PC, saracatinib (AZD0530), showed limited clinical efficacy as monotherapy in a phase II trial (Lara et al., 2009).
Endothelin-1 Receptor Antagonists
The pathogenesis of osteoblastic bone metastasis, which frequently occur in mCRPC, is characterized by dysregulation of both bone resorption and formation (Guise et al., 2006). In particular, a role has been identified for the vasoactive peptide endothelin-1 (ET-1), produced by metastatic cancer cells in the microenvironment of new-formed bone, through the stimulation of the endothelin A receptor (ETaR) and its downstream pathways in osteoblastic cells (Yin et al., 2003). Atrasentan (ABT-627), an ETaR antagonist, reduced osteoblastic bone metastases, and bone tumor burden in in vitro and in vivo pre-clinical models (Yin et al., 2003), demonstrating an additive anti-tumor effect in combination with taxanes (Akhavan et al., 2006; Banerjee et al., 2007). Despite positive effects of atrasentan monotherapy in delaying median time to disease and PSA progression, as observed in a double-blinded, randomized, placebo-controlled phase II clinical trial (Carducci et al., 2003), data from two phase III studies carried out with this agent in either non-metastatic or metastatic disease failed to show a significant benefit in time to progression (Carducci et al., 2007; Nelson et al., 2008). Similarly, the phase III SWOG 0421 trial of atrasentan plus docetaxel as first-line therapy was closed early due to failure in reaching the primary endpoints (OS and PFS). Also zibotentan (ZD4054), another ETaR antagonist, presented discordant data among a phase II trial (James et al., 2010) and two of the subsequent phase III trials. The ENTHUSE clinical trial program consists of three phase III clinical studies designed to evaluate zibotentan monotherapy in men with metastatic (ENTHUSE M1 trial 14) and non-metastatic (ENTHUSE M0 trial 15) CRPC, as well as its combination with docetaxel as first-line treatment (ENTHUSE M1C trial 33). Both ENTHUSE studies 14 (Nelson et al., 2011) and 15 (not published) were stopped following the negative results to meet primary efficacy endpoints, while ENTHUSE study 33 will be continued and full results are expected.
Radiopharmaceuticals
Unlike strontium-89 and samarium-153, beta-emitting radiopharmaceuticals approved for palliation of bone metastasis-related pain (National Comprehensive Cancer Network (NCCN), 2011), radium-223 (alpharadin) targets bone metastasis with higher energy and shorter track length alpha-radiation. This allows hematopoietic bone marrow cells to be partly spared from damage due to radiation (Nilsson et al., 2007). A phase II trial reported minimum myelotoxicity and a significant effect on bone-alkaline phosphatase concentrations in patients treated with radium-223 versus placebo (Nilsson et al., 2007). The subsequent phase III ALSYMPCA trial was prematurely stopped in June 2011 after a preplanned interim efficacy analysis showing a significant 2.8-month OS benefit in the radium-223 arm over placebo arm (HR = 0.699). Based on these results approval procedures are ongoing.
Immunotherapy
In addition to sipuleucel-T, further immunotherapeutic strategies are being explored with the aim to induce a specific T-cell response against PC (Gerritsen and Sharma, 2012). However expensive costs and complex procedures represent limiting factors for the application of these new options in clinical practice. Updated results of a phase II study of a PSA-targeted poxviral vaccine, PROSTVAC-VF (rV-PSA), for patients with mCRPC, reported a 44% reduction in the death rate, and an 8.5-month improvement in median OS despite a similar PFS (Kantoff et al., 2010b). To confirm these positive data, the phase III study PROSPECT was recently initiated in patients with asymptomatic or minimally symptomatic mCRPC. GVAX is a cell-based vaccine consisting of LNCaP and PC-3 prostate cell lines, genetically engineered to secrete high levels of GM-CSF. These cells are injected intradermally in order to initiate an antiprostate immune response (Gerritsen and Sharma, 2012). Despite promising results of a phase II study (Higano et al., 2008), two phase III clinical trials, VITAL-1 and 2, were both terminated early due to futility (VITAL-1) and increased death rates (VITAL-2) in the GVAX arms (Small et al., 2009). The fully human antibody ipilimumab blocks a negative regulator of T cells, the cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), leading to an increased anti-tumor immune response. Early results of phase I/II clinical trials testing ipilimumab alone (Small et al., 2007) and in combination with GM-CSF (Fong et al., 2009) or radiotherapy (Slovin et al., 2009b) showed some activity. Therefore, two phase III placebo-controlled trials are being evaluated ipilimumab in CRPC patients either following radiotherapy after docetaxel chemotherapy or in chemo-naïve patients.
Conclusion
Prostate cancer management scenario is rapidly evolving thanks to the already approved and the emerging therapies in clinical development. Among new agents studied in phase III trials, cabazitaxel, abiraterone acetate, sipuleucel-T, MDV3100, and radium-223 have shown significant OS advantages, while denosumab has delayed time to first SRE and prolonged BMFS (Table 1). Therefore, these drugs have been or are going to be approved into clinical practice. Other agents are still under investigation in phase III trials and results are pending (Table 2). Among them, cabozantinib, custirsen, and dasatinib seem to be the most promising. However, even if all trials listed on Table 1 show positive results, they are not comparable because of heterogeneous study populations and control arms (i.e., cabazitaxel was tested versus mitoxantrone, other agents versus placebo). Further studies directly comparing these compounds are thus needed to better evaluate their clinical activity. Moreover, failure of various clinical trials testing treatment options for mCRPC (Table 3) reveals the complexity of research in this field and the related open questions. Firstly, while on one hand the availability of several novel compounds represents a meaningful tool against CRPC, on the other hand the use of multiple therapeutic strategies in these patients may confound study results, especially when OS is chosen as primary endpoint. This aspect should be taken into account when clinical trials are designed for this setting. Secondly, optimal timing, proper combination, and sequencing of the different therapeutic approaches need to be better defined. In fact, as the majority of innovative drugs have been tested in advanced stages of disease, it would be important to evaluate whether their earlier use could improve the outcomes. Moreover, until now clinical trials have been conducted in unselected populations, without regard on tumor genomic signature and molecular expression. In the near future, identification of different PC molecular subtypes through genomic and/or proteomic analyses, as well as prognostic and predictive markers, will allow us to exploit the potential differences in disease biology, in order to optimize therapy for each PC patient with individualized and more efficacious treatments.
Table 1. Positive phase III trials with emerging therapies for CRPC.
Table 2. Ongoing phase III trials with emerging targeted therapies for CRPC.
Table 3. Negative phase III trials with emerging targeted therapies for CRPC.
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.
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Keywords: castration-resistant prostate cancer, targeted therapy, hormonal therapy, anti-angiogenic therapy, bone targeting therapy, immunotherapy
Citation: Adamo V, Noto L, Franchina T, Chiofalo G, Picciotto M, Toscano G and Caristi N (2012) Emerging targeted therapies for castration-resistant prostate cancer. Front. Endocrin. 3:73. doi: 10.3389/fendo.2012.00073
Received: 30 January 2012; Paper pending published: 13 April 2012;
Accepted: 08 May 2012; Published online: 31 May 2012.
Edited by:
Carmen Priolo, Brigham and Women’s Hospital, USAReviewed by:
Daniele Santini, University Campus Bio-Medico, ItalyKevin Courtney, UT Southwestern Medical Center, USA
Copyright: © 2012 Adamo, Noto, Franchina, Chiofalo, Picciotto, Toscano and Caristi. This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
*Correspondence: Vincenzo Adamo, Integrated Therapies in Oncology Unit, Department of Human Pathology, University of Messina, Via Consolare Valeria 1, 98125 Messina, Italy. e-mail: vadamo@unime.it