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Cancer Med. 2013 April; 2(2): 243–252.
Published online 2013 February 24. doi:  10.1002/cam4.64
PMCID: PMC3639663

Is there a role for immune checkpoint blockade with ipilimumab in prostate cancer?

Abstract

Treatment for advanced prostate cancer has and will continue to grow increasingly complex, owing to the introduction of multiple new therapeutic approaches with the potential to substantially improve outcomes for this disease. Agents that modulate the patient's immune system to fight prostate cancer – immunotherapeutics – are among the most exciting of these new approaches. The addition of antigen-specific immunotherapy to the treatment of castration-resistant prostate cancer (CRPC) has paved the way for additional research that seeks to augment the activity of the immune system itself. The monoclonal antibody ipilimumab, approved in over 40 countries to treat advanced melanoma and currently under phase 2 and 3 investigation in prostate cancer, is thought to act by augmenting immune responses to tumors through blockade of cytotoxic T-lymphocyte antigen 4, an inhibitory immune checkpoint molecule. Ipilimumab has been studied in seven phase 1 and 2 clinical trials that evaluated various doses, schedules, and combinations across the spectrum of patients with advanced prostate cancer. The CRPC studies of ipilimumab to date suggest that the agent is active in prostate cancer as monotherapy or in combination with radiotherapy, docetaxel, or other immunotherapeutics, and that the adverse event profile is as expected given the safety data in advanced melanoma. The ongoing phase 3 program will further characterize the risk/benefit profile of ipilimumab in chemotherapy-naïve and -pretreated CRPC.

Keywords: Castration-resistant prostate cancer, checkpoint blockade, immune response, immunotherapy, ipilimumab

Rationale for Immunotherapy in Prostate Cancer

For men across the world, prostate cancer is the second most common cancer diagnosis and the sixth leading cause of cancer-related death 1. Most diagnoses (approximately 71%) occur in developed countries where routine prostate-specific antigen (PSA) screening is practiced; thus, the disease is frequently diagnosed in the asymptomatic stage 1,2. Even before the appearance of clinical symptoms, immune responses against prostate tumors are evidenced by intratumoral leukocyte infiltration and inflammatory pathway activation 3,4. Analyses of tissue samples from prostate tumors have revealed infiltrating leukocytes with a role in innate immunity (i.e., natural killer cells), as well as those with antigen-specific activity (i.e., effector and regulatory T cells), suggesting that the host immune system can mount a natural antitumor response that employs both the innate and adaptive branches 3,4. Persistence and progressive growth of the tumor in an immunocompetent environment suggests that, as has been shown for many solid tumors, at least some prostate cancer cells develop the ability to avoid or suppress the host immune response 4,5. This body of evidence supports the rationale for combating prostate cancer with immunotherapy, with the goal of promoting more effective tumor control by encouraging the host to mount an immunogenic response to prostate tumor cells 4,6.

Because tumor-associated antigens may not be adequately recognized by the immune system for a productive immune response to result 3,5, antigen-specific anticancer immunotherapy (tumor vaccines) is designed to enhance the immunogenicity of known tumor-associated antigens, with the goal of promoting a productive antitumor immune response. Tumor vaccines may or may not employ an adjuvant component to enhance the function of antigen presenting cells (APCs) and immune effectors such as T cells 7. In 2010, sipuleucel-T (PROVENGE®; Dendreon, Seattle, WA) garnered the first national regulatory approval (by the United States Food and Drug Administration [FDA]) of a tumor vaccine and is now indicated for treatment of castration-resistant prostate cancer (CRPC) in patients with asymptomatic or minimally symptomatic disease 8,9. For prostate cancer oncologists and urologists, this approval helped to validate immunotherapy as a treatment approach with the potential to provide significant clinical benefits, and several other tumor vaccines are now under investigation for CRPC.

Targeting specific tumor-associated antigens is only one therapeutic approach with the potential to tip the balance from immune tolerance to immune activation against the tumor. Some preclinical and clinical evidence suggests that the CRPC tumor cells or the surrounding microenvironment are capable of suppressing the activity of infiltrating T effector cells, leading to immune tolerance toward the tumor in spite of an antigen-specific immune response 7,10,11. With the aim of overcoming this tolerance and augmenting immune responses to CRPC tumors, cancer researchers are investigating inhibition of molecules or pathways that dampen immune responses (so-called immune checkpoint receptors), in an effort to modulate the immune system itself to fight cancer 4,6.

Interestingly, standards of care like androgen deprivation therapy, radiotherapy, and chemotherapy 12 have been observed to alter the immune milieu of prostate cancer or the host, although the underlying pathways are not completely understood 4,6,7,10,13. Preclinical and preliminary clinical evidence suggest that radiotherapy and/or chemotherapy may augment immunotherapy-induced immunologic responses on a molecular level, possibly through antigen release from dying tumor cells 14,15,16 or by direct modulation of immune effector molecules 17. This evidence for synergy supports the rationale for investigating multimodal therapies involving immunotherapy and other anticancer agents with potentially immunosupportive mechanisms of action. Whether a particular combination, timing, or schedule maximizes clinical benefit of immunotherapy-containing regimens is a subject of ongoing research.

CTLA-4 Blockade in Prostate Cancer

When APCs present antigens to T cells, the costimulatory interaction between APC-expressed B7 and T-cell–expressed CD28 is indispensable for a productive immune response to the antigen. To keep these responses in check, T-cell activation induces cell surface expression of immune checkpoint receptors, which has the net effect of downregulating T-cell activity 1820. This process is thought to underlie the induction of peripheral tolerance. Cytotoxic T-lymphocyte antigen 4 (CTLA-4), the most extensively studied of these immune checkpoint receptors, binds to B7 with higher avidity than does CD28; thus, CTLA-4 competitively inhibits CD28-mediated T-cell activation and subsequently dampens the T-cell response (Fig. 1) 18. Blockade of CTLA-4 signaling preserves the CD28-B7 costimulatory signal and thus the T-cell activation signal, which augments the resulting T-cell-mediated immune responses.

Figure 1
Role of CTLA-4 in T-cell activation and molecular consequence of CTLA-4 blockade. AP, adapter protein; APC, antigen presenting cell; ARF-1, ADP ribosylation factor 1; BCL-2, B cell lymphoma–associated protein 2; BCL-XL, B cell lymphoma–associated ...

Ipilimumab (YERVOYTM; Bristol-Myers Squibb, Princeton, NJ) is a fully human IgG1 monoclonal antibody against CTLA-4 21. Two randomized phase 3 trials of ipilimumab in advanced melanoma have reported overall survival benefit over control arms, with a side-effect profile that was managed with proactive treatment guidelines as outlined in the individual protocols 2224. In 2011, the agent was approved in the United States as monotherapy at a dose of 3 mg/kg for treatment of unresectable or metastatic melanoma 24. The agent has since been approved as an advanced melanoma treatment in over 40 countries.

Due to its potentially broadly applicable mechanism of action, ipilimumab has also been under investigation in several other solid tumor settings, including CRPC. In fact, the first in-human study of ipilimumab was in prostate cancer: an investigation of a single 3 mg/kg dose of ipilimumab in 14 patients with hormone-refractory prostate cancer 25. Ipilimumab as a single dose had acceptable pharmacokinetic and safety profiles, but only two of the 14 patients experienced PSA declines of >50%. Results have since been reported for six other clinical studies of ipilimumab in CRPC. Together, these seven trials encompassed 240 patients across multiple settings of advanced CRPC, roughly 20% of whom had progressed on or relapsed after docetaxel (Table 1) 2535.

Table 1
Summary of phase 1/2 data for ipilimumab in CRPC

Reflecting the dose-finding nature of many of these trials, the studies utilized multiple doses (ranging from 0.5 to 10 mg/kg as either monotherapy or in combination studies) and schedules (ranging from a single dose of ipilimumab to recurring doses every 3 weeks for four cycles). In the phase 1 and 2 trials in CRPC, ipilimumab was active whether used as monotherapy 25,28 or with other interventions such as radiotherapy 26, docetaxel 27, or other immunotherapeutics with different mechanisms of action 2935. Notably, one study in 43 chemotherapy-eligible patients compared ipilimumab monotherapy (3 mg/kg, every 4 weeks, for four doses) with ipilimumab plus a single 75 mg/m2 dose of docetaxel on day 1; this small study did not reveal a clear difference in safety or PSA response (around 15%) between the two groups 27.

Clinical investigation in CRPC with the antigen-specific therapies sipuleucel-T 9 and PROSTVAC® (Bavarian Nordic, Kvistgaard, Denmark) 36 revealed little overall impact on delaying progression of disease, but the reported benefits in overall survival may represent a slowing of tumor growth 7,26. In phase 2 reports of ipilimumab, although efficacy endpoints also varied amongst the studies, declines in PSA were consistently noted (15–20%) at doses of ≥3 mg/kg. All trials utilized the PSA Working Group 2 criteria 37. These response rates suggest that a subset of patients with CRPC may be responsive to therapy with ipilimumab, although none of the data reported to date have revealed specific characteristics of this subset. However, these studies did report various patterns of PSA declines, occurring at treatment onset, after a short period of stable disease, or within 6 months after an initial rise in PSA levels. Some immediate responses (within 1 month of initiating treatment) were noted, and some late responses (after 6 months of treatment) were also observed 26,27. In some cases, responses to ipilimumab lasted for 1 year or more 26,27. Although these phase 2 data require further verification in phase 3 trials, these observed patterns do suggest that an individual's immune response to cancerous cells may be dynamic and, in a select number of patients, durable over the course of disease.

In the CRPC trials, the side effects associated with ipilimumab therapy were common and inflammatory in nature (reflective of the immunologic mechanism of action). Table 2 provides incidences of these immune-related adverse events (irAEs) from the largest phase 2 trial, in which ipilimumab was used as monotherapy at 10 mg/kg (CA184-017) 26. Commonly reported side effects in the CRPC studies included gastrointestinal events such as colitis, diarrhea, rash or pruritus, hepatitis, or endocrinopathies. These endocrinopathies included adrenal insufficiency, hyper- or hypothyroidism, hypophysitis, or hypopituitarism. Interestingly, endocrinopathies leading to adrenally insufficient states (and suppressed androgen production) may also provide an indirect mechanism for tumor control, but as PSA responses to ipilimumab have been reported in the absence of changes in adrenal hormones 30, it is more likely that tumor responses are directly mediated by an ipilimumab-induced immune response. The phase 1 and 2 studies in CRPC did not report any safety issues that were unexpected given the safety data previously reported for ipilimumab 22,23. Though these side effects were severe in some instances, they were typically addressed through interventions outlined in the individual trial protocols, as was done in the melanoma studies. In study CA184-017, corticosteroids and other immunosuppressive agents, as well as hormone replacement therapy for endocrine side effects, were utilized at the discretion of the investigators 26.

Table 2
Common treatment-related adverse events observed with ipilimumab monotherapy at 10 mg/kg in a phase 2 study 26

Only one of the phase 2 studies in CRPC reported a dose-limiting toxicity (one case of grade 4 sarcoid alveolitis in a patient who received 5 mg/kg of ipilimumab and GVAX) 35, but this has not been recapitulated in other studies of ipilimumab monotherapy or combination therapy at 10 mg/kg 26,2930,3335. Phase 2 dose-ranging studies for ipilimumab in advanced melanoma suggested that the risk/benefit profile was more favorable at 10 mg/kg than it was for 3 mg/kg 16. Although it is not known whether these results are translatable to prostate cancer, when taken together, the reports in melanoma, and the overall tolerability of the 10-mg/kg dose in CRPC trials where it was evaluated, suggest that 10 mg/kg is appropriate for further study of ipilimumab in CRPC.

Open Questions, Ongoing Trials, and Future Directions

Ongoing research in prostate cancer has broadened, and it is continuing to augment the therapeutic choices available to treat this disease. Immunotherapy is a promising but relatively recent addition, and while the concept of immunotherapy in CRPC was solidified with the US approval of sipuleucel-T, the ideal fit for immunotherapy in the CRPC treatment paradigm is a matter of continued study (Fig. 2) 3840.

Figure 2
Anticancer agents US- or EU-approved or under phase 3 investigation for castration-resistant prostate cancer (CRPC). Data from http://www.fda.gov 38, http://www.ema.europa.eu , and http://www.clinical.trials.gov 40.

In an effort to understand in which settings ipilimumab might provide benefit in CRPC, it is under phase 2 and 3 investigation in both the chemotherapy-naïve and -pretreated settings (Table 3). In addition, other antigen-specific approaches are the subjects of ongoing clinical investigation (reviewed in Cha 7). It is hoped that these studies will help answer some of the questions that the medical community has regarding immunotherapy in CRPC.

Table 3
Summary of ipilimumab clinical trials in CRPC

Treating physicians must always consider the question of risk/benefit when considering a therapeutic approach, and for immunotherapy, more data is needed to firmly address this issue. In the case of ipilimumab, phase 2 studies in CRPC suggest that PSA declines may occur in roughly 15–20% of patients. However, in the phase 3 trials of ipilimumab in melanoma, some responses to ipilimumab therapy initially appeared as disease progression (e.g., increases in total tumor burden or number of lesions) 16,22,23. If the response patterns seen in the phase 3 studies are suggestive of what can be expected in CRPC, it is possible that in some cases the benefit with ipilimumab may not be readily apparent for several weeks or months. It is for this reason that the phase 3 clinical trials of ipilimumab specify confirmation of disease progression 41,42.

The experience with irAEs associated with ipilimumab therapy in CRPC is limited to phase 1 and 2 data, but the agent's clinical development in melanoma has provided more extensive characterization of side effects and how to proactively manage them 22,23. Prompt treatment with corticosteroids or other immunosuppressive therapy, skipping a dose of ipilimumab, or in some cases discontinuation of ipilimumab therapy permitted resolution of the majority of severe events in a matter of days to weeks 22. It was also noted that prophylactic budesonide does not reduce the incidence of grade ≥2 diarrhea during therapy with ipilimumab for advanced melanoma 17. In the phase 1/2 reports for CRPC, ipilimumab's side-effect profile did not greatly differ from that reported for melanoma, but there is always a potential for patients with CRPC to experience side effect incidence or severity not anticipated from experience in other tumor types; for example, pelvic irradiation in older patients with CRPC might predispose them to side effects such as colitis. The phase 3 clinical trials in CRPC will help answer these questions and clarify whether the current side effect management guidelines, established in the phase 3 melanoma trials, will benefit patients with CRPC.

Finally, even though the phase 2 data in CRPC supports the use of 10 mg/kg as the phase 3 investigational dose, it is not yet clear whether this dose provides the ideal risk/benefit profile for CRPC. The phase 3 trials in CRPC will not utilize doses lower than 10 mg/kg, and it is uncertain what the risk/benefit profile of a lower dose would be.

Physicians must also consider whether a given therapy is the right choice for an individual patient. Currently, the prostate cancer community does not know to what extent different types of immunotherapy will be best suited for different subsets of patients, as heretofore no clinical or molecular parameters have clearly emerged as biomarkers. Encouragingly, however, studies of ipilimumab and ipilimumab-based combination therapy in melanoma and CRPC have identified new leads. Antibody and T-cell responses to NY-ESO-1 43, high baseline expression of immune markers such as FoxP3 and indoleamine 2,3-dioxygenase 44, increases in tumor-infiltrating lymphocytes, and changes in expression of immune-related genes 44 have all been correlated with clinical activity or benefit of ipilimumab. High baseline frequency of differentiated CD8+ T cells, high baseline frequency of CD4+ T cells that express CTLA-4 or PD-1, and low pretreatment frequencies of differentiated CD4+ or regulatory T cells have been associated with significantly longer survival following ipilimumab therapy 45. Furthermore, analysis of CD4+ and CD8+ T cells from ipilimumab-treated patients correlated low baseline expression of Ki67, a marker for T-cell proliferation, and eomesodermin, a transcription factor associated with effector T-cell function, with relapse or irAEs from ipilimumab therapy 46. Ongoing ipilimumab studies in multiple tumor types are evaluating various clinical and molecular parameters as biomarkers for survival or other clinical benefit, safety, or immunologic competence.

Chronic use of immunosuppressive corticosteroids, a therapeutic option among solid tumors unique to prostate cancer, may also be detrimental to ipilimumab's activity, and sustaining an active and durable immune response after ipilimumab treatment may benefit from delaying the initiation of corticosteroid-heavy regimens. There is currently no appropriate analysis to determine to what extent prolonged corticosteroid use and its sequence in CRPC treatment affect ipilimumab activity.

As mentioned above, their nonoverlapping mechanisms of action suggest the potential for combination therapy between multiple immunotherapy approaches, particularly antigen-specific therapies such as sipuleucel-T and antigen-independent therapies such as ipilimumab. To further explore the utility of such combinations, phase 1 or 2 studies pairing ipilimumab in regimens with sipuleucel-T, off-the-shelf prostate cancer vaccines, and/or adjuvants such as granulocyte macrophage colony-stimulating growth factor (GM-CSF) are complete or underway 31,32. One recent study, a phase 1 dose escalation trial of ipilimumab given concurrently with a fixed dose of GM-CSF–transduced allogeneic prostate cancer cells, reported that the higher doses (3 mg/kg and 5 mg/kg) were tolerated well in most patients and produced some PSA declines of >50% in seven patients (25% of patients in the 3 mg/kg or 5 mg/kg cohorts) 32. Although these trials have not and will not directly address how the sequence of therapies may affect results, as data from these studies and the phase 3 trials mature, clarification of issues above will further our understanding of the ideal placement for ipilimumab, and possibly other immunotherapy, into the CRPC treatment paradigm.

Acknowledgments

The authors take full responsibility for the content of this publication and confirm that it reflects their viewpoint and medical expertise. Professional medical writing and editorial assistance was provided by Rebecca Goldstein, Ph.D., at StemScientific and was funded by Bristol-Myers Squibb.

Financial support: Edward Cha, Conquer Cancer Foundation Young Investigator Award 2011.

Conflict of Interest

None declared.

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