Current and Emerging Therapies for Bone Metastatic Castration-Resistant Prostate Cancer

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the Cancer Therapy Advisor take:

There is now a wide variety of treatment options for patients with metastatic castration-resistant prostate cancer and as new treatment therapies are developed out of the growing knowledge of the disease, overall survival rates have improved for some patients.

The authors of this journal article reviewed approved agents for metastatic prostate cancer in the United States and discussed them in the context of recent developments in the understanding of the disease’s biology and bone metastasis.

They also discussed the ways in which underlying mechanisms may represent opportunities for therapeutic intervention and the new challeneges in treatment that are born from the development of different therapy options. The authors also highlight treatment options that target androgen synthesis and utilization or the microenvironment that can improve the rate of overall survival in patients with metastatic castration-resistant prostate cancer.

The authors also explain the ways in which determining how factors from the primary tumor can aid the creation of premetastatic niches and how prostate cancer cells parasitize niches in the bone microenvironment could yield new therapies to treat mCRPC.

In addition the authors explain how improved patient stratification and the administration of optimal therapy sequencing also aids the novel treatment development for this disease type. 

New developments in mCRPC have resulted in several new therapies.
New developments in mCRPC have resulted in several new therapies.

Background:A paucity of therapeutic options is available to treat men with metastatic castration-resistant prostate cancer (mCRPC). However, recent developments in our understanding of the disease have resulted in several new therapies that show promise in improving overall survival rates in this patient population.

Methods:Agents approved for use in the United States and those undergoing clinical trials for the treatment of mCRPC are reviewed. Recent contributions to the understanding of prostate biology and bone metastasis are discussed as well as how the underlying mechanisms may represent opportunities for therapeutic intervention. New challenges to delivering effective mCRPC treatment will also be examined.

Results: New and emerging treatments that target androgen synthesis and utilization or the microenvironment may improve overall survival rates for men diagnosed with mCRPC.

Determining how factors derived from the primary tumor can promote the development of premetastatic niches and how prostate cancer cells parasitize niches in the bone microenvironment, thus remaining dormant and protected from systemic therapy, could yield new therapies to treat mCRPC. Challenges such as intratumoral heterogeneity and patient selection can potentially be circumvented via computational biology approaches.

Conclusions:The emergence of novel treatments for mCRPC, combined with improved patient stratification and optimized therapy sequencing, suggests that significant gains may be made in terms of overall survival rates for men diagnosed with this form of cancer.


Prostate cancer is the second most common cancer in American men with approximately 233,000 newly diagnosed cases in 2014.1

With an aging population, the incidence of prostate cancer is likely to continue to increase. Patients whose disease is detected at an early stage benefit from a range of treatment strate­gies, including radiotherapy and prostatectomy, with survival rates near 100%.2

However, the clinical real­ity is that many men present with advanced stages of the disease. Currently, the main treatment option for men with advanced cancer is hormone therapy. Historic contributions from Huggins and Hodges3 in 1941 revealed that removing androgens could inhibit the progression of prostate cancer.

These ear­ly observations paved the way for the development of androgen-deprivation therapy — either surgically or chemically — which has remained the standard treatment for men with advanced disease for the last 70 years. Despite the initial response to androgen deprivation for most men, the disease typically pro­gresses to a castration-resistant state within 18 to 24 months.4

Castration-resistant prostate cancer (CRPC) is defined by disease progression that, despite chem­ical castration, is often indicated by rising levels of prostate-specific antigen (PSA).5

The development of resistance to hormonal intervention and why the disease progresses is not fully understood, although some mechanisms have been demonstrated, with the majority focusing on the continued androgen recep­tor (AR) activity in addition to TMPRSS2/ERG fusion, PTEN, Nkx3.1, and EGR1. As the disease progresses, the CRPC ultimately metastasizes (mCRPC).

Patients with mCRPC have a poor prognosis and a predicted survival rate of fewer than 2 years from the initial time of progression, comprising a large portion of the 30,000 prostate cancer-related deaths per year.6,7 Currently, mCRPC is an incurable disease and represents a major clinical hurdle.

Prostate cancer preferentially metastasizes to bone.8 As the disease transitions from castration sensitive to castration resistant, the incidence of bone metastasis increases, with more than 90% of patients with mCRPC developing bone metastases.9,10

Patients with mCRPC who are symptomatic are at a high risk for skeletal-related events (SREs), including sponta­neous fracture and spinal cord compression, that are a source of significant pain and decreased quality of life.11

Pain from the metastases is a major com­ponent of the disease and is an important aspect to be considered regarding a patient's treatment regi­men.

Depending on the level of pain, medications ranging from ibuprofen to morphine are prescribed.12 Because prostate to bone metastases are primarily bone-forming sclerotic lesions, bone scanning us­ing technetium-99m is often preferred for diagnosis due to the incorporation of the radionuclide tracer into regions of new bone formation by osteoblasts.13

Magnetic resonance imaging (MRI) and positron emission tomography (PET)/computed tomography (CT) are also used for detection. A trial comparing 18F–sodium fluoride PET/CT, 18F-fluorodeoxyglucose PET/CT, MRI, and technetium-99m identified strengths for each modality.14

However, the ability to detect occult or micrometastases less than 5 mm remains a current limitation for each imaging technique. 

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