- Research article
- Open Access
Temporal and geographic variation in the systemic treatment of advanced prostate cancer
BMC Cancer volume 18, Article number: 258 (2018)
Several systemic treatments have been shown to increase survival for patients with metastatic castration-resistant prostate cancer. This study sought to characterize variation in use of the six “focus drugs” (docetaxel, abiraterone, enzalutamide, sipuleucel-T, radium-223, and cabazitaxel) that have been approved by the Food and Drug Administration for the treatment of metastatic castration-resistant prostate cancer during the years 2010–2015. We hypothesized that the use of these treatments would vary over time and by region of the country.
We used Clinformatics DataMart™ Database (OptumInsight, Eden Prairie, MN), a de-identified claims database from a national insurance provider. Our sample included patients with prostate cancer who received any of the six drugs. We describe changes in usage patterns over time and geographic region of the United States via detailed descriptive statistics. We explore both patterns of first line therapy and sequence of treatments in our database.
Our final analysis included 4275 patients with a mean age of 74 years. Docetaxel was the most commonly used first-line therapy in 2010 (97%), 2011 (66%), and 2012 (49%). Abiraterone was the most commonly used first-line therapy in 2013 (56%), 2014 (46%), and 2015 (34%). Approximately 14% of our study cohort received ≥3 of the 6 drugs throughout their disease course. There was marked geographic variation in use of each of the drugs.
Variation in treatment patterns were found with respect to both time and geographic location. Prescription rates of abiraterone outpaced docetaxel as the most commonly prescribed drug after 2013 when it became widely available. However, some regions of the country still lagged behind and prescribed less than would be expected.
Prostate cancer, one of the leading causes of cancer death in men in the United States, is treated with androgen deprivation therapy (ADT) in its advanced form of metastatic disease . Most patients with metastatic prostate cancer will require additional treatments beyond ADT when their cancer progresses to castration-resistant disease, the lethal form of prostate cancer. The Food & Drug Administration (FDA) approved docetaxel in 2004 for the treatment of patients with metastatic castration-resistant prostate cancer (mCRPC) based on its ability to improve overall survival . Since 2010, five new therapies have been FDA-approved to treat patients with mCRPC. Sipuleucel-T and cabazitaxel were each approved in 2010 [3, 4]. Abiraterone and enzalutamide were approved in 2011 and 2012, respectively, [5,6,7,8] and most recently, radium-223 was approved in 2013 after showing an improvement in overall survival in men with symptomatic bone metastases .
Due to the rapid emergence of these new therapies, which we refer to as our “focus drugs,” little is known about their adoption since approval and there is limited guidance on their use. Importantly, with the exception of docetaxel, the average wholesale price for each of these medications is greater than $8000 a month and insurance coverage for these treatments are included under different forms of payment structures within payer programs. Abiraterone and enzalutamide are relatively well tolerated oral medications and are typically covered through prescription drug plans with patient co-payments and without direct office reimbursements. Docetaxel and cabazitaxel are associated with greater side effects and are therefore more difficult for some patients to tolerate but are covered in a different part of the health plan and may cost less to patients out of pocket due to lack of co-payments. Similarly, radium-223 and sipuleucel-T are not chemotherapy agents but are delivered intravenously and require specialized centers to administer. Therefore, use is likely to be influenced by whether a practice invested in the infrastructure needed to deliver these specialty medications (for example, radium-223 requires existence of a nuclear medicine facility).
To better understand the real-world use of these treatments, we sought to characterize initial treatment patterns of the six focus drugs subsequent to FDA-approval in a large sample of patients with prostate cancer covered by a national private insurance provider. We expected that adoption of all of the focus drugs, except docetaxel, would gradually increase with time after FDA-approval and that the use of docetaxel would consequently decline as the newer agents were substituted for docetaxel. We expected that the oral medications (abiraterone and enzalutamide) would gradually outpace intravenous medications despite the decreased revenue to practices since they can be more widely prescribed by physicians and allow some physicians without access to infusion centers or tertiary care centers to keep their patients for longer. However, we expected to see geographical differences in adoption of the newer agents with a preference in rural communities for oral therapies due to difficulty in frequent travel required for intravenous chemotherapy. We also hypothesized that many patients would be prescribed more than one drug at a time despite the lack of evidence for benefit for combination therapy. We use the claims database of a large national insurance provider to explore these hypotheses.
Data for this study was obtained from the Clinformatics Data Mart (CDM), a de-identified database (OptumInsight, Eden Prairie, MN) from a large, national US health insurer. This database includes administrative health claims data of approximately 61 million unique patients across the United States, including enrollment records, medical claims, and prescription claims, from 2001 to the latest data available (currently June 2015). Among patients 65 years of age and older, three quarters of patients in the OptumInsight database have Medicare Advantage plans while the rest are enrolled through private insurance plans. The database is updated every six to twelve months, and each member is assigned one unique identification number regardless of a break in coverage.
Participants and sample selection
To identify patients with prostate cancer in the OptumInsight Claims Database (OCD), the diagnosis fields (DIAG1 – DIAG5) within the medical claims data were matched against 185, the International Statistical Classification of Diseases and Related Health Problems (ICD) 9-CM for a prostate cancer diagnosis. Patients with a 185 diagnosis during the study period of January 1, 2010 to June 30, 2015 who received one of the six focus drugs were included. To identify patients who received any of the focus drugs, we matched national drug codes (NDC), brand names and Healthcare Common Procedure Coding System (HCPCS) codes associated with the six focus drugs against appropriate fields within the medical claims and pharmacy claims data. Patient demographic variables such as age, race, geographic location, and education level are available by matching on patient identification numbers across data files. In order to be considered for analysis of drug treatment patterns and in order to identify “first drug” for patients with advanced prostate cancer, we further required continuous enrollment of 180 days prior to receipt of one of the focus drugs (abiraterone, enzalutamide, docetaxel, cabazitaxel, sipuleucel-T, or radium-223), with no claim for one of the six drugs during that 180 days. Continuous enrollment was defined as less than 30 days break in coverage. In order to identify patients who had metastatic disease, the following ICD-9-CM codes were included: 196.x, 197.x, 198.x, 198.80, 198.81, 198.82, and 198.89. We refer the reader to the Additional file 1: supplementary materials for a detailed description of our sample selection methods.
For each patient in our cohort, we identified pharmacy and medical claims for the six focus drugs over follow-up periods. Among these claims, we defined first-line therapy for each patient as the focus drug associated with the first claim with respect to time. We construct line plots of therapy administration rates and first-line therapy administration rates stratified by year to observe temporal patterns in treatment. In addition, we calculate 95% confidence intervals (based on the Wilson estimate) for the first-line therapy administration rates by year and tabulate the claims by therapy and year. To test for geographical variation in treatment, we carried out a chi-squared test of independence between first-line of therapy and geographical region.
To identify patients who received more than one drug concurrently, we implemented a search algorithm to find therapy sequences containing at least two overlapping sequences that met the following criteria: a claim for a focus drug is registered between two claims for a different focus drug, the difference between the two claims being no more than five weeks apart. We carried out a sensitivity analysis to the choice of “five weeks” as a time window to assess the robustness of our findings.
We identified 295,525 patients with prostate cancer over the study period January 1, 2010 to June 30, 2015 and 5659 patients who received one of the six focus drugs during that time. The final study cohort of patients included 4275 patients who were continuously enrolled for 180 days before receipt of first focus drug. The mean age of patients was 74 (standard deviation, S.D. 9). Further descriptive characteristics can be found in Table 1. All variables were significantly different in distribution (p < 0.05) between the larger prostate cancer sample and our selected sample of patients who received any one of the focus drugs. Age, education level, household income, region, insurance product, and presence of metastatic disease were strongly significant (p < 0.001) due to the large sample size. However, observed differences among some of these variables across the two groups may not be practically relevant.
Figure 1 illustrates a time indexed plot of the proportion of patients in our sample that received each drug as first-line therapy in a given year and the most commonly prescribed first-line drugs. Docetaxel was the most common first-line therapy in 2010 (97.1%), 2011 (66.0%), and 2012 (48.9%). Abiraterone was the second most common first-line therapy in 2011 (24.5%) and 2012 (31.8%), but became the most commonly prescribed first-line therapy in 2013 (56.3%), 2014 (45.8%), and 2015 (34.2%). In contrast to the oral agents, abiraterone and enzalutamide, the usage of sipuleucel-T did not rapidly increase over time despite FDA-approval in 2010. Details for each drug frequency can be found in Table 2.
We were able to determine the total number of distinct focus drugs that a patient received throughout their course of treatment for patients who started their first treatment in a given year. In 2011, 57.3% (n = 377) of patients received one therapy over the course of treatment and 42.7% (n = 281) received at least two. The proportion of patients receiving more than one drug throughout their course of treatment increased for those patients who started a drug in 2012; 50.4% (n = 403) of patients who started a treatment in 2012 received one therapy over the course of treatment, 48.6% (n = 397) went on to receive more than one focus drug during treatment and 21.4% (n = 170) received at least three. The majority of these drugs were given sequentially and not concurrently. We only report the frequencies for 2011 and 2012 since follow-up is shorter for patients who started therapy after 2012. There were 88 patients identified who received more than one of the six focus drugs concurrently; Fig. 2 illustrates claims patterns for 50 randomly selected patients who received more than one of the six focus drugs concurrently during follow-up. The most common combination was docetaxel plus either abiraterone (19%) or enzalutamide (10%). Sipuleucel-T plus either abiraterone (10%) or enzalutamide (11%) was also seen as well as radium-223 plus abiraterone (8%) or enzalutamide (13%). We also observed two patients who received three drugs concurrently (one patient received abiraterone, enzalutamide, and docetaxel concurrently; one patient received abiraterone, enzalutamide, and cabazitaxel concurrently).
We were able to demonstrate administration rates of the focus drugs as first-line therapy by geographic division in 2014, the first year that all focus drugs were FDA-approved for their most updated indication. These rates are shown in Table 3. Figure 3 illustrates the expected versus the observed counts under the assumption of independence between therapy and geographic division. The calculation of the expected frequency takes into account the distribution of patients included across different geographical regions. A chi-squared test yielded a p-value < 0.001, indicating evidence supporting a difference in administration rates across regions. For example, the average rate of use for abiraterone as a first-line therapy in 2014 was 45.8%. However, among patients in our cohort belonging to the Pacific division (AK, CA, HI, OR and WA), 61.9% of patients received abiraterone as a first-line therapy in 2014 in contrast to 26.7% of patients belonging to the West North Central division (IA, KS, MN, MO, NE, ND, and SD), indicating significant geographic regional differences in preference for first-line therapy in 2014.
This study found that the most common treatment prescribed between 2010 and 2015 among the six novel agents for advanced prostate cancer was abiraterone. Notable temporal patterns emerged throughout the observed period, including the declining preference of docetaxel as first-line treatment over time, likely a consequence with the approval of abiraterone in 2011, and a decline of abiraterone use when enzalutamide was FDA-approved toward the end of 2012. These patterns indicate a potential substitution effect of abiraterone for docetaxel and later enzalutamide for abiraterone. We would expect with longer times on the market, the frequency of use of abiraterone and enzalutamide may begin to mirror the therapy that is preferred by patients and providers as first-line treatment rather than being driven by the timing of FDA-approval of treatments. Even though the adoption of the oral agents increased with time, as we predicted, we were surprised that the use of sipuleucel-T and radium-223 did not increase the longer they were available despite clinical trials showing excellent tolerance of therapy. This could be due to the more complicated administration of those treatments. Another observation we made was that there was a substantial number of patients we identified who were prescribed more than one focus drug concurrently, a practice that is not evidence-based and may be associated with unexpected side effects as well as high costs. What is perhaps more unsettling is that our observation of frequency of concurrent use is likely to be an underestimation of the actual frequency of this practice considering our strict criteria for identifying concurrent use of therapies. Finally, we observed significant variation in regards to adoption of these agents by region of the country. Some regions appeared to favor intravenous agents and some the oral agents as first-line treatment. There were also regions of the country that used a higher than expected rate of sipuleucel-T and radium-223 while others used lower than expected rates.
This the first study to our knowledge that describes the contemporary treatment patterns for advanced prostate cancer and includes all six focus drugs in a large cohort of patients. Most standard clinical trials do not investigate drug sequences within the same trial but tend to focus on one medication. Large observational studies done with large databases allow the investigation of several patterns of drugs manufactured by different pharmaceutical companies in concert. This enables comparison of not just one drug but of the entire drug sequence and in the future, potential outcomes corresponding to those different drug sequences. Some studies have shown emerging practice patterns for systemic therapy in patients with mCRPC, such as medical oncologists prescribing more oral therapy and chemotherapy than urologists,  and evidence that prescriptions for abiraterone and enzalutamide vary geographically across the United States . However, comparable studies demonstrating variation among all six focus drugs and relative variation in large datasets are lacking. While the temporal variation that we observed was somewhat expected as the use of a drug increases from the time a drug is introduced, the rate of change was not the same for each treatment. Moreover, there are no data in the literature with concrete evidence of the temporal changes. The geographic variation was also important to illustrate. Geography is a non-clinical factor that has been shown in the literature to influence variation in health care practices in several conditions, including treatment of back pain,  tonsillectomy,  and other surgical and cardiac procedures,  but has not been described in the systemic treatment of advanced prostate cancer. While geographic variation may be an independent contributor to variation, geographic variation in treatment patterns may be a result of other factors associated with geography, such as rural/urban differences, patient income, race, and health system factors.
Another potential contributor to geographic variation that has not been well-described in prostate cancer treatment may result from physicians and hospitals. Physicians from different specialties (e.g. medical oncology and urology) treat patients with advanced prostate cancer, and therefore different guidelines and national organizations are involved in guideline recommendations [15, 16]. Physician practices may get reimbursed higher for intravenous chemotherapy as opposed to oral medications that are dispensed through pharmacies, and whether a practice has invested in the infrastructure necessary to deliver specialty medications such as sipuleucel-T or radium-223 is likely to affect referral for these two treatments. Literature has shown that urology practices invested in radiation technology are more likely to treat patients with radiation than practices that do not, even in patients with a low likelihood of benefit from definitive treatment . In addition, considering the high cost of treatment options for mCRPC, financial considerations for the patient become important factors as well. Some patients have tremendous out of pocket expenditures for certain treatment options that can lead to significant financial toxicity, despite the fact that they may have insurance coverage [18,19,20]. Except for docetaxel, each of the studied agents has an average wholesale price of at least $8000 a month and different insurance plans have varying coverage and co-pays for medications that are administered intravenously versus oral drugs. Thus, the out-of-pocket costs for oral drugs may be substantially higher than that for chemotherapy and thus income level is likely to factor in to treatment decisions. We expect to further evaluate these important non-clinical variables and their influence on treatment patterns in future studies. However, the most important first step was to define the landscape of treatment patterns adopted over time.
Due to the nature of observational research, there were limitations inherent to analyzing data using a large medical claims database such as accounting for missing or unknown variables. Table 1 demonstrated that the variables we describe had very few unknown values and thus we do not expect this small number to substantially impact our results. Second, a limitation in identifying our cohort was ensuring that patients who had a diagnosis of prostate cancer received one of the focus drugs for prostate cancer rather than for another diagnosis. Since docetaxel is the only focus drug in our study that is approved for use in other cancers and is typically a salvage treatment in other cancers, we expect that observations of patients using docetaxel for other cancers concurrent with a prostate cancer diagnosis will be uncommon and thus not influence the results substantially. Third, there were limitations in identifying treatment codes since reporting of some treatment codes can be delayed. To handle this limitation, we developed an algorithm based on timing of administration and cost of drug that is explained in our Additional file 1: Supplementary Materials for sample selection. Fourth, the database does not include information about denied claims so it is difficult to know if denials factored into observed patterns of treatments. To address this limitation, we obtained the Coverage Summary and Policy Guidelines for the private insurer which included all of our focus drugs as covered treatments and did not differentiate coverage based on Local Coverage Determinations. Thus, we expect there would not have been a systematic denial of coverage for any of the included treatments and the majority of the geographic variation we detected is likely due to other factors such as patient, provider, or hospital factors, rather than claim denials. We expect that among patients included in OptumInsight who are all insured by the same private insurer, coverage for certain treatments are similar across the country. And finally, another limitation was in regards to generalizing the results of an insured cohort of patients to a broader population of patients, which is an inherent limitation to working with a dataset that is limited to patients who are privately insured. While our results may not be generalizable to uninsured patients, results are likely to be applicable to other commercially insured populations. We plan to conduct future studies to address payer-level variables that affect treatment patterns. Despite these limitations, several research teams have conducted important studies using similar statistical methods to analyze data through the Optum platform, including one study by Hershman et al. investigating socioeconomic factors associated with adherence to breast cancer therapy,  and another by Abraham et al. evaluating gastrointestinal bleeding associated with different anticoagulant medications .
In future work, we expect to repeat our analyses with longer time of follow-up and to investigate patient and external factors that may influence patterns of treatment, such as the factors that may underlie the geographic variation we observed. Understanding the determinants of this geographic variation is essential to minimizing disparities in treatment delivery. We also expect to repeat this work in broader reaching datasets such as Medicare in order to investigate patterns of care in patients who may not be able to afford private health insurance. As recommendations for using these focus drugs expand, [23, 24] identifying treatment variation and determinants of that variation, geographical or otherwise, become even more important so that implementation of best practices in the use of these treatments across the country can be optimized and tailored to different regions and practices.
In summary, we were able to identify the patterns of use of novel agents for advanced prostate cancer and demonstrate that abiraterone and enzalutamide have largely replaced intravenous therapy docetaxel as the first-line treatment of advanced prostate cancer. We also observed significant geographic variation in use of treatments for advanced prostate cancer. Describing this current landscape of treatment use is the first step in understanding treatment variation so that our future studies can identify patient and provider characteristics associated with variation and investigate the comparative effectiveness of treatment outcomes in order to identify highest value care.
Androgen deprivation therapy
Food & Drug Administration
metastatic castration-resistant prostate cancer
Clinformatics Data Mart
OptumInsight Claims Database
- ICD 9-CM:
International Statistical Classification of Diseases and Related Health Problems
National drug codes
Healthcare Common Procedure Coding System
New England: Connecticut, Maine, New Hampshire, Rhode Island, Vermont, Massachusetts
Middle Atlantic: New Jersey, New York, Pennsylvania
South Atlantic: Delaware, Washington D.C., Florida, Georgia, Maryland, North Carolina, South Carolina, Virginia, West Virginia
East North Central: Illinois, Indiana, Michigan, Ohio, Wisconsin
East South Central: Alabama, Kentucky, Mississippi, Tennessee
West North Central: Iowa, Kansas, Minnesota, Missouri, Nebraska, North Dakota, South Dakota
West South Central: Arkansas, Louisiana, Oklahoma, and Texas
Mountain: Arizona, Colorado, Idaho, Montana, Nevada, New Mexico, Utah, Wyoming
Pacific: Alaska, California, Hawaii, Oregon, Washington
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Dr. Bhramar Mukherjee is funded by the University of Michigan Comprehensive Cancer Center Core Grant - P30 CA 046592. The funding body had no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.
Availability of data and materials
The data that support the findings of this study are available from OptumInsight, but restrictions apply to the availability of these data, which were used under license for the current study, and so are not publicly available. Data are however available from the authors upon reasonable request and with permission of OptumInsight.
MC and JE are co-first-authors.
Ethics approval and consent to participate
On 4/19/2016, a representative of the University of Michigan Medical School Institutional Review Boards (IRBMED) determined that this study does not meet the regulatory definition of research involving human subjects. This study involved de-identified data that cannot be linked to a specific individual by the investigator(s) directly or indirectly through a coding system. In accordance with OHRP guidance on this subject (See http://www.hhs.gov/ohrp/policy/cdebiol.html), IRB approval is not required as the data cannot be tracked to a human subject. In addition, since this study did not meet regulatory definition of research involving human subjects, informed consent does not apply. The tracking number for this study was: HUM00113888.
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Caram, M.E.V., Estes, J.P., Griggs, J.J. et al. Temporal and geographic variation in the systemic treatment of advanced prostate cancer. BMC Cancer 18, 258 (2018). https://doi.org/10.1186/s12885-018-4166-3
- Prostate cancer
- Novel agents
- Care delivery
- Claims data