Representation of Minorities and Elderly in Cancer Clinical Trials at a Single Institution-The William Beaumont Hospital Experience

Mohammed Ibrahim*, Foluso Ogunleye, Jennifer Roye, Siddhartha Yadav, Diane Townsel and Zhou Yu

The Beaumont Health Haematology and Oncology Consortium and Ishmael Jaiyesimi DO Beaumont Health System, Royal Oak, Michigan, USA

*Corresponding Author:
Mohammed Ibrahim MD
3577 W. 13 Mile Road, Suite 202a, Royal
Oak, MI 48073, USA
Tel: 2485514975
Fax: 2485513154
E-mail: [email protected]

Received date: February 21, 2017; Accepted date: February 23, 2017; Published date: February 25, 2017

Citation: Ibrahim M, Ogunleye F, Roye J, et al. Representation of Minorities and Elderly in Cancer Clinical Trials at a Single Institution – The William Beaumont Hospital Experience. J Cancer Epidemiol Prev. 2017, 2:1.

 
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Abstract

Background: Disparities in the enrollment of minorities and elderly in cancer clinical trials have been reported in large national studies. We studied patient enrollment in clinical trials at William Beaumont Hospital for the years 2002 to 2013.

Methods: We obtained data on patient enrollment in cancer clinical trials for the time period of 2002 to 2013 from William Beaumont Hospital Community Clinical Oncology Program and Cancer Clinical Trials Office. We acquired data on cancer incidence at William Beaumont Hospital for the years 2002 to 2013 from the Beaumont Cancer Registry. Enrollment rate was calculated as the ratio of trial enrollment to the cancer incidence for different races and ethnicities, age groups and genders.

Results: The overall enrollment rate for the years 2002 to 2013 for all patients was 3.5%. The enrollment rate for men was significantly lower at 1.2% compared to 5.4% for women (p<0.001). The enrollment rates were similar for white and minority patients at 3.8% and 3.6% respectively. The enrollment rate was highest for the age group 31-49 years (6.9%) and lowest for the age group of over 75 years (0.8%).

Conclusions: The overall enrollment rate remains low. Enrollment rates were low, but similar for both white and minority patients. Increasing availability and access to clinical trials should increase enrollment rates for all patients. More efforts are needed to address the significantly low enrollment rates in all groups of patients, especially those over the age of 65 years.

Keywords

Minorities; Disparities; Cancer clinical trials

Introduction

Cancer is one of the leading causes of death worldwide. In 2016, it is estimated that 1,685,210 new cases of cancer will be diagnosed in the US and 595,690 people will succumb to their disease [1]. Cancer is the second most common cause of death in the United States, behind only coronary artery disease, and accounts for nearly 1 in 4 deaths [1]. In the US, cancer related deaths have declined overall from 2003 to 2012 by 1.8% per year among men and 1.4% per year among women [2]. However, certain ethnic and racial groups continue to suffer from a disproportionately higher incidence of cancer and have significantly worse outcomes. African American men, for instance, have a higher incidence of prostate cancer as well as higher risk of dying from their disease [3]. African American women have a higher incidence of triple negative breast cancer compared to other racial and ethnic groups [3]. A higher incidence of liver cancer has been found in Asian and Pacific Islander populations [2]. It is critical to have adequate representation of minorities in clinical trials in order to better understand disease biology and optimize treatment options. Unfortunately, several studies have shown that minorities are under-represented in cancer clinical trials [4-6]. The objectives of our study were to evaluate the enrollment of minorities and the elderly in our clinical trials and use this information to formulate an action plan to address any disparities [5].

Methods

We obtained Institutional Review Board (IRB) approval for this study. We acquired data on patient enrollment in cancer treatment clinical trials from the Community Clinical Oncology Program (CCOP) and the Cancer Clinical Trials Office (CCTO) at William Beaumont Hospital for the years 2002 to 2013. We collected data on patient demographics including race/ethnicity, age, gender, type of clinical trial and disease site. Patients under 18 years of age were excluded. Data on cancer incidence was obtained from the Beaumont Cancer Registry for the years 2002 to 2013. Enrollment in cancer trials was examined for 4 major cancer types: colorectal, lung, breast and prostate. We assigned patients into 1 of 6 mutually exclusive racial/ethnicity categories: White, Black, Hispanic, Asian, Native Hawaiian and American Indian.

Statistics

Enrollment rate was calculated as the ratio of trial enrollment to cancer incidence for different racial/ethnicity, age and gender groups, as recently described by Zullig et al. [6] Odds ratio was calculated for each group with 95% confidence intervals. P values were calculated using Fisher’s exact test. All tests were 2 sided. Data analysis was performed using SPSS version 21 statistical software [6].

Results

A total of 55,408 patients over 18 years of age were diagnosed with cancer at William Beaumont Hospital from 2002 to 2013. Of these 55,408 patients 1,924 patients were enrolled in cancer clinical trials, yielding an enrollment rate of 3.5%. Race was not reported in 5,209 of the 55,408 patients who were diagnosed with cancer. Race was also not reported in 9 of the 1,924 patients enrolled in clinical trials. The enrollment rate for minority patients (3.6%) was similar to that for the white population (3.8%) [OR 0.94, 95% CI 0.81-1.10]. Enrollment rate for Blacks, Hispanics, Asians and Native Hawaiian patients was 3.5%, 7.6%, 3.4% and 5.6% respectively. Table 1 shows the cancer incidence and enrollment rates, odds ratios with 95% confidence intervals and p values for different racial and ethnic groups. The mean age of diagnosis with cancer was 64 years, whereas the mean age at enrollment in clinical trials was 45.9 years. Patients over the age of 65 years were significantly less likely to be enrolled in cancer treatment trials compared to patients under the age of 65 years. The enrollment rate was 1.8% for patients over 65 years compared to 5.2% for patients under the age of 65 years [OR 0.34, 95% CI 0.31-0.37]. Table 2 shows the enrollment rates with odds ratios for the different age groups. On further stratification of age groups, patients in the age group of 31-49 years had the highest enrollment rate (6.9%), while patients over the age of 75 years had the lowest enrollment rate (0.8%). Patients in the age group of 65 -74 years had an enrollment rate of only 2.9% compared to an enrollment rate of 6.9% for patients in the age group of 31-49 years [OR 0.40, 95% CI 0.35-0.46] [7]. The enrollment rate for women (5.4%) was substantially higher than that of men (1.2%) [OR 4.51, 95% CI 3.99-5.10]. White women had significantly higher enrollment rate of 6% compared to white men (1.3%), [OR 4.92, 95% CI 4.31- 5.61]. Black women (4.5%) and black men (2.2%) also had higher enrollment rates than white men ([OR 3.57, 95% CI 2.85-4.48] for black women and [OR 1.75, 95% CI 1.26 -2.43] for black men respectively). We compared enrollment rates for men and women over and under the age of 65 years. Men under the age of 65 years had an enrollment rate of only 1.6%. Women under 65 had a significantly higher enrollment rate of 7.9% when compared to men under the age of 65 [OR 5.39, 95% CI 4.60-6.32]. Women over the age of 65 also had higher enrollment rate (2.7%) than men under the age of 65 years [OR 1.74, 95% CI 1.45-2.08]. Men over the age of 65 years had an even lower enrollment rate of 1% [OR 0.62, 95% CI 0.49-0.77] when compared to men under the age of 65 years. Table 2 provides more information regarding combined race and sex, race and age and age and gender subgroup analyses. We analysed cancer incidence and enrollment data for 4 major cancer types: breast, colorectal, prostate and lung cancer. On average, we have 12-15 breast cancer trials, 2-3 colon cancer trials, 3-4 lung cancer trials and 3-4 prostate cancer trials that are open annually. The overwhelming majority of these trials are NCI supported and funded cooperative group studies. 11,923 patients were diagnosed with breast cancer during the years 2002 to 2013, of which 1,333 patients were enrolled in clinical trials, yielding an enrollment rate of 11.2%. The enrollment rates were similar for both black (13.1%) and white (12.8%) patients in breast cancer trials. The enrollment rates were 8 much lower in trials for lung cancer (1.2%), colorectal cancer (2.7%) and prostate cancer (1.8%) as shown in Table 3. Black patients had higher enrollment rates compared to white patients in colorectal and prostate cancer trials. Table 3 provides information on overall and race-based enrollment in breast, colorectal, prostate and lung cancer trials.

  Cancer incidence Patients enrolled Enrollment Rate- % OR (95 % CI) P value
All Patients 55408 1924 3.5    
Male 25473 316 1.2 Referent  
Female 29931 1607 5.4 4.51(3.99-.10) <0.001
Not documented 4 1      
White, non-Hispanic 44707 1715 3.8 Referent  
All minorities 5492 200 3.6 0.94 (0.81-.10) 0.5
Black 4354 152 3.5 0.90 (0.76-.07) 0.256
Hispanic 275 21 7.6 2.07(1.32-.24) 0.001
Asian 772 26 3.4 0.87(0.58-.29) 0.501
American Indian 73 0 0    
Native Hawaiian 18 1 5.6 1.47(0.19-1.08) 0.506
Not documented 5209 9      

Table 1: Cancer incidence and accrual data in cancer clinical trials at Beaumont Health System (2002-2013) based on race, age and gender.

  Cancerincidence Patientsenrolled Enrollmentrate % OR (95% CI) pvalue
Age (Elderly vs Younger patients)
<65 years 26781 1395 5.2 referent  
>65 years 28609 529 1.8

0.34(0.31-0.37)

<0.001
Age stratified
31-49 years 749 4 51 6 6.9 referent  
18-30 years 872 41 4.7 0.66(0.48-0.92) 0.014
50-64 years 18415 838 4.6 0.64(0.57-0.72) <0.001
65-74 years 13951 405 2.9 0.40(0.35-0.46) <0.001
>75 years 14658 124 0.8 0.11(0.09-0.14) <0.001
Race and Gender
White male 20618 265 1.3 referent  
White female 24085 1450 6 4.92 (4.31-5.61) <0.001
Black male 1883 42 2.2 1.75(1.26-2.43) <0.001
Black female 2471 110 4.5 3.75(2.85-4.48) <0.001
Race and Age
White <65 years 21125 1231 5.8 referent  
White >65 years 23570 484 2.1

0.33(0.30-.37)

<0.001
Black >65 years 2113 33 1.6

0.25(0.180.36)

<0.001
Black <65 years 2239 119 5.3

0.90(0.74-.10)

0.34
Age and gender
Male <65 years 11379 178 1.6 referent  
Male >65 years 14089 138 1 0.62(0.49-0.77) <0.001
Female >65years 14516 391 2.7 1.74(1.45-2.08) <0.001
Female <65years 15402 1216 7.9 5.39(4.60-6.32) <0.001

Table 2: Cancer incidence and accrual data in cancer clinical trials at Beaumont HealthSystem (2002-2013), based on race, age and gender.

  Cancerincidence Patientsenrolled Enrolmentrate % OR (95% CI) pvalue
Cancer Type
Breast 11923 1333 11.2 referent  
Colorectal 4557 122 2.7 0.21(0.18-0.26) <0.001
Lung 6459 80 1.2 0.10(0.07-0.12) <0.001
Prostate 7373 131 1.8 0.14(0.12-0.17) <0.001
Cancer Type and Race
Colorectal-white 3749 102 2.7 referent  
Colorectal-black 402 20 5 1.87(1.14-3.05) 0.018
Lung-white 5361 75 1.4 referent  
Lung-black 544 5 0.9 0.65(0.26-1.62) 0.44
Breast-white 9412 1208 12.8 referent  
Breast-black 883 116 13.1 1.02(0.83-1.26) 0.797
Prostate-white 5622 107 1.9 referent  
Prostate-black 692 24 3.5 1.85(1.18-2.90) 0.01

Table 3: Cancer incidence and accrual data for white and minority patients in breast,colon, prostate and lung cancer clinical trials at Beaumont Health System (2002-2013).

Discussion

In our study, we found that the overall enrollment rate in cancer treatment clinical trials was only 3.5%. This is similar to the low enrollment rates of less than 5% noted in other large studies [4-7]. The enrollment rate for women (5.4%) was significantly higher than that of men (1.2%) Though women represented 54% of patients diagnosed with cancer, they accounted for over 80% of the enrolees in our cancer treatment trials. There is a preponderance of breast cancer trials at our institution and this accounted for the significantly higher proportion of women enrolled in cancer clinical trials in our institution, compared to men. In our study, 11% of patients diagnosed with cancer and 10% of enrolees in cancer clinical trials belonged to a minority subgroup. Our catchment area includes the densely-populated Oakland, Macomb and Wayne counties, that centre around the city of Detroit in south-eastern Michigan and account for 40% of Michigan’s population. In addition, we also serve Lenawee, Monroe, Washtenaw, Livingston, Genessee, Lapeer and St Clair counties. Although Detroit’s suburbs are predominantly white, nearby urban and suburban communities exist that have diverse racial and ethnic populations in proximity (within a 30-minute drive or less) to our hospitals. Our overall catchment area includes a minority population of 19%. 12.8% of the population in our overall catchment area is African American, 2.3% is Hispanic, 2.4% is Asian, 0.2% is American Indian and 1.2% is multiracial. Though the overall enrollment rates were low, we did not find a statistically significant difference in the enrollment of minority patients compared to white patients. Several initiatives have been started at our institution to address the low enrollment rates in the minorities. One of the first initiatives was the development of a minority outreach program. A previous study by Vicini et al. [8] from our institution looked at minority participant accrual by the Beaumont CCTO from 1988 to 2010. This study found that the development of the CCOP lead to a ten-fold increase in clinical trial accrual (p=0.001). The minority outreach program, initiated in 2003, targeted metropolitan Detroit areas and provided bilingual cancer education including information on screening and prevention, which helped improve accrual of minorities in our clinical trials to 11% by 2010 [8] The minority outreach program and the CCTO at Beaumont have engaged in fruitful collaborations with various community leaders and faith-based organizations in the Metro Detroit area, especially those that serve minorities. Educational materials and resources including clinical trials information, American Cancer Society pamphlets and NCI resource pamphlets are provided to the communities. Many of the educational materials are also provided in Spanish and Arabic to serve the needs of the non-English speaking population. The “Cancer Clinical 10 Trials Awareness Week- Fruit Tray Sunday” program was initiated in 2014. This program involved community awareness programs in various churches in metro Detroit area, targeting African American, Hispanic and Arab American populations. In addition to advice on healthy diet and exercise, these programs have helped introduce and explain the concept and importance of clinical trials. Second, a diverse, multilingual staff at our CCTO assists patients navigate through the clinical trial process, scheduling appointments, insurance authorizations and transportation, and provides social support. After discussion of the clinical trial process with their physicians, patients meet with the staff at the CCTO where the clinical trial protocol is reviewed again in more detail. Patients are educated on the rationale of the study, the type and duration of treatment, need for additional testing or procedures, the randomization process, the major and minor risks including need for more doctor and clinic visits and time off from work as well as possible benefits. Patients are informed about their right to decline participation in a clinical trial without any consequences to their medical care. They are also informed that they can decide to stop participation in the clinical trial at any time. They are provided with contact information for the CCTO office so they have an ongoing resource to answer any additional questions. Once patients understand and agree to the clinical trial, their written consent is obtained. We suspect that other factors may also influence clinical trial participation and may play a bigger role than race and ethnicity alone, such as educational level, insurance status, access to health care, transportation issues, social support and income level.

It is critical to recognize the disparities in age with regards to clinical trial enrollment. Patients over the age of 65 account for over 60% of all cancer cases in the US, but are only 25% of the participants in clinical trials [9]. Similarly, in our study cohort patients over the age of 65 accounted for 52% of all cancer diagnoses, but were only 27% of patients in clinical trials. Patients over the age of 65 and especially those over the age of 75 are under-represented in our clinical trials. The enrollment rates for patients in the age group of 65-74 (2.9%) and over 75 (0.8%) are significantly lower compared to their younger counterparts. Several studies have examined the incidence of cancer in the elderly and the causes of poor enrollment in cancer clinical trials [10-14]. Elderly patients are likely to have significant comorbid illnesses, which may preclude their participation in clinical trials [12-14]. Physicians attitudes regarding the elderly population can also be a barrier to trial enrollment. Physicians may consider patients’ medical co-morbidities, cognitive factors, toxicity concerns, costs, transportation and compliance to be prohibitive [12-14]. Also, physicians may have concerns about insurance coverage for clinical trials, although Medicare does cover routine clinical trial costs [15]. We not only studied enrollment of patients over the age of 65, but also looked at gender and race-based enrollment in that age group. We found that overall enrollment of elderly patients is uniformly low, regardless of race or gender. In our study, the enrollment rates were significantly lower for both white and black patients over the age of 65 (2.1% and 1.6% respectively), compared to the population of white patients under the age of 65 (5.8%) as shown in Table 2. Similarly, both men and women over the age of 65 had lower enrollment rates of 1% and 2.7% compared to women under the age of 65 (7.9%) [12].

Strategies to increase the enrollment of elderly patients should include relaxing eligibility criteria. In one study, for instance, it was found that if the exclusion criteria related to organ system abnormalities and performance status were relaxed, the participation of elderly patients would approach 60%, in line with the cancer incidence in this population [9]. Another strategy would be to increase the number of clinical trials targeting the elderly population, with careful selection of patients. In addition, physician education is necessary to help overcome the attitudinal beliefs regarding elderly patients. In some trials, the incidence and severity of toxicity from chemotherapy was not significantly higher in the elderly than that observed in the younger population, as long as patients were carefully selected [16,17]. Thus, physicians concern about tolerability of treatment may be unfounded for many patients. Breast cancer trials had heavy accrual in our institution compared to colorectal, prostate and lung cancer trials. Breast cancer patients accounted for 21% of all new cancers diagnosed during 2002 to 2013, but represented 69% of enrolees in cancer clinical trials. This underscores the fact that the single main factor that affects clinical trial enrollment is the availability of clinical trials. Strategies that increase the number of cancer clinical trials in our institution will lead to increased enrollment of all patients. In a recent review by Unger et al., barriers to clinical trial participation were discussed [18] These included structural (clinic access and availability of clinical trials), clinical (eligibility requirements), attitudinal (both physician and patient’s attitudes regarding the clinical trial process), demographic and socioeconomic factors.18 Several studies have shown that even if patients have access to cancer care, the lack of an 13 available clinical trial precludes participation for 50% of patients [19-23]. Even if a clinical trial was available, stringent eligibility criteria, mostly related to comorbid illnesses, resulted in exclusion of approximately 20% of patients [19-23]. Physician attitudes also play a very important role in clinical trial participation. In addition to those specific to elderly patients discussed above, such attitudes may include concerns about interference with physician-patient relationship [24,25]. uncertainty regarding the randomization process, lack of incentives [27] and concerns about extra workload [25,27]. Patient attitudes include concerns about experimentation and randomization [26,28] toxicity of treatments, [29] mistrust of medical science due to past abuses [30], transportation issues [19,31] and cost. [31,32] Socioeconomic status also plays a significant role in trial enrollment. In one study, patients earning less than $50,000 per year were 27% less likely to participate in clinical trials compared to those earning higher salaries [33]. Several actions have been taken at our institution to increase overall accrual to clinical trials. The most important activity has been the frequent educational sessions provided to Medical Oncology, Radiation Oncology and Surgical Oncology physicians. CCTO staff provides information on open clinical trials at various tumour board meetings. In addition, the physicians are provided with updated pocket handbooks every month, which serve as a reference for currently open clinical trials to which they may refer their patients. The CCTO staff helps physicians and patients navigate the path to the clinical trials in an expeditious manner. Other activities included the “Cancer Clinical Trials Awareness Day” that was organized at Michigan’s Capitol, Lansing, in June 2014 to 14 increase the awareness of clinical trial activity in the state. The “Royal Oak Coffee with CCTO” event helped create an open dialogue between the CCTO staff and patients, visitors, physicians, community leaders and other Beaumont staff regarding the mission, events and resources the CCTO must offer. The “Lunch and Learn-Improving Health Professionals’ Understanding of Clinical Trials” program at the Beaumont, Royal Oak campus also helped disseminate information about clinical trials to physicians, nurses and other health care staff. The “Eat Healthy, Be Active” workshops, organized by the CCTO’s community health educator along with other organizations, included discussions on clinical trials in addition to healthy lifestyle resources and tips on cancer prevention. One of these workshops was targeted to residents of a Senior Living apartment facility, which aimed to help increase the enrollment of the elderly in clinical trials. Our study is unique in many ways. We looked at clinical trial enrollment only from our institution. Our intention was to study our current accrual patterns so that we could plan and implement strategies to address any disparities and improve overall enrollment. We plan on using this data to guide decisions regarding the allocation of available resources of the Beaumont-NCORP (National Cancer Institute Community Oncology Research program) and CCTO in the future. We believe that the combination of a dedicated minority outreach program and a well-trained CCTO staff that provides both education and support to patients and physicians helps improve accrual for both minorities and the overall population. Other institutions can utilize a similar approach to address the disparities in their accrual. Our data also underscore the idea that the 15 biggest hurdle to clinical trial enrollment is the lack of availability of a clinical trial. The heavy accrual in our breast cancer trials compared to other trials is one example. Our study had some limitations. We only studied enrollment in clinical trials for adults over the age of 18 years and did not study data for the paediatric population. The paediatric population in general has much higher rates of enrollment in cancer clinical trials than the adult population, especially for those under the age of 15 years, where enrollment rates are typically reported as being greater than 50% [34,35]. Also, race was not reported in 5,209 of the 55,408 patients who were diagnosed with cancer. Race was also not reported in 9 patients in clinical trials. The reasons for this could be several. In our databases, patients self-identified their race. Either race was not asked for or documented for these patients, patients declined to disclose their race or they belonged to a race that is not one of the Federal government-recognized categories. The city of Dearborn, located in Wayne county, Michigan is home to the largest concentration of Arab Americans in the U.S, including Lebanese, Yemenis, Iraqis and Palestinians, but the Middle Eastern ancestry is not a federally recognized race or ethnicity. In most cases, Middle Eastern patients have been considered as Caucasian. It is also unclear how multi-racial patients were reported in the database. Information on factors such as socioeconomic status, insurance status, or educational level was not collected and may influence the results as well. Also, there is a preponderance of breast cancer trials in our institution. This leads to heavy accrual of both white and minority women compared to their male counterparts. Lastly, we only included cancer treatment-related trials in our analysis and excluded other trials on cancer screening, prevention, genetic and bio16 bank studies, etc. It is unclear if the enrollment patterns would differ if these patients were also studied. The future of Oncology depends on well designed, properly matched clinical trials that have rapid accrual of patients of all age, social and demographic groups. More efforts are needed to increase enrollment of all cancer patients to clinical trials in general and the elderly in particular.

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