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Development of a Financial Literacy Course for Patients With Newly Diagnosed Cancer
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Development of a Financial Literacy Course for Patients With Newly Diagnosed Cancer

Veena Shankaran, MD, MS; Hannah Linden, MD; Jordan Steelquist, BA; Kate Watabayashi, BA; Karma Kreizenbeck, BA; Tony Leahy, JD; and Karen Overstreet, JD
This paper describes results from a patient survey regarding treatment-related financial experiences and interest in a financial literacy course.

OBJECTIVES: Although patients with cancer often face serious financial hardships, few studies have reported on strategies to mitigate this burden. Improving literacy about the financial aspects of cancer care may decrease the negative financial impact of cancer diagnosis and treatment. We obtained input from patient stakeholders on the perceived value and optimal design of a financial literacy program in the advanced cancer setting.

STUDY DESIGN: Prospective cohort survey.

METHODS: A series of semi-structured interviews were conducted, during which patients with either colorectal or breast cancer were asked to describe the impact of cancer on their finances and employment, to state their preferences about discussing costs with their providers, and to give input on development of a financial literacy course.

RESULTS: Twenty-one patients (76% Caucasian) completed interviews, the majority of whom had Medicare or commercial insurance (71%). Lost income from early retirement or disability was the most financially burdensome experience for 67% of patients. The majority of patients (76%) reported that a financial literacy course would be helpful in navigating the cost of cancer care. Most preferred the course be administered at diagnosis in a live group format.

CONCLUSIONS: Feedback from patients with cancer supported the development of a group financial literacy course that addresses barriers to discussing cost concerns, employment changes during cancer, and available resources for financial assistance.

Am J Manag Care. 2017;23(3 Suppl):S58-S64
Takeaway Points

We explored attitudes around the development of a financial literacy program for patients with cancer. 
  • Lost income from early retirement or disability was the most financially burdensome experience for 67% of patients with breast or colon cancer in our study. 
  • Over 75% of patients reported that a financial literacy course would be helpful in navigating the cost of cancer care. 
  • Major topics to cover in the financial literacy course include employment issues, barriers to discussing costs, and resources for financial assistance.
The term “financial toxicity” has gained traction in the oncology community in recent years and captures the spectrum of financial hardships faced by cancer survivors (eg, loss of productivity, high out-of-pocket [OOP] spending, depletion of savings, medical debt, bankruptcy). Recent evidence suggests that patients who experience financial toxicity are at risk for decreased treatment adherence, poorer quality of life, and worse survival.1-4 The growing intersection between the financial and clinical aspects of cancer care thus represents an emerging challenge in oncology.

Despite an improved understanding of the problem of financial toxicity, there is a relative lack of research and guidance on how best to help families deal with the cost of cancer care. Organizations, such as the American Society of Clinical Oncology (ASCO), have called for increased communication between patients and oncologists about the cost of cancer care.5,6 We agree, but also believe that addressing this problem will require a comprehensive and multifaceted approach that targets various factors that contribute to financial toxicity: lack of awareness about how to navigate the costs of care, lack of budget planning, high OOP spending on cancer therapy, and difficulty in managing other fixed expenses (Figure). We propose that aligning patients with organizations and resources to help navigate the cost of their care may help to decrease and prevent their financial stress and burden.

In partnership with the nonprofit organization Consumer Education and Training Services (CENTS), which specializes in financial literacy and education for various groups throughout western Washington state, we are developing a financial literacy course targeted to patients with cancer. We intend for this course to provide not only basic information about health insurance, disability, and employment benefits, but also to provide 1-on-1 budget planning with a trained specialist. Because stakeholder input is important in the development of meaningful interventions, we conducted a qualitative survey-based study with the goal of obtaining feedback from patients regarding their financial experiences during treatment, interest level in a financial literacy course, desired course content, and perspectives on communicating about costs with their providers.


We conducted semi-structured, in-person interviews with patients with advanced cancer being treated at 2 University of Washington clinical sites (Harborview Medical Center [HMC] and Seattle Cancer Care Alliance [SCCA], both in Seattle). HMC is a county hospital with a large immigrant and uninsured population. SCCA is the outpatient clinical oncology arm of the University of Washington. The study protocol was approved by the institutional review boards at these institutions.

Patient Population

We identified patients 18 years or older with either metastatic breast cancer or colorectal cancer on active treatment at either HMC or SCCA. These cancers were chosen as they are both common diseases with many expensive treatment options.

Patient Interviews

The interview guide was developed in collaboration with CENTS, adopting many questions previously tested and used in a study assessing the financial experiences of patients with colon cancer.7 In order to maximize patient comfort and encourage feedback, an experienced nonclinical interviewer conducted all inperson interviews, transcribed them, and kept detailed field notes. Demographic and clinical information was obtained from review of the patients’ electronic health records. Participants received a $20 gift card incentive for their participation in the interview.

Data Analysis

This was a qualitative study using descriptive statistics to understand characteristics of the study population. Means, medians, and proportions were used to describe the types of financial challenges patients faced, levels of pre- and postdiagnosis financial stress, barriers to communication with providers, preference for a financial literacy course, and desired course structure and content. To identify the major topics that would inform a financial literacy course, the principal investigator (author VS) actively reviewed and re-reviewed all transcripts and field notes in detail and identified recurring key themes by counting the frequencies of various constructs. Through iterative reading, provocative quotations and illustrative examples were established. Investigators then discussed the interview results with the CENTS project volunteers to inform the financial literacy course development.


A total of 21 patients across both institutions (HMC and SCCA) met eligibility criteria and completed in-person interviews. The majority of participants (mean age = 56 years) were women with breast cancer (76%) and were either commercially insured or had Medicare with a supplement plan (66%) (Table 1). Most patients were also highly educated and married (57%).

Knowledge and Resource Gaps Identified Through Patient Interviews

Key topics that were identified as important to address in developing the financial literacy course include: 1) implications of cancer on employment and income, 2) challenges in navigating and understanding health insurance plans and bills, and 3) barriers and fears about discussing costs with healthcare providers.

Implications of Cancer Diagnosis on Employment and Income

The majority of patients in this study were employed prior to diagnosis (86%) and transitioned to unemployment, retirement, or disability as a result of cancer diagnosis (Table 2). A significant proportion of patients (67%) reported lost income as one of the most burdensome financial aspects of treatment relative to other aspects (eg, costs associated with chemotherapy, diagnostics, transportation). Although there was some evidence of poor financial health in patients before diagnosis (19%), approximately 75% of all patients experienced a major financial hardship—including accrual of debt and nonadherence to cancer treatment due to cost concerns—following diagnosis as a result of cancer-related spending. The proportion of patients with total annual income greater than $50,000 was 62% before diagnosis and 48% following diagnosis. Financial stress was measured before and after diagnosis using a 5-point Likert scale. The mean financial stress level was significantly higher post diagnosis (3.5) compared with pre-diagnosis (2.05) (P = .0009).

Patients reported frustration with the inability to work during treatment and attributed many of the difficulties in paying the OOP expenses to the decline in income. Patients’ inability to advance their careers, invest in retirement, and accumulate savings for the family were seen as major stress factors. As one participant stated, “Even if I survive the cancer, my quality of life will not be as good because my retirement plan has suffered.” The inability to work also seemed to have an impact on patients from a psychological standpoint: “It has been hard to go from the ‘breadwinner’ in the family to having to rely on others.” From a logistic standpoint, several patients reported lack of transparency about the process of filing for disability and were unaware that they would qualify for Social Security disability benefits. At the same time, the process of filing for disability took longer than anticipated, during which period, several individuals faced significant financial hardship: one reported becoming homeless and staying in shelters during this period. Additionally, transitioning back to the workforce from disability was a deterrent for many who worried about a gap in insurance benefits during this time as they went from Medicare coverage back to an employer-based health plan.

Challenges in Navigating and Understanding Health Insurance Plans and Bills

Most patients in this study had either commercial insurance or Medicare with a supplemental plan (66%); however, there were 6 patients (29%)—the majority from HMC—with either Medicaid or institutional charity care coverage. Patients consistently reported difficulty in understanding paperwork and feeling overwhelmed by Medicare and Medicaid applications, although social workers were usually able to provide guidance and support. Patients also described confusion understanding bills and explanation of benefits and perceived the frequent delays in rendering coverage decisions as “unfair.” Despite the recent Affordable Care Act legislation prohibiting health plans from instituting lifetime coverage limits, many patients also reported fears about hitting a “cap” in spending and being “kicked off” their insurance plan. Finally, many patients reported lack of knowledge about how to navigate between potential insurance plans and how to anticipate higher OOP spending in the “donut hole,” which created tension for some worrying about how to budget other monthly expenses. Switching between insurance plans (eg, moving to a spouse’s plan or transitioning to Medicare) was often associated with large changes in co-payments for chronic medications; these unanticipated changes led to financial difficulties for many patients.

Barriers and Fears About Discussing Costs With Healthcare Providers

Patients were asked a series of questions about their preferences in communicating about costs with their oncologists. Only 12 patients (57%) actually discussed treatment costs with their physicians, which is consistent with previous studies.8 Of the 9 patients (43%) who did not discuss treatment costs, 6 reported a treatment-related financial burden of 3 or higher (on a 5-point Likert scale). Information about treatment costs was also not readily available to patients; only 2 patients (10%) reported having prior knowledge of expected costs prior to treatment. Interestingly, only 11 patients (52%) actually believed that physicians should discuss the anticipated costs of treatment with patients prior to making a treatment decision.

When asked more open-ended questions about these discussions, patient responses were mixed. Some patients felt that prior knowledge about anticipated costs would help with short-term and long-term financial planning (eg, monthly budgets, life insurance policy purchasing) and some were amenable to the idea of cheaper treatment alternatives as long as they were “similar in effectiveness” or talking to providers about how to “get the best treatment for less.” One patient stated that “the more information about costs that are exchanged, the more we feel in control.” Other patients viewed prior knowledge of treatment costs as a way of talking to their physicians about “spacing out CT scans” or “evaluating how to avoid duplicating lab draws and imaging tests…the costs of which can add up over time.”

Nevertheless, many patients were strongly against the idea of discussing costs with providers because: 1) cost information would have been overwhelming at diagnosis or 2) they were concerned that discussing costs could influence the physician to offer less-effective treatment. Provocative statements around these concepts include the following:

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