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Supportive Care in Cancer

, Volume 27, Issue 5, pp 1697–1708 | Cite as

“It still affects our economic situation”: long-term economic burden of breast cancer and lymphedema

  • Lorraine T. DeanEmail author
  • Shadiya L. Moss
  • Yusuf Ransome
  • Livia Frasso-Jaramillo
  • Yuehan Zhang
  • Kala Visvanathan
  • Lauren Hersch Nicholas
  • Kathryn H. Schmitz
Open Access
Original Article

Abstract

Purpose

Financial toxicity after breast cancer may be exacerbated by adverse treatment effects, like breast cancer-related lymphedema. As the first study of long-term out-of-pocket costs for breast cancer survivors in the USA with lymphedema, this mixed methods study compares out-of-pocket costs for breast cancer survivors with and without lymphedema.

Methods

In 2015, 129 breast cancer survivors from Pennsylvania and New Jersey completed surveys on demographics, economically burdensome events since cancer diagnosis, cancer treatment factors, insurance, and comorbidities; and prospective monthly out-of-pocket cost diaries over 12 months. Forty participants completed in-person semi-structured interviews. GLM regression predicted annual dollar amount estimates.

Results

46.5% of participants had lymphedema. Mean age was 63 years (SD = 8). Average time since cancer diagnosis was 12 years (SD = 5). Over 98% had insurance. Annual adjusted health-related out-of-pocket costs excluding productivity losses totaled $2306 compared to $1090 (p = 0.006) for those without lymphedema, or including productivity losses, $3325 compared to $2792 (p = 0.55). Interviews suggested that the cascading nature of economic burden on long-term savings and work opportunities, and insufficiency of insurance to cover lymphedema-related needs drove cost differences. Higher costs delayed retirement, reduced employment, and increased inability to access lymphedema care.

Conclusions

Long-term cancer survivors with lymphedema may face up to 112% higher out-of-pocket costs than those without lymphedema, which influences lymphedema management, and has lasting impact on savings and productivity. Findings reinforce the need for actions at policy, provider, and individual patient levels, to reduce lymphedema costs. Future work should explore patient-driven recommendations to reduce economic burden after cancer.

Keywords

Breast cancer Lymphedema Financial toxicity Economic burden 

Introduction

Nearly half of cancer survivors experience financial distress [1]. Cancer-related financial toxicity, the harmful personal economic burden caused by cancer treatment [2], affects nearly half of cancer survivors [1] and is present even among those with health insurance [2, 3, 4, 5, 6]. Costs of cancer care are even higher for those with adverse treatment effects [7, 8, 9, 10, 11, 12], such as breast cancer-related lymphedema [13, 14], and comorbidities [3, 15].

Breast cancer-related lymphedema affects up to 35% [16, 17] of the 3.5 million breast cancer survivors in the USA (2016) [18]. Breast cancer-related lymphedema is a chronic inflammatory condition that arises when there is disruption of lymphatic flow due to surgery, adjuvant radiation, and some forms of chemotherapy, infection, obesity, or other trauma to the lymphatic system [17, 19], leading to buildup of lymphatic fluid in the upper body, especially the arms, breast, and torso [20, 21]. The arm swelling and altered lymphatic function caused by lymphedema may affect a breast cancer survivor’s ability to complete activities of daily living and maintain employment, leading to psychosocial distress, secondary comorbidities [19, 22, 23, 24], and limited work and career opportunities [25, 26, 27].

Previous work has estimated that incremental costs due to lymphedema for US cancer survivors at $14,877 (excluding cancer-related costs) in the first 2 years after cancer treatment initiation [13]; however, these estimates are nearly 15 years old, focused on only the short-term costs, and predate the 2010 Affordable Care Act that expanded coverage for cancer-related care and banned refusal of coverage for those who might have a pre-existing condition [28]. A patient’s decision about whether or not to expend resources on medical care versus other competing needs is driven by out-of-pocket costs. Yet, previous estimates rely on claims and administrative data, which neglect the impact of out-of-pocket costs. Altogether, data on out-of-pocket costs of lymphedema management is lacking for US-based samples and overlooks the long-term impact of cost and indirect costs, such as lost productivity.

To address gaps in this research topic and expand on previous inquiry, we conducted a prospective longitudinal explanatory mixed methods study. This is the first study in the USA to quantitatively compare long-term out-of-pocket direct and indirect costs among women with breast cancer-related lymphedema to those without a lymphedema diagnosis, integrating qualitative data to offer insight into what makes costs different comparing those with or without lymphedema.

Methods

Sample

From May to September of 2015, 258 women were screened by phone for eligibility to the PAL Social Economic and Quality of Life (PAL SEQL) follow-up study. Recruits were identified from prior participants of the Physical Activity and Lymphedema (PAL) trial (n = 295) [29, 30] who were still alive or participants who were ineligible (n = 163) for the ongoing Women in Steady Exercise Research (WISER) Survivor Study (ClinicalTrials.gov #NCT01515124) [31], but met requirements for entry into PAL. All participants who had agreed to be contacted about future studies and had up-to-date contact information were contacted. Eligibility criteria included women with stages I–III invasive breast cancer, completion of active breast cancer treatment, > 1 lymph node removed, and current residents of Pennsylvania or New Jersey. Those with active cancer, or who were pregnant or planning to become pregnant in the next 6 months were excluded. Of those screened, 37 were ineligible, and 96 declined or dropped out due to lack of time to commit to a longitudinal study. Figure 1 describes the conceptual overview of the mixed methods study design.
Fig. 1

Conceptual overview of mixed methods approach. This figure shows the flow of the explanatory sequential design of the mixed methods study, which begins with quantitative out-of-pocket costs data collection for all 129 participants, followed by qualitative interviews of 40 randomly selected participants, which were integrated to interpret the cost differences identified between those who had lymphedema and those who did not have lymphedema

Ethical considerations and informed consent

The Institutional Review Board of the University of Pennsylvania approved the study. Written informed consent was obtained from all individual participants. Participants completed a measurement visit at baseline and 6 months that included measures of upper extremity lymphedema severity.

Measures

Demographics

Participants self-reported current age, US census-defined race, and socio-economic position. Consumer credit was included because cancer diagnosis has been associated with increased bankruptcy rates [6, 32], which would have an impact on a patient’s consumer credit rating for up to 10 years. Self-reported health insurance was classified as public (Medicaid or Medicare), private, or none. Participants reporting both public and private insurance were counted in both categories.

Costs and productivity losses over 12 months (cost diary)

The data collection instrument developed was based on Goossens’ cost diary [33], a validated tool for cost-effectiveness analysis. Participants were instructed to report direct, indirect, and productivity costs related to their overall healthcare including the following: co-payments for outpatient physician visits, physical and occupational therapy visits, complementary and integrative therapy visits, emergency department visits, hospitalizations, labs, X-rays, and tests; wellness resources (e.g., gym memberships); all lymphedema-specific healthcare needs (compression garments, bandages) for lymphedema in any part of the body; medications or other health-related product that a participant identified; and health insurance premiums if paid out-of-pocket (Appendix I in the supplementary material). All out-of-pocket costs were collected in continuous dollar amounts.

Similar to methods used in previously published cost studies of adverse effects of cancer treatment [14], participants reported 12 months of cost data. This was captured through a 3-month retrospective cost diary, then six monthly prospective cost diaries, followed by an estimation of projected costs in the upcoming 3 months. For the 3-month retrospective and 6-month prospective data collection, participants were encouraged to use personal calendars, insurance statements, and receipts to aid in recall. The following 3-month projection was designed to capture any regularly occurring appointment co-pays, such as those for annual check-ups, that did not fall in the earlier time windows that out-of-pocket costs data were being prospectively recorded. Altogether, participants supplied 12 months of cost data and each cost was summed across all the data collection points. For each itemized question, participants with lymphedema designated which costs were related to lymphedema. We considered 12-month costs including and excluding productivity costs to differentiate direct medical and non-medical, and indirect cost domains [34]. Productivity losses for work and for home were calculated based on methods used in a previously published paper that estimated economic burden for US cancer survivors [35] based on self-reported days unable to perform usual activities or hours of help needed to carry out daily activities. For work productivity losses, the adjusted mean number of missed workdays was multiplied by the US Bureau of Labor Statistics estimates for the median hourly wage ($16.87) based on a 6-h workday. For household productivity losses, the mean number of hours that someone needed help was multiplied by the daily household productivity rate ($43.37 per day) based on the consumer price index.

Subjective ratings of economic burden

At baseline, participants completed a self-administered survey on economic burden using 12 items adapted from the Breast Cancer Finances Survey [36, 37], a validated survey of economically burdensome events among breast cancer survivors that assesses burden related to long-term survival.

Cancer history and treatments

Participants self-reported completing chemotherapy and/or radiation therapy and/or hormone therapy after cancer surgery, and year of breast cancer diagnosis. Self-report of breast cancer treatment has been validated as over 90% accurate [38]. Whether patients underwent multiple adjuvant treatment modalities is more important than the details of treatment; thus, we modeled the total number of types of treatments.

Health conditions and lymphedema

Participants self-reported any of 23 comorbidities and previous diagnosis of breast cancer-related lymphedema. To measure upper extremity lymphedema severity, interlimb volume difference measurements between the affected and unaffected arms were taken using perometry (Juzo, Germany), and were adjusted for humidity, barometric pressure, and time of day. Women who wore compression garments were asked to remove them for at least 1 h prior to perometry assessment.

Qualitative data collection

As depicted in Fig. 1, the explanatory sequential design [39] of this mixed methods study included 30-min qualitative interviews at the end of monthly prospective out-of-pocket cost data collection. This method entails first collecting quantitative data, and then collecting qualitative data to inform and provide context for quantitative findings. This approach used data from semi-structured interviews to explore what might drive cost differences between breast cancer survivors with and without lymphedema, and capture ways in which long-term economic burden might affect breast cancer survivors that might not be easily quantifiable with a cost diary approach alone. A standardized semi structured interview guide (Appendix II in the supplementary material), developed by the study PI, included questions on economic challenges, supports utilized, lasting impact and resource gaps after participants’ breast cancer diagnosis. The study PI and a trained research assistant conducted interviews with a subset of 40 participants who were purposively sampled to ensure equal representation across three sampling categories: lymphedema status, socioeconomic position (high school or less vs. college or more), and age group (over 65 and under 65). The sample included 40 participants to ensure at least 10 participants per each sampling category and the potential to reach saturation of themes. Participants were randomly selected using a random number generator and placed into each sampling category until there were at least ten in each category.

Data analysis

For quantitative analysis of the entire study sample, baseline statistical differences between demographic characteristics were calculated using Chi-squared test and Fischer’s statistic for demographic categories with less than five respondents, and non-parametric Ranksum test for non-normally continuously distributed variables. A generalized linear model (GLM) with the power 0.5 link and negative binomial family was used to account for over dispersion because the cost outcome variables contained several zeros and the variance exceeded the mean distribution, which is common with health care cost data. After the model was fitted, the marginal effects of the total cost for those with and without lymphedema were calculated and graphed, adjusted for each covariate at its mean. Two separate GLM models were estimated: one for the total cost including and one for the total cost excluding productivity costs.

For qualitative analysis of the 40 interviewees, verbatim interview transcripts were inputted into MAXQDA software program for qualitative analysis. First, structural codes based on interview questions and domains of economic burden among cancer survivors documented in the literature were identified. Additional codes were included after transcripts were reviewed for themes. The research team organized these codes into a codebook, which was used for thematic coding. Each fifth transcript was double coded and discrepancies were discussed and resolved among the research team. Quotes were collected to illustrate key findings and ensure that conclusions were consistent with the data.

Results

The 129 participants who completed data for the study are described in Table 1. Across the entire sample, the mean age was 63 and the average time since cancer diagnosis was 12 years. Just under half (46.5%) of participants had been diagnosed with lymphedema. There was no statistically significant difference by lymphedema status in mean age, race, education, social status, wealth, credit score, type of insurance, or number of economically burdensome events. A significantly greater percentage of women with lymphedema were in a lower income category (p = 0.02) compared to those without lymphedema. Cancer stage at diagnosis, type of adjuvant treatments, and number of comorbidities did not differ by lymphedema status, but those with lymphedema were on average 3 years farther out from diagnosis (p = 0.002) and had greater interlimb difference (p < 0.001).
Table 1

Participant baseline characteristics

N = 129

BCRL yes, n = 60 (46.51%)

BCRL no, n = 69 (54.49%)

p value

Demographics

 Age in years, M (SD)

65 (8)

62 (8)

0.11

 Race

  

0.32

  White

35 (57.4)

41 (60.3)

 

  Black

24 (39.3)

26 (38.2)

 

  Other

2 (3.3)

0 (0.0)

 

 Education completed

  

0.35

  High school

17 (27.9)

13 (19.1)

 

  College

26 (42.6)

29 (42.7)

 

  Graduate school

17(27.9)

26 (38.2)

 

 Income

  

0.02

  ≤ $30,000

8 (13.1)

11 (16.2)

 

  $30,001–$70,000

30 (49.2)

18 (26.5)

 

  > $70,000

19 (31.2)

35 (51.5)

 

 Total cash assets

  

0.60

  ≤ $4999

17 (27.9)

16 (23.5)

 

  $5000–$49,999

16 (26.2)

13 (19.1)

 

  $50,000–$499,999

13 (21.3)

19 (27.9)

 

  ≥ 500,000

9 (14.8)

13 (19.1)

 

 Consumer credit quality (n = 123)

  

0.12

  Poor/fair

18 (31.6)

12 (18.2)

 

  Good/very good

22 (38.6)

24 (36.4)

 

  Excellent

17 (29.8)

30 (45.5)

 

 Insurance type

   

  Public

21 (34.4)

19 (27.9)

0.43

  Private

49 (80.3)

53 (77.9)

0.74

  None

1 (1.6)

2 (2.9)

0.62

 Economic burden score [range 0–12] (SD)

3 (3)

2 (4)

0.95

Cancer diagnosis and treatment variables

 Cancer stage at diagnosis

  

0.09

  Stage 0

9 (14.8)

10 (14.7)

 

  Stage 1

11 (18.0)

22 (32.4)

 

  Stage 2

11 (16.2)

19 (31.2)

 

  Stage 3

9 (14.8)

6 (8.8)

 

  Missing

13 (21.3)

19 (27.9)

 

 Years since cancer diagnosis (SD)

13 (6)

10 (3)

0.002

 Number of adjuvant treatment modalities (SD)

2 (1)

2 (1)

0.13

  Radiation

51 (83.6)

53 (77.9)

0.42

  Chemotherapy

51 (83.6)

46 (67.7)

0.05

  Hormonal therapy

29 (47.5)

34 (50)

0.79

 Comorbidities

1 (1)

1 (1)

0.46

 Interlimb difference (%)

9.3 (13.4)

− 0.8 (6.1)

< 0.001

BCRL breast cancer-related lymphedema

Figure 2 compares the average dollar amount difference, with and without productivity losses, for those who did not have lymphedema and those who did, controlling for age, race, socioeconomic position, type of cancer treatments, comorbidities, years since cancer diagnosis, and type of insurance. Excluding productivity losses, participants with lymphedema are estimated to have an average $2306 in out-of-pocket costs per year compared to $1090 for those without lymphedema (p = 0.006), or 112% higher costs (Fig. 2a). Including productivity losses, participants with lymphedema are estimated to have an average $3325 in out-of-pocket costs per year compared to $2792 for those without lymphedema (p = 0.55), or 19% higher costs (Fig. 2b). Among those reporting having lymphedema, Fig. 3 shows that nearly 50% of total costs were attributed to lymphedema.
Fig. 2

Adjusted annual out-of-pocket costs (marginal effects) for breast cancer survivors without or with lymphedema. a Mean annual out-of-pocket costs, excluding productivity losses, and 95% confidence intervals. The bar graphs in this figure compare mean annual out-of-pocket costs excluding productivity losses of $2306 for long-term breast cancer survivors with lymphedema and $1090 without lymphedema, adjusted for age, race, education, income, cash assets, consumer credit quality, interlimb difference, number of cancer adjuvant treatment modalities, years since diagnosis, number of comorbid conditions, and public or private insurance. b Mean annual out-of-pocket costs, including productivity losses, and 95% confidence intervals. The bar graphs in this figure compare mean annual out-of-pocket costs including productivity losses of $3325 for long-term breast cancer survivors with lymphedema and $2792 without lymphedema, adjusted for age, race, education, income, cash assets, consumer credit quality, interlimb difference, number of cancer adjuvant treatment modalities, years since diagnosis, number of comorbid conditions, and public or private insurance

Fig. 3

Proportion of total costs attributed to lymphedema-related needs, among those with lymphedema. The bar graphs show that 47% and 50% of cost, excluding and including productivity losses, respectively, for patients with lymphedema were costs directly relating to lymphedema needs

Table 2 contains illustrative quotes that demonstrate the three major themes that emerged from the qualitative interviews comparing breast cancer survivors across lymphedema status. These interviews provide further insight into the burden of higher costs associated with lymphedema.
  • Theme 1: Economic burden is cumulative and cascades over time; managing an adverse treatment effect presents ongoing challenges. The use of savings to cover medical costs and additional loans or debt to cover medical costs was common in all respondent interviews. For some women, covering medical costs compromised their ability to manage basic needs like utility bills. Women with lymphedema were more likely to relay that the upfront costs associated with cancer set off a cascade of financial challenges that continues to affect their current economic situation. Participants described current effects such as decreased ability to help family, support their children’s educational endeavors, and retire. Ongoing costs for lymphedema care needs exacerbated economic burden and compromised participants’ ability to obtain care for their current lymphedema needs.

  • Theme 2: Lymphedema care needs are unlikely to be covered by insurance, which contributes to higher long-term costs and compromises a patient’s ability to manage lymphedema symptoms. Respondents in both groups reported out-of-pocket health care costs and shifting costs to other parties (including family, employers, social service organizations, and advocacy groups). Participants described the need to use leftovers of patients’ medications to cope with their economic burden. Women who did not have lymphedema were more likely to report out-of-pocket costs accrued closer to the period of their cancer treatment for supplemental insurance, co-pays, and treatment, while women with lymphedema reported additional ongoing long-term out-of-pockets costs for lymphedema care in the form of ongoing physical therapy, lymphedema specialists, sleeves, and garments that were not covered by insurance. Even participants with private insurance did not always receive necessary lymphedema-specific care because of the cost burden. Changes in insurance, especially when changes in status led to less lymphedema coverage, further stymied their ability to manage ongoing lymphedema needs.

  • Theme 3: Productivity losses have long-term impact: breast cancer diagnosis may have influenced work opportunities and long-term earning potential, and breast cancer-related lymphedema may further decrease productivity losses at work. Both sets of participants spoke about long-term productivity losses. In some cases, women missed out on educational opportunities, modified work schedules, experienced job loss, pursued voluntary early retirement, or went back to work sooner than medically recommended. These experiences framed their subsequent health and lifestyles and still affect them currently. Women in both sets recalled needing additional help for duties around the house. Women with lymphedema were less likely to return to employment after cancer because of their additional physical challenges.

Table 2

Illustrative quotes from research participants by lymphedema status

Theme

Sub theme

Respondents with lymphedema

Respondents with no lymphedema

Theme 1: Economic burden is cumulative and cascades over time; managing an adverse treatment effect presents ongoing challenges

Use of assets, loans and lasting impact of cost accrual

I had to take my 401 K money and like pay bills, buy medicine because I did not have any medical coverage … all the moneys that I had saved up that would have sustained me [as a retiree] was gone … in terms of the money that I would have wanted to contribute [to retirement and children’s college funds], you know, I wasn’t able to and when I was able to-- I’m 61 so I’ll never get caught up with that so, yeah. – age 60; private insurance

So I went for a long time just basically on my savings and family helping me. – age 52; private insurance

So and I was able to get a small loan and pay off some bills. So, you know, that helped. – age 69; public & private insurance

It still affects our economic situation … we still feel the effects of the economic problems …. We had the co-pays. We had [lymphedema] therapies, different therapies... Massage. And, of course, you know, the sleeves … it seems like we can never, ever catch up to have a little bit extra. – age 56; private insurance

Balancing health costs with utility bill costs

It was just like, just a lot of financial burden so it was stressful where I would have liked to have had the experience while I was convalescing to be like not worried about are my lights gonna get shut off? And sometimes that happened and it was just rough. – age 60; private insurance

… So I was no longer able to work, ‘cause I had three surgeries … And then I had to do chemo and then I did radiation … I had my lights cut off. I had my water shut off. I had my gas shut off. And I would have to go up to the hospital and get slips to get them cut back on … And they would cut my lights off for, like, maybe $100...

– age 69; public & private insurance

Increased costs due to lymphedema-specific health needs

So having to go to physical therapy, it’s $30 each time I go … So I have had to actually ceased going because I just do not have the money. – age 62; private insurance

 

I just ordered my replacement sleeve on Monday, and I had to give my credit card for $420 before they would put in that order … This was one sleeve and glove – age 66; public insurance

Theme 2: Lymphedema care needs are unlikely to be covered by insurance, which contributes to higher long-term costs, and lack of management of lymphedema symptoms

Insufficiency of Medicaid to cover lymphedema needs

The physical therapy is covered with my Medicare and the secondary insurance, but if I were to get any garments, or new bandages, and everything, I am gonna have to do the out of pocket stuff, and I know that ran into, like, $95 for the bandages, and then the tape that you buy to wrap the bandages, the Ace, that runs to, like, $5 a roll. – age 73; public & private insurance

I pay for supplemental insurance to cover it, and I am dealing with... Medicare telling me what I can and cannot take … My supplemental insurance, to help cover the doctors and stuff, is $227 a month, and then your supplemental to cover your drugs is another $45 a month. And of course, Medicare’s not free. I know everybody acts like it is, but it’s not. Last time I looked, it was $166 bucks every three months. – age 73; public insurance

I cannot basically afford to buy the compression sleeve... And insurance does not cover it … I had [private insurance that] did give me one sleeve. Right after that, they changed my health insurance [to Medicare], so it went from getting the sleeve to not getting the sleeve. – age 68; public insurance

Out-of-pocket costs that are not covered by insurance

Right after my diagnosis and treatment and surgery, I had lymphedema and severe cording and banding... So I went to a [lymphedema] therapist, who at that time [the insurers] were not paying for that, it wasn’t reimbursed, so it was all out of pocket. – age 67; private insurance

The only thing that wasn’t covered was … a shot that was $100 and for-- I think for someone that’s not employed, that would be a difficult fee for them to have to pay – age 55; private insurance

When you’re first diagnosed, you have to go to a bunch of specialists, and the specialists are $25 apiece. When you’re going three times a week … it does add up, even with insurance. – age 56; private insurance

Theme 3: Productivity losses have long-term impact: breast cancer diagnosis may have influenced work opportunities and long-term earning potential and breast cancer-related lymphedema may further decrease productivity losses at work

Loss of career opportunities

I actually, I was teaching first grade at the time, which is very physically challenging, and I decided at the end of that school year, in June I retired – age 66; public insurance

When I went back, [the university] had taken away my financial aid, and consequently I was not able to complete my PhD. That’s an enormous hit. Consequently, although I am teaching at the University level … they will not hire me full time because I do not have the PhD. That would not have happened had I not had cancer... I also had chemo brain at that point... I mean, I still was getting good grades, but it was much harder work, but I also had no money, and we could not afford it, so I quit [the PhD program]. I have regretted that all these years. – age 59; private insurance

I lost my job ‘cause I got diagnosed with breast cancer so financially it was very difficult … I was out of work for almost a year … with the chemo … I was really sick and then I went back against the doctor’s orders ‘cause I needed to make money... When I came back to work that’s when they expected me to resume all of the duties... full force and … I got fired... – age 60; private insurance

I used to do work with a lady with catering and stuff right and I could not use my arm because it was always in pain with the lymphedema … It was a setback …. I stopped [working]. – age 63; private insurance

Needing help with daily activities

I just went around my normal household duties, and only thing I didn’t do-- I don’t think I did any ironing. – age 81; public insurance

During the first year, during treatment and immediately following, one, I was out of work for six months. Two, I needed help with childcare, transportation for children, housekeeping, meal prep. – age 60; private insurance

Taking time off from work

Well, the surgery, I was-- I think I was out of work for maybe a month. For the lymphedema treatments, I just would go after work. I had to maybe leave early for work and leave early for radiation and that was about six weeks I think – age 63; private insurance

After I had my [breast cancer surgery] surgery, I wound up back in the hospital with a severe infection... because I did not get, or I did not understand, or I did not hear the proper way to keep it draining. And it backed up, and I wound up in the hospital for another four days with that. – age 73; public insurance

I would schedule my chemo on a Friday, so it would give me Saturday and Sunday if I needed it. And, for my radiation, my employer would let me leave like at one o’clock every day... – age 60; public insurance

I didn’t go back to work until part-time in November. So from June to November. And then, full-time, I guess, December or January … so we had the loss of salary plus additional outlay. – age 60; private insurance

Discussion

Study results suggest that the economic burden of breast cancer continues long after diagnosis. Women with lymphedema experience a higher burden, with or without indirect cost considerations. In the long term, women report losses to economic opportunity due to their cancer and lymphedema diagnoses. Despite the expansion of cancer-related insurance coverage under the Affordable Care Act, breast cancer survivors, with and without lymphedema, still face significant financial need.

Breast cancer survivors with lymphedema faced up to 112% higher total out-of-pocket costs when excluding productivity losses and up to 19% higher total out-of-pocket costs when including productivity losses, compared to those without lymphedema. The average out-of-pocket costs estimated in this study are lower than the roughly $11,000 per year previously estimated for US women [13]; however, previous estimates are based on costs closer to the time of treatment, when overall healthcare needs may be higher, and are based on women of working age, who would not have out-of-pockets subsidized by Medicare. These estimates are based on insurance claims, and not patient out-of-pocket costs, which may also contribute to why previous estimates differ from those found in the present study. Even though our costs are lower than previously estimated, the study provides evidence that costs for women with lymphedema remain significantly elevated long after cancer treatment. On average, there is a $500–$1215 difference. These economic burdens occur even among those who have health insurance.

Although nearly all of the women in the sample had some form of insurance, changes and challenges with insurance consistently complicated issues for both women who had lymphedema and those who did not. Studies conducted before the 2010 Affordable Care Act reported that financial burden created worry and anger when tools for lymphedema management were not covered by insurance [40]. The present study suggests that these challenges persist even after the Affordable Care Act, which has the potential to expand health insurance coverage for cancer-related care [41] and for cancer survivors [42, 43]. For women cancer survivors with lymphedema, who continued to manage a disease long after completing cancer treatment, these challenges persisted due to ongoing needs for lymphedema care. Women who did not have lymphedema reported insurance challenges related to coverage of cancer treatment and co-pays at the time of treatment but did not report challenges with current care.

Insurance coverage of lymphedema care varied over time and changed based on insurer. Previous findings suggest persistently high costs for cancer survivors who are insured by public insurance [44], which are particularly relevant because coverage for lymphedema treatment varies for public insurance [45]. Medicare covers: medically necessary manual lymph drainage performed by physical or occupational therapists, compression bandaging services, patient education on lymphedema self-care and lymphatic decongestion exercises, and pneumatic compression devices, but not for all compression self-management equipment (such as bandages). Medicaid expands on that coverage, with a few states covering compression garments and bandages. Switching from private to public insurance often posed the most problems when public and private insurance covered lymphedema differently such that patients’ needs were no longer met. When patients could not cover their costs, family members or social service organizations were sometimes able to help, but often patients simply went without the care they needed. Other studies have suggested that high out-of-pocket costs will cause patients to use compression garments that no longer apply sufficient pressure to manage lymphedema [46], which participants in our study corroborated. Interview participants reported that lack of coverage for lymphedema-related costs contributed to less lymphedema management and exacerbation of lymphedema.

This study confirmed that higher costs can only be partly attributed to lymphedema, above and beyond the presence of other comorbidities. Interview data suggest that higher costs for women with lymphedema stemmed from cumulatively high economic burden that cascaded over time and prevented women from fully recovering financially. It also highlighted that examining only financial costs due to lymphedema underestimates its full cumulative effect of economic burden on ability to afford other basic needs. Use of savings and retirement to cover lymphedema and healthcare costs can affect women long term and have intergenerational effects. Managing breast cancer-related lymphedema presents ongoing challenges, and adherence can be difficult due to ongoing costs. Having access to additional resources through family, credit, or savings is often leveraged, but may never be recovered, especially for those with ongoing lymphedema management needs.

The findings of this study are especially timely given the recent calls to reduce financial toxicity in US cancer patients through individual-level strategies, as encouraging healthier behaviors [47] and greater financial disclosure [48, 49]. But these strategies put the onus on patients to act in order to reduce cost, rather than pointing to healthcare systems to change to reduce costs. This approach may widen disparities since patients with the greatest resources will be able to afford better health, thus reducing costs is paramount. Some scholars have explored healthcare provider-driven recommendations to reduce economic burden [50]. Other scholars have called for introducing screening for financial toxicity, as well as a multi-level approach to reducing economic burden [51], and redesigning sick leave policies to better accommodate chronic disease needs [46]. For mitigating lymphedema costs in particular, advocates have supported the Lymphedema Treatment Act, which would amend Title XVIII (Medicare) of the Social Security Act to cover certain lymphedema compression treatment items as durable medical equipment under Medicare. Some states, including California, Louisiana, North Carolina, and Virginia, have issued their own laws, but the Act has not found success at the US Congressional level. A 2016 report found that expanding insurance coverage in one state had a less than 0.1% impact on insurance claims, while lowering costs for lymphedema treatment and lymphedema-related hospitalizations [52]. Our findings reinforce the need for actions at policy, provider, and individual patient levels, especially for those with lymphedema.

This analysis consisted of a small sample from one geographic area, the majority of whom had insurance, which may limit the external validity of the findings, especially given that insurance policies differ regionally. Responses may be different from women living in regions with other insurance offerings. Cost diaries pose a time burden on participants to complete, which may have led to missing entries: monthly text-based, e-mail, and phone messaging was used to remind participants to complete their diaries. Participants were also allowed to send in receipts and medical visit bill summaries in lieu of writing them into the cost diaries themselves. Nonetheless, the data that were collected comprehensively covered cost domains in real time, with over a 90% response rate in each month of data collected. Cost data collection was not prospective throughout, and the 3-month retrospective data may have been biased due to recall; to minimize the potential for bias, participants were asked to use supporting documents to aid in recall. The final 3 months were based on projected costs due to regular ongoing medical visits or needs, leading to underestimated costs because unexpected healthcare needs would not be included. Cost diaries may not comprehensively capture the various domains of direct, indirect, psychosocial, and time costs and only measure costs over the period of observation; thus, we used qualitative data to supplement our understanding of how and when various types of costs were incurred during the course of survivorship. These challenges mean that the cost estimates are conservative, and that actual out-of-pocket costs are likely higher than reported here. There may have been other clinical factors to consider that may influence cost, like cancer severity [53] as the initial economic shock that set patients on different financial trajectories. Data on stage at cancer diagnosis were excluded from the regression analysis due to a high percentage of missing data (16%), although available data suggest no difference in stage of diagnosis by lymphedema status. As a voluntary research study, those experiencing the greatest economic or health challenges may not have had time to enroll and participate, meaning that our results may underestimate economic burden. Results may not be generalizable to those with higher cancer stage, older age, or other tumor sites other than the breast, but breast cancer is among the most economically burdensome cancers.

Breast cancer survivors with lymphedema face higher costs than those who do not have lymphedema, even many years after cancer diagnosis. Although women with and without lymphedema experience a similar number of economically burdensome events and comorbidities, high out-of-pocket costs for women with breast cancer-related lymphedema lead to a cascade of other economic challenges that persist long after cancer treatment. Future work should explore patient-driven recommendations to reduce economic burden after cancer.

Notes

Funding information

This work was supported by the National Center for Research Resources and the National Center for Advancing Translational Sciences (NCATS) of the National Institutes of Health through grant 1UL1TR001079 (statistical consultation); the National Cancer Institute grant K01CA184288 (Lorraine T. Dean); the National Institute of Mental Health grant R25MH083620 (Lorraine T. Dean, Yusuf Ransome); the Sidney Kimmel Cancer Center grant P30CA006973 (Lorraine T. Dean, Kala Visvanathan, Yuehan Zhang); Johns Hopkins University Center for AIDS Research grant P30AI094189 (Lorraine T. Dean); the National Institute on Drug Abuse grant T32DA031099 (Shadiya L. Moss), National Institutes of Mental Health K01MH111374 (Yusuf Ransome); the National Institute on Aging grant K01AG04176 (Lauren Hersch Nicholas); and the National Cancer Institute grants R01CA106851 and 1U54CA155850-01 (Kathryn H. Schmitz).

Compliance with ethical standards

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

Informed consent

Informed consent was obtained from all individual participants included in the study.

Conflict of interest

The authors declare that they have no conflict of interest.

Supplementary material

520_2018_4418_MOESM1_ESM.docx (31 kb)
ESM 1 (DOCX 31 kb)
520_2018_4418_MOESM2_ESM.docx (17 kb)
ESM 2 (DOCX 16 kb)

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Copyright information

© The Author(s) 2018

Open Access This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors and Affiliations

  • Lorraine T. Dean
    • 1
    • 2
    Email author
  • Shadiya L. Moss
    • 3
  • Yusuf Ransome
    • 4
  • Livia Frasso-Jaramillo
    • 5
  • Yuehan Zhang
    • 6
  • Kala Visvanathan
    • 1
    • 2
  • Lauren Hersch Nicholas
    • 2
    • 5
  • Kathryn H. Schmitz
    • 7
  1. 1.Department of Epidemiology, Johns Hopkins Bloomberg School of Public HealthJohns Hopkins UniversityBaltimoreUSA
  2. 2.Department of OncologyJohns Hopkins School of MedicineBaltimoreUSA
  3. 3.Department of Epidemiology, Mailman School of Public HealthColumbia UniversityNew YorkUSA
  4. 4.Department of Social & Behavioral SciencesYale School of Public HealthNew HavenUSA
  5. 5.Department of Health Policy & Management, Johns Hopkins Bloomberg School of Public HealthJohns Hopkins UniversityBaltimoreUSA
  6. 6.Department of General Internal Medicine, University of Pennsylvania Perelman School of MedicineUniversity of PennsylvaniaPhiladelphiaUSA
  7. 7.Department of Public Health Sciences, Pennsylvania State University College of MedicinePennsylvania State UniversityHersheyUSA

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