Introduction
Older adults are heterogeneous in terms of health, functional, psychological, social, and economic status [1]. With increasing age the levels of frailty increase and there is decline in physiologic function that influences both the risks and benefits of treatment [2]. Studies show that under-treatment in older adults with cancer is common and is related to age and comorbidities [3‐8]. Evidence also shows greater variation in treatments offered by oncologists [9‐12] to older adults with declining health, suggesting difficulty in identifying and recommending the most appropriate treatment for this population.
A previous systematic review of cancer treatment decision-making showed that few studies have focused on older adults aged 70+ [13]. Furthermore, although recent studies explored factors influencing the treatment decision-making process from the perspectives of older adults with cancer [14, 15], none explored the influence of frailty, comorbidity, or functional status while they have been shown to be associated with treatment tolerability and outcomes [16‐18]. In addition, few studies explored support needed to enhance the quality of the treatment decision-making process for older adults, their family members, oncologists and family physicians. The aims of this study were to examine the treatment decision-making process from all four perspectives, as well to explore how comorbidity, frailty, and functional status influenced the decision-making process.
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Patients and methods
Study design
We conducted a mixed method multi-perspective longitudinal study [19‐21]. Older adults with cancer were invited to complete two semi-structured interviews and surveys: one after the treatment decision had been made [up to six months after the decision] and one 3–6 months later to allow examination of changes over time. The other participants (family members, oncologist and family physician) were invited to participate in one semi-structured interview. Multi-perspective interviews were used as they can provide complementary and contradictory perspectives [22].
The study was approved by each participating institution’s research ethics board. All participants provided written informed consent.
Study participants
Older adults with cancer aged ≥70 with advanced breast, prostate, colorectal, and lung cancer and who made a treatment decision about palliative chemotherapy in the previous six months at the Princess Margaret Cancer Centre, University Health Network or the Odette Cancer Centre, Sunnybrook Health Sciences Centre, both in Toronto Canada between July 2014 and August 2015 were eligible.
Purposeful sampling was used to maximize opportunities to develop concepts and identify relationships among concepts [23]. The process of data collection and analysis was cyclical to allow time for reflection and opportunity to refine questions.
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The older adult sample was stratified by age (70–79 and 80+) to ensure adequate representation from the oldest adults, as treatment benefits and risks differ with increasing comorbidity, frailty and age. The number of participants was guided by data saturation in each stratum.
Sixty-seven older adults were invited to participate; 38 agreed and 29 declined. The most common reason for decline was that the older adult was not interested. Six patients did not complete the first interview. While 6 agreed to participate they were not interviewed for various reasons. Reasons included: change of mind (n = 1), family member disapproval (n = 1), or declining health (n = 4). Three patients slightly younger than 70 were recruited at the Odette Cancer Centre by mistake; they were retained as their experiences were similar to other participant’s experiences.
At the end of the first older adult interview the other participants were identified and recruited subsequently. All but one invited family member participated. Fifteen family physicians agreed to participate, seven refused and the other older adults did not have one. Thirteen oncologists participated and three declined. Eleven older adults passed away and two withdrew before the second interview.
Interviews
Semi-structured interviews were conducted using topic guides (see Supplemental information file 1). The interviews included questions about health and treatment recommendations, factors that influenced the treatment decision-making process, information needs, support needs, and the influence of comorbidities and functional status on the treatment decision-making process. Twenty-two participants were interviewed by the telephone as per the patients’ wishes; six were interviewed at home and four were interviewed in the cancer centers. All family members and family physicians were interviewed by telephone. The oncologists were interviewed in their office. All interviews were audio-recorded and transcribed verbatim and field notes were written to provide context for the interview. Interviews were conducted by the PI and trained nursing students. Most interviews lasted between 15 and 60 min.
Member checking was used to validate our findings [23] by sending all participants the summary of their interview findings with a return envelope for corrections.
Survey and chart data
Older adults were asked to complete a survey after both interviews to obtain social demographic information, and information on health, frailty (using the Vulnerable Elder Survey (VES) -13 items [24]), and the decision making (the 1 item Control Preferences Scale [25] to assess decisional preferences and Satisfaction with Decision Scale [26] which is a sum of the six items and ranges 6–30 with higher scores indicating more satisfaction). Two initial and seven follow-up surveys were missing for reasons including patients’ death and not receiving surveys back.
Cancer diagnosis, comorbid conditions and the Eastern Cooperative Oncology Group performance status [27] closest to the interview date were abstracted from the chart.
Data analysis
Interviews were transcribed verbatim and analyzed with support of NVivo v.10 using a thematic analysis approach [28]. The PI and research assistant read the transcripts to explore emerging themes. We used constant comparison to identify the themes and data from each perspective. Initially data from each perspective was analyzed separately and in the next step as case studies around the older adult [19]. The findings were discussed with the research team to reach peer consensus.
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Descriptive statistics were used to summarize survey results and describe the characteristics of older adults. The VES-13 was used to categorize patients into frail (score of ≥3) and non-frail to explore whether the treatment decision-making process was different.
Results
Twenty-three men and nine women participated (see Table 1 and Supplemental information Table 1). Eighteen were aged 70–79, 11 were aged 80+ and 3 were aged 63–69. Four older adults had breast cancer, 11 had prostate cancer, six had colorectal cancer, and 11 had lung cancer. Seven patients lived alone. All participants were satisfied with their treatment decision-making process using the Satisfaction with Decision-making scale (mean 25.4 (SD 2.7) for age 70–79 and mean 25.7 (SD 4.5) age 80+). There were 9 persons in the “young old” group frail (VES-13 score ≥ 3). In the “old old” group 6 were frail. Of the 27 family members who participated in this study, 14 were children, 10 were spouses and 1 was a friend who had become the caregiver. Female participants had more often a child as their caregiver (7/9 participants) compared to the male participants who had more spouses as caregivers (8/23).
Table 1
Study participants characteristics
Characteristic
|
Young old:
n = 21
|
Aged 80 years and older
n = 11
|
|---|---|---|
Sex | ||
Woman | 5 (24 %) | 4 (36 %) |
Man | 16 (76 %) | 7 (64 %) |
Living alone | 5 (24 %) | 3 (27 %) |
Cancer type | ||
Breast | 3 (14 %) | 1 (9 %) |
Colorectal | 4 (19 %) | 1 (9 %) |
Prostate | 7 (33 %) | 4 (36 %) |
Lung | 7 (33 %) | 5 (45 %) |
Interview with family member | 16 (76 %) | 9 (82 %) |
Interview with oncologist | 18 (86 %) | 10 (91 %) |
Interview with family physician | 12 (57.1 %) | 6 (55 %) |
Themes according to participant group
Themes per participant group are reported in Supplemental information Table 2 with citations and are summarized below.
Older adults
All but four patients accepted the recommended treatment. There were no differences in the treatment decision-making process based on age, frailty or comorbidities. The following three themes to describe the older adults’ treatment decision-making processes emerged:
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Relationship with the oncologist
The most common reason for accepting chemotherapy was based on their relationship and their trust in the oncologist as expert to recommend the best treatment. The older adults felt that their oncologists were generally supportive and took the time to explain things to them and answer their questions. However, about a third of older adults felt that they were often being rushed by their oncologist and the appointments were too short to allow them to express their concerns and ask their questions. One-third of the patients sought advice from their family physicians regarding their disease and treatment.
Perceived benefits and harms/discomfort
There were many older adults that accepted the oncologists’ recommended chemotherapy as they saw chemotherapy as the last resort to prolong life. Others accepted chemotherapy to maintain quality of life. Comorbidity and functional status did not play any role in the treatment decision-making process for most patients despite some older adults reporting having several other diseases. Travel to the hospital did influence decisions of older adults who were dependent on family.
Treatment experiences of important others/family influences
Four patients described how others’ positive chemotherapy experiences made them accept chemotherapy, reasoning that if it worked for others and they were doing well it made the decision easier to accept it. Two accepted chemotherapy because their family told them to accept and one patient who initially did not want chemotherapy changed her mind after her family was upset and wanted her to try it.
Family members
The following themes emerged from interviews with family members:
Trust in the oncologist
The family members trusted the oncologist to give the best treatment recommendations based on his/her expertise. They often searched online for more information. They were unsatisfied with the opportunities for telephone contact because of the miscommunications or contradicting information with regard to follow-up care.
Perceived benefits and harms
Family members wanted treatment to prolong life and they indicated that they were not always clear on what the intended outcome of the treatment was. They mentioned that they would like more information about the actual goal, whether that was reduction in a specific symptom or stabilizing the disease etc. However, several family members did not feel comfortable asking explicit questions about prognosis.
Family physicians
Lack of involvement
Family physicians reported not being involved in the treatment decision-making process and some voiced that they would like to be more involved in the care of their patients and be involved earlier than only being included at the end-of-life stage. Family physicians reported that patients usually did not come back for advice regarding treatment. However, those older adults that did come to see them often lacked the details on the treatment that was suggested and thus they could not provide support with the treatment decision-making process.
Oncologists
“easy decision”
The majority of the oncologists stated that coming up with their treatment recommendation was easy and that most patients did not have a hard time making a decision. Several oncologists stated that they do take functional status (performance status) into consideration when assessing for treatment suitability. Some oncologists used dose-reduction due to patients’ age. The challenges of formulating treatment was balancing risks and benefits of treatment and to help patients, particularly for those who were eager for treatment, understand the importance of the risk-benefit balance.
Comparison of the four perspectives
Several discrepancies between the four participant groups were noted (see Table 2 and Supplemental information Table 3) and are described below.
Table 2
Summary table of the influence of functional status, frailty and comorbidity on the treatment decision-making process
Domains
|
Older Adult
|
Family member
|
Cancer Specialist
|
Family physician
|
|---|---|---|---|---|
Functional status
| Prolonging life is most important, for others maintaining quality of life is important | Prolonging life is most important | Most patients were fit, performance status is taken into account | Not involved |
Comorbidity
| Other health conditions do not play a role in the chemotherapy decision | Other health conditions do not play a role in the chemotherapy decision | Comorbidity is taken into account but most patients were fit so it did not play an important role | Not contacted for the patient’s medical history, some feel the patient’s comorbidity is underappreciated by oncologists |
Frailty
| Not mentioned by patients | Not mentioned by family members (but they do describe weakened states after the start of chemotherapy) | Not mentioned by all except one | Not contacted for any information with regard to health and functional status |
Different perspectives on frailty and function
Older adults stated they were in good shape, and reported no major concerns other than fatigue. Older adults did not mention frailty. No family member mentioned frailty; although they did often describe a weakened state after starting chemotherapy. Only one oncologist stated that the decision about what treatment to recommend was challenging due to the patient’s frail status.
Different perspectives on comorbidity
Most patients stated they had good health, and denied having any major comorbidities. Those with comorbidities mentioned they were being treated for them and thus comorbidity played no role in their treatment decision-making process. Family members also indicated that comorbidities played no role in the treatment decision-making process. In contrast, some family physicians stated that comorbidities were often not sufficiently taken into account in the cancer treatment decision-making process. Oncologists spoke of most patients as fit patients and therefore comorbidity had no influence on the treatment decision-making process. Although several patients denied having any comorbidities and stated they had good health, their family physician described these same patients’ as having multiple comorbidities and health issues. Oncologists did not always mention these multiple comorbidities. Despite oncologists and patients reporting good health there was a substantial proportion who were classified as frail on the VES-13, which was only due to age alone (aged 85+) in two patients.
Differences in who made the decision
Almost all patients stated that they made the treatment decision themselves. However, they also talked about ‘leaving it up to the specialist’. Of note, most older adults indicated on the Control Preferences Scale a desire to make their own decision after seriously considering their doctor’s opinion. Oncologists indicated that patients made their own decisions. Lastly, differences in perspectives were observed between family members. Spouses of patients spoke of “his/her decision” because it is “his/her life” or “his/her body”. These decisions were usually made in the moment. Contrastingly, children spoke of “we decisions”, and they took time to think and discuss the treatments recommended at home. Children were often more actively involved in finding additional information about the treatment decision to be made than spouses.
(Mis)communication
Several older adults and family members voiced their dissatisfaction with their family physician due to delays in diagnosis/wrong diagnoses. However, these family physicians did not seem to be aware of this dissatisfaction. Some older adults accepted chemotherapy to ‘get better’ and ‘to cure cancer’ while these patients were receiving chemotherapy with palliative intent.
Many oncologists felt that it was not useful to contact family physicians as they are not experienced and cannot add value to the discussion or are not interested. Conversely, some family physicians felt that they were not given the opportunity to get involved in the treatment decision-making process nor included in the discussion regarding patients’ treatment goal, prognosis, and transition from active treatment to palliative/end-of-life care.
Suggestions for improvement
While most older adults were satisfied and had few suggestions, several family members (particularly children) and family physicians had several suggestions to improve care. These are summarized in Table 3.
Table 3
Participants’ Suggestions for Improvement
Patient
|
Family member
|
Oncologist
|
Family physician
|
|---|---|---|---|
• More discussion about financial support in terms of travel costs during treatment. | • More written, understandable information about the recommended treatment | • More social work access | • Improvement on transportation and home care |
• Heads up if next appointment will involve decision-making so they can prepare and bring somebody; also, more time allocated for those appointments so that all questions can be asked | • More resources/directions on where to go online to find reliable information (e.g. provide a list of trustworthy websites). | • More support for patient assessment – no time in clinic to perform geriatric assessment (GA) | • More timely information about diagnosis, treatment (including actual drug and how it works), what side effects are and WHEN do they start |
• More clarification of medication terms | • More clarification with regard to medical terminology | • Get family physicians involved | • Opportunity to participate in discussion regarding end-of-life care |
• Listen to the patients | • Take time to sit down and listen to patients | • Each patient should be assigned a care navigator | • To be informed earlier if patients have no more treatment options; be informed by oncologist before hearing it from the patient |
• Nurses need to make more conversations | • More information on what treatment success means | • Be more informed about What treatment goal is | |
• Inform other patients that nurses are a source of support during TDMP | • Clinics should avoid appointment changes on short notice as it is very difficult for caregivers to arrange for time off work to come to appointments | • A paid patient navigator/manager (somebody with healthcare training such as a retired professional) should be assigned to each patient to help him/her navigate the system | |
• Each patient should be assigned a patient care coordinator/manager/navigator to help navigate the large, confusing system, which could be especially frightening for those who do not speak English. | • For patients with brain metastases, more consideration should be given in terms of who information is given to (if patient is confused) | • Oncologists need to understand psychosocial background and patient wishes | |
• More continuity in staff support (i.e. same nurse during each visit) | • Appointment reminders should be emailed to designated caregivers rather than to patients | • Oncologists should discuss more openly treatment goals – advanced care planning for patients | |
• Efforts should be made to ensure that phone numbers given to call for questions are helpful. Be sure there is someone to ask when questions arise | • Space and designated room in hospital for peer support (for patients and families). | ||
• Better communication and coordination to prevent contradicting treatment possibilities given to patients (fellows vs. oncologists) to avoid raising patients’ hopes only to be disappointed later when told something different. |
Changes over time
Half of the older adults were still on the same treatment regimen at the time of their second interview. Most of them were feeling better and noticed an improvement in functional status. All of them were satisfied with the information they received to support their treatment decision-making process, including the two patients who had to stop chemotherapy due to side effects. All but one patient stated they would have made the same decision if they were to go through the same treatment decision again.
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Discussion
We interviewed a series of older adults with advanced cancer along with their families, oncologists and family physicians to examine the treatment decision-making process and factors influencing it. Most accepted the treatment recommended by their oncologist based on trust. Surprisingly, comorbidity and functional status were not important factors influencing treatment decisions from the perspective of patients, families or oncologists in this study.
Our findings that most older adults and families accepted the treatment recommendation by the oncologist based on trust is in agreement with earlier studies [13]. The patient’s choice to follow the oncologists’ suggestions and place their trust in them aligns with the notion that there may exist a natural developmental tendency for older adults to desire less responsibility for medical decisions and to rely on the expertise of others. This is in agreement with the Socio-emotional Selectivity Theory (i.e. the selection and pursuit of goals change as one ages and time becomes limited [29]). As a result, interest in knowledge pursuit decreases, and older adults become less interested in problem-solving, planning, or information. However, this may change with increasing use of information technology (e.g. the Internet). Furthermore, only four patients declined the proposed treatment. This may be due to the two recruitment sites; both cancer centers are the largest comprehensive cancer centers in Canada and they attract patients that want a certain treatment not available or not offered in smaller hospitals as well as patients who want to be treated aggressively and therefore, are willing to travel to these famous cancer centers.
The decision to initiate chemotherapy in older adults is an important task facing oncologists and entails considering a number of factors including life expectancy, treatment benefit and tolerance, and availability of social support, along with considerations to minimize treatment toxicity [30‐32]. Recently the use of geriatric assessment has been recommended to help make chemotherapy treatment decisions in older adults [16, 33] by assessing the level of frailty and functional impairments as well as determining remaining life expectancy in the context of their other health conditions. Frailty was not a common theme brought up by oncologists. Many oncologists state that their patients were “fit enough” to undergo chemotherapy. However, research has shown that oncologists may overestimate the level of fitness of patients and that a frailty/geriatric assessment may give a better idea of the level of functioning of the patient [34] and none of the oncologists mentioned using any geriatric oncology guidelines or geriatric assessment tools to inform their treatment recommendation.
Older adults often have a long relationship with their family physicians whom they trust and who was often the health care professional investigating the symptoms leading to the cancer diagnosis and after referral there was a gap in communication. Improving the communication between the oncologist and family physician could improve quality of care at every stage of the disease and treatment as well as smooth transition for patients as they approach end-of-life [35, 36].
A strength of this study is our multi-perspective qualitative design and the first to explore the impact of frailty, comorbidity and function from each perspective. Results showed the advantages of using multiple perspectives as highlighted in the differences and discrepancies as well as agreements observed. However, generalizability of study findings must be made with caution. They were recruited at two highly specialized cancer centers that may attract different patients compared to other hospitals. Moreover, those who died or were too sick to participate in the second interview might have had different perspectives in terms of their satisfaction with the treatment decision-making process.
In conclusion, patients and family members were largely satisfied with their treatment decision-making process. Efforts to improve communication between oncologists and family physicians and between oncologists and patient and their families are needed to enhance the quality of the treatment decision-making process.
Acknowledgments
The authors would like to thank all staff at the Princess Margaret Cancer Centre and the Odette Cancer Centre for their support.
Compliance with ethical standards
Funding
This study was funded by an Innovation grant (grant # 702,050) from the Canadian Cancer Society Research Institute. Dr. Puts is supported by a Canadian Institutes of Health Research New Investigator Award.
Conflict of interest
None.
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