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01.02.2012 | Review Article | Ausgabe 2/2012 Open Access

Supportive Care in Cancer 2/2012

The unfulfilled promise: a systematic review of interventions to reduce the unmet supportive care needs of cancer patients

Zeitschrift:
Supportive Care in Cancer > Ausgabe 2/2012
Autoren:
Mariko Carey, Sylvie Lambert, Rochelle Smits, Chris Paul, Rob Sanson-Fisher, Tara Clinton-McHarg

Psychosocial impact of cancer and its treatment

The psychosocial impact of a diagnosis of cancer is widely acknowledged. Rates of clinically significant distress have been reported to be between 25% and 45% among people with cancer [1, 2]. Cancer treatment can bring about changes in body image and sexual functioning [3]. Symptoms, such as pain and fatigue, can lead to a diminished capacity to fulfill the usual social, vocational, and family roles [3]. The effects of cancer and its treatment may, therefore, be far-reaching, impacting on a person’s physical, social, and emotional well-being. As such, a broad range of services and support may be needed to assist patients and their families to manage these effects.

Unmet supportive care needs are prevalent among cancer patients

The term supportive care needs is an umbrella term which covers the physical, informational, emotional, practical, social, and spiritual needs of an individual with cancer [4]. Unmet supportive care needs (unmet needs) are those needs which lack the level of service or support an individual perceives is necessary to achieve optimal well-being [4, 5]. Measures of unmet supportive care needs are able to capture concerns across a broad range of domains reflecting the multidimensional impact of cancer [5, 6]. Cancer patients have reported high levels of unmet need related to issues such as provision of information [5, 79], psychosocial support [5, 8, 10, 11], practical assistance [12, 13], and sexual issues [11, 14]. Cross-sectional research has also indicated that reporting higher levels of unmet need is associated with increased anxiety and poorer quality of life (QoL) among patients [6, 13, 15, 16]. Measures have been developed for cancer patients undergoing treatment [17], terminally ill cancer patients [18], and cancer survivors [19], as well as caregivers [2022]. The increased attention on measure development and description of unmet supportive care needs suggests that it is important to establish how these needs can be ameliorated.

Potential to reduce unmet needs through timely identification and tailored intervention

Typically, unmet need measures provide an indication of the relative importance of a need, rather than simply whether or not the need remains outstanding [23]. In this way, unmet need measures help to provide an indicator of an individual’s judgment regarding the significance of the need in relation to their psychosocial well-being. For researchers, clinicians, or other administrators, this method may also inform service prioritization [6, 24, 25].
It is plausible that unmet needs can be addressed through timely identification and provision of appropriate services or interventions. Given this potential, it is not surprising that research efforts have been directed towards the development and evaluation of interventions to reduce unmet needs among people with cancer. The aim of this review was to examine (a) trends in the number of publications on unmet supportive care for people with cancer since 2000 and (b) the effectiveness of all previous interventions developed to reduce unmet needs among people with cancer that employed methodologically rigorous study designs.

Methods

Definition of unmet needs

For the purpose of this review, an unmet need was defined as a necessary or desired action or resource that is required in order to achieve optimal well-being [5, 26].

Aim 1: examining trends in the number of unmet needs publications over time

Literature search

An electronic literature search was conducted using Medline using the terms “Health Services Needs and Demand or Needs Assessment or needs assessment.mp” OR “unmet needs.mp” AND “cancer.mp or Neoplasms.” Additional limits included publications between 2000 and 2010 and “all adult (19 plus years).” This search was restricted to one database only, as the intention was to provide an overview of trends only rather than a comprehensive search. The year 2000 was chosen as the beginning parameter of the search as several seminal papers were published on the unmet needs of cancer patients in this year [5, 17, 27]; therefore, it would be expected that interest in needs publication would increase from this point onwards.

Inclusion criteria for examination of trends in the number of publications on unmet needs

To provide an overview of the trends in the number of unmet needs publications over time, abstracts from Medline were reviewed. Studies which reported primary data on unmet supportive care needs for cancer patients or survivors were included. Both qualitative and quantitative published data were included. Studies were classified as “measurement” if they reported on the development or testing of a measure of unmet supportive care needs for people with cancer, “descriptive” if they reported on the prevalence or type of unmet needs experienced by people with cancer, or “intervention” if they reported on the evaluation of an intervention to reduce unmet supportive care needs.

Aim 2: systematic review of intervention studies

Literature search

An electronic literature search was conducted using Medline, CINAHL, PsychINFO, and Web of Science databases on 12 January 2011. The following combination of search terms was used: “intervention.mp OR intervention studies” OR “clinical trial(s)” OR “randomized controlled trial” AND “health services needs and demand” OR “health service needs” OR “needs assessment OR unmet needs.mp” AND “cancer.mp or neoplasms.” The search was limited to “all adults (19 plus years).” Researchers known to be conducting work in the area of unmet needs were also contacted by the authors to identify any additional publications which were under review or in press.

Inclusion and exclusion criteria

Publications were eligible for inclusion if they (a) tested the efficacy of an intervention to reduce unmet needs among adult cancer patients or survivors, (b) used a validated quantitative measure of unmet needs as the primary or secondary outcome, and (c) used a methodologically rigorous research design. The following research designs were included [28]:
Randomized controlled trials
These are studies where participants were randomly assigned to intervention or control groups.
Quasi-randomized controlled trials
These are studies which included a concurrent control group and where alternate assignment (or some other non-random method) was used to assign participants to intervention and control groups.
Controlled before and after designs
These are studies where measures were collected at an intervention and control site contemporaneously both before and after the intervention.
No restrictions on date of publication were used. Papers that were published in languages other than English; were dissertations, conference abstracts, or study protocols; were not relevant to cancer patients or survivors; were focused on children or adolescents with cancer; and were interventions that aimed to change provider behavior were excluded.
Assessment of publications against the inclusion criteria
Two authors independently examined all retained abstracts to identify publications that reported the results of methodologically rigorous intervention studies. Full-text versions of the remaining papers were reviewed independently by two authors to exclude intervention papers which were either not relevant to unmet needs or did not use a validated, quantitative measure of unmet need. Studies were then coded against the following quality criteria: concealment of allocation, whether outcomes were similar across groups at baseline, whether missing data were likely to affect results, and whether participants were blind to study allocation. Any discrepancies were discussed until an agreement was reached. The two authors then extracted the following information for each trial: aims and study design, setting and sample, description of the intervention, outcome measures used, and intervention results.

Results

Aim 1

As illustrated in Fig. 1, the majority of these studies have utilized descriptive methods, as opposed to measurement or intervention research. Despite some fluctuation, the number of descriptive studies per year has substantially increased from 2000 to 2010, while the number of intervention studies per year has remained low.

Aim 2

As shown in Fig. 2, eight studies from the literature search met the inclusion criteria. One additional randomized controlled trial (RCT) was identified through the authors’ research networks [29]. A high level of inter-rater agreement between the two authors for all coding stages was indicated by a kappa of 0.95. The study characteristics of the nine included trials are presented in Table 1.
Table 1
Randomized and quasirandomized controlled trials of interventions to reduce cancer patients’ unmet needs
Reference
Aim and study design
Setting and sample
Description of intervention
Needs measure
Results
McLachlan et al. 2001 [35]
To determine whether providing the health care team with a report on patients’ perceived cancer needs (primary outcome), QoL, and psychosocial information would reduce cancer needs
450 cancer patients (mixed cancer types) recruited from an outpatient clinic
For intervention participants, a computer-generated, one-page summary of their baseline survey results was generated immediately for discussion with their doctor. The intervention nurse was present at the consultation and, following the consultation, developed an individualized management plan based on the needs identified in the summary
CNQ short form
Of the 14 comparisons on the needs measure, the only difference found was on the spiritual need item at 6 months. This difference was in favor of the control group—mean improvement in spiritual needs was 6.6 lower in the intervention group compared to the control group
RCT
Country: Australia
The management plan followed prespecified referral pathways developed by a multidisciplinary team. The nurse implemented the management plan and initiated referrals as appropriate
Compared changes in domain scores at 2 and 6 months post-randomization
Control group participants received usual care, hence their health care team was not provided with a summary of their baseline results
Allen et al. 2002 [37]
To examine whether a problem-solving intervention for younger women with breast cancer was effective in reducing unmet needs and emotional distress
164 breast cancer patients aged 50 or younger identified from clinic records and recruited by telephone. Patients were also asked to nominate a primary support person who was also invited to participate
Intervention participants and their primary support person (if nominated), received a problem-solving intervention delivered over six sessions by an oncology nurse. The first and last sessions took place in the patient’s home or convenient location (2 h each). Four telephone sessions 2 weeks apart were scheduled in the intervening period
CARES
No statistically significant difference between the groups on the CARES global and subscale scores were observed at either follow-up assessment
RCT
Country: USA
The content of the intervention covered skills in defining and analyzing problems, generating alternative strategies to address the problem, deciding on a strategy, implementation of a strategy, and evaluation of its success
Compared changes in CARES scores at 4 and 8 months’ post-randomization
Post hoc subgroup analyses indicated that, compared to control group women with high problem-solving skills, experimental group women with high problem-solving skills had better scores on one subscale at 4-month follow-up and better scores on the global CARES scores on four out of the five subscales at 8-month follow-up. Conversely, control group participants who had poorer coping skills at baseline performed better than intervention group participants with poor coping skills at 8-month follow-up on three out of five subscales
Control group participants received unspecified usual care
Boyes et al. 2005 [36]
To examine the effect of providing medical oncologists immediate feedback about cancer patient’s self-reported psychosocial well-being on patients’ anxiety, depression, perceived needs, and physical symptoms
80 cancer patients (mixed cancer types) recruited from a medical oncology clinic
Both intervention and control participants completed the SCNS-34 via touch screen computer at four consecutive consultations (first, baseline visit and three follow-up visits or until the end of the chemotherapy course, depending on which occurred first)
SCNS-34 (short form)
No significant difference on any of the need domains between the arms at follow-up visits
Quasi-RCT
Country: Australia
For the intervention participants only, the computer-generated feedback report of their results was placed in the patient’s file and available for the doctor to discuss with the patient during the consultation
Compared average number of moderate or high needs per domain, across the visits
Aranda et al. 2006 [30]
To examine the effectiveness of a brief, nurse-delivered intervention designed to address the needs of women with advanced breast cancer
105 women with advanced breast cancer recruited from one of four participating outpatient clinics
Intervention participants received
Supportive Care Needs Survey (SCNS)
No significant differences between groups were found on any of the SCNS domain scores at 1 or 3 month follow-up
RCT
Country: Australia
 1. An hour face-to-face session with a breast care nurse. Needs identified by the SCNS were prioritized and tailored responses were provided, including coaching and practicing self-care strategies for identified issues. A self-care plan was provided, along with written information and a relaxation CD. A written summary of the session was provided to the treating doctor and placed in the medical record
Compared changes in domain scores at 1 and 3 months post-baseline
Post hoc analyses showed a greater decrease from baseline to follow-up in psychological needs for intervention participants with baseline psychological needs scores over 50 than for control participants with scores over 50 at baseline
 2. A follow-up, telephone session a week later with the nurse to check whether the strategies had been effective in addressing concerns, discuss lingering or new concerns, modify and reinforce self-care strategies or address new concerns as needed
Control group participants were also referred to a breast care nurse; however, he/she was not trained in the intervention procedures
McVean et al. 2007 [34]
To examine the acceptability and potential effectiveness of the Pathfinder Program, a telephone-based, volunteer-delivered support intervention
52 colorectal cancer patients recruited via a state-based cancer registry
Intervention participants were contacted by telephone at least twice by a trained volunteer, called a “Pathfinder”, once after completion of the initial survey at baseline and 3 months thereafter. Prior to the initial call, participants received a tailored summary of their baseline survey results. Pathfinders were also sent a letter summarizing participants’ survey results and, during the phone call, worked with participants to clarify their needs and identify strategies to address these. A copy of the summary was sent to the participant’s doctor with his/her permission. At the follow-up call, after the second survey, pathfinders reviewed the success of each strategy with participants
SCNS
The decrease in average number of needs from baseline to 3-month follow-up was greater for intervention than for control participants
Quasi-RCT (pilot)
Country: Australia
Control group participants received a letter informing them of their allocation to this group and received usual care
Nine-item colorectal cancer symptom checklist developed for the purpose of this study
Compared the decrease in mean SCNS needs from baseline to 3-month follow-up
Girgis et al. 2009a [31]
To examine the efficacy of two supportive care intervention models, telephone caseworker, and oncologists/GP, in decreasing anxiety, depression, and unmet needs and improving QoL
356 patients with nonlocalized breast or colorectal cancer were recruited from the NSW Central Cancer Registry
A baseline computer-assisted telephone interview (CATI) was used to generate a feedback sheet, which include a summary page of concerns and issues and suggestions for management strategies. This summary page was then forwarded to either a caseworker or oncologist/GP (according to group allocation). Participants did not receive copies of their own feedback sheets
SCNS-34 (short form)
Although a trend toward decreased needs in the telephone caseworker group was evident at 6 months, there were no significant differences in the percentage of participants experiencing at least one unmet need between the groups, across time
RCT
Country: Australia
Telephone caseworker—oncology nurses with telephone counseling training, based at the Cancer Council NSW helpline service telephoned participants to discuss reported issues identified on the feedback sheet and used the modified helpline database to refer them to appropriate resources/services. Caseworkers followed up at 6-week intervals to assess coping
10 items from the NA-ACP
Oncologist/GP—two hard copies of the feedback sheet generated from the CATIs were mailed to the participant’s nominated oncologist and GP for discussion at their next appointment. Clinicians were asked to keep one feedback sheet for their records and to return the second one to track which concerns were discussed and if any actions were taken
Compared percentage of participants experiencing at least one unmet supportive care need at 3 and 6 months post-baseline
Control group participants received standard care
King et al. 2009 [32]
To examine the effectiveness of an intervention designed to improve patient continuity of care
93 cancer patients (mixed cancer types) recruited from an outpatient clinic
Those allocated to receive the full intervention (arm 1) completed a 17-item continuity assessment. Patients were asked to tick a box indicating which items/issues they wished to discuss with the clinical team. Participants could list up to four additional issues. Feedback on the patient’s assessment was then provided to the clinical nurse specialist, and any resulting actions were documented
SCNS
A trend toward a greater reduction in unmet needs from the control group (highest) to the full intervention group (lowest) was observed at 6-week follow-up across the SCNS need domains; however, these differences were not statistically significant
Three-arm pilot RCT
Country: England
Those allocated to the partial intervention (arm 2) completed the 17-item checklist; however, no feedback was given to the clinical team
Compared unmet needs at baseline and 6 weeks post-intervention
Participants in the control arm (arm 3) received standard care
Scandrett et al. 2010 [33]
To examine whether feedback on a needs assessment to the clinical team improves documentation of needs, reported needs, and processes of care related to needs
451 cancer inpatients (mixed cancer types) were recruited from oncology service of an urban, academic tertiary care hospital
Intervention participants: (1) completed the NEST13+ by face-to-face interview on admission to the hospital and (2) NEST13+ responses were used to derive recommended clinical responses, which were communicated to their medical team the next day
NEST13+
No significant differences were found between groups in any dimension of the NEST13+ at discharge
Quasi-RCT
Country: USA
Usual-care participants completed a “sham” interview comprising of 12 questions about satisfaction with the admission process and facilities
Compared NEST13+ admission and discharge interviews
White et al. 2011 [29]
To examine the effectiveness of the Pathfinder Program, a telephone-based, volunteer-delivered support intervention, in reducing the prevalence of unmet supportive care needs and elevated levels of anxiety and depression among people with colorectal cancer over a 9-month period
653 colorectal cancer patients recruited via a state-based cancer registry
Participants completed surveys at baseline and at 3- and 6-month follow-up. After each of these surveys, intervention participants were contacted by a Pathfinder. The content of the intervention at each contact is described in McVean’s pilot study above
SCNS
No differences were found between the intervention and control groups for the proportion of moderate or high unmet needs at any follow-up
RCT
Country: Australia
Control group participants received a letter informing them of their allocation to this group and received usual care
Nine-item colorectal cancer symptom checklist developed for the purpose of this study
Compared percent of participants in the intervention and usual-care group with any priority unmet needs. Follow-up assessments were at 3, 6, and 9 months post-baseline
RCT randomized controlled trial
Study design
Two studies used a quasi-randomized controlled design, and the remaining studies were RCTs.
Concealment of allocation
Patients were the unit of randomization in all studies. Four of the seven RCTs reported that allocation was concealed when eligibility was being assessed [2932].
Baseline measurements similar
All studies reported that outcomes of interest were similar across groups at baseline, with the exception of the Scandrett study which reported that intervention participants had more needs than control participants in seven content areas [33].
Missing data unlikely to affect results
Missing data were adequately addressed in four studies [29, 31, 34, 35]. In King’s RCT [32], loss to follow-up was greater in the 2 intervention arms (16 and 12 participants, respectively) than in the control group (4 participants). In the remaining studies, insufficient information was provided to determine whether missing data were likely to affect results.
Knowledge of allocation to the intervention concealed
Only one study indicated that participants were blind to their allocation to the intervention or usual-care group [33].
Setting and sample
All studies reported that participants were cancer patients. Five studies included more than one cancer type in the sample [3133, 35, 36]. The remaining four studies focused on specific types of cancer including breast cancer [30, 37] and colorectal cancer [29, 34]. Three studies recruited participants from population-based cancer registries [29, 31, 34], one recruited oncology inpatients [33], and five recruited participants from outpatient cancer clinics [30, 32, 33, 3537].
Descriptions of interventions
With the exception of one study [37], all of the reviewed intervention studies included an initial identification of patient unmet needs, with feedback of identified needs provided to a health professional and/or the patient. Five of the studies included a structured clinical response intervention, tailored to address individual patient needs [2931, 34, 35]. Four of the interventions were delivered face-to-face only [32, 33, 35, 36], with the remainder delivered either by telephone only [29, 34] or a combination of face-to-face and telephone delivery [30, 31, 37]. Intervention agents included nurses [30, 32, 35, 37], physicians [36], general practitioners [31], trained volunteers [29, 34], telephone caseworkers [31], and multidisciplinary teams [33]. In some of the studies, there was more than one type of professional serving as the intervention agent. For instance, in the study by Girgis and colleagues, the intervention in arm 1 was delivered by a telephone caseworker, while the intervention in arm 2 was delivered by the patient’s general practitioner [31].
Outcome measures
Four studies used the original Supportive Care Needs Survey (SCNS) [29, 30, 32, 34]; two studies used the short form of the SCNS (SCNS-SF34) [31, 36], with one of these also using the Needs Assessment for Advanced Cancer Patients (NA-ACP) [31]; one study used the Cancer Rehabilitation Evaluation System (CARES) [37]; one study used the Needs of a social nature; Existential concerns; Symptoms; and Therapeutic interaction scales (NEST13) [33]; and one study used an earlier version of the SCNS, the Cancer Needs Questionnaire short form (CNQ) [35].
Effectiveness of unmet needs interventions for cancer patients
Six of the nine studies—four high-quality, large-scale trials [29, 31, 33, 35] and two pilot studies with fewer than 50 participants per group [32, 36]—failed to show a reduction in unmet needs for patients receiving an intervention, compared to usual care, at any follow-up time point. The remaining three studies found some intervention effect [30, 34, 37]. Aranda and colleagues’ trial of a nurse-led intervention, which focused on the development of self-care strategies for advanced breast cancer patients, demonstrated an effect on the psychological unmet needs subscale only of the SCNS for those patients who reported high unmet needs at baseline [30]. Similarly, post hoc subgroup analysis identified an intervention effect for those with high problem-solving skills at baseline in Allen’s trial [37]. A small pilot study undertaken by Macvean and colleagues reported a lower prevalence of overall unmet needs for colorectal cancer patients receiving an intervention [34]. However, these finding were not replicated in the full-scale trial [29]. Of those reporting an effect, no studies used the same unmet need measure or reported an intervention effect in the same unmet need domain.

Discussion

This review demonstrated that there has been increasing attention to unmet needs of cancer patients in the literature over time, with greater attention given to descriptive studies than intervention studies. While the literature search describing trends in types of unmet need publications was not intended to be systematic, the focus on descriptive research is concerning. Descriptive research has been invaluable in highlighting the unique needs of cancer patients and the necessary urgency to ameliorate these issues [5, 7, 9, 13]. It is generally accepted that the process of conducting descriptive research is simpler than for intervention studies, in terms of conceptualization, feasibility, and publishing [38]. While this may explain the trends observed in unmet needs research, it raises several issues. If it is not possible to change unmet needs, then there may be limited value in continuing to describe these needs. Conversely, if it is possible to change unmet needs, it could be argued that a greater emphasis on evaluating the effectiveness of strategies is warranted. A more appropriate balance in research effort is necessary to capitalize on available research funding, to develop a best-practice evidence base, and most importantly, to improve the psychosocial outcomes of cancer patients.
A total of nine intervention studies were identified. Six of the nine trials included in this review failed to demonstrate an intervention effect on unmet needs. Therefore, the results of this review suggest that, while it may be possible to reduce some patients’ unmet needs through supportive discussions, therapies, or referral, these changes have not been consistently demonstrated. Results of the reviewed intervention trials do not provide strong evidence for any particular approach for reducing levels of unmet need. In particular, testing of multiple subscale scores at multiple time points and the use of post hoc subgroup analyses in two of the three positive trials suggest the possibility of spurious results arising from type II errors [30, 37]. The third trial was a pilot study [34] and, although it demonstrated an intervention effect, this was not replicated in the full-scale RCT [29]. Given increasing interest in the assessment of and use of unmet needs measures for screening and tailoring interventions, it is timely to consider which factors may contribute to the mixed and limited findings observed across trials.

Potential explanations for mixed findings among intervention trials which aim reduce unmet needs among cancer patients

Psychometric rigor of unmet needs measures

While measures such as the SCNS have been psychometrically tested for validity and reliability [17, 39], sensitivity to change over time has not been well explored [6, 40]. It is possible that current measures of unmet need are not sufficiently sensitive to consistently identify small or isolated changes in unmet need. This may be due to the fact that these tools were originally designed to capture a wide breadth of concerns across an entire population, rather than being sensitive to the particular needs of an individual. Such psychometric design attributes may, therefore, limit the use of these instruments as individual screening devices or intervention outcome measures.

Appropriateness of measures for the selected sample

It should also be noted that, while all studies included in this review used the term “cancer patient,” some of the samples included may have consisted of cancer survivors. While definitions of survivorship vary [41, 42], treatment completion is often used as a defining point [43]. In particular, for the three studies that reported recruitment via population-based cancer registries [29, 31, 34], participants were at least 4–6 months post diagnosis at the time of study entry, and current treatment status was not clearly reported. It is, therefore, likely that many of these participants may have been “survivors” rather than patients. Since the needs of cancer survivors are known to be different from cancer patients [44], this suggests that studies which include survivors should use needs measures which have been specifically developed for the survivor population [6]. The SCNS, used in all three of the latter studies, was developed for a patient population (undergoing treatment) rather than a survivor population (post-treatment) [17]. Therefore, this measure may not have been appropriate to adequately capture the needs of these groups. Future research with cancer survivors should use measures specifically developed for this population such as the Survivors Unmet Need Survey (SUNS) [19] or the CaSUN [45].

Study samples are insufficient to find an intervention effect

It may be that, when using wide-ranging unmet needs measures such as the SCNS or CNQ, or for potentially heterogeneous samples involving multiple cancer types, large samples are required to identify small changes in particular patient needs. These measures may be more suited to identifying small changes in the population prevalence of domains of unmet need, rather than identifying small patient-specific changes. However, this theory is not supported by the studies reviewed here, given that the study with the largest and potentially most homogenous sample failed to find an effect [29].

Analysis of unmet needs

Items in unmet need measures can potentially be analyzed in a number of ways, and the scoring and analysis of these measures have evolved over time. Most studies in this review used domain scores as their outcome measure. On both the NA-ACP and the SCNS, domain scores are calculated by summing item scores [18, 46]. Therefore, similar scores at two follow-up points may not necessarily reflect that participants are endorsing the same needs at both time points [23]. Similarly, the approach of using subscale scores does not allow determination of whether specific needs have been reduced over time as a consequence of the intervention. Similar problems arise when the number of needs endorsed as unmet is used as an outcome measure rather than a domain score. This may hide the fact that needs may change over time, with different needs contributing to the prevalence count for an individual at any given time point.
An alternative to using subscale scores may be to examine changes in specific items of unmet needs. Without evidence of test–retest reliability at the item level, however, examining changes in prevalence of need by item is also problematic. Item-level test–retest reliability has not been demonstrated for any unmet needs measures for adult cancer patients [40]. This means that it is impossible to tell whether any change in number of people endorsing an item is due to the intervention or lack of test–retest reliability in the item.

Interventions tested are ineffective

It is possible that limited intervention effects observed across trials are a result of ineffective interventions. Descriptive studies have indicated that a range of sociodemographic, disease, physical, and psychological factors are associated with unmet needs [16]. Lack of effect may, therefore, indicate that the intervention is not powerful enough to address the many factors that may influence unmet needs. Similarly, the “dose” of the intervention may also have been inadequate to achieve an effect. A recent meta-analysis has found that longer-term interventions (minimum 12 weeks) had a greater impact on QoL of adults with cancer than short-term interventions (d = 1.19, d = 0.47) [47]. Intervention intensity and frequency were quite varied across the studies reviewed, ranging from single assessment and printed feedback to multiple sessions and multiple referrals. It is, however, difficult to assess the true intensity of any particular intervention, given that referral or feedback were a key part of the majority of both the effective [30, 34] and ineffective interventions [3133, 35, 36]. Limited data were provided on the consequences of the referrals. It is highly likely that this was variable both within and between studies.

Interventions are not delivered as intended

Lack of intervention effect may also reflect lack of adherence to key intervention components by patients or providers. For example, in McLachlan’s study, recommended services from the tailored management plan were declined by patients in 38% of instances [24]. Reasons reported for refusal of services included inappropriate timing of the referral and preferences for other forms of support including other formal services and informal support of self-management [24]. Similarly, in Boyes’ pilot study, only two of the four doctors involved in the study reported that they had discussed the feedback on needs with their patients during the consultation [36]. Given this low level of adherence to the intervention, the lack of effect may not be surprising.

Floor effects preclude demonstration of an intervention effect

Post hoc analysis in Aranda’s study indicated that an intervention effect may be possible if those who have high unmet needs at baseline are selectively targeted [30]. Similarly, Girgis and colleagues noted that participants in their trial reported higher levels of QoL and psychological well-being than expected [31]. The authors suggested that this may have contributed to the lack of intervention effect observed. This echoes a common criticism of psychological interventions to reduce distress, anxiety, and depression among cancer patients, whereby interventions to improve these outcomes are targeted at all patients rather than at those with demonstrated need at baseline [48]. This may reflect an assumption that all people with cancer have high levels of unmet supportive care needs.
However, selective targeting of high needs individuals poses its own challenges. These difficulties may include logistic and cost difficulties in screening large numbers of patients to identify a subset requiring intervention prior to commencing a trial. It may also reflect that there is no clear threshold for needs measure, which indicates clinical significance [23]. Therefore, by arbitrarily excluding those below a certain score, it is possible that some people who may benefit from an intervention may be excluded. Research focusing on the establishment of clinical significance of need measures may aid in the interpretation of scores and the application of such measures to assessing intervention effectiveness.

Needs reflect a desire for certainty and reassurance which cannot be met by the health care system

Longitudinal studies indicate that needs may change over time [25, 49, 50]. However, it is not clear from intervention studies whether needs can be reduced more rapidly or by a greater magnitude by intervention. Potentially life-threatening illnesses such as cancer are associated with high levels of uncertainty [51]. It is plausible that this uncertainty and desire for reassurance may be expressed as unmet psychological or information needs. If this is the case, it is possible that no amount of information, support, or service provision will be able to address this need. Therefore, during some phases of the illness trajectory, certain unmet needs may be endemic to the cancer experience [23]. In these circumstances, it may be important for providers to explore patient concerns, acknowledge uncertainties, and provide appropriate reassurance.

Lack of clarity regarding the nature of unmet needs

In addition to considering the possibility that unmet needs may reflect a desire which cannot be met, it is timely to also consider the nature of the concept of unmet need. The concept of “unmet needs” is a relatively new one, and there is little literature regarding the nature of the construct [23]. The concept of unmet needs appears to have arisen in the context of identifying the range of patient experiences which, if addressed, might ameliorate disease-related psychosocial impacts such as depression, anxiety, and poor QoL. While associations between these outcomes are supported by descriptive research [15, 16], there is no evidence of a causal relationship between unmet needs and patient psychosocial outcomes. It is possible that unmet need surveys, while being helpful in identifying particular patient concerns, are not appropriate as a focus for intervention development or outcome measurement.

Future directions

Given that there is increasing attention directed at describing the unmet needs of people with cancer, it is important to establish whether, and if so, how unmet needs can be reduced. There are several areas where future work could inform the development and testing of unmet need interventions. Firstly, to progress work in this field, it is necessary to develop clear guidelines about the scoring of unmet needs scales. Such guidelines should describe how needs should be scored for intervention trials so that it is possible to attribute change in needs to the intervention. This may necessitate examining test–retest reliability at the item level for existing scales. Further, to determine the magnitude of change needed to establish an intervention effect, the issues of sensitivity and clinical significance need to be considered. Unlike measures of anxiety or depression, criterion validity against a gold standard clinical interview cannot be used to determine clinical significance [23]. Greater clarity about the construct of unmet needs and its mechanism of operation would also assist in the development and design of appropriate interventions. One possible way forward may be to examine what level of needs predict future adverse outcomes such as greater health care utilization, poorer QoL, or greater risk of developing depression.

Limitations

It is possible that some relevant articles were missed by the current review. Articles published in languages other than English and unpublished articles, for example, may have been missed. The use of a funnel plot to assess publication bias was considered. However, given the relatively small number of studies included, it is likely that these results would have been unreliable [52].

Conclusions

This review indicates that most intervention trials have reported either no effect or limited effects on cancer patients’ unmet needs. The current literature does not allow conclusions to be drawn about whether these findings reflect problems with measurement, interventions, or sample selection or whether they indicate that needs are endemic parts of the sequelae of a cancer diagnosis. The inconclusive findings of the intervention studies suggest that further studies to describe unmet needs of cancer patients may have limited utility, if it cannot be demonstrated that these needs are modifiable.

Acknowledgements

Dr. Mariko Carey is supported by a Hunter Medical Research Institute (HMRI) postdoctoral fellowship, Dr Sylvie Lambert is supported by a NHMRC training fellowship, and Dr. Tara Clinton-McHarg is supported by a Leukaemia Foundation Australia postdoctoral fellowship.

Disclosures

None.

Open Access

This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
Open AccessThis is an open access article distributed under the terms of the Creative Commons Attribution Noncommercial License (https://​creativecommons.​org/​licenses/​by-nc/​2.​0), which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.

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