Patient experience of uncertainty in cancer genomics: a systematic review.

While genomics provides new clinical opportunities, its complexity generates uncertainties. This systematic review aimed to summarize what is currently known about the experience of uncertainty for adult patients undergoing cancer genomic testing. A search of five databases (2001 to 2018) yielded 6508 records. After removing duplicates, abstract/title screening, and assessment of full articles, ten studies were included for quality appraisal and data extraction. Qualitative studies were subjected to thematic analysis, and quantitative data were summarized using descriptive statistics. Cancer genomic results reduced uncertainty for patients regarding treatment decisions but did not reduce uncertainty in the risk context. Qualitative and quantitative data synthesis revealed four themes: (1) coexisting uncertainties, (2) factors influencing uncertainty, (3) outcomes of uncertainty, and (4) coping with uncertainty. Uncertainty can motivate, or be a barrier to, pursuing cancer genomic testing. Appraisal of uncertainty influences the patient experience of uncertainty, the outcome of uncertainty for patients, as well as the coping strategies utilized. While this systematic review found that appraisal of uncertainty is important to the patients' experience of uncertainty in the cancer genomic context, more mixed methods longitudinal research is needed to address the complexities that contribute to patient uncertainty across the process.

INTRODUCTION

There were an estimated 18.1 million new cases of cancer in 2018.[1] Cancer is caused by changes in genes either inherited from parents (germline), or developed over a person’s lifetime due to errors in cell division or exposures in their environment (somatic).[2] Cancer genetic testing focuses on single genes with a known function, for example BRCA1 and BRCA2 gene testing to identify risk of hereditary breast and ovarian cancer syndrome testing. Genomic testing refers to a broader investigation of genetic material with no specific gene target, for example multigene panel, genome sequencing, or exome sequencing, which include genes that are not fully understood in terms of cancer risk or management strategies.[3] Genomic testing provides hope for improvement in cancer prevention, by helping to identify individuals at increased risk of a broad range of cancers;[4] and reducing mortality and morbidity, through the identification of specific pathogenic variants to guide treatment.[5] Genomic testing also introduces challenges,[2] for example the uncertainty that is inherent in this new technology.[6]

Illness uncertainty, a patients’ inability to determine the meaning of illness-related events,[7] can be a result of ambiguity (conflicting, incomplete, or inadequate information); complexity (difficult to understand information); and unpredictability (likelihood or risk of future outcome of the disease).[7-9] Uncertainty in illness has been associated with anxiety, depression, and distress.[7,10,11]

The complexity of genomic testing introduces new scientific, practical, and personal uncertainties specific to this process.[6] Genomic testing can reveal variants that are (1) relevant to the target cancer versus secondary findings (relevant to other cancers or diseases), (2) clinically actionable versus non–clinically actionable (no proven treatments), and (3) of unknown or uncertain significance.[2,12] Treatments targeting actionable genomic results are often experimental. Thus, while reducing uncertainty can be a motivator for pursuing genomic testing,[13] results have the potential to increase uncertainty.

Existing uncertainty research has focused on patient uncertainty when undergoing single-gene testing (such as BRCA1/2 testing for specific hereditary cancer syndromes),[14-16] the uncertainty related to the science of genomics, or uncertainty experienced by health-care professionals in relation to interpreting results, and communicating uncertain information.[17] Little is known about the patient experience of uncertainty when undergoing cancer genomic testing, and the impact of this uncertainty on patient psychosocial outcomes. Furthermore, there has been no synthesis of the extant literature to aid identification of gaps and guide future research.

To meet this need, we conducted a systematic literature review aimed at identifying and synthesizing what is currently known about the patient experience of uncertainty when undergoing cancer genomic testing. Our review questions were:

What type of uncertainty do patients experience?

To what extent do patients experience uncertainty?

What are the factors that influence uncertainty?

What is the impact of uncertainty for these patients?

MATERIALS AND METHODS

Study design

This systematic review protocol was designed using the Preferred Reporting Items for Systematic Reviews (PRISMA) standards[18] and ENTREQ guidelines.[19] The review was registered with PROSPERO, registration CRD 42018084301.

Search strategy

A literature search of peer-reviewed publications was conducted using five databases (Scopus, Ovid MEDLINE, Embase, PsycINFO, and CINAHL). Search terms were a combination of keywords and MeSH terms relating to uncertainty, cancer, and genomics (Supplementary material). Qualitative, quantitative, and mixed methods studies (including hypothetical studies), published in English from January 2001 to June 2018, were included. The year 2001 was set as the outside date boundary because it was the year the initial sequencing and analysis of the human genome was completed,[20] marking an important milestone in the field of genetics.

Articles were excluded if they assessed uncertainty in the context of single-gene testing, for example BRCA1 or BRCA2 testing, or in relation to illnesses other than cancer; or focused on health-care professionals, or pediatric or adolescent populations. Unpublished reports, conference abstracts, systematic reviews, and dissertations were excluded. Reference lists of accepted articles were hand-searched for additional relevant publications.

Data extraction and assessment of study quality

Data extracted included study design, study objective, measures used, cancer genomic test, sample size and characteristics, and key findings. Data were extracted independently by two authors (N.B. and C.N.). A 30% overlap was extracted by a third author (P.B.) to ensure reliability. All studies included were evaluated using the Joanna Briggs Institute Critical Appraisal Tools,[21] for risk of bias across the study design, conduct, and analysis. One author (N.B.) independently assessed study quality with a 30% overlap assessed for quality by a second author (P.B.). Any disparities were resolved through discussion. No studies were excluded based on quality.

Analysis

Analysis was conducted using a three-stage synthesis process that combined qualitative and quantitative studies comprehensively and rigorously to answer the review questions.[22] As meta-analysis was not possible due to the heterogeneity of study outcomes, the first analysis focused on identifying and summarizing the quantitative data. The second analysis involved thematic synthesis[23] of the qualitative studies. Line-by-line coding of the results sections of an initial two qualitative studies was conducted (N.B., M.B., and P.B.) to develop a coding tree and themes. This coding structure was then applied to the remaining qualitative studies (N.B.) with new codes created and discussed by the authors. Finally, a matrix was used to compare the qualitative and quantitative findings from the first two stages to answer the review research questions.

RESULTS

The search strategy identified 6508 articles which were exported to EPPI-Reviewer 4. After removing duplicates, the remaining 5154 records were screened by title and abstract by two authors (N.B. and C.N.) with a 10% overlap. The two authors had an overall agreement rate of 98% (fixed marginal kappa of 0.97; free marginal kappa of 0.98). The full texts of 111 retained papers were retrieved for screening by three authors (N.B., C.N., and M.B.), with 10% double screened by the fourth author (PB) (Fig. 1). Of these, nine studies met eligibility criteria. One additional study was identified through a hand search of the eligible article reference lists, and ten studies were included for data extraction and quality assessment.

Fig. 1

Preferred Reporting Items for Systematic Reviews (PRISMA) flow diagram of the literature screening.

Article characteristics

Table 1 summarizes the ten included studies and their key findings regarding patient uncertainty. Only two studies assessed uncertainty as a primary outcome.[24,25] Two studies assessed hypothetical intention to undergo cancer genomic testing;[24,26] the remainder focused on participants’ experience while pursuing cancer genomic testing.[25,27-33] The majority of studies were quantitative (n = 5), cross-sectional (n = 6), and conducted in English-speaking Western countries (n = 8).

Table 1

Summary of studies with uncertainty findings (n = 10).

Study, design, and methods	Participant characteristics	Key uncertainty findings
Braithwaite, Sutton, Steggles[24] England Cross-sectional Quantitative—attitude toward uncertainty[24]	n = 292; Age range = 18–60 years (M = 35.11 years [SD 12.48] colon cancer sample; M = 37.76 years [SD 12.92] breast cancer sample); Breast cancer sample = 100% female; Colon cancer sample = gender not reported; Unaffected general population; Hypothetical predictive genetic testing for hereditary colon or breast cancer	15.75% of participants asked about genetic testing for cancer reported feeling unsure if they would participate in testing (15% colon cancer; 17% breast cancer). Overall attitude toward uncertainty mean score was 2.63 (SD 14.41) (M = 2.63 (SD 0.78) colon cancer; M = 2.64 (SD 0.83) breast cancer). Participants asked about colon cancer genetic testing attitude toward uncertainty was strongly correlated with behavioral intention (0.28, p < 0.01) and attitude toward testing (0.26, p < 0.01), and subjective norm (0.53, p < 0.01). Participants asked about breast cancer genetic testing attitude toward uncertainty was strongly correlated with behavioral intention (0.28, p < 0.01) and attitude toward testing (0.26, p < 0.01). Participants (colon cancer and breast cancer) with more positive attitudes about genetic testing (β 0.46, p < 0.001; β 0.54, p < 0.001), higher subjective norms (β 0.20, p < 0.01; β 0.22, p < 0.01), and more negative attitudes toward uncertainty (β 0.20, p < 0.01; β 0.28, p < 0.001) would be more likely to choose to participate in genetic testing.
Pellegrini, Rapti, Extra, et al.[32] France Cross-sectional Qualitative—interviews	n = 37; Age range = 35–69 years (M = 55 years); 100% female; 100% breast cancer; DNA microarrays	Factors that affected participant uncertainty included health-care professional and participant genetic literacy, as well as the type of result and a trust in science. • Participants were unclear on the meaning of genomic and gene expression. • Ten participants held misconception on the resemblance between the terms genomic and genetic, which generated fear of a hereditary risk, substantial uncertainty, and feelings of guilt toward their offspring. • “Not interpretable” results caused frustration and even more uncertainty about the future for some participants. • Good and poor signature participants felt certain that their treatment was the best for them, as it was directed by the test result. A poor signature directed to standard treatment, which women concluded was appropriate.
Holt, Bertelli, Humphreys, et al.[27] Wales Longitudinal Quantitative—Decision Conflict Scale (DCS)[35]	n = 39; Age range = 34–72 years (Mdn = 55 years); 100% female; 100% breast cancer; Oncotype DX 21-gene assay to predict chemotherapy benefit	Oncotype DX results significantly reduced participant uncertainty regarding their chemotherapy treatment decision (mean uncertainty subscale score change of −9.0, P = 0.004). • Initial uncertainty subscale score mean = 22.0 (95% CI, 14.6, 29.4) • Review uncertainty subscale score mean = 13.0 (95% CI, 8.0, 18.0)
Leventhal, Tuong, Peshkin, et al.[26] USA Cross-sectional Mixed methods—focus groups and pre- and post–focus group discussion surveys	n = 24; Age range = 28–77 years (M = 54.3 years SD12.3); 62% female; Hypothetical interest in SNP testing for colon cancer risk	Participants experienced uncertainty regarding future risk, clinical utility, potential reactions, and collateral damage. Uncertainty was a motivator (reduce uncertainty about personal and relatives’ cancer risk) or a barrier (uncertainties about insurance and privacy implications of results; uncertainty about limitations of SNP testing and clinical utility), for pursuing SNP testing. Factors that influenced uncertainty were health-care professionals (expertise), awareness of their limited genetic literacy, and personal or relatives’ previous experience with cancer. Some participants with a personal experience with cancer did consider that managing the uncertainty related to SNP risk information may not be worth the additional worry, while other participants (information seekers) valued risk information (even if uncertain), as it gave them a plan of action or risk management strategy.
Bradbury, Patrick-Miller, Egleston, et al.[28] USA Longitudinal Mixed methods—Multidimensional Impact of Cancer Risk Assessment (MICRA) questionnaire[34]	n = 49; Age range = 36–71 years (M = 52 years); 96% female; 78% personal history of cancer (71% breast cancer only); 25-gene next-generation sequencing	30% of those who declined to participate in the study were concerned about potential uncertainty or unclear utility of results. Participant baseline mean uncertainty subscale score was 7.5 (SD 4.2) (range 0–15), with no significant difference between those who had previously tested BRCA1/2 negative (M = 7.1, SD 4.5) and those who were BRCA1/2 untested (M = 8, SD 3.8). Making a less informed choice about proceeding with sequencing was associated with greater uncertainty (p = 0.06) after pretest counseling. Uncertainty did not significantly change from baseline, to pretest counseling, to post-test counseling among all participants or the subset that proceeded to sequencing. Participants experienced uncertainty regarding the collateral damage of testing and experienced conflicting uncertainty (decreasing one type of uncertainty, but increasing another). Participants felt that the type of result, their own genetic literacy, and the genetic counselor's approach and communication style influenced their experience of uncertainty when undergoing sequencing.
Hitch, Joseph, Guiltinan, et al[33] USA Cross-sectional Qualitative—interviews	n = 19; Age range = 18–90 years (M = 52.6 years); 68.4% female; 100% personal experience of cancer (type not specified); exome sequencing	Participants saw sequencing as a method of reducing their uncertainty about future risk. The potential of receiving a variant of uncertain significance (VUS) raised uncertainty about clinical utility. Some participants were uncertain how they would respond (emotionally and behaviorally) to results. Genetic literacy appeared to help give meaning to a VUS result. Health-care professional expertise and communication style influenced participant uncertainty. Participants were willing to experience uncertainty, if it meant that they knew all the information about themselves that their health-care professional knew. Previous experience with cancer and uncertainty led participants to believe that they would be able to cope with the potential uncertainty of sequencing results. Most participants expressed tolerance for the uncertainty involved in receiving VUS results; 16% of participants did not want to receive a VUS result, stating that uncertain information was not useful if it could not be clinically applied. Some participants predicted that they would respond to uncertain results by seeking more information (research literature, clinical trials, 2nd opinion), or by remaining optimistic. There was an acknowledgment that you cannot un-know the information that created the uncertainty. Some participants were hesitant to share results with their relatives if the results were less medically certain.
Levine, Julian, Bedard, et al.[29] Canada Longitudinal Quantitative—DCS[35]	n = 1000; Age range = 26–88 years (Mdn = 59 years); 99.5% female; 100% breast cancer; Oncotype DX 21-gene assay to predict chemotherapy benefit	42% of participants were unsure about chemotherapy before testing. Participants total DCS mean score significantly reduced from pretest (M = 34, SD 14) to post-test (M = 19, SD 13) (p < 0.001). Similar reductions were observed for the subscales of decisional uncertainty (pretest M = 53, SD 29; post-test M = 24, SD 23; p < 0.001), and factors affecting uncertainty (pretest M = 31, SD 13; post-test M = 19, SD 12; p < 0.001). Participants who chose no chemotherapy had a significantly greater mean reduction (mean change −17) in total DCS score than those who chose chemotherapy (mean change −13) (p = 0.015). Similarly, participants who chose no chemotherapy had a significantly greater mean reduction (mean change −30) in decision uncertainty than those who chose chemotherapy (mean change −23) (p = 0.0059).
Lumish, Steinfeld, Koval, et al[30] USA Cross-sectional Quantitative—MICRA[34]	n = 232; Age range = 21–88 years (M = 48.7 years); 96.5% female; 55.6% personal history of breast or ovarian cancer; variety of multigene panel tests	64.3% of participants in the cancer affected (CA)/VUS group receiving a VUS reported misunderstanding that result to be a negative result. Differences in MICRA uncertainty subscale scores were not significantly different between groups who received different types of genomic results (CA/mutation + M = 3.9, SD 4.2; CA/VUS M = 4.8, SD 5.3; CA/mutation—M = 4.2, SD 5.2; No CA/mutation + M = 9.6, SD 7.7; No CA/VUS M = 6.0, SD 7.3; No CA/mutation—M = 4.3, SD 5.3).
Esteban, Vilaro, Adrover, et al[31] Spain Longitudinal Quantitative—MICRA[34]	n = 187; Age range = 18–83 years (M = 50 years SD 13.35); 75% female; 44% colorectal cancer, 42% breast cancer, 4% endometrial cancer, 4% ovarian cancer, 5% unknown; 25-gene hereditary cancer panel	There were no differences in the levels of uncertainty at 1 week, 3 months, and 12 months among patients with a pathogenic variant, VUS, or negative result. Patients with a moderate penetrance pathogenic variant tended to have higher levels of uncertainty compared with carriers of a high penetrance pathogenic variant at 3 (22.00 vs. 7.06, p = 0.38) and 12 months (19.67 vs. 7.70, p = 0.25) after results disclosure. VUS carriers had lower levels of distress than patients with pathogenic variants at 1 week (2.33 vs. 7.13), 3 months (2.48 vs. 6.59), and 12 months (3.22 vs. 7.82) after disclosure (p < 0.01). VUS carriers did not differ from patients with a negative result across time. VUS carriers had higher levels of positive experience than patients with a pathogenic variant at 1 week (5.97 vs. 8.56), 3 months (6.47 vs. 8.93), and 12 months (6.31 vs. 8.22) after disclosure (p < 0.001). VUS carriers did not differ to patients with a negative result across time.
Solomon[25] USA and Canada Cross-sectional Qualitative—interviews	n = 27; Age range = 31–75 years (M not reported); 77.8% female; 62.9% personal history of cancer (type not specified); Testing for mismatch repair genes	Majority of participants felt that their results incorporated some aspects of uncertainty in relation to the variant itself and their diagnosis of Lynch syndrome (LS). VUS results lead to decisional uncertainty regarding risk management strategies and reproduction. VUS results also led to uncertainty about future risk of developing cancer. Some participants appraised uncertainty as a danger or health threat, while others appraised uncertainty as an opportunity or absence of health threat. A few participants appraised uncertainty as both a danger and an opportunity (a health threat but not as severe as a positive result). Appraisal of results relied heavily on guidance and interpretation by their health-care professional, as well as the participants’ genetic literacy. Many participants coped with their uncertainty by complying with recommended screening, or by being optimistic that their VUS result would be reclassified in the future. Participants who appraised their uncertain results as a danger coped by seeking information, reaching out to at-risk relatives in an attempt to protect them, and forming a plan of action based on high risk. Participants experienced a range of affective reactions to their uncertain results, including shock, regret, sadness, and disappointment. Some participants did also experience relief in that something genetic (although uncertain) was found.

CI confidence interval, SNP single-nucleotide polymorphism.

There was a scarcity of literature investigating the patient experience of uncertainty in cancer genomics, with only one or two studies published for each type of genomic test. As such we analyzed uncertainty across the range of genomic tests: genetic test for bowel/breast cancer susceptibility (hypothetical),[24] DNA microarray to direct treatment,[32] Oncotype DX 21-gene assay to predict chemotherapy benefit,[27,29] single-nucleotide polymorphism (SNP) testing for colorectal cancer susceptibility (hypothetical),[26] exome sequencing,[33] 25-gene test for cancer susceptibility,[28,31] multigene panel tests for cancer susceptibility,[30] and mismatch repair gene test for cancer susceptibility.[25]

Sample characteristics

There were a total of 1906 participants across all included studies, with the number of participants across the studies ranging from 19 to 1000. Participants’ ages across the ten studies ranged from 18–90 years. All studies comprised a majority female participant sample, and the seven studies that reported participants’ cancer diagnosis mainly included participants with a personal or family history of breast and/or ovarian cancer, and to a lesser extent colorectal cancer.

Uncertainty measures

Three separate measures of uncertainty were used. The attitude toward uncertainty scale[24] measures attitude toward uncertainty in the medical testing context, where higher scores (mean of seven items; possible range 1–5) reflect a negative attitude toward uncertainty. The Multidimensional Impact of Cancer Risk Assessment (MICRA) uncertainty subscale[34] measures uncertainties associated with testing results and future plans, where higher scores (sum of nine items; possible range 0–45) indicate greater uncertainty. The Decisional Conflict Scale[35] measures uncertainties about a course of action, factors contributing to uncertainty, and perceptions of effective decision making, where higher scores (mean of ten items multiplied by 25; possible range 0–100)[36] are associated with higher levels of uncertainty.

Extent of uncertainty

The quantitative synthesis showed that mean uncertainty scores were midrange for participants when deciding to undergo genomic testing for cancer risk information[28] and did not change post–result disclosure.[28,31] In the cancer treatment context, genomic results reduced participant treatment decisional uncertainty, i.e., to have (or not have) chemotherapy.[27,29]

Qualitative and quantitative synthesis

Synthesis of quantitative and qualitative results revealed four themes (Table 2): (1) coexisting uncertainties, (2) factors influencing uncertainty, (3) outcomes of uncertainty, and (4) coping with uncertainty.

Table 2

Quantitative and qualitative analysis matrix.

Review question	Quantitative synthesis	Qualitative synthesis	Theme
What types of uncertainty do patients experience when undergoing cancer genomic testing?	Participants experienced uncertainty about undergoing genomic testing,[24] concerned about potential uncertainty or unclear utility of results.[28] Participants with more negative attitudes toward uncertainty were more likely to choose to participate in hypothetical genomic testing for colon or breast cancer risk.[24]	Reducing uncertainty about personal and relatives’ cancer risk was a motivation for undergoing genomic testing.[26,33] When considering genomic testing participants experience multiple uncertainties (future risk,[25,26] clinical utility,[26,33] ambiguous results,[25] decisional uncertainty,[25] reactions to results,[26,33] and collateral damage[26,28]). Uncertainties are interrelated and conflicting; reducing one uncertainty can create a different uncertainty.[28] Some participants were willing to risk uncertainty for any risk information, while others felt it was not worth the additional worry.[26]	Coexisting uncertainties
To what extent do patients experience uncertainty when undergoing cancer genomic testing?	Participants undergoing genomic testing for risk information had midrange baseline mean uncertainty scores,[28] and uncertainty did not change over time.[28,31] Genomic results reduced treatment decision uncertainty.[27,29]
What are the factors that influence uncertainty in patients undergoing cancer genomic testing?	Attitude toward uncertainty was correlated with behavioral intention, subjective norm, and attitude toward testing.[24] A less informed choice about genomic testing was associated with greater uncertainty.[28] Previous experience with genetic testing did not influence participants' mean baseline uncertainty.[28] Genomic result (positive, negative, VUS) did not influence uncertainty in the risk context.[30,31] Moderate penetrance pathogenic variant carriers tended to have more uncertainty compared with high penetrance pathogenic variant carriers 12 months postresults.[31]	Factors affecting appraisal and experience of uncertainty include: • Health-care professionals’ credentials, communication approach and style.[25,26,28,32,33] • Genetic literacy (misconceptions; inadequate information).[25,26,28,32,33] • Previous experience with uncertainty, disease, and perceived self-efficacy in coping with uncertainty.[26,33] • Willingness to experience uncertainty to know all the information about themselves that their health-care professional know.[33] • Types of results can increase or decrease uncertainty. Some participants expressed a tolerance for the uncertainty involved in receiving VUS results;[33] however, VUS can also increase uncertainty about the future.[28,33] • A trust in science influenced treatment decisions certainty.[32] Experience of uncertainty depends on the appraisal of uncertainty.[25,26] Some participants appraise uncertainty as a danger or health threat, while others appraise uncertainty as an opportunity or absence of health threat. A few participants appraise uncertainty as both a danger and an opportunity (a health threat but not as severe as a positive result).[25]	Factors influencing uncertainty
What are the outcomes of uncertainty in patients undergoing cancer genomic testing?	Participants with uncertain genomic results had lower levels of distress and higher levels of positive experience than participants with pathogenic variants up to 12 months’ post–result disclosure. VUS carriers did not differ from participants with a negative result for both distress and positive experience following result disclosure.[31]	Uncertainty is ongoing, cannot un-know information that created uncertainty.[33] Sharing uncertain results with relatives would be difficult and hesitant to do so.[33] Participants who received uncertain results experienced a range affective reactions to their results, including shock, regret, sadness, and disappointment.[25,26,32] Some participants did also experience relief in that something genetic (although uncertain) was found.[25] Participants predicted they would cope with uncertain results by seeking more information, or by remaining optimistic.[33] Participants coped with their uncertainty by complying with recommended screening, or by being optimistic that their VUS result would be reclassified in the future. Where participants appraised their uncertain results as a danger, they coped by seeking information, reaching out to at-risk relatives in an attempt to protect them, and forming a plan of action based on high risk.[25]	Outcomes of uncertainty Coping with uncertainty

VUS variant of uncertain significance, M mean, Mdn median.

Coexisting uncertainties

Multiple interrelated uncertainties can exist for patients considering or undergoing cancer genomic testing. Uncertainty can be a motivation for[26,33] or barrier to[24,28] pursuing cancer genomic testing. When hypothetically considering genomic testing for cancer risk, 15.75% of participants of one study were unsure if they would pursue genomic testing for breast and colon cancer risk.[24] These participants reported on average a somewhat negative attitude toward uncertainty (M = 2.63, SD 14.41); those with a more negative attitude toward uncertainty were more likely to choose to pursue testing,[24] motivated by a desire to reduce uncertainty related to their own and their relatives’ future risk of cancer.[26,33]

“I’d like to know if that’s where I’m headed. Maybe there’s nothing I could do about it—that doesn’t matter. I think there’s a benefit to knowing as much as you can about yourself.”[26]

Undergoing (or considering) genomic testing can create uncertainties about future risk,[25,26] clinical utility,[26,28,33] collateral damage,[26,28] potential emotional and behavioral reactions to results,[26,33] as well as decisional uncertainty.[25] Ambiguity surrounding the meaning of a variant of uncertain significance (VUS) result can create uncertainty about future risk for participants,[25] due to conflicting views and interpretation, and lack of conclusive information about the variant. Thus, some participants were motivated against undergoing genomic testing by high perceived uncertainty regarding clinical utility of genomic results, particularly if the results indicated a small increased cancer risk or were of uncertain significance.[26,33]

“So it’s just—it is an ambiguity, and it makes me wonder, you know like I said, do I really have it or not?”[25]

“Unless you might have something that will impact your health in the future, I don’t know if it’s good or useful for just anybody to get to see their whole genetic makeup.”[33]

Participants who received VUS results experienced further uncertainty related to decision making around reproduction and preventive surgery.[25]

Participants expressed uncertainty about potential collateral damage or negative implications of undergoing genomic testing, such as impact on insurance, employment, and privacy.[26,28] Participants also acknowledged that they were uncertain about how they would react to their genomic results, stating that results could have a negative impact on their emotions and also behavior.[26,33]

“I guess I’m concerned that in some ways I might change the way that I’m living my life now unintentionally. Not even consciously, but having that knowledge may potentially change what I’m doing now that I don’t actually want to change.…”[33]

The above uncertainties are interrelated and can be in conflict. Acknowledging that the science is still evolving, participants reported feeling both certainty and uncertainty from their genomic results, and that decreasing one uncertainty can increase another type of uncertainty.[28,32]

“There’s a black cloud over my head if I don’t get the testing because it’s like you’re constantly wondering what is causing it, but it’s a little black cloud if I get it the testing and they find something because then I know it’s genetic and there’s nothing I can do....”[28]

Factors influencing uncertainty

A number of factors influenced participants’ experience of uncertainty related to genomic testing. Information seekers showed higher tolerance for uncertainty, preferring to know as much as possible about their risks even if that information is uncertain.[26,33,37] Some participants also had a preference for knowing their genomic information (even uncertain results) over paternalistic secrecy, stating that if medical professionals know genomic results, that information should be shared with the individual.[33]

Participants’ own genomic literacy[25,26,28,32,33] influenced their experience of uncertainty, with high literacy helping to give meaning to uncertain results.[33] However, misconceptions about results and inadequate information caused confusion and uncertainty about the future for some participants,[25,26,32] as well as difficulty making decisions.[28] Bradbury and colleagues[28] found that making a less informed choice (which was defined as inadequate knowledge and a decision discordant with attitudes toward testing) about genomic testing was associated with greater uncertainty prior to testing. While previous experience with uncertainty and disease led some participants to believe they could cope with the uncertainty related to genomic testing,[26,33] Bradbury and colleagues[28] found that previous experience with genetic testing was not associated with participants’ mean baseline uncertainty scores.

Health professionals’ credentials, and communication approach and style when discussing genomic results,[25,26,28,32,33] also influenced participants’ uncertainty. Participants preferred to have a genetic counselor rather than a medical geneticist or oncologist explain their germline genomic results,[33] and found that uncertainty was increased when health-care professionals provided too much information causing information overload, or used genetic/medical language, such as “not interpretable.”[28,32]

A trust in science influenced patients’ experience of uncertainty about treatment decisions based on genomic results, with trusting participants feeling more certain about their targeted or standard treatment.[32] These participants trusted the science, therefore any genomic result was reassuring and reduced uncertainty to some extent.[32]

“The tests showed that in any case, I had to be given docetaxel, which was the only possible option, and therefore I wasn’t included in the trial protocol. So in the end I underwent the normal, well-known procedure, which is quite reassuring.”[32]

The influence of the type of genomic result and participant uncertainty was mixed. While the quantitative synthesis showed no difference in uncertainty levels between participants who received positive, negative, or uncertain genomic results,[30,31] the qualitative synthesis found decreases in disease and risk uncertainty for participants who received negative or positive genomic results, but increased uncertainty about the future for participants receiving a VUS result.[25,28,32,33]

“It’s just that I don’t know…I know I’ve got something, but I don’t know what and I don’t know what it means.”[25]

Some participants expressed tolerance for the uncertainty involved in receiving VUS results;[33] others who received uncertain genomic results subsequently reported feeling more uncertain.[28,33] Participants’ experience of uncertain results depended on whether they appraised the uncertainty attached to the result as a danger, an opportunity, or both.[25,26] Those who appraised the uncertainty as a danger considered their VUS as a health threat (i.e., assumed high risk). Those who appraised uncertainty as an opportunity held hope for a positive outcome (i.e., not developing cancer). Some participants appraised the VUS as both an opportunity and a danger, seeing it as a health threat but not as serious a threat as a positive result.

Outcomes of uncertainty

Lumish and colleagues[30] reported that participants receiving uncertain genomic results misinterpreted their VUS result as a negative result. Esteban and colleagues[31] reported that participants who receive uncertain genomic results have similar psychological reactions as participants who receive negative genomic results, including lower levels of distress and higher levels of positive experience compared with those who receive a positive genomic result.

Participants who received uncertain genomic results experienced a range of affective reactions to their results, including frustration, shock, regret, sadness, disappointment, and further uncertainty about the future.[25,26,32] Some participants acknowledged that once you experience uncertainty, you cannot go back to being oblivious.[33]

“I can’t un-know that information.”[33]

Some participants did also experience a sense of relief that something (however uncertain) was detected.[25]

“Yeah, it was a relief in yeah okay I do have something that it’s not my fault I got cancer and the other part of me was like this doesn’t mean anything.”[25]

Uncertainty also influenced participants’ decisions regarding communicating genomic results to relatives. Participants assessed whether the information would be more harmful than useful to their relatives, and judged uncertain results to be more potentially harmful and difficult to communicate, generating hesitancy to share such results with relatives.[33]

“...if it was going to do more harm than good by telling them certain results, there is a slight chance I would not tell them.”[33]

Coping with uncertainty

Participants were mostly individuals with a personal and/or family history of cancer. Having experienced cancer-related uncertainty, they were willing to risk more uncertainty for the chance of some certainty about their cancer, and/or future risk. Previous experience of coping with uncertainty gave participants a sense of self-efficacy to be able to cope with more uncertainty if that was the outcome of genomic testing.[26,33]

Prior to receiving genomic results, participants felt that they would respond to uncertain results by seeking more information, or by remaining optimistic about a positive future outcome.[25,33] Subsequently many participants did cope with their uncertainty by seeking more information and by remaining optimistic that their VUS would be reclassified in the future. Researching what was known about their uncertain result and what clinical trials were available based on that result helped participants cope with the uncertainty of their genomic results.[25,33]

“I didn’t want to get a second opinion because it was a big deal to get a genetic work-up, and I trusted the geneticist. I went to the Internet, though, and started doing some research on my own.”[25]

Some participants felt that their faith or positive attitude helped them to be resilient enough to cope with uncertainty, through believing that the positive outcome would occur.[33] Some participants appraised uncertain genomic results as an opportunity, believing that advances in science would provide more certain answers in the future.[25]

“I feel that there is a seed of hope that I could be completely normal. Some information could come out in five years, ten years, twenty years, that could make me interpret these results differently.”[25]

Additionally, participants coped with uncertainty by complying with recommended screening, sharing risk information with relatives, or by forming a plan of action based on high risk cancer assumptions.[25,26,33] Participants who appraised an uncertain genomic result as a danger self-identified as high risk or as having a positive result and acted accordingly in terms of risk reduction strategies.[25]

“And getting my ovaries out, that was a hard decision but the thing is I don’t want to die of something that doesn’t do anything. I would rather just go ahead and get them out. I want to live. Definitely safe vs. sorry, absolutely.”[25]

Regardless of whether participants appraised the uncertainty as an opportunity or danger, coping strategies involved having a plan. Participants believed that they could intervene with their behavior to reduce their risk with surveillance and management plans.[25,26]

“You know the thing is you need to get a plan in place, like get a surveillance plan in place, know what you’re going to be doing and that gives me more comfort. To think every year, okay I’m going to have a colonoscopy and you know I’m going to let the doctors know about it….”[25]

Some participants coped with uncertainty by sharing their genomic information with relatives, stating that this gave them a sense of protecting their relatives with risk information.[25]

DISCUSSION

This systematic review provides a synthesis of the existing research on the patient experience of uncertainty related to cancer genomic testing. Overall, our findings highlight the multiplicity of coexisting uncertainties involved in genomic testing for patients, supporting what has been found in the literature on the experience of uncertainty in patients who are pursuing cancer genetic testing.[12,15,16,38-44]

To ensure that the findings of this systematic review were grounded in the data, we focused only on the data from the papers included in the review during the analysis, rather than using theories or frameworks to guide analysis. It is important however to discuss these results in the context of the well-known theories and frameworks of uncertainty. Our results align with Han’s taxonomy of sequencing uncertainty.[6] For instance the source of patient’s uncertainty may relate to the imprecise nature and usefulness of genomic results, or the complexity with which results are delivered. Scientific uncertainty felt by some patients may be a result of low genomic literacy, while personal uncertainty may occur as a consequence of not knowing how they may react psychologically to their genomic results.

Our results suggest that how a patient appraises uncertainty, as either a danger, opportunity, or both, has implications initially for whether patients will decide to pursue cancer genomic testing; and subsequently for the impact of uncertainty for patients, as well as the coping strategies engaged to deal with their uncertainty. This appraisal of uncertainty as opportunity or danger is supported by Mishel’s[7] uncertainty in illness theory, which states that the experience of uncertainty is neutral until the implications of uncertainty are determined by the patient. When uncertainty is appraised as a danger, strategies to reduce the uncertainty, such as information seeking, are engaged. When uncertainty is seen as an opportunity, strategies to maintain uncertainty or reframe the uncertainty into a positive outcome, such as focusing on the positive aspects of unknowns, are implemented.[7,45] Similarly, this systematic review found that those who viewed their uncertain cancer genomic results as an opportunity remained hopeful that research would evolve and provide a more certain result in the future; while those who appraised their uncertain cancer genomic result as a danger acted to reduce their uncertainty by implementing risk management action plans based on a high risk or positive result.

Appraisal involves evaluation of uncertainty, which is influenced by personality, previous experience, knowledge, contextual cues, and beliefs.[7,45] Simpkin et al. [46] and Biesecker et al. [45,47] have discussed the importance of more effectively communicating the practical and scientific uncertainties of genomics with patients to better manage patient expectations and subsequent uncertainties postresults. This systematic review also found that health-care professionals can help reduce patient uncertainty by communicating in lay language.

This review highlighted that there is currently limited published research on the patient experience of uncertainty when pursuing cancer genomic testing. To more comprehensively assess the limited research available, two hypothetical studies were included in this systematic review. We recognize the limitations of hypothetical studies, and that findings may not be generalizable to real clinical situations. However, participants’ responses regarding the types of uncertainty they expected to experience and the factors influencing that uncertainty are likely representative of their actual opinions and attitudes.[24,26] It should also be noted that patient experiences of uncertainty reported in the hypothetical studies were similar to those reported in studies reporting on real-life use of testing.

Due to the scarcity of literature on any one type of genomic test, we included studies on a variety of genomic tests in a cancer context. There did not appear to be differences in the experience of uncertainty across the test types, for example exome sequencing compared with SNP testing. The only difference that emerged was as a result of the purpose of the genomic testing: providing risk information versus treatment indications, where genomic results decreased decisional uncertainty for patients in the cancer treatment context, compared with no change in uncertainty for patients receiving cancer risk genomic results.[27-29,31]

Much of what we know about the psychosocial issues of cancer patients related to genetic or genomic testing is from an overrepresented female and breast cancer perspective.[48] Similarly, the majority of research investigating patient uncertainty in relation to cancer genomic has focused on females with a personal or family history of breast cancer, highlighting a bias in the literature and a need for future research to include a more diverse range of cancer patients. Future research should include patients with rarer cancers, or cancers with fewer treatment options, to understand more clearly how cancer genomic testing compounds or mitigates disease uncertainty.

Mishel’s reconceptualized uncertainty in illness theory[8] suggests that uncertainty evolves over time, stating that the longer a patient lives with a chronic illness and continual uncertainty, the more positively they appraise their uncertainty. For example, an initial appraisal of uncertainty as danger may evolve into appraisal of uncertainty as opportunity over time. This is supported in the cancer genetic literature by Halbert and colleagues[49] finding that women experiencing uncertainty had received their BRCA results more recently than women who were not experiencing uncertainty. Of the few studies included in our systematic review that did follow patients over time, most focused on the receipt of uncertain genomic results only[27-29] and only one reported on psychosocial outcomes of uncertainty.[31] Further longitudinal research focusing on uncertainty is needed to understand the how the experience of uncertainty changes over time, and the impact of that uncertainty.

Conclusion

This systematic review highlights the need for more mixed methods longitudinal research to understand the experience of patient uncertainty across the genomic testing process (e.g., waiting for and receiving results, and making treatment/risk management decisions), as well as the long-term psychosocial impacts of uncertainty for a broad range of cancer patients. The evidence highlights that while patients approach genomic testing as a disease uncertainty reduction strategy, genomic testing can also raise its own uncertainties for patients. It appears that appraisal of uncertainty as a danger, an opportunity, or both, is important in how the patient experiences uncertainty, as well the impact that uncertainty will have for them and the coping strategies that they utilize.

Supplementary Material