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editorial
. 2021 Dec 13;15:ed119. doi: 10.3332/ecancer.2021.ed119

How aging of the global population is changing oncology

Yan Fei Gu 1, Frank P Lin 2,3, Richard J Epstein 1,2,4,a
PMCID: PMC8816510  PMID: 35211208

Abstract

Population aging is causing a demographic redistribution with implications for the future of healthcare. How will this affect oncology? First, there will be an overall rise in cancer affecting older adults, even though age-specific cancer incidences continue to fall due to better prevention. Second, there will be a wider spectrum of health functionality in this expanding cohort of older adults, with differences between “physiologically older” and “physiologically younger” patients becoming more important for optimal treatment selection. Third, greater teamwork with supportive care, geriatric, mental health and rehabilitation experts will come to enrich oncologic decision-making by making it less formulaic than it is at present. Success in this transition to a more nuanced professional mindset will depend in part on the development of user-friendly computational tools that can integrate a complex mix of quantitative and qualitative inputs from evidence-based medicine, functional and cognitive assessments, and the personal priorities of older adults.

Keywords: clinical decision-making, demography, longevity, quality of life, supportive care


Epidemiologic shifts with impacts on health are occurring worldwide [13]. Life expectancies in most countries are rising, reflecting improvements in public health [4, 5], while birth rates are declining with urbanization [69]. This upending of the population age pyramid is now raising healthcare concerns due to an expected higher burden of age-related disabilities and diseases [10, 11] with consequent reduction in ‘health span’ [12, 13]. An inconvenient question is thus raised: does this global transition to a super-aging society [1416] imply a need to change how medicine is practised today [17, 18]?

Cancer care is a timely focus for this debate [19]. Over the next forty years cancer will create the highest productivity burden of all disease groups as quantified by disability-adjusted life years, and will also overtake ischemic heart disease as the leading cause of death [2022]. Even as age-standardized cancer mortality is declining due to better prevention, total cancer diagnoses and death rates are continuing to rise, with population aging the single main cause [23, 24].

Policies have been created to improve cancer care for older adults [2527] in response to the realization that standard guidelines cannot define optimal management for all circumstances [28, 29]. Such guidelines have largely been based on the heuristic of late-phase randomized trial endpoints, especially overall survival [30], but there are weaknesses of this model from the viewpoint of older patients with cancer [3133]. First, most trials have elected to treat younger and fitter patients with maximally tolerated drug doses, but by doing so have raised doubts whether the reported benefits are applicable to older people [34, 35]. Second, although randomized prospective trials are much respected in evidential terms, their credibility has been eroded by human factors. For example, despite the need to frame research questions with equipoise [36], positive results from clinical trials are favored by most involved parties – pharmaceutical companies [37], physicians [38], patients [39] and the press [40] – with only insurers and government agencies querying this tendency [41, 42].

Dominance of clinical research by industry [43] has likewise selected for biases due to non-publication of negative studies [44, 45], and trial designs favoring statistically significant outcomes [46, 47] – even though many such outcomes provide little real-world benefit to patients [48], especially if older [49]. This is consistent with the impression that average trial gains have tended to reduce in recent decades [50, 51], in part due to regulatory frameworks that have made therapeutic incrementalism the safest commercial strategy [52]. These caveats serve to remind us that clinical decisions should be made not by evidence alone, but by honest and self-critical discussion between doctors and patients [53], including older adults with cancer [54].

How treatment decisions are becoming less influenced by chronological age

As the cohort of older adults with cancer enlarges, a widening spectrum of patient fitness versus frailty is to be expected [55], complicating therapeutic decision-making. A controversy often raised in this context is that the costliest phase of care tends to be the last year [56, 57], with even older patients often being prescribed anticancer therapy in the last month of life [5860]. The solution to this would not seem to lie in implementing policies based on age, which is an unreliable predictor of health status [61], but in applying functional measures [62]. These include metrics of pre-morbid fitness – as approximated by estimated remaining life years without cancer [63] – and of daily activities or coping [64], as assessed by tools such as comprehensive geriatric assessment, which includes an evaluation of comorbidities [6567].

A “physiological age” so derived could be factored into evidence-based cancer and treatment expectations (e.g., estimated remaining life years with cancer, without and with treatment, plus quality of life with or without treatment] to create a decisional process that is not arbitrarily distorted by age [68, 69]. Assessing older patients with cancer in this function-based way should reduce risks of both over- and under-treatment [70, 71]. These risks include those from overreliance on the metric traditionally used by oncologists to assess fitness for drug trials, patient performance status [72]. In relinquishing these imperfect predictors of well-being, however, doctors will need to substitute more informative algorithms or endpoints (Figure 1).

Figure 1. Comparison of the traditional chronological view of aging with a physiological (or “functional”, “biological”, etc.) viewpoint adapted for patients with a cancer diagnosis.

Figure 1.

How cancer epidemiology is changing as populations are aging

Mortality from smoking-related malignancies is still rising, but these cancers should decrease as living standards and education improve [73]. In contrast, the epidemic of ‘lifestyle cancers’ due to overweight and under-exercise shows no hint of abating [74]. As population aging proceeds, lifestyle-related cancers may diverge into two strata: a younger group which more often has cardiovascular disease or diabetes, and an older group whose main risk factor is age alone [75]. The functional extremes, or stereotypes, of older adults with cancer – i.e., physiologically older or physiologically younger – illustrate the breadth of the wellness-illness spectrum in older individuals [76], highlighting the notion of health-related quality of life [77]. Physiologically older patients with cancer are by definition less fit than average for their age, based on non-cancer comorbidity [78, 79]. An estimate of physiological age is derivable by actuarial calculation of an individual’s likely death x years before or after the population’s mean life expectancy [80].

Physiologically older vs. younger patients with cancer may also be separated by a wealth-health gradient that steepens with age [81]. The former cohort tends more often to be male, with more comorbidities, fewer financial resources, and more smoking- or inflammation-induced cancers, such as those of the lung, upper esophagus, stomach, bladder or rectum [82]. Physiologically younger patients tend to be more educated or affluent, and more prone to late-onset lifestyle malignancies such as those of the prostate, breast, endometrium, proximal colon, HPV-positive oropharynx, thyroid, or gastro-oesophageal junction; or melanoma, glioma or myeloma [74]. Since the latter patients tend to have fewer competing causes of death [83], they may in future come to comprise the dominant ‘older’ cohort (Figure 2).

Figure 2. Pathogenetic and socioeconomic interplays relevant to the changing physiological age-specificity of cancer demographics.

Figure 2.

How fewer remaining life years are translating into more patient choices

Doctors have always modified treatment decisions on a holistic basis – for example, by deciding against morbid surgeries in favor of more conservative even if less curative interventions [84, 85], or by minimizing use of toxic chemotherapies [86]. Such decisions are often justified by patient frailty [31, 87]; however, non-frail older patients may also not receive the most effective therapies due to perceptions that benefits are less worthwhile in individuals with shorter life expectancy [88]. This is analogous to doubts over the use of cancer screening in older adults [89, 90], and represents one aspect of a controversy familiar to oncologists – namely, whether doing (or costing) more, in treatment terms, necessarily means doing better [91].

Demand will remain strong in all older patient groups for treatment modalities which are perceived, rightly or wrongly, to offer more hope of durable disease control with acceptable toxicity – e.g., molecularly-targeted drugs [92] and immune checkpoint inhibitors [93]. The spectrum of tumors in physiologically older patients tends to be more responsive to immunotherapies [94], even if only in a minority [95], whereas those in the physiologically younger group more often respond to hormonal or targeted drug therapies [96]. The higher educational profile of physiologically younger patients [97, 98] will likely favor interest in personalized oncology – i.e., targeted ‘smart drugs’ which are scientifically plausible [99] but not always empirically testable [100, 101]. So-called theranostic use of 177Lu-PSMA-617 radionuclide therapy to treat prostate cancer [102] is one example of a targeted treatment modality that may in future become more widely sought by some older patients – for example, when standard options are exhausted, or are anticipated to be poorly tolerated [103].

This ‘healthy aging’ cohort also seems likely to embrace mechanism-based non-pharmacologic health initiatives as anticancer interventions [104106], with these including dietary modification – i.e., caloric restriction [107], fasting or weight loss [108], which inhibit insulin-like growth factor-1/Akt-mediated cancer cell survival [109] – and vigorous daily exercise, which blocks tumors via its effects on AMPK or mTOR signaling [110]. For young and fit patients similar to those recruited for trials, heuristic decision-making based on randomized trials showing survival benefit is appropriate, and for older patients such benefits also remain important [111]. Additional considerations may be prized by older adults, however [112]: these include humanistic prioritization of quality of life [113, 114], holistic balancing of mechanistic interventions with decisional autonomy [115117], and hermeneutic notions of acceptance and finitude [118, 119] (Figure 3). Hence, one challenge is how to encourage older patients to include these value-adding endpoints in their decision-making without feeling that they are neglecting life-threatening survival priorities.

Figure 3. Decision-making schematic showing influence of survival gains balanced with other factors including mechanistic interventions, quality of life strategies, and personal priorities.

Figure 3.

How the needs of older patients with cancer are driving greater medical teamwork

The decision-making style of each older cancer patient will vary, ranging from independent to passive [120], but emotion remains a significant factor [121] with reassurance a frequent need [122]. This hints at the influence of incrementalist thinking among patients with cancer, such that even a one-month survival gain persuades many to request more toxic treatments [123], presumably due to fear [124]. Most patients worry about disease recurrence, and look to their oncologist as the ultimate defender against such contingencies [125, 126]; the mantra of whatever can be done will be done, and only the best is good enough, thus becomes a path of least resistance for physicians, and is further reinforced by litigation concerns. Such positivity appears to improve mood and quality of life for newly diagnosed patients with cancer by reducing prognostic awareness [127]. In the longer term, however, decision-making based on risk aversion and anticipated regret [128130] – a response to threatened losses, as used by auctioneers to drive up offers from competing bidders [131, 132] – appears to undermine patient returns [133, 134].

This maladaptive positive feedback loop can be prevented by a team approach incorporating an initial discussion of goals [135]. By admitting fear factors and frequent sources of decision regret [136], older adults may become more able to consider a full range of coping options [137]. Early involvement of supportive, geriatric and/or mental health experts has thus become a standard of care [138-142] which is appreciated by older patients with cancer who value autonomy and dignity [143, 144]. For selected patients, religious professionals can also contribute to this team effort [145] – in part, perhaps, because religious people may accept better than doctors that death is a normal part of life, as distinct from its usual secular interpretation as a loss of life or an end to life [146]. Hence, as the age of cancer diagnosis rises, demand for professionals to work together is also likely to rise [147, 148], leading to more cross-disciplinary teamworking and better patient care.

To achieve this vision of a ‘geriatric tumor board’ [149], it will be ideal to develop computational algorithms able to integrate subspecialty metrics with individualised patient priorities as in Figure 3 [150]. By bridging these qualitative and quantitative dimensions, a validated algorithm could help to give older patients with cancer – plus their carers and doctors – confidence to move away from a cure-seeking to a more cost-effective cure-and-support-seeking culture [151]. As such, this could be a step away from the paradox that cancer costs rise further as knowledge grows, which trend is the opposite of that seen in technological progress as per Moore’s Law [152]. However, artificial intelligence approaches to even simple oncological decisions have still to mature [153], suggesting that a quantum leap in digital technologies will be needed to quantify subjective inputs [154]. Device-reported data [155, 156] for monitoring health outcomes in real time [157, 158] provide a fresh dimension of functional analysis for older adults with cancer, but this goal is still far from realization [159]. If and when innovative software eventually yields a systems medicine approach to shared decision-making [160, 161], utilization by third-party payers could create a virtuous pathway to better synergistic team care of older patients [162165].

Conclusions

The problems of the modern era have taught the importance of contingency planning. Population aging is a serious and imminent challenge for global healthcare cultures; treating an expanding group of older patients with widely varying fitness levels will demand deep changes to contemporary practices. Steps to ease this transition include the adoption of more informative patient metrics, greater use of function-based assessments, valuing and embracing the personal and spiritual priorities of older patients, and development of informatic infrastructures that can smoothly blend a mix of specialist assessments and patient preferences into 21st-century multidisciplinary cancer care.

Conflicts of interest and funding

All authors declare no support from any organisation for the submitted work, no financial relationships with any organisations that might have an interest in the submitted work, and no other relationships or activities that could appear to have influenced the submitted work.

Authors’ contributions

The manuscript was conceived and drafted by RJE, was read, criticised and revised through multiple drafts by YFG and FPL, and finally rewritten and approved by all authors. All authors are medical oncologists and PhDs, with FPL having additional expertise in medical informatics, and RJE in drug targeting and clinical trials. The clinical experience of the authors has taken place in Australia, China, Hong Kong, the UK, the USA and Singapore.

Acknowledgments

Kind support from the family of the late Mr Frank Wolf, and from The St Vincent’s Hospital Curran Foundation, is gratefully acknowledged.

References

  • 1.Khan HTA. Population ageing in a globalized world: risks and dilemmas? J Eval Clin Pract. 2019;25(5):754–760. doi: 10.1111/jep.13071. [DOI] [PubMed] [Google Scholar]
  • 2.Song Z, Ferris TG. Baby boomers and beds: a demographic challenge for the ages. J Gen Intern Med. 2018;33(3):367–369. doi: 10.1007/s11606-017-4257-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.England K, Azzopardi-Muscat N. Demographic trends and public health in Europe. Eur J Public Health. 2017;27(suppl_4):9–13. doi: 10.1093/eurpub/ckx159. [DOI] [PubMed] [Google Scholar]
  • 4.Foreman KJ, Marquez N, Dolgert A, et al. Forecasting life expectancy, years of life lost, and all-cause and cause-specific mortality for 250 causes of death: reference and alternative scenarios for 2016–40 for 195 countries and territories. Lancet. 2018;392(10159):2052–2090. doi: 10.1016/S0140-6736(18)31694-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Seals DR, Justice JN, LaRocca TJ. Physiological geroscience: targeting function to increase healthspan and achieve optimal longevity. J Physiol. 2016;594(8):2001–2024. doi: 10.1113/jphysiol.2014.282665. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Mitteldorf JJ, Goodnight C. Post-reproductive life span and demographic stability. Biochemistry [Mosc] 2013;78(9):1013–1022. doi: 10.1134/S0006297913090071. [DOI] [PubMed] [Google Scholar]
  • 7.Bhasin S, Kerr C, Oktay K, et al. The implications of reproductive aging for the health, vitality and economic welfare of human societies. J Clin Endocrinol Metab. 2019;104(9):3821–3825. doi: 10.1210/jc.2019-00315. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Seltzer N. Beyond the great recession: labor market polarization and ongoing fertility decline in the United States. Demography. 2019;56(4):1463–1493. doi: 10.1007/s13524-019-00790-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Vollset SE, Goren E, Yuan CW, et al. Fertility, mortality, migration, and population scenarios for 195 countries and territories from 2017 to 2100: a forecasting analysis for the Global Burden of Disease Study. Lancet. 2020;396(10258):1285–1306. doi: 10.1016/S0140-6736(20)30677-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Harper S. Economic and social implications of aging societies. Science. 2014;346(6209):587–591. doi: 10.1126/science.1254405. [DOI] [PubMed] [Google Scholar]
  • 11.Prince MJ, Wu F, Guo Y, et al. The burden of disease in older people and implications for health policy and practice. Lancet. 2015;385(9967):549–562. doi: 10.1016/S0140-6736(14)61347-7. [DOI] [PubMed] [Google Scholar]
  • 12.Selman C, Swindell WR. Putting a strain on diversity. EMBO J. 2018;37(22):e100862. doi: 10.15252/embj.2018100862. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Fulop T, Larbi A, Khalil A, et al. Are we ill because we age? Front Physiol. 2019;10:1508. doi: 10.3389/fphys.2019.01508. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Nomura K, Karita K, Araki A, et al. For making a declaration of countermeasures against the falling birth rate from the Japanese Society for Hygiene: summary of discussion in the working group on academic research strategy against an aging society with low birth rate. Environ Health Prev Med. 2019;24(1):14. doi: 10.1186/s12199-019-0768-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Kim KW, Kim OS. Super aging in South Korea unstoppable but mitigatable: a sub-national scale population projection for best policy planning. Spat Demogr. 2020;8(2):155–173. doi: 10.1007/s40980-020-00061-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Suzuki T. Health status of older adults living in the community in Japan: recent changes and significance in the super-aged society. Geriatr Gerontol Int. 2018;18(5):667–677. doi: 10.1111/ggi.13266. [DOI] [PubMed] [Google Scholar]
  • 17.Akashi H, Ishizuka A, Lee S, et al. The role of the G20 economies in global health. Glob Health Med. 2019;1(1):11–15. doi: 10.35772/ghm.2019.01008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Nakatani H. Population aging in Japan: policy transformation, sustainable development goals, universal health coverage, and social determinates of health. Glob Health Med. 2019;1(1):3–10. doi: 10.35772/ghm.2019.01011. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Winckworth-Prejsnar K, McCanney J, Schatz AA, et al. Policy challenges and opportunities to address changing paradigms in cancer care delivery. J Natl Compr Canc Netw. 2019;17(5):424–431. doi: 10.6004/jnccn.2019.7299. [DOI] [PubMed] [Google Scholar]
  • 20.Mattiuzzi C, Lippi G. Current cancer epidemiology. J Epidemiol Glob Health. 2019;9(4):217–222. doi: 10.2991/jegh.k.191008.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Global Burden of Disease Cancer C, Fitzmaurice C, Akinyemiju TF, et al. Global, regional, and national cancer incidence, mortality, years of life lost, years lived with disability, and disability-adjusted life-years for 29 cancer groups, 1990 to 2016: a systematic analysis for the global burden of disease study. JAMA Oncol. 2018;4(11):1553–1568. doi: 10.1001/jamaoncol.2018.2706. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Wu TY, Chung CH, Lin CN, et al. Lifetime risks, loss of life expectancy, and health care expenditures for 19 types of cancer in Taiwan. Clin Epidemiol. 2018;10:581–591. doi: 10.2147/CLEP.S155601. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Aunan JR, Cho WC, Soreide K. The biology of aging and cancer: a brief overview of shared and divergent molecular hallmarks. Aging Dis. 2017;8(5):628–642. doi: 10.14336/AD.2017.0103. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Nolen SC, Evans MA, Fischer A, et al. Cancer-incidence, prevalence and mortality in the oldest-old A comprehensive review. Mech Ageing Dev. 2017;164:113–126. doi: 10.1016/j.mad.2017.05.002. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Kadambi S, Loh KP, Dunne R, et al. Older adults with cancer and their caregivers - current landscape and future directions for clinical care. Nat Rev Clin Oncol. 2020;17(12):742–755. doi: 10.1038/s41571-020-0421-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Extermann M, Brain E, Canin B, et al. Priorities for the global advancement of care for older adults with cancer: an update of the International Society of Geriatric Oncology Priorities Initiative. Lancet Oncol. 2021;22(1):e29–e36. doi: 10.1016/S1470-2045(20)30473-3. [DOI] [PubMed] [Google Scholar]
  • 27.Biganzoli L, Battisti NML, Wildiers H, et al. Updated recommendations regarding the management of older patients with breast cancer: a joint paper from the European Society of Breast Cancer Specialists [EUSOMA] and the International Society of Geriatric Oncology [SIOG] Lancet Oncol. 2021;22(7):e327–e340. doi: 10.1016/S1470-2045(20)30741-5. [DOI] [PubMed] [Google Scholar]
  • 28.Woolf SH, Grol R, Hutchinson A, et al. Clinical guidelines: potential benefits, limitations, and harms of clinical guidelines. BMJ. 1999;318(7182):527–530. doi: 10.1136/bmj.318.7182.527. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.van Baalen S, Boon M. An epistemological shift: from evidence-based medicine to epistemological responsibility. J Eval Clin Pract. 2015;21(3):433–439. doi: 10.1111/jep.12282. [DOI] [PubMed] [Google Scholar]
  • 30.Benjamin DM, Mandel DR, Barnes T, et al. Can oncologists predict the efficacy of treatments in randomized trials? Oncologist. 2021;26(1):56–62. doi: 10.1634/theoncologist.2020-0054. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Ethun CG, Bilen MA, Jani AB, et al. Frailty and cancer: implications for oncology surgery, medical oncology, and radiation oncology. CA Cancer J Clin. 2017;67(5):362–377. doi: 10.3322/caac.21406. [DOI] [PubMed] [Google Scholar]
  • 32.Feliu J, Heredia-Soto V, Girones R, et al. Can we avoid the toxicity of chemotherapy in elderly cancer patients? Crit Rev Oncol Hematol. 2018;131:16–23. doi: 10.1016/j.critrevonc.2018.08.008. [DOI] [PubMed] [Google Scholar]
  • 33.Al-Mansour Z, Pang L, Bathini V. Novel cancer therapeutics in geriatrics: what is unique to the aging patient? Drugs Aging. 2019;36(1):1–11. doi: 10.1007/s40266-018-0619-2. [DOI] [PubMed] [Google Scholar]
  • 34.Dunn C, Wilson A, Sitas F. Older cancer patients in cancer clinical trials are underrepresented Systematic literature review of almost 5000 meta- and pooled analyses of phase III randomized trials of survival from breast, prostate and lung cancer. Cancer Epidemiol. 2017;51:113–117. doi: 10.1016/j.canep.2017.11.002. [DOI] [PubMed] [Google Scholar]
  • 35.Ludmir EB, Mainwaring W, Lin TA, et al. Factors associated with age disparities among cancer clinical trial participants. JAMA Oncol. 2019;5(12):1769–1773. doi: 10.1001/jamaoncol.2019.2055. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36.Fries JF, Krishnan E. Equipoise, design bias, and randomized controlled trials: the elusive ethics of new drug development. Arthritis Res Ther. 2004;6(3):R250–R255. doi: 10.1186/ar1170. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Lexchin J. Those who have the gold make the evidence: how the pharmaceutical industry biases the outcomes of clinical trials of medications. Sci Eng Ethics. 2012;18(2):247–261. doi: 10.1007/s11948-011-9265-3. [DOI] [PubMed] [Google Scholar]
  • 38.Ahn R, Woodbridge A, Abraham A, et al. Financial ties of principal investigators and randomized controlled trial outcomes: cross sectional study. BMJ. 2017;356:i6770. doi: 10.1136/bmj.i6770. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Sandman L, Liliemark J. From evidence-based to hope-based medicine? Ethical aspects on conditional market authorization of and early access to new cancer drugs. Semin Cancer Biol. 2017;45:58–63. doi: 10.1016/j.semcancer.2017.05.009. [DOI] [PubMed] [Google Scholar]
  • 40.Haque W, Alvarenga M, Hsiehchen D. Nonresearch pharmaceutical industry payments to oncology physician editors. Oncologist. 2020;25(6):e986–e989. doi: 10.1634/theoncologist.2019-0828. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41.Brogan AP, DeMuro C, Barrett AM, et al. Payer perspectives on patient-reported outcomes in health care decision making: oncology examples. J Manag Care Spec Pharm. 2017;23(2):125–134. doi: 10.18553/jmcp.2017.23.2.125. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Ismail Z, Peacock SJ, Kovacic L, et al. Cost-effectiveness impacts cancer care funding decisions in british Columbia, Canada, evidence from 1998 to 2008. Int J Technol Assess Health Care. 2017;33(4):481–486. doi: 10.1017/S0266462317000642. [DOI] [PubMed] [Google Scholar]
  • 43.Buchkowsky SS, Jewesson PJ. Industry sponsorship and authorship of clinical trials over 20 years. Ann Pharmacother. 2004;38(4):579–585. doi: 10.1345/aph.1D267. [DOI] [PubMed] [Google Scholar]
  • 44.Knox KS, Adams JR, Djulbegovic B, et al. Reporting and dissemination of industry versus non-profit sponsored economic analyses of six novel drugs used in oncology. Ann Oncol. 2000;11(12):1591–1595. doi: 10.1023/a:1008309817708. [DOI] [PubMed] [Google Scholar]
  • 45.Peppercorn J, Blood E, Winer E, et al. Association between pharmaceutical involvement and outcomes in breast cancer clinical trials. Cancer. 2007;109(7):1239–1246. doi: 10.1002/cncr.22528. [DOI] [PubMed] [Google Scholar]
  • 46.Clifford TJ, Barrowman NJ, Moher D. Funding source, trial outcome and reporting quality: are they related? Results of a pilot study. BMC Health Serv Res. 2002;2(1):18. doi: 10.1186/1472-6963-2-18. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47.Liang F, Zhu J, Mo M, et al. Role of industry funders in oncology RCTs published in high-impact journals and its association with trial conclusions and time to publication. Ann Oncol. 2018;29(10):2129–2134. doi: 10.1093/annonc/mdy305. [DOI] [PubMed] [Google Scholar]
  • 48.Ocana A, Tannock IF. When are "positive" clinical trials in oncology truly positive? J Natl Cancer Inst. 2011;103(1):16–20. doi: 10.1093/jnci/djq463. [DOI] [PubMed] [Google Scholar]
  • 49.Kilari D, Mohile SG. Management of cancer in the older adult. Clin Geriatr Med. 2012;28(1):33–49. doi: 10.1016/j.cger.2011.10.003. [DOI] [PubMed] [Google Scholar]
  • 50.Cressman S, Browman GP, Hoch JS, et al. A time-trend economic analysis of cancer drug trials. Oncologist. 2015;20(7):729–736. doi: 10.1634/theoncologist.2014-0437. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51.Gyawali B, de Vries EGE, Dafni U, et al. Biases in study design, implementation, and data analysis that distort the appraisal of clinical benefit and ESMO-Magnitude of Clinical Benefit Scale [ESMO-MCBS] scoring. ESMO Open. 2021;6(3):100117. doi: 10.1016/j.esmoop.2021.100117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52.Soleimani F, Zenios S. Disrupting incrementalism in health care innovation. Ann Surg. 2011;254(2):203–208. doi: 10.1097/SLA.0b013e3182251538. [DOI] [PubMed] [Google Scholar]
  • 53.Haynes RB, Devereaux PJ, Guyatt GH. Physicians' and patients' choices in evidence based practice. BMJ. 2002;324(7350):1350. doi: 10.1136/bmj.324.7350.1350. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Vallet-Regi M, Manzano M, Rodriguez-Manas L, et al. Management of cancer in the older age person: an approach to complex medical decisions. Oncologist. 2017;22(3):335–342. doi: 10.1634/theoncologist.2016-0276. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Nguyen H, Moreno-Agostino D, Chua KC, et al. Trajectories of healthy ageing among older adults with multimorbidity: a growth mixture model using harmonised data from eight ATHLOS cohorts. PLoS One. 2021;16(4):e0248844. doi: 10.1371/journal.pone.0248844. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 56.Garrido MM, Prigerson HG, Bao Y, et al. Chemotherapy use in the months before death and estimated costs of care in the last week of life. J Pain Symptom Manage. 2016;51(5):875–881. doi: 10.1016/j.jpainsymman.2015.12.323. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57.Langton JM, Reeve R, Srasuebkul P, et al. Health service use and costs in the last 6 months of life in elderly decedents with a history of cancer: a comprehensive analysis from a health payer perspective. Br J Cancer. 2016;114(11):1293–1302. doi: 10.1038/bjc.2016.75. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 58.Pitson G, Matheson L, Garrard B, et al. Population-based analysis of radiotherapy and chemotherapy treatment in the last month of life within regional Australia. Intern Med J. 2020;50(5):596–602. doi: 10.1111/imj.14377. [DOI] [PubMed] [Google Scholar]
  • 59.Hu J, Aprikian AG, Vanhuyse M, et al. Cancer drug use in the last month of life in men with castration-resistant prostate cancer. J Oncol Pract. 2019;15(6):e510–e519. doi: 10.1200/JOP.18.00626. [DOI] [PubMed] [Google Scholar]
  • 60.Cheung MC, Earle CC, Rangrej J, et al. Impact of aggressive management and palliative care on cancer costs in the final month of life. Cancer. 2015;121(18):3307–3315. doi: 10.1002/cncr.29485. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 61.Artz AS. Biologic vs physiologic age in the transplant candidate. Hematology Am Soc Hematol Educ Program. 2016;2016(1):99–105. doi: 10.1182/asheducation-2016.1.99. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 62.Soto-Perez-de-Celis E, Li D, Yuan Y, et al. Functional versus chronological age: geriatric assessments to guide decision making in older patients with cancer. Lancet Oncol. 2018;19(6):e305–e316. doi: 10.1016/S1470-2045(18)30348-6. [DOI] [PubMed] [Google Scholar]
  • 63.Ploussard G, Albrand G, Rozet F, et al. Challenging treatment decision-making in older urologic cancer patients. World J Urol. 2014;32(2):299–308. doi: 10.1007/s00345-013-1158-4. [DOI] [PubMed] [Google Scholar]
  • 64.Colloca G, Di Capua B, Bellieni A, et al. Biological and functional biomarkers of aging: definition, characteristics, and how they can impact everyday cancer treatment. Curr Oncol Rep. 2020;22(11):115. doi: 10.1007/s11912-020-00977-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 65.Pamoukdjian F, Liuu E, Caillet P, et al. How to optimize cancer treatment in older patients: an overview of available geriatric tools. Am J Clin Oncol. 2019;42(2):109–116. doi: 10.1097/COC.0000000000000488. [DOI] [PubMed] [Google Scholar]
  • 66.O'Donovan A, Leech M. Personalised treatment for older adults with cancer: the role of frailty assessment. Tech Innov Patient Support Radiat Oncol. 2020;16:30–38. doi: 10.1016/j.tipsro.2020.09.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Overcash J, Ford N, Kress E, et al. Comprehensive geriatric assessment as a versatile tool to enhance the care of the older person diagnosed with cancer. Geriatrics [Basel] 2019;4(2):39. doi: 10.3390/geriatrics4020039. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68.Gomes F, Lewis A, Morris R, et al. The care of older cancer patients in the United Kingdom. Ecancermedicalscience. 2020;14:1101. doi: 10.3332/ecancer.2020.1101. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 69.Tranvag EJ, Norheim OF, Ottersen T. Clinical decision making in cancer care: a review of current and future roles of patient age. BMC Cancer. 2018;18(1):546. doi: 10.1186/s12885-018-4456-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.DuMontier C, Loh KP, Bain PA, et al. Defining undertreatment and overtreatment in older adults with cancer: a scoping literature review. J Clin Oncol. 2020;38(22):2558–2569. doi: 10.1200/JCO.19.02809. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71.Djulbegovic B, Elqayam S, Dale W. Rational decision making in medicine: implications for overuse and underuse. J Eval Clin Pract. 2018;24(3):655–665. doi: 10.1111/jep.12851. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 72.Simcock R, Wright J. Beyond performance status. Clin Oncol [R Coll Radiol] 2020;32(9):553–561. doi: 10.1016/j.clon.2020.06.016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 73.Arnold M, Rutherford MJ, Bardot A, et al. Progress in cancer survival, mortality, and incidence in seven high-income countries 1995–2014 [ICBP SURVMARK-2]: a population-based study. Lancet Oncol. 2019;20(11):493–505. doi: 10.1016/S1470-2045(19)30456-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74.Friedenreich CM, Ryder-Burbidge C, McNeil J. Physical activity, obesity and sedentary behavior in cancer etiology: epidemiologic evidence and biologic mechanisms. Mol Oncol. 2021;15(3):790–800. doi: 10.1002/1878-0261.12772. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 75.Cortes-Ibanez FO, Nagaraj SB, Cornelissen L, et al. Prediction of incident cancers in the lifelines population-based cohort. Cancers [Basel] 2021;13(9):2133. doi: 10.3390/cancers13092133. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76.Balducci L, Dolan D. Palliative care of cancer in the older patient. Curr Oncol Rep. 2016;18(12):70. doi: 10.1007/s11912-016-0557-2. [DOI] [PubMed] [Google Scholar]
  • 77.Galvin AE, Friedman DB, Hebert JR. Focus on disability-free life expectancy: implications for health-related quality of life. Qual Life Res. 2021;30(8):2187–2195. doi: 10.1007/s11136-021-02809-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 78.Grippo F, Desesquelles A, Pappagallo M, et al. Multi-morbidity and frailty at death: a new classification of death records for an ageing world. Popul Stud [Camb] 2020;74(3):437–449. doi: 10.1080/00324728.2020.1820558. [DOI] [PubMed] [Google Scholar]
  • 79.Ezzatvar Y, Ramirez-Velez R, Saez de Asteasu ML, et al. Physical function and all-cause mortality in older adults diagnosed with cancer: a systematic review and meta-analysis. J Gerontol A Biol Sci Med Sci. 2020;76(8):1447–1453. doi: 10.1093/gerona/glaa305. [DOI] [PubMed] [Google Scholar]
  • 80.Verduzco-Aguirre HC, Gomez-Moreno C, Chavarri-Guerra Y, et al. Predicting life expectancy for older adults with cancer in clinical practice: implications for shared decision-making. Curr Oncol Rep. 2019;21(8):68. doi: 10.1007/s11912-019-0821-3. [DOI] [PubMed] [Google Scholar]
  • 81.McMaughan DJ, Oloruntoba O, Smith ML. Socioeconomic status and access to healthcare: interrelated drivers for healthy aging. Front Public Health. 2020;8:231. doi: 10.3389/fpubh.2020.00231. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 82.Zhang YB, Pan XF, Chen J, et al. Combined lifestyle factors, incident cancer, and cancer mortality: a systematic review and meta-analysis of prospective cohort studies. Br J Cancer. 2020;122(7):1085–1093. doi: 10.1038/s41416-020-0741-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83.Ezzatvar Y, Ramirez-Velez R, Saez de Asteasu ML, et al. Cardiorespiratory fitness and all-cause mortality in adults diagnosed with cancer systematic review and meta-analysis. Scand J Med Sci Sports. 2021;31(9):1745–1752. doi: 10.1111/sms.13980. [DOI] [PubMed] [Google Scholar]
  • 84.Revenig LM, Canter DJ, Taylor MD, et al. Too frail for surgery? Initial results of a large multidisciplinary prospective study examining preoperative variables predictive of poor surgical outcomes. J Am Coll Surg. 2013;217(4):665–70 e1. doi: 10.1016/j.jamcollsurg.2013.06.012. [DOI] [PubMed] [Google Scholar]
  • 85.Boulahssass R, Gonfrier S, Ferrero JM, et al. Predicting early death in older adults with cancer. Eur J Cancer. 2018;100:65–74. doi: 10.1016/j.ejca.2018.04.013. [DOI] [PubMed] [Google Scholar]
  • 86.Lewis MA. ASCO 2021’s Best Trials Proved We Can Do More With Less. Medscape; 2021. [14/7/21]. [Google Scholar]
  • 87.Baltatzis M, Rodriquenz MG, Siriwardena AK, et al. Contemporary management of pancreas cancer in older people. Eur J Surg Oncol. 2021;47(3 Pt A):560–568. doi: 10.1016/j.ejso.2020.08.007. [DOI] [PubMed] [Google Scholar]
  • 88.de Boer AZ, de Glas NA, Marang-van de Mheen PJ, et al. Effect of omission of surgery on survival in patients aged 80 years and older with early-stage hormone receptor-positive breast cancer. Br J Surg. 2020;107(9):1145–1153. doi: 10.1002/bjs.11568. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 89.Kotwal AA, Walter LC. Cancer screening among older adults: a geriatrician's perspective on breast, cervical, colon, prostate, and lung cancer screening. Curr Oncol Rep. 2020;22(11):108. doi: 10.1007/s11912-020-00968-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 90.Schoenborn NL, Huang J, Sheehan OC, et al. Influence of age, health, and function on cancer screening in older adults with limited life expectancy. J Gen Intern Med. 2019;34(1):110–117. doi: 10.1007/s11606-018-4717-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 91.Attena F. Too much medicine? Scientific and ethical issues from a comparison between two conflicting paradigms. BMC Public Health. 2019;19(1):97. doi: 10.1186/s12889-019-6442-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 92.Hebar A, Valent P, Selzer E. The impact of molecular targets in cancer drug development: major hurdles and future strategies. Expert Rev Clin Pharmacol. 2013;6(1):23–34. doi: 10.1586/ecp.12.71. [DOI] [PubMed] [Google Scholar]
  • 93.Fox B, de Toro Carmena M, Alvarez Alvarez R, et al. Efficacy and safety of immune checkpoint inhibitor immunotherapy in elderly cancer patients. Clin Transl Oncol. 2020;22(4):555–562. doi: 10.1007/s12094-019-02161-4. [DOI] [PubMed] [Google Scholar]
  • 94.Rzeniewicz K, Larkin J, Menzies AM, et al. Immunotherapy use outside clinical trial populations: never say never? Ann Oncol. 2021;32(7):866–880. doi: 10.1016/j.annonc.2021.03.199. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 95.Elias R, Odejide O. Immunotherapy in older adults: a checkpoint to palliation? Am Soc Clin Oncol Educ Book. 2019;39:e110–e20. doi: 10.1200/EDBK_238795. [DOI] [PubMed] [Google Scholar]
  • 96.Battisti NML, Liposits G, De Glas NA, et al. Systemic therapy of common tumours in older patients: challenges and opportunities. A young International Society of Geriatric Oncology review paper. Curr Oncol Rep. 2020;22(10):98. doi: 10.1007/s11912-020-00958-z. [DOI] [PubMed] [Google Scholar]
  • 97.Ingleby FC, Woods LM, Atherton IM, et al. Describing socio-economic variation in life expectancy according to an individual's education, occupation and wage in England and Wales: an analysis of the ONS Longitudinal Study. SSM Popul Health. 2021;14:100815. doi: 10.1016/j.ssmph.2021.100815. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 98.Balachandran A, James KS, van Wissen L, et al. Can changes in education alter future population ageing in Asia and Europe? J Biosoc Sci. 2021;30:1–13. doi: 10.1017/S0021932021000134. [DOI] [PubMed] [Google Scholar]
  • 99.Seligson ND, Knepper TC, Ragg S, et al. Developing drugs for tissue-agnostic indications: a paradigm shift in leveraging cancer biology for precision medicine. Clin Pharmacol Ther. 2021;109(2):334–342. doi: 10.1002/cpt.1946. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 100.Tonelli MR. Clinical judgement in precision medicine. J Eval Clin Pract. 2018;24(3):646–648. doi: 10.1111/jep.12892. [DOI] [PubMed] [Google Scholar]
  • 101.Ozdogan M, Papadopoulou E, Tsoulos N, et al. Comprehensive tumor molecular profile analysis in clinical practice. BMC Med Genomics. 2021;14(1):105. doi: 10.1186/s12920-021-00952-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 102.Sartor O, de Bono J, Chi KN, et al. Lutetium-177-PSMA-617 for metastatic castration-resistant prostate cancer. N Engl J Med. 2021;385:1091–1103. doi: 10.1056/NEJMoa2107322. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 103.Leibowitz R, Davidson T, Gadot M, et al. A retrospective analysis of the safety and activity of Lutetium-177-prostate-specific membrane antigen radionuclide treatment in older patients with metastatic castration-resistant prostate cancer. Oncologist. 2020;25(9):787–792. doi: 10.1634/theoncologist.2020-0100. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 104.White MC, Holman DM, Boehm JE, et al. Age and cancer risk: a potentially modifiable relationship. Am J Prev Med. 2014;46(3 Suppl 1):S7–S15. doi: 10.1016/j.amepre.2013.10.029. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 105.Holliday R. Aging is no longer an unsolved problem in biology. Ann N Y Acad Sci. 2006;1067:1–9. doi: 10.1196/annals.1354.002. [DOI] [PubMed] [Google Scholar]
  • 106.Li Y, Schoufour J, Wang DD, et al. Healthy lifestyle and life expectancy free of cancer, cardiovascular disease, and type 2 diabetes: prospective cohort study. BMJ. 2020;368:l6669. doi: 10.1136/bmj.l6669. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 107.Carmona JJ, Michan S. Biology of healthy aging and longevity. Rev Invest Clin. 2016;68(1):7–16. [PubMed] [Google Scholar]
  • 108.Dorling JL, Martin CK, Redman LM. Calorie restriction for enhanced longevity: the role of novel dietary strategies in the present obesogenic environment. Ageing Res Rev. 2020;64:101038. doi: 10.1016/j.arr.2020.101038. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 109.Duran-Ortiz S, List EO, Basu R, et al. Extending lifespan by modulating the growth hormone/insulin-like growth factor-1 axis: coming of age. Pituitary. 2021;24(3):438–456. doi: 10.1007/s11102-020-01117-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 110.Pozuelo-Carrascosa DP, Alvarez-Bueno C, Cavero-Redondo I, et al. Cardiorespiratory fitness and site-specific risk of cancer in men: a systematic review and meta-analysis. Eur J Cancer. 2019;113:58–68. doi: 10.1016/j.ejca.2019.03.008. [DOI] [PubMed] [Google Scholar]
  • 111.Stegmann ME, Brandenbarg D, Reyners AKL, et al. Treatment goals and changes over time in older patients with noncurable cancer. Support Care Cancer. 2021;29(7):3849–3856. doi: 10.1007/s00520-020-05945-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 112.Puts MTE, Strohschein FJ, Del Giudice ME, et al. Role of the geriatrician, primary care practitioner, nurses, and collaboration with oncologists during cancer treatment delivery for older adults: a narrative review of the literature. J Geriatr Oncol. 2018;9(4):398–404. doi: 10.1016/j.jgo.2018.04.008. [DOI] [PubMed] [Google Scholar]
  • 113.Firkins J, Hansen L, Driessnack M, et al. Quality of life in ‘chronic’ cancer survivors: a meta-analysis. J Cancer Surviv. 2020;14(4):504–517. doi: 10.1007/s11764-020-00869-9. [DOI] [PubMed] [Google Scholar]
  • 114.Mead KH, Raskin S, Willis A, et al. Identifying patients' priorities for quality survivorship: conceptualizing a patient-centered approach to survivorship care. J Cancer Surviv. 2020;14(6):939–958. doi: 10.1007/s11764-020-00905-8. [DOI] [PubMed] [Google Scholar]
  • 115.Thiessen M, Sinclair S, Tang PA, et al. Information access and use by patients with cancer and their friends and family: development of a grounded theory. J Med Internet Res. 2020;22(10):e20510. doi: 10.2196/20510. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 116.Al Achkar M, Marchand L, Thompson M, et al. Unmet needs and opportunities for improving care for patients with advanced lung cancer on targeted therapies: a qualitative study. BMJ Open. 2020;10(3):e032639. doi: 10.1136/bmjopen-2019-032639. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 117.Bijlsma RM, Wouters RHP, Wessels H, et al. Managing unsolicited findings in genomics: a qualitative interview study with cancer patients. Psychooncology. 2018;27(4):1327–1333. doi: 10.1002/pon.4676. [DOI] [PubMed] [Google Scholar]
  • 118.Yang W, Staps T, Hijmans E. Existential crisis and the awareness of dying: the role of meaning and spirituality. Omega (Westport) 2010;61(1):53–69. doi: 10.2190/OM.61.1.c. [DOI] [PubMed] [Google Scholar]
  • 119.Stanic J, Perrenoud B, Rochat E, et al. Experiences of newly diagnosed cancer patients in confronting the finitudes of life: a qualitative systematic review protocol. JBI Database System Rev Implement Rep. 2018;16(12):2288–2294. doi: 10.11124/JBISRIR-2017-003621. [DOI] [PubMed] [Google Scholar]
  • 120.De Silva D, Ranasinghe W, Bandaragoda T, et al. Machine learning to support social media empowered patients in cancer care and cancer treatment decisions. PLoS One. 2018;13(10):e0205855. doi: 10.1371/journal.pone.0205855. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 121.Treffers T, Putora PM. Emotions as social information in shared decision-making in Oncology. Oncology. 2020;98(6):430–437. doi: 10.1159/000505341. [DOI] [PubMed] [Google Scholar]
  • 122.Mighton C, Carlsson L, Clausen M, et al. Development of patient ‘profiles’ to tailor counseling for incidental genomic sequencing results. Eur J Hum Genet. 2019;27(7):1008–1017. doi: 10.1038/s41431-019-0352-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 123.Weiss J, Kirchberger MC, Heinzerling L. Therapy preferences in melanoma treatment-willingness to pay and preference of quality versus length of life of patients, physicians, healthy individuals and physicians with oncological disease. Cancer Med. 2020;9(17):6132–6140. doi: 10.1002/cam4.3191. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 124.Greer JA, Applebaum AJ, Jacobsen JC, et al. Understanding and addressing the role of coping in palliative care for patients with advanced cancer. J Clin Oncol. 2020;38(9):915–925. doi: 10.1200/JCO.19.00013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 125.Abernethy AP, Grubbs SS. Managing cumulative expectations in oncology: challenges and potential solutions. Am Soc Clin Oncol Educ Book. 2014;34:e140–e144. doi: 10.14694/EdBook_AM.2014.34.e140. [DOI] [PubMed] [Google Scholar]
  • 126.Shah M, Ferguson A, Corn PD, et al. Developing workshops to enhance hope among patients with metastatic breast cancer and oncologists: a pilot study. JCO Oncol Pract. 2021;17(6):e785–e93. doi: 10.1200/OP.20.00744. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 127.Nipp RD, Greer JA, El-Jawahri A, et al. Coping and prognostic awareness in patients with advanced cancer. J Clin Oncol. 2017;35(22):2551–2557. doi: 10.1200/JCO.2016.71.3404. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 128.Brewer NT, DeFrank JT, Gilkey MB. Anticipated regret and health behavior: a meta-analysis. Health Psychol. 2016;35(11):1264–1275. doi: 10.1037/hea0000294. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 129.Maguire R, Hanly P, Drummond FJ, et al. Regret and fear in prostate cancer: the relationship between treatment appraisals and fear of recurrence in prostate cancer survivors. Psychooncology. 2017;26(11):1825–1831. doi: 10.1002/pon.4384. [DOI] [PubMed] [Google Scholar]
  • 130.Vickers AJ. Decisional conflict, regret, and the burden of rational decision making. Med Decis Making. 2017;37(1):3–5. doi: 10.1177/0272989X16657544. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 131.Reimann M, Nenkov GY, MacInnis D, et al. The role of hope in financial risk seeking. J Exp Psychol Appl. 2014;20(4):349–364. doi: 10.1037/xap0000027. [DOI] [PubMed] [Google Scholar]
  • 132.Bennett M, Mullard R, Adam MTP, et al. Going, going, gone: competitive decision-making in Dutch auctions. Cogn Res Princ Implic. 2020;5(1):62. doi: 10.1186/s41235-020-00259-w. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 133.Hoverman JR. Rethinking clinical oncology drug research in an era of value-based cancer care: a role for chemotherapy pathways. Cancer Med. 2020;9(15):5306–5311. doi: 10.1002/cam4.3193. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 134.Massa I, Balzi W, Altini M, et al. The challenge of sustainability in healthcare systems: frequency and cost of diagnostic procedures in end-of-life cancer patients. Support Care Cancer. 2018;26(7):2201–2208. doi: 10.1007/s00520-018-4067-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 135.Bernacki RE, Block SD, American College of Physicians High Value Care Task F. Communication about serious illness care goals: a review and synthesis of best practices. JAMA Intern Med. 2014;174(12):1994–2003. doi: 10.1001/jamainternmed.2014.5271. [DOI] [PubMed] [Google Scholar]
  • 136.Nicolai J, Buchholz A, Seefried N, et al. When do cancer patients regret their treatment decision? A path analysis of the influence of clinicians' communication styles and the match of decision-making styles on decision regret. Patient Educ Couns. 2016;99(5):739–746. doi: 10.1016/j.pec.2015.11.019. [DOI] [PubMed] [Google Scholar]
  • 137.Wen FH, Chen JS, Chang WC, et al. Accurate prognostic awareness and preference states influence the concordance between terminally ill cancer patients' states of preferred and received life-sustaining treatments in the last 6 months of life. Palliat Med. 2019;33(8):1069–1079. doi: 10.1177/0269216319853488. [DOI] [PubMed] [Google Scholar]
  • 138.Greer JA, Jacobs JM, El-Jawahri A, et al. Role of patient coping strategies in understanding the effects of early palliative care on quality of life and mood. J Clin Oncol. 2018;36(1):53–60. doi: 10.1200/JCO.2017.73.7221. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 139.Maltoni M, Scarpi E, Dall'Agata M, et al. Systematic versus on-demand early palliative care: a randomised clinical trial assessing quality of care and treatment aggressiveness near the end of life. Eur J Cancer. 2016;69:110–118. doi: 10.1016/j.ejca.2016.10.004. [DOI] [PubMed] [Google Scholar]
  • 140.Ryan S, Wong J, Chow R, et al. Evolving definitions of palliative care: upstream migration or confusion? Curr Treat Options Oncol. 2020;21(3):20. doi: 10.1007/s11864-020-0716-4. [DOI] [PubMed] [Google Scholar]
  • 141.Vanbutsele G, Pardon K, Van Belle S, et al. Effect of early and systematic integration of palliative care in patients with advanced cancer: a randomised controlled trial. Lancet Oncol. 2018;19(3):394–404. doi: 10.1016/S1470-2045(18)30060-3. [DOI] [PubMed] [Google Scholar]
  • 142.Brighton LJ, Bristowe K. Communication in palliative care: talking about the end of life, before the end of life. Postgrad Med J. 2016;92(1090):466–470. doi: 10.1136/postgradmedj-2015-133368. [DOI] [PubMed] [Google Scholar]
  • 143.van Leeuwen KM, van Loon MS, van Nes FA, et al. What does quality of life mean to older adults? A thematic synthesis. PLoS One. 2019;14(3):e0213263. doi: 10.1371/journal.pone.0213263. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 144.Staats K, Grov EK, Husebo BS, et al. Dignity and loss of dignity: experiences of older women living with incurable cancer at home. Health Care Women Int. 2020;41(9):1036–1058. doi: 10.1080/07399332.2020.1797035. [DOI] [PubMed] [Google Scholar]
  • 145.Balducci L. Geriatric oncology, spirituality, and palliative care. J Pain Symptom Manage. 2019;57(1):171–175. doi: 10.1016/j.jpainsymman.2018.05.009. [DOI] [PubMed] [Google Scholar]
  • 146.Gillman J. Memoirs and the Ars Moriendi. J Pastoral Care Counsel. 2019;73(3):160–168. doi: 10.1177/1542305019863012. [DOI] [PubMed] [Google Scholar]
  • 147.Kaasa S, Loge JH, Aapro M, et al. Integration of oncology and palliative care: a Lancet Oncology Commission. Lancet Oncol. 2018;19(11):e588–e653. doi: 10.1016/S1470-2045(18)30415-7. [DOI] [PubMed] [Google Scholar]
  • 148.Evans CJ, Ison L, Ellis-Smith C, et al. Service delivery models to maximize quality of life for older people at the end of life: a rapid review. Milbank Q. 2019;97(1):113–175. doi: 10.1111/1468-0009.12373. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 149.Wildes TM, O'Donovan A, Colloca GF, et al. Tumour boards in geriatric oncology. Age Ageing. 2018;47(2):168–170. doi: 10.1093/ageing/afx171. [DOI] [PubMed] [Google Scholar]
  • 150.Stacey D, Legare F, Lewis K, et al. Decision aids for people facing health treatment or screening decisions. Cochrane Database Syst Rev. 2017;4:CD001431. doi: 10.1002/14651858.CD001431.pub5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 151.Iijima K, Arai H, Akishita M, et al. Toward the development of a vibrant, super-aged society: the future of medicine and society in Japan. Geriatr Gerontol Int. 2021;21:601–613. doi: 10.1111/ggi.14201. [DOI] [PubMed] [Google Scholar]
  • 152.Alvarnas J. From the editor-in-chief: oncology in the time of ‘Moore's Law’. Am J Manag Care. 2019;25(5 Spec No.):SP140. [PubMed] [Google Scholar]
  • 153.Lohr S. What Ever Happened to IBM’s Watson? The New York Times; 2021. [16/7/21]. [Google Scholar]
  • 154.Chin-Yee B, Upshur R. Three problems with big data and artificial intelligence in medicine. Perspect Biol Med. 2019;62(2):237–256. doi: 10.1353/pbm.2019.0012. [DOI] [PubMed] [Google Scholar]
  • 155.Adriaans DJ, Dierick-van Daele AT, van Bakel M, et al. Digital self-management support tools in the care plan of patients with cancer: review of randomized controlled trials. J Med Internet Res. 2021;23(6):e20861. doi: 10.2196/20861. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 156.Ostropolets A, Zhang L, Hripcsak G. A scoping review of clinical decision support tools that generate new knowledge to support decision making in real time. J Am Med Inform Assoc. 2020;27(12):1968–1976. doi: 10.1093/jamia/ocaa200. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 157.Berry DL, Blonquist TM, Patel RA, et al. Exposure to a patient-centered, Web-based intervention for managing cancer symptom and quality of life issues: impact on symptom distress. J Med Internet Res. 2015;17(6):e136. doi: 10.2196/jmir.4190. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 158.Lavallee DC, Chenok KE, Love RM, et al. Incorporating patient-reported outcomes into health care to engage patients and enhance care. Health Aff (Millwood) 2016;35(4):575–582. doi: 10.1377/hlthaff.2015.1362. [DOI] [PubMed] [Google Scholar]
  • 159.Kelly CJ, Karthikesalingam A, Suleyman M, et al. Key challenges for delivering clinical impact with artificial intelligence. BMC Med. 2019;17(1):195. doi: 10.1186/s12916-019-1426-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 160.Apweiler R, Beissbarth T, Berthold MR, et al. Whither systems medicine? Exp Mol Med. 2018;50(3):e453. doi: 10.1038/emm.2017.290. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 161.Josfeld L, Keinki C, Pammer C, et al. Cancer patients' perspective on shared decision-making and decision aids in oncology. J Cancer Res Clin Oncol. 2021;147(6):1725–1732. doi: 10.1007/s00432-021-03579-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 162.Shahrokni A, Alexander K, Wildes TM, et al. Preventing treatment-related functional decline: strategies to maximize resilience. Am Soc Clin Oncol Educ Book. 2018;38:415–431. doi: 10.1200/EDBK_200427. [DOI] [PubMed] [Google Scholar]
  • 163.DuMontier C, Loh KP, Soto-Perez-de-Celis E, et al. Decision making in older adults with cancer. J Clin Oncol. 2021;39(19):2164–2174. doi: 10.1200/JCO.21.00165. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 164.Lin FP, Groza T, Kocbek S, et al. Cancer care treatment outcome ontology: a novel computable ontology for profiling treatment outcomes in patients with solid tumors. JCO Clin Cancer Inform. 2018;2:1–14. doi: 10.1200/CCI.18.00026. [DOI] [PubMed] [Google Scholar]
  • 165.Cesario A, D'Oria M, Calvani R, et al. The role of artificial intelligence in managing multimorbidity and cancer. J Pers Med. 2021;11(4):314. doi: 10.3390/jpm11040314. [DOI] [PMC free article] [PubMed] [Google Scholar]

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