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Biologic, psychological, and social health needs in cancer care: how far have we come? F. Sch u lte

In 2007, th e U .S. In stitu te o f M ed icin e d eliv ered a re p o rt titled C a n cer C are f o r the W hole P atient: M e etin g P sy c h o so c ia l H ea lth N e e d s 1, in w h ich gaps in th e p ro v isio n o f p sy ch o so cial care for ca n cer p a ­ tien ts w ere identified. T he re p o rt h ig h lig h ted that, desp ite a b u rg e o n in g evid en ce b ase d em o n stratin g th e effectiv en ess o f a v a rie ty o f p sychosocial health in terv e n tio n s for p atien ts an d su rv iv o rs o f cancer, th e p sy ch o so cial health n eed s o f patients w ere not b ein g ad e q u a te ly m et. T h at re p o rt b ro u g h t to the fo refro n t th e n ec essity not sim ply to co n sid er the psychosocial needs o f cancer patients, but to carefully in teg ra te p sy ch o so cial asse ssm e n t an d su b sequent tre a tm e n t w ith m an ag em en t o f the physical needs o f each patien t. In essence, one set o f n ee d s cannot be co n ceiv ed w ith o u t the other. C an ce r care for the “w hole p a tie n t” m u st co n sid er biologic, psy ch o lo g i­ cal, an d social factors. T h e article titled “T he influence o f c h e m o th e ra­ p y -in d u ced n eu ro to x ic ity on psychological distress an d sleep d istu rb an ce in ca n cer p atien ts” by H ong an d c o lle a g u e s th a t a p p e a rs in th is issue o f C u r­ ren t O n co lo g y is a p rim e exam ple o f the in tricate re la tio n s h ip b e tw e e n p h y sic a l a n d p sy c h o so c ia l sy m p to m s in ca n cer care. T he article explores the re la tio n sh ip s o f c h e m o th e rap y -in d u c ed p e rip h e ra l n eu ro to x ic ity ( c i p n ) w ith p sychosocial d istress and re d u c e d sleep q u a lity in n ew ly d ia g n o se d ca n c e r p atients. S pecifically, the study sam pled 706 new ly d iag n o sed ca n c e r p atien ts b etw e en 18 and 70 years o f age u n d erg o in g ca n cer th era p y at four in stitu tio n s across C h in a. P atients com pleted m easu res designed to o p eratio n aliz e p erip h e ral neurotoxicity, an x iety and d ep ressio n , and sleep quality. R esults rev ealed that, a fte r co n tro llin g for age, sex, edu catio n level, social su p p o rts, fatig ue, d isease stage, and tu m o u r site, p a tie n t-re p o rte d n e u ro to x ic ity w as th e m o st sig n ifican t p re d ic to r o f d epression and an x iety ; c i p n also sign ifican tly p re d ic ted sleep quality. U nfo rtu n ately , this research w as not longitudinal in desig n , lim itin g the ab ility o f the authors to d e­ te rm in e cau satio n . Q u estio n s m ig h t therefore arise

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ab o u t w h e th e r p a tie n ts e x p e rie n c in g g re a te r p s y ­ chosocial d istre ss— including d ep ressio n , anxiety , and p o o r sleep— are m ore likely to re p o rt g re ater self-perceived p erip h eral n eu ro to x ic ity o r w h eth er c i p n leads to an in cre ased freq u en c y o f psy ch o so cial difficulties. T he p o ten tial to u n d ersta n d causatio n is fu rth e r affected by the inclusion o f a self-rep o rt m easu re o f c i p n co m p risin g only tw o item s, w hich p re clu d es a b ro a d e r clin ic a l p ic tu re o f a d d itio n al chem otherapy side effects that m ight also be affecting psychosocial sym ptom s. N ev erth eless, th is research em phasizes a significant lin k betw een chem otherapyin d u ced n eu ro to x icity an d p sychosocial sym ptom s. M ost notable is the fin d in g th at the relatio n sh ip ex­ ten d s over and above th o se o f o th er v ariab les k n o w n to affect m ood and anxiety, including social supp o rts an d fatigue. Today, alm ost 7 years since the Institute o f M ed i­ cine rep o rt, research continues to overw helm in g ly support an association o f the p revalence o f p sycho so ­ cial sym ptom s w ith the physical side effects o f cancer treatm ent. H as care for the cancer patient becom e bet­ ter integrated w ith resp ect to assessing, m onitoring, and treatin g the “w hole p atien t”— that is, including the biologic, psychological, and social needs? B ased on th e ir re se a rc h fin d in g s, H o n g e t al. co n c lu d e th at ongoing assessm ent o f peripheral neuropathies should be em phasized. A s health care practitioners and academ ics, w e have an ongoing responsibility to recognize, m onitor, docum ent, and treat psychosocial sym ptom s across the cancer continuum . S ince the early 2 0 0 0 s, a trem e n d o u s m ovem en t has b eg u n to screen for psychosocial d istress in all c a n c e r p atien ts. P sy ch o so cial d istre ss is now a c ­ k n o w ledged in tern a tio n ally as “th e 6th v ital sign ”2. T he co st o f u n id e n tifie d p sy c h o so c ia l d istre ss in ca n c e r p atien ts, su rv iv o rs, an d fam ilies is severe. P atien ts ex p e rie n c in g m u ltip le stre sso rs ca n h ave m ore d ifficu lty m ak in g decisions and ad h e rin g to tre a tm e n t reco m m en d atio n s. T h ey ca n also strain the re so u rces o f o ncology team s by re q u irin g m ore h ealth care p erso n n el tim e to deal w ith non m ed ical

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21 , N u m b e r 4 , A u g u s t 2014

Copyright © 2014 Multimed Inc. Following publication in Current Oncology, the full text of each article is available immediately and archived in PubMed Central (PMC).

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concerns3. Further, w hen psychosocial distress is not addressed, the ways that patients w ith cancer and their fam ilies cope w ith the disease is affected. Beyond the direct im pact on patient and family, the cost o f unidentified psychosocial distress is a public health concern. Patients and fam ilies who do not receive the help they need are at risk o f developing chronic m ental health issues that w ill ultim ately require tim e, resources, and financial expenditures from the health care system 4. Psychosocial care should not be considered a luxury— it is a necessity.

2008. [Available online at: http://books.nap.edu/openbook. php?record_id=11993; cited March 26, 2014] 2. Bultz BD, Carlson LE. Emotional distress: the sixth vital sign in cancer care. J Clin Oncol 2005;23:6440-1. 3. Kazak AE, Cant MC, Jensen MM, et al. Identifying psycho­ social risk indicative of subsequent resource use in families of newly diagnosed pediatric oncology patients. J Clin Oncol 2003;21:3220-5. 4. Chiles JA, Lambert MJ, Hatch AL. The impact of psycho­ logical interventions on medical cost offset: a meta-analytic review. Clin Psychol Sci Pract 1999;6:204-220.

T he a u th o r has no fin a n c ia l c o n flic t o f in te re st to declare.

C orrespondence to: Fiona Schulte, A lberta C hil­ dren’s Hospital, 2888 Shaganappi Trail NW, Calgary, A lberta T3B 6A8. E -m ail: fiona.schulte@ albertahealthservices.ca

REFERENCES

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CONFLICT OF INTEREST DISCLOSURES

1. Adler NE, Page AEK. Institute o f Medicine: Cancer Care fo r the Whole Patient: M eeting Psychosocial Health Needs. Washington, DC: The National Academies Press;

D epartm ents o f O ncology and Paediatrics, Uni­ versity o f Calgary; A lberta C hildren’s Hospital Research Institute; and Haem atology, Oncology and T ransplant P rogram , A lb e rta C h ild re n ’s Hospital, Calgary, AB.

I C urrent O ncology— V olume 21, N umber 4, A ugust 2014 | Copyright © 2014 Multimed Inc. Following publication in Current Oncology, the full text of each article is available immediately and archived in PubMed Central (PMC).

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Biologic, psychological, and social health needs in cancer care: how far have we come?

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