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Psychiatric, behavioral, and cognitive disorders in patients with extracranial cancers

Published online by Cambridge University Press:  23 July 2018

Gabriella Pravettoni
Affiliation:
Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy Psycho-Oncology Division, European Institute of Oncology, Milan, Italy
Bernardo Dell’Osso
Affiliation:
Department of Pathophysiology and Transplantation, University of Milan, Milan, Italy Department of Mental Health, Fondazione IRCCS Ca’ Granda Policlinico, Milan, Italy Department of Psychiatry and Behavioral Sciences, Bipolar Disorders Clinic, Stanford University, Stanford, California, USA “Aldo Ravelli” Research Center for Experimental Brain Therapeutics, Department of Health Sciences, University of Milan, Milan, Italy
Tommaso Bocci
Affiliation:
Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy Unit of Clinical Neurophysiology, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, Milan, Italy
Francesca Cortese
Affiliation:
Unit of Clinical Neurophysiology, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, Milan, Italy Department of Medical-Surgical Sciences and Biotechnologies, Sapienza University of Rome, Latina, Italy
Roberta Ferrucci
Affiliation:
Unit of Clinical Neurophysiology, Fondazione IRCCS Ca’ Granda, Ospedale Maggiore Policlinico, Milan, Italy “Aldo Ravelli” Research Center for Experimental Brain Therapeutics, Department of Health Sciences, University of Milan, Milan, Italy
Valentina Lampis
Affiliation:
Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy
Chiara Rosci
Affiliation:
Neurology Section, ASST Santi Paolo e Carlo, Milan, Italy
Alberto Priori*
Affiliation:
“Aldo Ravelli” Research Center for Experimental Brain Therapeutics, Department of Health Sciences, University of Milan, Milan, Italy Neurology Section, ASST Santi Paolo e Carlo, Milan, Italy
*
*Address for correspondence: Prof. Alberto Priori, Clinica Neurologica, Università degli Studi di Milano, Polo Universitario San Paolo, Via A. Di Rudinì 8, 20122 Milano, Italy. (Email: [email protected])

Abstract

Patients with cancer may report neuropsychiatric abnormalities including cognitive impairment, behavioral disturbances, and psychiatric disorders that potentially worsen their quality of life, reduce their treatment response, and aggravate their overall prognosis. Neuropsychiatric disturbances have a different pathophysiology, including immuno-inflammatory and neuroendocrine mechanisms, as a consequence of oncologic treatments (chemo- and radio-therapy). Among clinicians involved in the management of such patients, psychiatrists need to pay particular attention in recognizing behavioral disturbances that arise in oncologic patients, and determining those that may be effectively treated with psychotropic medications, psychotherapeutic interventions, and an integration of them. Through the contribution of different clinicians actively involved in the management of oncological patients, the present review is ultimately aimed at updating psychiatrists in relation to the pathophysiological mechanisms responsible for the onset of cognitive, affective, and behavioral syndromes in these patients, along with epidemiologic and clinical considerations and therapeutic perspectives.

Type
Review
Copyright
© Cambridge University Press 2018 

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References

1. Dantzer, R, O’Connor, JC, Freund, GG, Johnson, RW, Kelley, KW. From inflammation to sickness and depression: when the immune system subjugates the brain. Nat Rev Neurosci. 2008; 9(1): 4656.Google Scholar
2. Lee, BN, Dantzer, R, Langley, KE, et al. A cytokine-based neuroimmunologic mechanism of cancer-related symptoms. Neuroimmunomodulation. 2004; 11(5): 279292.Google Scholar
3. Miller, AH, Ancoli-Israel, S, Bower, JE, Capuron, L, Irwin, MR. Neuroendocrine-immune mechanisms of behavioral comorbidities in patients with cancer. J Clin Oncol. 2008; 26(6): 971982.Google Scholar
4. Dantzer, R. Cytokine-induced sickness behavior: where do we stand? Brain Behav Immun. 2001; 15(1): 724.Google Scholar
5. Bouchard, LC, Antoni, MH, Blomberg, BB, et al. Postsurgical depressive symptoms and proinflammatory cytokine elevations in women undergoing primary treatment for breast cancer. Psychosom Med. 2016; 78(1): 2637.Google Scholar
6. Schaefer, M, Horn, M, Schmidt, F, et al. Correlation between sICAM-1 and depressive symptoms during adjuvant treatment of melanoma with interferon-alpha. Brain Behav Immun. 2004; 18(6): 555562.Google Scholar
7. Capuron, L, Ravaud, A, Neveu, PJ, Miller, AH, Maes, M, Dantzer, R. Association between decreased serum tryptophan concentrations and depressive symptoms in cancer patients undergoing cytokine therapy. Mol Psychiatry. 2002; 7(5): 468473.Google Scholar
8. Wirleitner, B, Neurauter, G, Schrocksnadel, K, Frick, B, Fuchs, D. Interferon-gamma-induced conversion of tryptophan: immunologic and neuropsychiatric aspects. Curr Med Chem. 2003; 10(16): 15811591.Google Scholar
9. Denz, H, Orth, B, Weiss, G, et al. Weight loss in patients with hematological neoplasias is associated with immune system stimulation. Clin Investig. 1993; 71(1): 3741.Google Scholar
10. Huang, A, Fuchs, D, Widner, B, Glover, C, Henderson, DC, Allen-Mersh, TG. Tryptophan and quality of life in colorectal cancer. Adv Exp Med Biol. 2003; 527: 353358.Google Scholar
11. Iwagaki, H, Hizuta, A, Tanaka, N, Orita, K. Decreased serum tryptophan in patients with cancer cachexia correlates with increased serum neopterin. Immunol Invest. 1995; 24(3): 467478.Google Scholar
12. Zuliani, L, Graus, F, Giometto, B, Bien, C, Vincent, A. Central nervous system neuronal surface antibody associated syndromes: review and guidelines for recognition. J Neurol Neurosurg Psychiatry. 2012; 83(6): 638645.Google Scholar
13. Du, Y.J., et al. Sputum interleukin-6, tumor necrosis factor-alpha and Salivary cortisol as new biomarkers of depression in lung cancer patients. Prog Neuropsychopharmacol Biol Psychiatry. 2013; 47: 6976.Google Scholar
14. Botwinick, I.C., et al. A biological basis for depression in pancreatic cancer. HPB (Oxford). 2014; 16(8): 740743.Google Scholar
15. Hufner, K., et al. Levels in neurotransmitter precursor amino acids correlate with mental health in patients with breast cancer. Psychoneuroendocrinology. 2015; 60: 2838.Google Scholar
16. Fukami, Y., et al. [Following sensory neuropathy, anti-Hu antibody-positive paraneoplastic neurological syndrome presenting with limbic encephalitis occurs after complete remission]. Rinsho Shinkeigaku. 2013; 53(4): 287292.Google Scholar
17. Funaguchi, N., et al. [Paraneoplastic neurological syndrome accompanied by severe central hypoventilation and expression of anti-Hu antibody in a patient with small cell lung cancer]. Nihon Kokyuki Gakkai Zasshi. 2008; 46(4): 314318.Google Scholar
18. Gultekin, S.H., et al. Paraneoplastic limbic encephalitis: neurological symptoms, immunological findings and tumour association in 50 patients. Brain. 2000; 123(Pt 7): 14811494.Google Scholar
19. Dalmau, J., et al. Clinical analysis of anti-Ma2-associated encephalitis. Brain. 2004; 127(Pt 8): 18311844.Google Scholar
20. Dogan Onugoren, M., et al. Limbic encephalitis due to GABAB and AMPA receptor antibodies: a case series. J Neurol Neurosurg Psychiatry. 2015; 86(9): 965972.Google Scholar
21. Fras, I., Litin, E.M., Pearson, J.S. Comparison of psychiatric symptoms in carcinoma of the pancreas with those in some other intra-abdominal neoplasms. Am J Psychiatry. 1967; 123(12): 15531562.Google Scholar
22. Ferlay, J., et al. Breast and cervical cancer in 187 countries between 1980 and 2010. Lancet. 2012; 379(9824): 13901391.Google Scholar
23. Bernal, F, Graus, F, Pifarre, A, Saiz, A, Benyahia, B, Ribalta, T. Immunohistochemical analysis of anti-Hu-associated paraneoplastic encephalomyelitis. Acta Neuropathol. 2002; 103(5): 509515.Google Scholar
24. Voltz, R, Dalmau, J, Posner, JB, Rosenfeld, MR. T-cell receptor analysis in anti-Hu associated paraneoplastic encephalomyelitis. Neurology. 1998; 51(4): 11461150.Google Scholar
25. Kayser, MS, Kohler, CG, Dalmau, J. Psychiatric manifestations of paraneoplastic disorders. Am J Psychiatry. 2010; 167(9): 10391050.Google Scholar
26. Irani, SR, Bera, K, Waters, P, et al. N-Methyl-D-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexes. Brain. 2010; 133(Pt 6): 16551667.Google Scholar
27. Dalmau, J, Gleichman, AJ, Hughes, EG, et al. Anti-NMDA-receptor encephalitis: case series and analysis of the effects of antibodies. Lancet Neurol. 2008; 7(12): 10911098.Google Scholar
28. Dalmau, J, Lancaster, E, Martinez-Hernandez, E, Rosenfeld, MR, Balice-Gordon, R. Clinical experience and laboratory investigations in patients with anti-NMDAR encephalitis. Lancet Neurol. 2011; 10(1): 6374.Google Scholar
29. Olney, JW, Farber, NB. Glutamate receptor dysfunction and schizophrenia. Arch Gen Psychiatry. 1995; 52(12): 9981007.Google Scholar
30. Olney, JW, Farber, NB. NMDA antagonists as neurotherapeutic drugs, psychotogens, neurotoxins, and research tools for studying schizophrenia. Neuropsychopharmacology. 1995; 13(4): 335345.Google Scholar
31. Holsboer, F. Corticotropin-releasing hormone modulators and depression. Curr Opin Investig Drugs. 2003; 4(1): 4650.Google Scholar
32. Swaab, DF, Bao, AM, Lucassen, PJ. The stress system in the human brain in depression and neurodegeneration. Ageing Res Rev. 2005; 4(2): 141194.Google Scholar
33. Pace, TW, Hu, F, Miller, AH. Cytokine-effects on glucocorticoid receptor function: relevance to glucocorticoid resistance and the pathophysiology and treatment of major depression. Brain Behav Immun. 2007; 21(1): 919.Google Scholar
34. Raison, CL, Miller, AH. When not enough is too much: the role of insufficient glucocorticoid signaling in the pathophysiology of stress-related disorders. Am J Psychiatry. 2003; 160(9): 15541565.Google Scholar
35. Walker, J, Waters, RA, Murray, G, et al. Better off dead: suicidal thoughts in cancer patients. J Clin Oncol. 2008; 26(29): 47254730.Google Scholar
36. Fras, I, Litin, EM, Pearson, JS. Comparison of psychiatric symptoms in carcinoma of the pancreas with those in some other intra-abdominal neoplasms. Am J Psychiatry. 1967; 123(12): 15531562.Google Scholar
37. Holland, JC. Managing depression in the patient with cancer. CA Cancer J Clin. 1987; 37(6): 366371.Google Scholar
38. Green, AI, Austin, CP. Psychopathology of pancreatic cancer. A psychobiologic probe. Psychosomatics. 1993; 34(3): 208221.Google Scholar
39. Brown, JH, Paraskevas, F. Cancer and depression: cancer presenting with depressive illness: an autoimmune disease? Br J Psychiatry. 1982; 141(3): 227232.Google Scholar
40. Li, R, Hou, J, Xu, Q, et al. High level interleukin-6 in the medium of human pancreatic cancer cell culture suppresses production of neurotransmitters by PC12 cell line. Metab Brain Dis. 2012; 27(1): 91100.Google Scholar
41. Felger, JC, Li, Z, Haroon, E, et al. Inflammation is associated with decreased functional connectivity within corticostriatal reward circuitry in depression. Mol Psychiatry. 2015; 21(10): 13581365.Google Scholar
42. Hampson, JP, Zick, SM, Khabir, T, Wright, BD, Harris, RE. Altered resting brain connectivity in persistent cancer related fatigue. Neuroimage Clin. 2015; 8: 305313.Google Scholar
43. Zick, SM, Zwickey, H, Wood, L, et al. Preliminary differences in peripheral immune markers and brain metabolites between fatigued and non-fatigued breast cancer survivors: a pilot study. Brain Imaging Behav. 2014; 8(4): 506516.Google Scholar
44. Benveniste, H, Zhang, S, Reinsel, RA, et al. Brain metabolomic profiles of lung cancer patients prior to treatment characterized by proton magnetic resonance spectroscopy. Int J Clin Exp Med. 2012; 5(2): 154164.Google Scholar
45. Corsellis, JA, Goldberg, GJ, Norton, AR. “Limbic encephalitis” and its association with carcinoma. Brain. 1968; 91(3): 481496.Google Scholar
46. Lancaster, E. The diagnosis and treatment of autoimmune encephalitis. J Clin Neurol. 2016; 12(1): 113.Google Scholar
47. Restivo, A, Carta, MG, Farci, AM, Saiu, L, Gessa, GL, Agabio, R. Risk of thiamine deficiency and Wernicke’s encephalopathy after gastrointestinal surgery for cancer. Support Care Cancer. 2016; 24(1): 7782.Google Scholar
48. Ahles, TA, Saykin, AJ, Furstenberg, CT, et al. Neuropsychologic impact of standard-dose systemic chemotherapy in long-term survivors of breast cancer and lymphoma. J Clin Oncol. 2002; 20(2): 485493.Google Scholar
49. Brezden, CB, Phillips, KA, Abdolell, M, Bunston, T, Tannock, IF. Cognitive function in breast cancer patients receiving adjuvant chemotherapy. J Clin Oncol. 2000; 18(14): 26952701.Google Scholar
50. Wefel, JS, Lenzi, R, Theriault, R, Buzdar, AU, Cruickshank, S, Meyers, CA. ‘Chemobrain’ in breast carcinoma? a prologue. Cancer. 2004; 101(3): 466475.Google Scholar
51. van Dam, FS, Schagen, SB, Muller, MJ, et al. Impairment of cognitive function in women receiving adjuvant treatment for high-risk breast cancer: high-dose versus standard-dose chemotherapy. J Natl Cancer Inst. 1998; 90(3): 210218.Google Scholar
52. Ahles, TA, Saykin, AJ. Candidate mechanisms for chemotherapy-induced cognitive changes. Nat Rev Cancer. 2007; 7(3): 192201.Google Scholar
53. Koppelmans, V, Breteler, MM, Boogerd, W, Seynaeve, C, Gundy, C, Schagen, SB. Neuropsychological performance in survivors of breast cancer more than 20 years after adjuvant chemotherapy. J Clin Oncol. 2012; 30(10): 10801086.Google Scholar
54. Schagen, SB, Wefel, JS. Chemotherapy-related changes in cognitive functioning. EJC Suppl. 2013; 11(2): 225232.Google Scholar
55. Schagen, SB, Hamburger, HL, Muller, MJ, Boogerd, W, van Dam, FS. Neurophysiological evaluation of late effects of adjuvant high-dose chemotherapy on cognitive function. J Neurooncol. 2001; 51(2): 159165.Google Scholar
56. Jansen, CE, Miaskowski, C, Dodd, M, Dowling, G, Kramer, J. A metaanalysis of studies of the effects of cancer chemotherapy on various domains of cognitive function. Cancer. 2005; 104(10): 22222233.Google Scholar
57. Wefel, JS, Schagen, SB. Chemotherapy-related cognitive dysfunction. Curr Neurol Neurosci Rep. 2012; 12(3): 267275.Google Scholar
58. Jatoi, A, Kahanic, SP, Frytak, S, et al. Donepezil and vitamin E for preventing cognitive dysfunction in small cell lung cancer patients: preliminary results and suggestions for future study designs. Support Care Cancer. 2005; 13(1): 6669.Google Scholar
59. Von, Ah D, Storey, S, Jansen, CE, Allen, DH. Coping strategies and interventions for cognitive changes in patients with cancer. Semin Oncol Nurs. 2014; 29(4): 288299.Google Scholar
60. Ferguson, RJ, Ahles, TA, Saykin, AJ, et al. Cognitive-behavioral management of chemotherapy-related cognitive change. Psychooncology. 2007; 16(8): 772777.Google Scholar
61. Hoffman, CJ, Ersser, SJ, Hopkinson, JB, Nicholls, PG, Harrington, JE, Thomas, PW. Effectiveness of mindfulness-based stress reduction in mood, breast- and endocrine-related quality of life, and well-being in stage 0 to III breast cancer: a randomized, controlled trial. J Clin Oncol. 2012; 30(12): 13351342.Google Scholar
62. Baumann, FT, Bloch, W, Weissen, A, et al. Physical activity in breast cancer patients during medical treatment and in the aftercare—a review. Breast Care (Basel). 2013; 8(5): 330334.Google Scholar
63. Culos-Reed, SN, Carlson, LE, Daroux, LM, Hately-Aldous, S. A pilot study of yoga for breast cancer survivors: physical and psychological benefits. Psychooncology. 2006; 15(10): 891897.Google Scholar
64. Ostuzzi, G, Benda, L, Costa, E, Barbui, C. Efficacy and acceptability of antidepressants on the continuum of depressive experiences in patients with cancer: systematic review and meta-analysis. Cancer Treat Rev. 2015; 41(8): 714724.Google Scholar
65. Mehta, RD, Roth, AJ. Psychiatric considerations in the oncology setting. CA Cancer J Clin. 2015; 65(4): 300314.Google Scholar
66. Mitchell, AJ, Chan, M, Bhatti, H, et al. Prevalence of depression, anxiety, and adjustment disorder in oncological, haematological, and palliative-care settings: a meta-analysis of 94 interview-based studies. Lancet Oncol. 2011; 12(2): 160174.Google Scholar
67. Valente, SM, Saunders, JM, Cohen, MZ. Evaluating depression among patients with cancer. Cancer Pract. 1994; 2(1): 6571.Google Scholar
68. Mitchell, AJ, Ferguson, DW, Gill, J, Paul, J, Symonds, P. Depression and anxiety in long-term cancer survivors compared with spouses and healthy controls: a systematic review and meta-analysis. Lancet Oncol. 2013; 14(8): 721732.Google Scholar
69. Bottomley, A. Depression in cancer patients: a literature review. Eur J Cancer Care (Engl). 1998; 7(3): 181191.Google Scholar
70. Krebber, AM, Buffart, LM, Kleijn, G, et al. Prevalence of depression in cancer patients: a meta-analysis of diagnostic interviews and self-report instruments. Psychooncology. 2014; 23(2): 121130.Google Scholar
71. Derogatis, LR, Morrow, GR, Fetting, J, et al. The prevalence of psychiatric disorders among cancer patients. JAMA. 1983; 249(6): 751757.Google Scholar
72. Robinson, S, Kissane, DW, Brooker, J, Burney, S. A systematic review of the demoralization syndrome in individuals with progressive disease and cancer: a decade of research. J Pain Symptom Manage. 2015; 49(3): 595610.Google Scholar
73. Miller, K, Massie, MJ. Depression and anxiety. Cancer J. 2006; 12(5): 388397.Google Scholar
74. Rustad, JK, David, D, Currier, MB. Cancer and post-traumatic stress disorder: diagnosis, pathogenesis and treatment considerations. Palliat Support Care. 2012; 10(3): 213223.Google Scholar
75. Watts, S, Leydon, G, Birch, B, et al. Depression and anxiety in prostate cancer: a systematic review and meta-analysis of prevalence rates. BMJ Open. 2014; 4(3): e003901.Google Scholar
76. Watts, S, Prescott, P, Mason, J, McLeod, N, Lewith, G. Depression and anxiety in ovarian cancer: a systematic review and meta-analysis of prevalence rates. BMJ Open. 2015; 5(11): e007618.Google Scholar
77. Lydiatt, WM, Moran, J, Burke, WJ. A review of depression in the head and neck cancer patient. Clin Adv Hematol Oncol. 2009; 7(6): 397403.Google Scholar
78. Massie, MJ. Prevalence of depression in patients with cancer. J Natl Cancer Inst Monogr. 2004;(32): 5771.Google Scholar
79. Colleoni, M, Mandala, M, Peruzzotti, G, Robertson, C, Bredart, A, Goldhirsch, A. Depression and degree of acceptance of adjuvant cytotoxic drugs. Lancet. 2000; 356(9238): 13261327.Google Scholar
80. Prieto, JM, Blanch, J, Atala, J, et al. Psychiatric morbidity and impact on hospital length of stay among hematologic cancer patients receiving stem-cell transplantation. J Clin Oncol. 2002; 20(7): 19071917.Google Scholar
81. Anguiano, L, Mayer, DK, Piven, ML, Rosenstein, D. A literature review of suicide in cancer patients. Cancer Nurs. 2012; 35(4): E14E26.Google Scholar
82. Llorente, MD, Burke, M, Gregory, GR, et al. Prostate cancer: a significant risk factor for late-life suicide. Am J Geriatr Psychiatry. 2005; 13(3): 195201.Google Scholar
83. Ryan, H, Schofield, P, Cockburn, J, et al. How to recognize and manage psychological distress in cancer patients. Eur J Cancer Care (Engl). 2005; 14(1): 715.Google Scholar
84. Stagno, D, Stiefel, F, Rousselle, I, Guex, P. [Diagnosis and treatment of depression in patients with cancer]. Rev Med Suisse. 2005; 1(5): 350353.Google Scholar
85. Ramasubbu, R, Taylor, VH, Samaan, Z, et al. The Canadian Network for Mood and Anxiety Treatments (CANMAT) task force recommendations for the management of patients with mood disorders and select comorbid medical conditions. Ann Clin Psychiatry. 2012; 24(1): 91109.Google Scholar
86. Rayner, L, Price, A, Hotopf, M, Higginson, IJ. The development of evidence-based European guidelines on the management of depression in palliative cancer care. Eur J Cancer. 2011; 47(5): 702712.Google Scholar
87. De Fazio, P, Barberi, A, Caglioti, F, Pierfrancesco, T, Piersandro, T, Segura-Garcia, C. Mental adjustment to cancer: the role of anxious and depressive symptoms under treatment. Int J Psychiatry Med. 2013; 46(4): 375386.Google Scholar
88. Fisch, MJ, Loehrer, PJ, Kristeller, J, et al. Fluoxetine versus placebo in advanced cancer outpatients: a double-blinded trial of the Hoosier Oncology Group. J Clin Oncol. 2003; 21(10): 19371943.Google Scholar
89. Holland, JC, Romano, SJ, Heiligenstein, JH, Tepner, RG, Wilson, MG. A controlled trial of fluoxetine and desipramine in depressed women with advanced cancer. Psychooncology. 1998; 7(4): 291300.Google Scholar
90. Thekdi, SM, Trinidad, A, Roth, A. Psychopharmacology in cancer. Curr Psychiatry Rep. 2015; 17(1): 529.Google Scholar
91. Kim, SW, Shin, IS, Kim, JM, et al. Effectiveness of mirtazapine for nausea and insomnia in cancer patients with depression. Psychiatry Clin Neurosci. 2008; 62(1): 7583.Google Scholar
92. Moss, EL, Simpson, JS, Pelletier, G, Forsyth, P. An open-label study of the effects of bupropion SR on fatigue, depression and quality of life of mixed-site cancer patients and their partners. Psychooncology. 2006; 15(3): 259267.Google Scholar
93. Minton, O, Richardson, A, Sharpe, M, Hotopf, M, Stone, P. Drug therapy for the management of cancer-related fatigue. Cochrane Database Syst Rev. 2010;(7): CD006704.Google Scholar
94. Grassi, L, Caruso, R, Hammelef, K, Nanni, MG, Riba, M. Efficacy and safety of pharmacotherapy in cancer-related psychiatric disorders across the trajectory of cancer care: a review. Int Rev Psychiatry. 2014; 26(1): 4462.Google Scholar
95. Saarto, T, Wiffen, PJ. Antidepressants for neuropathic pain. Cochrane Database Syst Rev. 2007;(4): CD005454.Google Scholar
96. Smith, EM, Pang, H, Cirrincione, C, et al. Effect of duloxetine on pain, function, and quality of life among patients with chemotherapy-induced painful peripheral neuropathy: a randomized clinical trial. JAMA. 2013; 309(13): 13591367.Google Scholar
97. Kroenke, K, Theobald, D, Wu, J, Loza, JK, Carpenter, JS, Tu, W. The association of depression and pain with health-related quality of life, disability, and health care use in cancer patients. J Pain Symptom Manage. 2010; 40(3): 327341.Google Scholar
98. Reutfors, J, Wingard, L, Brandt, L, et al. Risk of breast cancer in risperidone users: a nationwide cohort study. Schizophr Res. 2017; 182: 98103.Google Scholar
99. Froes Brandao, D, Strasser-Weippl, K, Goss, PE. Prolactin and breast cancer: the need to avoid undertreatment of serious psychiatric illnesses in breast cancer patients: a review. Cancer. 2016; 122(2): 184188.Google Scholar
100. Gaston, C, Kolesar, J. Clinical significance of CYP2D6 polymorphisms and tamoxifen in women with breast cancer. Clin Adv Hematol Oncol. 2008; 6(11): 825833.Google Scholar
101. Nevels, RM, Gontkovsky, ST, Williams, BE. Paroxetine—the antidepressant from hell? Probably not, but caution required. Psychopharmacol Bull. 2016; 46(1): 77104.Google Scholar
102. Thangathurai, D, Roby, J, Roffey, P. Treatment of resistant depression in patients with cancer with low doses of ketamine and desipramine. J Palliat Med. 2010; 13(3): 235.Google Scholar
103. Zanicotti, CG, Perez, D, Glue, P. Mood and pain responses to repeat dose intramuscular ketamine in a depressed patient with advanced cancer. J Palliat Med. 2012; 15(4): 400403.Google Scholar
104. Fan, W, Yang, H, Sun, Y, et al. Ketamine rapidly relieves acute suicidal ideation in cancer patients: a randomized controlled clinical trial. Oncotarget. 2017; 8(2): 23562360.Google Scholar
105. Schagen, SB, van Dam, FS, Muller, MJ, Boogerd, W, Lindeboom, J, Bruning, PF. Cognitive deficits after postoperative adjuvant chemotherapy for breast carcinoma. Cancer. 1999; 85(3): 640650.Google Scholar
106. Tchen, N, Juffs, HG, Downie, FP, et al. Cognitive function, fatigue, and menopausal symptoms in women receiving adjuvant chemotherapy for breast cancer. J Clin Oncol. 2003; 21(22): 41754183.Google Scholar
107. Ahles, TA, Root, JC, Ryan, EL. Cancer- and cancer treatment-associated cognitive change: an update on the state of the science. J Clin Oncol. 2012; 30(30): 36753686.Google Scholar
108. O’Farrell, E, MacKenzie, J, Collins, B. Clearing the air: a review of our current understanding of “chemo fog.”. Curr Oncol Rep. 2013; 15(3): 260269.Google Scholar
109. Thomas, SA, Tomeh, N, Theard, S. Fluorouracil-induced hyperammonemia in a patient with colorectal cancer. Anticancer Res. 2015; 35(12): 67616763.Google Scholar
110. Kagawa, Y, Kato, T, Naito, A, et al. [A case of consciousness disturbance caused by hyperammonemia during a mFOLFOX6 regimen for metastatic colon cancer]. Gan To Kagaku Ryoho. 2015; 42(12): 21602162.Google Scholar
111. Loblaw, DA, Virgo, KS, Nam, R, et al. Initial hormonal management of androgen-sensitive metastatic, recurrent, or progressive prostate cancer: 2006 update of an American Society of Clinical Oncology practice guideline. J Clin Oncol. 2007; 25(12): 15961605.Google Scholar
112. Miyamoto, H, Rahman, MM, Chang, C. Molecular basis for the antiandrogen withdrawal syndrome. J Cell Biochem. 2004; 91(1): 312.Google Scholar
113. Bussiere, JR, Beer, TM, Neiss, MB, Janowsky, JS. Androgen deprivation impairs memory in older men. Behav Neurosci. 2005; 119(6): 14291437.Google Scholar
114. Cherrier, MM, Rose, AL, Higano, C. The effects of combined androgen blockade on cognitive function during the first cycle of intermittent androgen suppression in patients with prostate cancer. J Urol. 2003; 170(5): 18081811.Google Scholar
115. Salminen, EK, Portin, RI, Koskinen, A, Helenius, H, Nurmi, M. Associations between serum testosterone fall and cognitive function in prostate cancer patients. Clin Cancer Res. 2004; 10(22): 75757582.Google Scholar
116. Wefel, JS, Lenzi, R, Theriault, RL, Davis, RN, Meyers, CA. The cognitive sequelae of standard-dose adjuvant chemotherapy in women with breast carcinoma: results of a prospective, randomized, longitudinal trial. Cancer. 2004; 100(11): 22922299.Google Scholar
117. Hurria, A., et al. Effect of adjuvant breast cancer chemotherapy on cognitive function from the older patient's perspective. Breast Cancer Res Treat. 2006; 98(3): 343348.Google Scholar
118. Schagen, S.B., et al. Change in cognitive function after chemotherapy: a prospective longitudinal study in breast cancer patients. J Natl Cancer Inst. 2006; 98(23): 17421745.Google Scholar
119. Ahles, T.A., et al. Longitudinal assessment of cognitive changes associated with adjuvant treatment for breast cancer: impact of age and cognitive reserve. J Clin Oncol. 2010; 28(29): 44344440.Google Scholar
120. Paulino, A.C., et al. Long-term effects in children treated with radiotherapy for head and neck rhabdomyosarcoma. Int J Radiat Oncol Biol Phys. 2000; 48(5): 14891495.Google Scholar
121. Jim, H.S., et al. Cognitive functioning in breast cancer survivors: a controlled comparison. Cancer. 2009; 115(8): 17761783.Google Scholar
122. Phillips, K.M., et al. Cognitive functioning after cancer treatment: a 3-year longitudinal comparison of breast cancer survivors treated with chemotherapy or radiation and noncancer controls. Cancer. 2012; 118(7): 19251932.Google Scholar
123. Shibayama, O., et al. Association between adjuvant regional radiotherapy and cognitive function in breast cancer patients treated with conservation therapy. Cancer Med. 2014; 3(3): 702709.Google Scholar
124. Ernst, T, Chang, L, Cooray, D, et al. The effects of tamoxifen and estrogen on brain metabolism in elderly women. J Natl Cancer Inst. 2002; 94(8): 592597.Google Scholar
125. Eberling, JL, Wu, C, Tong-Turnbeaugh, R, Jagust, WJ. Estrogen- and tamoxifen-associated effects on brain structure and function. Neuroimage. 2004; 21(1): 364371.Google Scholar
126. Abayomi, OK. Pathogenesis of cognitive decline following therapeutic irradiation for head and neck tumors. Acta Oncol. 2002; 41(4): 346351.Google Scholar
127. Smedler, AC, Bolme, P. Neuropsychological deficits in very young bone marrow transplant recipients. Acta Paediatr. 1995; 84(4): 429433.Google Scholar
128. Geinitz, H, Zimmermann, FB, Stoll, P, et al. Fatigue, serum cytokine levels, and blood cell counts during radiotherapy of patients with breast cancer. Int J Radiat Oncol Biol Phys. 2001; 51(3): 691698.Google Scholar
129. Quesnel, C, Savard, J, Ivers, H. Cognitive impairments associated with breast cancer treatments: results from a longitudinal study. Breast Cancer Res Treat. 2009; 116(1): 113123.Google Scholar
130. Alcorso, J, Sherman, KA, Koelmeyer, L, Mackie, H, Boyages, J. Psychosocial factors associated with adherence for self-management behaviors in women with breast cancer-related lymphedema. Support Care Cancer. 2016; 24(1): 139146.Google Scholar
131. Kanani, R, Davies, EA, Hanchett, N, Jack, RH. The association of mood disorders with breast cancer survival: an investigation of linked cancer registration and hospital admission data for South East England. Psychooncology. 2016; 25(1): 1927.Google Scholar
132. Moynihan, JA, Ader, R. Psychoneuroimmunology: animal models of disease. Psychosom Med. 1996; 58(6): 546558.Google Scholar
133. Renzi, C, Vadilonga, V, Gandini, S, et al. Stress exposure in significant relationships is associated with lymph node status in breast cancer. PLoS One. 2016; 11(2): e0149443.Google Scholar
134. Ader, R, Cohen, N, Felten, D. Psychoneuroimmunology: interactions between the nervous system and the immune system. Lancet. 1995; 345(8942): 99103.Google Scholar
135. Reiche, EM, Nunes, SO, Morimoto, HK. Stress, depression, the immune system, and cancer. Lancet Oncol. 2004; 5(10): 617625.Google Scholar
136. O’Leary, A. Stress, emotion, and human immune function. Psychol Bull. 1990; 108(3): 363382.Google Scholar
137. Segerstrom, SC, Miller, GE. Psychological stress and the human immune system: a meta-analytic study of 30 years of inquiry. Psychol Bull. 2004; 130(4): 601630.Google Scholar
138. McGregor, BA, Antoni, MH. Psychological intervention and health outcomes among women treated for breast cancer: a review of stress pathways and biological mediators. Brain Behav Immun. 2009; 23(2): 159166.Google Scholar
139. Cruess, DG, Antoni, MH, McGregor, BA, et al. Cognitive-behavioral stress management reduces serum cortisol by enhancing benefit finding among women being treated for early stage breast cancer. Psychosom Med. 2000; 62(3): 304308.Google Scholar
140. Andersen, BL, Yang, HC, Farrar, WB, et al. Psychologic intervention improves survival for breast cancer patients: a randomized clinical trial. Cancer. 2008; 113(12): 34503458.Google Scholar
141. Cohen, M, Numa, M. Posttraumatic growth in breast cancer survivors: a comparison of volunteers and non-volunteers. Psychooncology. 2011; 20(1): 6976.Google Scholar
142. Gotay, CC, Ransom, S, Pagano, IS. Quality of life in survivors of multiple primary cancers compared with cancer survivor controls. Cancer. 2007; 110(9): 21012109.Google Scholar
143. Fioretti, C, Smorti, A. Narrating positive versus negative memories of illness: does narrating influence the emotional tone of memories? Eur J Cancer Care (Engl). 2017 May; 26(3): e12524.Google Scholar
144. Romundstad, S, Svebak, S, Holen, A, Holmen, J. A 15-year follow-up study of sense of humor and causes of mortality: the Nord-Trondelag Health Study. Psychosom Med. 2016; 78(3): 345353.Google Scholar
145. Lutgendorf, SK, Sood, AK. Biobehavioral factors and cancer progression: physiological pathways and mechanisms. Psychosom Med. 2011; 73(9): 724730.Google Scholar
146. Schwarz, N. Emotion, cognition, and decision making. Cognition & Emotion. 2000; 14(4): 433440.Google Scholar
147. Segerstrom, SC. Individual differences, immunity, and cancer: lessons from personality psychology. Brain Behav Immun. 2003; 17(Suppl 1): S92S97.Google Scholar
148. Pirl, WF, Roth, AJ. Diagnosis and treatment of depression in cancer patients. Oncology (Williston Park). 1999; 13(9): 12931301; discussion 1301–1302, 1305–1306.Google Scholar
149. Orom, H, Homish, DL, Homish, GG, Underwood, W 3rd. Quality of physician-patient relationships is associated with the influence of physician treatment recommendations among patients with prostate cancer who chose active surveillance. Urol Oncol. 2015; 32(4): 396402.Google Scholar
150. Renzi, C, Riva, S, Masiero, M, Pravettoni, G. The choice dilemma in chronic hematological conditions: why choosing is not only a medical issue? A psycho-cognitive perspective. Crit Rev Oncol Hematol. 2015; 99: 134140.Google Scholar
151. Pravettoni, G, Mazzocco, K, Gorini, A, Curigliano, G. Understanding cognitive processes behind acceptance or refusal of phase I trials. Crit Rev Oncol Hematol. 2016; 100: 6973.Google Scholar