Colorectal Cancer in Elderly Patients with Surgical Indication: State of the Art, Current Management, Role of Frailty and Benefits of a Geriatric Liaison
Abstract
:Highlights
- (1)
- Individualizing interventions in the colorectal cancer elderly population undergoing elective surgery could boost the benefits of fast-track pathways (as ERAS program), which may be gained by CGA-guided care and a geriatric liaison or co-management.
- (2)
- CGA should be the first step towards a multidisciplinary network which would give the patient access to a personalized pre-habilitation and rehabilitation program.
1. Background
1.1. Epidemiology
1.2. Risk Factors
1.3. Screening for Colorectal Cancer
1.4. Colorectal Cancer Management
2. Characteristics of Elderly Colorectal Cancer Population That Undergo Surgery
2.1. General Colorectal Cancer Characteristics
2.1.1. Disease Presentation
2.1.2. Complications and Post-Surgical Survival
2.2. Geriatric Syndromes
2.2.1. Functional Dependency
2.2.2. Frailty
2.2.3. Cognitive Impairment and Mental Health
2.2.4. Malnutrition and Social Support
3. Multidisciplinary Team and Comprehensive Interventions in Colorectal Cancer Patients
3.1. Benefits of a Geriatrics Liaison
3.2. Benefits of Exercise Programs
3.3. Benefits of Psychotherapeutic Interventions
4. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Conflicts of Interest
References
- Howlader, N.; Noone, A.; Krapcho, M.; Garshell, J.; Miller, D.; Altekruse, S.; Kosary, C.; Yu, M.; Ruhl, J.; Tatalovich, Z.; et al. SEER Cancer Statistics Review, 1975–2018; National Cancer Institute: Bethesda, MD, USA, 2020. Available online: https://seer.cancer.gov/csr/1975_2017/ (accessed on 30 January 2021).
- Arnold, M.; Sierra, M.S.; Laversanne, M.; Soerjomataram, I.; Jemal, A.; Bray, F. Global patterns and trends in colorectal cancer incidence and mortality. Gut 2017, 66, 683–691. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Ouakrim, D.A.; Pizot, C.; Boniol, M.; Malvezzi, M.; Boniol, M.; Negri, E.; Bota, M.; Jenkins, M.A.; Bleiberg, H.; Autier, P.J.B. Trends in colorectal cancer mortality in Europe: Retrospective analysis of the WHO mortality database. BMJ 2015, 351:h4970. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Bray, F.; Ferlay, J.; Soerjomataram, I.; Siegel, R.L.; Torre, L.A.; Jemal, A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J. Clin. 2018, 68, 394–424. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Dekker, E.; Tanis, P.J.; Vleugels, J.L.A.; Kasi, P.M.; Wallace, M.B. Colorectal cancer. Lancet 2019, 394, 1467–1480. [Google Scholar] [CrossRef]
- Bosman, F.T.; Carneiro, F.; Hruban, R.H.; Theise, N.D. WHO Classification of Tumours of the Digestive System, 4th ed.; World Health Organization, International Agency for Research on Cancer: Geneva, Switzerland, 2010. [Google Scholar]
- Henrikson, N.B.; Webber, E.M.; Goddard, K.A.; Scrol, A.; Piper, M.; Williams, M.S.; Zallen, D.T.; Calonge, N.; Ganiats, T.G.; Janssens, A.C.; et al. Family history and the natural history of colorectal cancer: Systematic review. Genet. Med. Off. J. Am. Coll. Med Genet. 2015, 17, 702–712. [Google Scholar] [CrossRef] [Green Version]
- Siegel, R.L.; Miller, K.D.; Goding Sauer, A.; Fedewa, S.A.; Butterly, L.F.; Anderson, J.C.; Cercek, A.; Smith, R.A.; Jemal, A. Colorectal cancer statistics, 2020. CA Cancer J. Clin. 2020, 70, 145–164. [Google Scholar] [CrossRef] [Green Version]
- Wolf, A.M.D.; Fontham, E.T.H.; Church, T.R.; Flowers, C.R.; Guerra, C.E.; LaMonte, S.J.; Etzioni, R.; McKenna, M.T.; Oeffinger, K.C.; Shih, Y.T.; et al. Colorectal cancer screening for average-risk adults: 2018 guideline update from the American Cancer Society. CA Cancer J. Clin. 2018, 68, 250–281. [Google Scholar] [CrossRef]
- Labianca, R.; Nordlinger, B.; Beretta, G.D.; Mosconi, S.; Mandala, M.; Cervantes, A.; Arnold, D.; Group, E.G.W. Early colon cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 2013, 24 (Suppl. 6), vi64–vi72. [Google Scholar] [CrossRef]
- Jafari, M.D.; Jafari, F.; Halabi, W.J.; Nguyen, V.Q.; Pigazzi, A.; Carmichael, J.C.; Mills, S.D.; Stamos, M.J. Colorectal Cancer Resections in the Aging US Population: A Trend Toward Decreasing Rates and Improved Outcomes. JAMA Surg. 2014, 149, 557–564. [Google Scholar] [CrossRef] [Green Version]
- Papamichael, D.; Audisio, R.A.; Glimelius, B.; de Gramont, A.; Glynne-Jones, R.; Haller, D.; Kohne, C.H.; Rostoft, S.; Lemmens, V.; Mitry, E.; et al. Treatment of colorectal cancer in older patients: International Society of Geriatric Oncology (SIOG) consensus recommendations 2013. Ann. Oncol. 2013, 26, 463–476. [Google Scholar] [CrossRef]
- Simon, K. Colorectal cancer development and advances in screening. Clin. Interv. Aging 2016, 11, 967–976. [Google Scholar] [CrossRef] [Green Version]
- Moreno, C.C.; Mittal, P.K.; Sullivan, P.S.; Rutherford, R.; Staley, C.A.; Cardona, K.; Hawk, N.N.; Dixon, W.T.; Kitajima, H.D.; Kang, J.; et al. Colorectal Cancer Initial Diagnosis: Screening Colonoscopy, Diagnostic Colonoscopy, or Emergent Surgery, and Tumor Stage and Size at Initial Presentation. Clin. Colorectal Cancer 2016, 15, 67–73. [Google Scholar] [CrossRef]
- Force, U.P.S.T. Screening for Colorectal Cancer: US Preventive Services Task Force Recommendation Statement. JAMA 2016, 315, 2564–2575. [Google Scholar] [CrossRef]
- Rex, D.K.; Boland, C.R.; Dominitz, J.A.; Giardiello, F.M.; Johnson, D.A.; Kaltenbach, T.; Levin, T.R.; Lieberman, D.; Robertson, D.J. Colorectal Cancer Screening: Recommendations for Physicians and Patients from the U.S. Multi-Society Task Force on Colorectal Cancer. Am. J. Gastroenterol. 2017, 112, 1016–1030. [Google Scholar] [CrossRef]
- van Hees, F.; Habbema, J.D.; Meester, R.G.; Lansdorp-Vogelaar, I.; van Ballegooijen, M.; Zauber, A.G. Should colorectal cancer screening be considered in elderly persons without previous screening? A cost-effectiveness analysis. Ann. Intern. Med. 2014, 160, 750–759. [Google Scholar] [CrossRef]
- van Leeuwen, B.L.; Pahlman, L.; Gunnarsson, U.; Sjovall, A.; Martling, A. The effect of age and gender on outcome after treatment for colon carcinoma. A population-based study in the Uppsala and Stockholm region. Crit. Rev. Oncol. Hematol. 2008, 67, 229–236. [Google Scholar] [CrossRef] [PubMed]
- Colorectal Cancer Collaborative Group. Surgery for colorectal cancer in elderly patients: A systematic review. Lancet 2000, 356, 968–974. [Google Scholar] [CrossRef]
- Sell, N.M.; Qwaider, Y.Z.; Goldstone, R.N.; Stafford, C.E.; Cauley, C.E.; Francone, T.D.; Ricciardi, R.; Bordeianou, L.G.; Berger, D.L.; Kunitake, H. Octogenarians present with a less aggressive phenotype of colon adenocarcinoma. Surgery 2020, 168, 1138–1143. [Google Scholar] [CrossRef]
- Serra-Rexach, J.A.; Jimenez, A.B.; Garcia-Alhambra, M.A.; Pla, R.; Vidan, M.; Rodriguez, P.; Ortiz, J.; Garcia-Alfonso, P.; Martin, M. Differences in the therapeutic approach to colorectal cancer in young and elderly patients. Oncologist 2012, 17, 1277–1285. [Google Scholar] [CrossRef] [Green Version]
- Townsley, C.A.; Selby, R.; Siu, L.L. Systematic review of barriers to the recruitment of older patients with cancer onto clinical trials. J. Clin. Oncol. Off. J. Am. Soc. Clin. Oncol. 2005, 23, 3112–3124. [Google Scholar] [CrossRef]
- Pallis, A.G.; Papamichael, D.; Audisio, R.; Peeters, M.; Folprecht, G.; Lacombe, D.; Van Cutsem, E. EORTC Elderly Task Force experts’ opinion for the treatment of colon cancer in older patients. Cancer Treat. Rev. 2010, 36, 83–90. [Google Scholar] [CrossRef] [PubMed]
- Abraham, N.S.; Young, J.M.; Solomon, M.J. Meta-analysis of short-term outcomes after laparoscopic resection for colorectal cancer. Br. J. Surg. 2004, 91, 1111–1124. [Google Scholar] [CrossRef] [PubMed]
- Braga, M.; Vignali, A.; Gianotti, L.; Zuliani, W.; Radaelli, G.; Gruarin, P.; Dellabona, P.; Di Carlo, V. Laparoscopic versus open colorectal surgery: A randomized trial on short-term outcome. Ann. Surg. 2002, 236, 759–766. [Google Scholar] [CrossRef]
- Lacy, A.M.; Garcia-Valdecasas, J.C.; Delgado, S.; Castells, A.; Taura, P.; Pique, J.M.; Visa, J. Laparoscopy-assisted colectomy versus open colectomy for treatment of non-metastatic colon cancer: A randomised trial. Lancet 2002, 359, 2224–2229. [Google Scholar] [CrossRef]
- Fujii, S.; Tsukamoto, M.; Fukushima, Y.; Shimada, R.; Okamoto, K.; Tsuchiya, T.; Nozawa, K.; Matsuda, K.; Hashiguchi, Y. Systematic review of laparoscopic vs open surgery for colorectal cancer in elderly patients. World J. Gastrointest. Oncol. 2016, 8, 573–582. [Google Scholar] [CrossRef]
- Hinoi, T.; Kawaguchi, Y.; Hattori, M.; Okajima, M.; Ohdan, H.; Yamamoto, S.; Hasegawa, H.; Horie, H.; Murata, K.; Yamaguchi, S.; et al. Laparoscopic versus open surgery for colorectal cancer in elderly patients: A multicenter matched case-control study. Ann. Surg. Oncol. 2015, 22, 2040–2050. [Google Scholar] [CrossRef]
- Kannan, U.; Reddy, V.S.; Mukerji, A.N.; Parithivel, V.S.; Shah, A.K.; Gilchrist, B.F.; Farkas, D.T. Laparoscopic vs open partial colectomy in elderly patients: Insights from the American College of Surgeons-National Surgical Quality Improvement Program database. World J. Gastroenterol. 2015, 21, 12843–12850. [Google Scholar] [CrossRef]
- Bircan, H.Y.; Koc, B.; Ozcelik, U.; Adas, G.; Karahan, S.; Demirag, A. Are there any differences between age groups regarding colorectal surgery in elderly patients? BMC Surg. 2014, 14, 44. [Google Scholar] [CrossRef] [Green Version]
- Grosso, G.; Biondi, A.; Marventano, S.; Mistretta, A.; Calabrese, G.; Basile, F. Major postoperative complications and survival for colon cancer elderly patients. BMC Surg. 2012, 12 (Suppl 1), S20. [Google Scholar] [CrossRef] [Green Version]
- Marusch, F.; Koch, A.; Schmidt, U.; Steinert, R.; Ueberrueck, T.; Bittner, R.; Berg, E.; Engemann, R.; Gellert, K.; Arbogast, R.; et al. The impact of the risk factor “age” on the early postoperative results of surgery for colorectal carcinoma and its significance for perioperative management. World J. Surg. 2005, 29, 1013–1021; discussion 1021–1012. [Google Scholar] [CrossRef]
- Kunitake, H.; Zingmond, D.S.; Ryoo, J.; Ko, C.Y. Caring for octogenarian and nonagenarian patients with colorectal cancer: What should our standards and expectations be? Dis. Colon Rectum 2010, 53, 735–743. [Google Scholar] [CrossRef]
- Engel, A.F.; Oomen, J.L.; Knol, D.L.; Cuesta, M.A. Operative mortality after colorectal resection in the Netherlands. Br. J. Surg. 2005, 92, 1526–1532. [Google Scholar] [CrossRef]
- Faiz, O.; Haji, A.; Bottle, A.; Clark, S.K.; Darzi, A.W.; Aylin, P. Elective colonic surgery for cancer in the elderly: An investigation into postoperative mortality in English NHS hospitals between 1996 and 2007. Colorectal Dis. Off. J. Assoc. Coloproctol. Great Br. Irel. 2011, 13, 779–785. [Google Scholar] [CrossRef]
- Dekker, J.W.; Gooiker, G.A.; Bastiaannet, E.; van den Broek, C.B.; van der Geest, L.G.; van de Velde, C.J.; Tollenaar, R.A.; Liefers, G.J.; Steering Committee of the ‘Quality Information System Colorectal Cancer’ Project. Cause of death the first year after curative colorectal cancer surgery; a prolonged impact of the surgery in elderly colorectal cancer patients. Eur. J. Surg. Oncol. J. Eur. Soc. Surg. Oncol. Br. Assoc. Surg. Oncol. 2014, 40, 1481–1487. [Google Scholar] [CrossRef]
- Dekker, J.W.; van den Broek, C.B.; Bastiaannet, E.; van de Geest, L.G.; Tollenaar, R.A.; Liefers, G.J. Importance of the first postoperative year in the prognosis of elderly colorectal cancer patients. Ann. Surg. Oncol. 2011, 18, 1533–1539. [Google Scholar] [CrossRef] [Green Version]
- Magnuson, A.; Sattar, S.; Nightingale, G.; Saracino, R.; Skonecki, E.; Trevino, K.M. A Practical Guide to Geriatric Syndromes in Older Adults With Cancer: A Focus on Falls, Cognition, Polypharmacy, and Depression. Am. Soc. Clin. Oncol. Educ. Book. Am. Soc. Clin. Oncology. Annu. Meet. 2019, 39, e96–e109. [Google Scholar] [CrossRef]
- Reuben, D.B.; Rubenstein, L.V.; Hirsch, S.H.; Hays, R.D. Value of functional status as a predictor of mortality: Results of a prospective study. Am. J. Med. 1992, 93, 663–669. [Google Scholar] [CrossRef]
- Wedding, U.; Rohrig, B.; Klippstein, A.; Pientka, L.; Hoffken, K. Age, severe comorbidity and functional impairment independently contribute to poor survival in cancer patients. J. Cancer Res. Clin. Oncol. 2007, 133, 945–950. [Google Scholar] [CrossRef]
- Hamaker, M.E.; Prins, M.C.; Schiphorst, A.H.; van Tuyl, S.A.; Pronk, A.; van den Bos, F. Long-term changes in physical capacity after colorectal cancer treatment. J. Geriatr. Oncol. 2015, 6, 153–164. [Google Scholar] [CrossRef]
- Ronning, B.; Wyller, T.B.; Jordhoy, M.S.; Nesbakken, A.; Bakka, A.; Seljeflot, I.; Kristjansson, S.R. Frailty indicators and functional status in older patients after colorectal cancer surgery. J. Geriatr. Oncol. 2014, 5, 26–32. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Clegg, A.; Young, J.; Iliffe, S.; Rikkert, M.O.; Rockwood, K. Frailty in elderly people. Lancet 2013, 381, 752–762. [Google Scholar] [CrossRef] [Green Version]
- Hoogendijk, E.O.; Afilalo, J.; Ensrud, K.E.; Kowal, P.; Onder, G.; Fried, L.P. Frailty: Implications for clinical practice and public health. Lancet 2019, 394, 1365–1375. [Google Scholar] [CrossRef]
- Fried, L.P.; Tangen, C.M.; Walston, J.; Newman, A.B.; Hirsch, C.; Gottdiener, J.; Seeman, T.; Tracy, R.; Kop, W.J.; Burke, G.; et al. Frailty in older adults: Evidence for a phenotype. J. gerontology. Ser. A Biol. Sci. Med Sci. 2001, 56, M146–M156. [Google Scholar] [CrossRef] [PubMed]
- Rockwood, K.; Song, X.; MacKnight, C.; Bergman, H.; Hogan, D.B.; McDowell, I.; Mitnitski, A. A global clinical measure of fitness and frailty in elderly people. CMAJ Can. Med Assoc. J. 2005, 173, 489–495. [Google Scholar] [CrossRef] [Green Version]
- Collard, R.M.; Boter, H.; Schoevers, R.A.; Oude Voshaar, R.C. Prevalence of frailty in community-dwelling older persons: A systematic review. J. Am. Geriatr. Soc. 2012, 60, 1487–1492. [Google Scholar] [CrossRef]
- Mohile, S.G.; Dale, W.; Somerfield, M.R.; Schonberg, M.A.; Boyd, C.M.; Burhenn, P.S.; Canin, B.; Cohen, H.J.; Holmes, H.M.; Hopkins, J.O.; et al. Practical Assessment and Management of Vulnerabilities in Older Patients Receiving Chemotherapy: ASCO Guideline for Geriatric Oncology. J. Clin. Oncol. Off. J. Am. Soc. Clin. Oncol. 2018, 36, 2326–2347. [Google Scholar] [CrossRef]
- Morley, J.E.; Vellas, B.; van Kan, G.A.; Anker, S.D.; Bauer, J.M.; Bernabei, R.; Cesari, M.; Chumlea, W.C.; Doehner, W.; Evans, J.; et al. Frailty consensus: A call to action. J. Am. Med Dir. Assoc. 2013, 14, 392–397. [Google Scholar] [CrossRef] [Green Version]
- Extermann, M.; Aapro, M.; Bernabei, R.; Cohen, H.J.; Droz, J.P.; Lichtman, S.; Mor, V.; Monfardini, S.; Repetto, L.; Sorbye, L.; et al. Use of comprehensive geriatric assessment in older cancer patients: Recommendations from the task force on CGA of the International Society of Geriatric Oncology (SIOG). Crit. Rev. Oncol. Hematol. 2005, 55, 241–252. [Google Scholar] [CrossRef]
- Balducci, L.; Extermann, M. Management of cancer in the older person: A practical approach. Oncologist 2000, 5, 224–237. [Google Scholar] [CrossRef]
- Saliba, D.; Elliott, M.; Rubenstein, L.Z.; Solomon, D.H.; Young, R.T.; Kamberg, C.J.; Roth, C.; MacLean, C.H.; Shekelle, P.G.; Sloss, E.M.; et al. The Vulnerable Elders Survey: A tool for identifying vulnerable older people in the community. J. Am. Geriatr. Soc. 2001, 49, 1691–1699. [Google Scholar] [CrossRef] [Green Version]
- Bellera, C.A.; Rainfray, M.; Mathoulin-Pelissier, S.; Mertens, C.; Delva, F.; Fonck, M.; Soubeyran, P.L. Screening older cancer patients: First evaluation of the G-8 geriatric screening tool. Ann. Oncol. 2012, 23, 2166–2172. [Google Scholar] [CrossRef]
- Fagard, K.; Leonard, S.; Deschodt, M.; Devriendt, E.; Wolthuis, A.; Prenen, H.; Flamaing, J.; Milisen, K.; Wildiers, H.; Kenis, C. The impact of frailty on postoperative outcomes in individuals aged 65 and over undergoing elective surgery for colorectal cancer: A systematic review. J. Geriatr. Oncol. 2016, 7, 479–491. [Google Scholar] [CrossRef]
- Sáez-López, P.; Filipovich Vegas, E.; Martinez Peromingo, J.; Jimenez Mola, S. Colorectal cancer in the elderly. Surgical treatment, chemotherapy, and contribution from geriatrics. Rev. Esp. De Geriatr. Y Gerontol. 2017, 52, 261–270. (In Spanish) [Google Scholar] [CrossRef]
- Robinson, T.N.; Walston, J.D.; Brummel, N.E.; Deiner, S.; Brown, C.H., IV; Kennedy, M.; Hurria, A. Frailty for Surgeons: Review of a National Institute on Aging Conference on Frailty for Specialists. J. Am. Coll. Surg. 2015, 221, 1083–1092. [Google Scholar] [CrossRef] [Green Version]
- Gupta, S.K.; Lamont, E.B. Patterns of presentation, diagnosis, and treatment in older patients with colon cancer and comorbid dementia. J. Am. Geriatr. Soc. 2004, 52, 1681–1687. [Google Scholar] [CrossRef]
- Derogatis, L.R.; Morrow, G.R.; Fetting, J.; Penman, D.; Piasetsky, S.; Schmale, A.M.; Henrichs, M.; Carnicke, C.L., Jr. The prevalence of psychiatric disorders among cancer patients. JAMA 1983, 249, 751–757. [Google Scholar] [CrossRef]
- Massie, M.J. Prevalence of depression in patients with cancer. J. Natl. Cancer Inst. Monogr. 2004, 2004, 57–71. [Google Scholar] [CrossRef]
- Peng, Y.N.; Huang, M.L.; Kao, C.H. Prevalence of Depression and Anxiety in Colorectal Cancer Patients: A Literature Review. Int. J. Environ. Res. Public Health 2019, 16. [Google Scholar] [CrossRef] [Green Version]
- Lloyd, S.; Baraghoshi, D.; Tao, R.; Garrido-Laguna, I.; Gilcrease, G.W., 3rd; Whisenant, J.; Weis, J.R.; Scaife, C.; Pickron, T.B.; Huang, L.C.; et al. Mental Health Disorders are More Common in Colorectal Cancer Survivors and Associated With Decreased Overall Survival. Am. J. Clin. Oncol. 2019, 42, 355–362. [Google Scholar] [CrossRef]
- Mols, F.; Schoormans, D.; de Hingh, I.; Oerlemans, S.; Husson, O. Symptoms of anxiety and depression among colorectal cancer survivors from the population-based, longitudinal PROFILES Registry: Prevalence, predictors, and impact on quality of life. Cancer 2018, 124, 2621–2628. [Google Scholar] [CrossRef] [Green Version]
- Zhang, A.Y.; Cooper, G.S. Recognition of Depression and Anxiety among Elderly Colorectal Cancer Patients. Nurs. Res. Pract. 2010, 2010, 693961. [Google Scholar] [CrossRef] [PubMed]
- Arends, J.; Bachmann, P.; Baracos, V.; Barthelemy, N.; Bertz, H.; Bozzetti, F.; Fearon, K.; Hutterer, E.; Isenring, E.; Kaasa, S.; et al. ESPEN guidelines on nutrition in cancer patients. Clin. Nutr. 2017, 36, 11–48. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Arends, J.; Baracos, V.; Bertz, H.; Bozzetti, F.; Calder, P.C.; Deutz, N.E.P.; Erickson, N.; Laviano, A.; Lisanti, M.P.; Lobo, D.N.; et al. ESPEN expert group recommendations for action against cancer-related malnutrition. Clin. Nutr. 2017, 36, 1187–1196. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Zhang, X.; Edwards, B.J. Malnutrition in Older Adults with Cancer. Curr. Oncol. Rep. 2019, 21, 80. [Google Scholar] [CrossRef]
- Kenis, C.; Bron, D.; Libert, Y.; Decoster, L.; Van Puyvelde, K.; Scalliet, P.; Cornette, P.; Pepersack, T.; Luce, S.; Langenaeken, C.; et al. Relevance of a systematic geriatric screening and assessment in older patients with cancer: Results of a prospective multicentric study. Ann. Oncol. 2013, 24, 1306–1312. [Google Scholar] [CrossRef]
- Haviland, J.; Sodergren, S.; Calman, L.; Corner, J.; Din, A.; Fenlon, D.; Grimmett, C.; Richardson, A.; Smith, P.W.; Winter, J.; et al. Social support following diagnosis and treatment for colorectal cancer and associations with health-related quality of life: Results from the UK ColoREctal Wellbeing (CREW) cohort study. Psycho-Oncology 2017, 26, 2276–2284. [Google Scholar] [CrossRef]
- Kristjansson, S.R.; Nesbakken, A.; Jordhøy, M.S.; Skovlund, E.; Audisio, R.A.; Johannessen, H.O.; Bakka, A.; Wyller, T.B. Comprehensive geriatric assessment can predict complications in elderly patients after elective surgery for colorectal cancer: A prospective observational cohort study. Crit. Rev. Oncol. Hematol. 2010, 76, 208–217. [Google Scholar] [CrossRef] [Green Version]
- Ommundsen, N.; Wyller, T.B.; Nesbakken, A.; Bakka, A.O.; Jordhoy, M.S.; Skovlund, E.; Rostoft, S. Preoperative geriatric assessment and tailored interventions in frail older patients with colorectal cancer: A randomized controlled trial. Colorectal Dis. Off. J. Assoc. Coloproctol. Great Br. Irel. 2018, 20, 16–25. [Google Scholar] [CrossRef]
- Reisinger, K.W.; van Vugt, J.L.; Tegels, J.J.; Snijders, C.; Hulsewé, K.W.; Hoofwijk, A.G.; Stoot, J.H.; Von Meyenfeldt, M.F.; Beets, G.L.; Derikx, J.P.; et al. Functional compromise reflected by sarcopenia, frailty, and nutritional depletion predicts adverse postoperative outcome after colorectal cancer surgery. Ann. Surg. 2015, 261, 345–352. [Google Scholar] [CrossRef] [Green Version]
- Tan, K.Y.; Kawamura, Y.J.; Tokomitsu, A.; Tang, T. Assessment for frailty is useful for predicting morbidity in elderly patients undergoing colorectal cancer resection whose comorbidities are already optimized. Am. J. Surg. 2012, 204, 139–143. [Google Scholar] [CrossRef]
- Kehlet, H. Fast-track colorectal surgery. Lancet 2008, 371, 791–793. [Google Scholar] [CrossRef]
- Vlug, M.S.; Wind, J.; Hollmann, M.W.; Ubbink, D.T.; Cense, H.A.; Engel, A.F.; Gerhards, M.F.; van Wagensveld, B.A.; van der Zaag, E.S.; van Geloven, A.A.; et al. Laparoscopy in combination with fast track multimodal management is the best perioperative strategy in patients undergoing colonic surgery: A randomized clinical trial (LAFA-study). Ann. Surg. 2011, 254, 868–875. [Google Scholar] [CrossRef]
- Varadhan, K.K.; Neal, K.R.; Dejong, C.H.; Fearon, K.C.; Ljungqvist, O.; Lobo, D.N. The enhanced recovery after surgery (ERAS) pathway for patients undergoing major elective open colorectal surgery: A meta-analysis of randomized controlled trials. Clin. Nutr. 2010, 29, 434–440. [Google Scholar] [CrossRef]
- Gonzalez-Ayora, S.; Pastor, C.; Guadalajara, H.; Ramirez, J.M.; Royo, P.; Redondo, E.; Arroyo, A.; Moya, P.; Garcia-Olmo, D. Enhanced recovery care after colorectal surgery in elderly patients. Compliance and outcomes of a multicenter study from the Spanish working group on ERAS. Int. J. Colorectal Dis. 2016, 31, 1625–1631. [Google Scholar] [CrossRef] [Green Version]
- Rubenstein, L.Z.; Stuck, A.E.; Siu, A.L.; Wieland, D. Impacts of geriatric evaluation and management programs on defined outcomes: Overview of the evidence. J. Am. Geriatr. Soc. 1991, 39, 8S–16S. [Google Scholar] [CrossRef]
- Wildiers, H.; Heeren, P.; Puts, M.; Topinkova, E.; Janssen-Heijnen, M.L.; Extermann, M.; Falandry, C.; Artz, A.; Brain, E.; Colloca, G.; et al. International Society of Geriatric Oncology consensus on geriatric assessment in older patients with cancer. J. Clin. Oncol. Off. J. Am. Soc. Clin. Oncol. 2014, 32, 2595–2603. [Google Scholar] [CrossRef] [Green Version]
- Soto-Perez-de-Celis, E.; Aapro, M.; Muss, H. ASCO 2020: The Geriatric Assessment Comes of Age. Oncologist 2020, 25, 909–912. [Google Scholar] [CrossRef]
- Jones, T.S.; Jones, E.L.; Richardson, V.; Finley, J.B.; Franklin, J.L.; Gore, D.L.; Horney, C.P.; Kovar, A.; Morin, T.L.; Robinson, T.N. Preliminary data demonstrate the Geriatric Surgery Verification program reduces postoperative length of stay. J. Am. Geriatr. Soc. 2021. [Google Scholar] [CrossRef]
- Shahrokni, A.; Tin, A.L.; Sarraf, S.; Alexander, K.; Sun, S.; Kim, S.J.; McMillan, S.; Yulico, H.; Amirnia, F.; Downey, R.J.; et al. Association of Geriatric Comanagement and 90-Day Postoperative Mortality Among Patients Aged 75 Years and Older With Cancer. JAMA Netw. Open 2020, 3, e209265. [Google Scholar] [CrossRef]
- Ghignone, F.; van Leeuwen, B.L.; Montroni, I.; Huisman, M.G.; Somasundar, P.; Cheung, K.L.; Audisio, R.A.; Ugolini, G.; International Society of Geriatric Oncology Surgical Task Force. The assessment and management of older cancer patients: A SIOG surgical task force survey on surgeons’ attitudes. Eur. J. Surg. Oncol. J. Eur. Soc. Surg. Oncol. Br. Assoc. Surg. Oncol. 2016, 42, 297–302. [Google Scholar] [CrossRef]
- Lee, D.Y.; Kwak, J.M. Comprehensive Approach for Older Cancer Patients: New Challenge in an Aging Society. Ann. Coloproctol. 2020, 36, 289–290. [Google Scholar] [CrossRef] [PubMed]
- Shipway, D.; Koizia, L.; Winterkorn, N.; Fertleman, M.; Ziprin, P.; Moorthy, K. Embedded geriatric surgical liaison is associated with reduced inpatient length of stay in older patients admitted for gastrointestinal surgery. Future Healthc. J. 2018, 5, 108–116. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Ramírez-Martín, R.; JA, G.M.; JL, M.M.; González-Montalvo, J.I. The efficiency of «Cross-speciality Geriatrics» in the co-management of patients older than 80 years admitted to the General Surgery Service. Economic Results. Rev. Esp. Geriatr. Gerontol. 2021, 56, 87–90. [Google Scholar] [CrossRef] [PubMed]
- Tarazona-Santabalbina, F.J.; Llabata-Broseta, J.; Belenguer-Varea, A.; Alvarez-Martinez, D.; Cuesta-Peredo, D.; Avellana-Zaragoza, J.A. A daily multidisciplinary assessment of older adults undergoing elective colorectal cancer surgery is associated with reduced delirium and geriatric syndromes. J. Geriatr. Oncol. 2019, 10, 298–303. [Google Scholar] [CrossRef]
- Indrakusuma, R.; Dunker, M.S.; Peetoom, J.J.; Schreurs, W.H. Evaluation of preoperative geriatric assessment of elderly patients with colorectal carcinoma. A retrospective study. Eur. J. Surg. Oncol. J. Eur. Soc. Surg. Oncol. Br. Assoc. Surg. Oncol. 2015, 41, 21–27. [Google Scholar] [CrossRef]
- Patel, A.V.; Friedenreich, C.M.; Moore, S.C.; Hayes, S.C.; Silver, J.K.; Campbell, K.L.; Winters-Stone, K.; Gerber, L.H.; George, S.M.; Fulton, J.E.; et al. American College of Sports Medicine Roundtable Report on Physical Activity, Sedentary Behavior, and Cancer Prevention and Control. Med. Sci. Sports Exerc. 2019, 51, 2391–2402. [Google Scholar] [CrossRef] [Green Version]
- Schmid, D.; Leitzmann, M.F. Association between physical activity and mortality among breast cancer and colorectal cancer survivors: A systematic review and meta-analysis. Ann. Oncol. 2014, 25, 1293–1311. [Google Scholar] [CrossRef]
- Schmitz, K.H.; Campbell, A.M.; Stuiver, M.M.; Pinto, B.M.; Schwartz, A.L.; Morris, G.S.; Ligibel, J.A.; Cheville, A.; Galvão, D.A.; Alfano, C.M. Exercise is medicine in oncology: Engaging clinicians to help patients move through cancer. CA Cancer J. Clin. 2019, 69, 468–484. [Google Scholar] [CrossRef] [Green Version]
- Schmitz, K.H.; Courneya, K.S.; Matthews, C.; Demark-Wahnefried, W.; Galvao, D.A.; Pinto, B.M.; Irwin, M.L.; Wolin, K.Y.; Segal, R.J.; Lucia, A.; et al. American College of Sports Medicine roundtable on exercise guidelines for cancer survivors. Med. Sci. Sports Exerc. 2010, 42, 1409–1426. [Google Scholar] [CrossRef]
- Lynch, B.M.; van Roekel, E.H.; Vallance, J.K. Physical activity and quality of life after colorectal cancer: Overview of evidence and future directions. Expert Rev. Qual. Life Cancer Care 2016, 1, 9–23. [Google Scholar] [CrossRef] [Green Version]
- McGettigan, M.; Cardwell, C.R.; Cantwell, M.M.; Tully, M.A. Physical activity interventions for disease-related physical and mental health during and following treatment in people with non-advanced colorectal cancer. Cochrane Database Syst. Rev. 2020, 5, CD012864. [Google Scholar] [CrossRef] [Green Version]
- Pollan, M.; Casla-Barrio, S.; Alfaro, J.; Esteban, C.; Segui-Palmer, M.A.; Lucia, A.; Martin, M. Exercise and cancer: A position statement from the Spanish Society of Medical Oncology. Clin. Transl. Oncol. Off. Publ. Fed. Span. Oncol. Soc. Natl. Cancer Inst. Mex. 2020, 22, 1710–1729. [Google Scholar] [CrossRef] [Green Version]
- Berkel, A.E.M.; Bongers, B.C.; Kotte, H.; Weltevreden, P.; de Jongh, F.H.C.; Eijsvogel, M.M.M.; Wymenga, A.N.M.; Bigirwamungu-Bargeman, M.; van der Palen, J.; van Det, M.J.; et al. Effects of Community-based Exercise Prehabilitation for Patients Scheduled for Colorectal Surgery With High Risk for Postoperative Complications: Results of a Randomized Clinical Trial. Ann. Surg. 2021. [Google Scholar] [CrossRef]
- Carli, F.; Charlebois, P.; Stein, B.; Feldman, L.; Zavorsky, G.; Kim, D.J.; Scott, S.; Mayo, N.E. Randomized clinical trial of prehabilitation in colorectal surgery. Br. J. Surg. 2010, 97, 1187–1197. [Google Scholar] [CrossRef]
- Dronkers, J.J.; Lamberts, H.; Reutelingsperger, I.M.; Naber, R.H.; Dronkers-Landman, C.M.; Veldman, A.; van Meeteren, N.L. Preoperative therapeutic programme for elderly patients scheduled for elective abdominal oncological surgery: A randomized controlled pilot study. Clin. Rehabil. 2010, 24, 614–622. [Google Scholar] [CrossRef]
- Minnella, E.M.; Ferreira, V.; Awasthi, R.; Charlebois, P.; Stein, B.; Liberman, A.S.; Scheede-Bergdahl, C.; Morais, J.A.; Carli, F. Effect of two different pre-operative exercise training regimens before colorectal surgery on functional capacity: A randomised controlled trial. Eur. J. Anaesthesiol. 2020, 37, 969–978. [Google Scholar] [CrossRef]
- Awasthi, R.; Minnella, E.M.; Ferreira, V.; Ramanakumar, A.V.; Scheede-Bergdahl, C.; Carli, F. Supervised exercise training with multimodal pre-habilitation leads to earlier functional recovery following colorectal cancer resection. Acta Anaesthesiol. Scand. 2019, 63, 461–467. [Google Scholar] [CrossRef]
- Chia, C.L.; Mantoo, S.K.; Tan, K.Y. ‘Start to finish trans-institutional transdisciplinary care’: A novel approach improves colorectal surgical results in frail elderly patients. Colorectal Dis. Off. J. Assoc. Coloproctology Great Br. Irel. 2016, 18, O43–O50. [Google Scholar] [CrossRef]
- Souwer, E.T.D.; Bastiaannet, E.; de Bruijn, S.; Breugom, A.J.; van den Bos, F.; Portielje, J.E.A.; Dekker, J.W.T. Comprehensive multidisciplinary care program for elderly colorectal cancer patients: “From prehabilitation to independence”. Eur. J. Surg. Oncol. J. Eur. Soc. Surg. Oncol. Br. Assoc. Surg. Oncol. 2018, 44, 1894–1900. [Google Scholar] [CrossRef]
- Bousquet-Dion, G.; Awasthi, R.; Loiselle, S.E.; Minnella, E.M.; Agnihotram, R.V.; Bergdahl, A.; Carli, F.; Scheede-Bergdahl, C. Evaluation of supervised multimodal prehabilitation programme in cancer patients undergoing colorectal resection: A randomized control trial. Acta Oncol. 2018, 57, 849–859. [Google Scholar] [CrossRef] [Green Version]
- Carli, F.; Bousquet-Dion, G.; Awasthi, R.; Elsherbini, N.; Liberman, S.; Boutros, M.; Stein, B.; Charlebois, P.; Ghitulescu, G.; Morin, N.; et al. Effect of Multimodal Prehabilitation vs Postoperative Rehabilitation on 30-Day Postoperative Complications for Frail Patients Undergoing Resection of Colorectal Cancer: A Randomized Clinical Trial. JAMA Surg. 2020, 155, 233–242. [Google Scholar] [CrossRef] [PubMed]
- Gillis, C.; Li, C.; Lee, L.; Awasthi, R.; Augustin, B.; Gamsa, A.; Liberman, A.S.; Stein, B.; Charlebois, P.; Feldman, L.S.; et al. Prehabilitation versus rehabilitation: A randomized control trial in patients undergoing colorectal resection for cancer. Anesthesiology 2014, 121, 937–947. [Google Scholar] [CrossRef] [PubMed]
- Minnella, E.M.; Bousquet-Dion, G.; Awasthi, R.; Scheede-Bergdahl, C.; Carli, F. Multimodal prehabilitation improves functional capacity before and after colorectal surgery for cancer: A five-year research experience. Acta Oncol. 2017, 56, 295–300. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Campbell, K.L.; Winters-Stone, K.M.; Wiskemann, J.; May, A.M.; Schwartz, A.L.; Courneya, K.S.; Zucker, D.S.; Matthews, C.E.; Ligibel, J.A.; Gerber, L.H.; et al. Exercise Guidelines for Cancer Survivors: Consensus Statement from International Multidisciplinary Roundtable. Med. Sci. Sports Exerc. 2019, 51, 2375–2390. [Google Scholar] [CrossRef] [PubMed] [Green Version]
- Lim, S.H.; Chan, S.W.C.; Chow, A.; Zhu, L.; Lai, J.H.; He, H.G. Pilot trial of a STOMA psychosocial intervention programme for colorectal cancer patients with stomas. J. Adv. Nurs. 2019, 75, 1338–1346. [Google Scholar] [CrossRef] [PubMed]
- Bryan, S.; Dukes, S. The Enhanced Recovery Programme for stoma patients: An audit. Br. J. Nurs. 2010, 19, 831–834. [Google Scholar] [CrossRef]
- Chaudhri, S.; Brown, L.; Hassan, I.; Horgan, A.F. Preoperative intensive, community-based vs. traditional stoma education: A randomized, controlled trial. Dis. Colon Rectum 2005, 48, 504–509. [Google Scholar] [CrossRef]
- Cheung, Y.L.; Molassiotis, A.; Chang, A.M. The effect of progressive muscle relaxation training on anxiety and quality of life after stoma surgery in colorectal cancer patients. Psycho-Oncology 2003, 12, 254–266. [Google Scholar] [CrossRef]
- Danielsen, A.K.; Burcharth, J.; Rosenberg, J. Patient education has a positive effect in patients with a stoma: A systematic review. Colorectal Dis. Off. J. Assoc. Coloproctology Great Br. Irel. 2013, 15, e276–e283. [Google Scholar] [CrossRef]
- Son, H.; Son, Y.J.; Kim, H.; Lee, Y. Effect of psychosocial interventions on the quality of life of patients with colorectal cancer: A systematic review and meta-analysis. Health Qual. Life Outcomes 2018, 16, 119. [Google Scholar] [CrossRef]
- Hoon, L.S.; Chi Sally, C.W.; Hong-Gu, H. Effect of psychosocial interventions on outcomes of patients with colorectal cancer: A review of the literature. Eur. J. Oncol. Nurs. 2013, 17, 883–891. [Google Scholar] [CrossRef]
- Ohlen, J.; Sawatzky, R.; Pettersson, M.; Sarenmalm, E.K.; Larsdotter, C.; Smith, F.; Wallengren, C.; Friberg, F.; Kodeda, K.; Carlsson, E. Preparedness for colorectal cancer surgery and recovery through a person-centred information and communication intervention-A quasi-experimental longitudinal design. PLoS ONE 2019, 14, e0225816. [Google Scholar] [CrossRef] [Green Version]
- Louro, A.C.; Castro, J.F.; Blasco, T. Effects of a positive emotion-based adjuvant psychological therapy in colorectal cancer patients: A pilot study. Psicooncologia 2016, 13, 113–125. [Google Scholar]
- Ellis, J.; Lin, J.; Walsh, A.; Lo, C.; Shepherd, F.A.; Moore, M.; Li, M.; Gagliese, L.; Zimmermann, C.; Rodin, G. Predictors of referral for specialized psychosocial oncology care in patients with metastatic cancer: The contributions of age, distress, and marital status. J. Clin. Oncol. Off. J. Am. Soc. Clin. Oncol. 2009, 27, 699–705. [Google Scholar] [CrossRef]
- Newell, S.A.; Sanson-Fisher, R.W.; Savolainen, N.J. Systematic review of psychological therapies for cancer patients: Overview and recommendations for future research. J. Natl. Cancer Inst. 2002, 94, 558–584. [Google Scholar] [CrossRef]
Author, yr. | Sample (n) | Age (yr.) | Setting | Frailty Measure | Frailty Prevalence | Outcomes & Results |
---|---|---|---|---|---|---|
Kristjansson el al. (2010) [69] | 178 | Mean: 80 SD: 6 Range: 70–94 | Hospitalization Elective surgery | CGA (Frail: ≥1 domain affected)
| F: 76 (43%) NF: 102 (57%) | 30-Day Postoperative Complications Any complication (Clav. I–IV) RR 1.59, 95% CI (1.25–2.01) F: 58 (76%), NF: 59 (48%) Severe Complications (Clav. ≥II) RR 1.75, 95% CI (1.28, 2.41) F: 47 (62%), NF: 36 (35%) |
Ommundsen et al. (2014) [70] | 178 | Age Groups: 70–79 (50%) 80–89 (44%) ≥90 (6%) | Hospitalization Elective surgery | CGA (Frail: ≥1 domain affected)
| F: 76 (43%) NF: 102 (57%) | 5-Year Survival F: 18 (24%), NF: 67 (66%) p < 0.001 |
Reisinger et al. (2015) [71] | 153 * | >70 | Hospitalization Elective surgery | GFI (Frail: ≥5/15)
| F: 39 (26%) NF: 114 (75%) | Postoperative Sepsis OR 3.96, 95% CI (1.14–13.83) F: 6 (15.4%), NF: 5 (4.4%) p = 0.03 |
Tan et al. (2012) [72] | 83 | Mean: 81 Range: 75–93 | Hospitalization Elective surgery | Fried Criteria (Frail: ≥3/5)
| F: 23 (28%) NF: 60 (72%) | Major Postoperative Complications (Clav. ≥ II) OR 4.083, 95% CI (1.433–11.638) F: 11 (47.8%), NF: 11 (18.3%) p = 0.006 |
Author, yr. | Sample (n; Groups) | Age (yr.) † | Design | Type of Program & Setting | Assessments & Interventions | Benefits ‡ |
---|---|---|---|---|---|---|
Shipway et al., 2018 [84] | 682 CG: 203 IG: 479 | >60 CG: 73 (60–100) IG: 73 (60–94) | Single-center before-after study | Embedded Geriatric Liaison Hospitalization Elective & Emergency GI surgery | Preoperative CGA - Comorbidity - Medication - Nutrition Status - Exercise Tolerance - Cognitive Function - Frailty - Depression Assessment - Functional Capacity - Social Circumstances - Screening Investigations Postoperative Follow-Up - Ward Rounds (selected patients) - Discharge Plan - Geriatrician-led rehabilitation ward (selected patients) | LOS (All Surgeries) All Patients Mean Reduction: 3.1 days 95% CI (0.7–5.5), p = 0.007 Patients ≥ 75 years Mean Reduction: 3 days 95% CI (0.2–5.8), p = 0.045 LOS (Elective Surgery) All Patients Mean Reduction: 1.3 days 95%CI (−1.4–4.03) Patients ≥ 75 years Mean Reduction: 5.2 days 95% CI (−1.7–12.1), p = 0.099 |
Tarazona- Santabalbina et al., 2019 [86] | 310 CG: 107 IG: 203 | ≥ 70 CG: 75 ± 5 IG: 76 ± 5 | Single-center retrospective cohort study | In-Hospital Program Elective CRC Surgery | 8-Hour Ward Assessment/intervention - Pressure Ulcers - Pain - Urinary Continence - Constipation - Delirium Daily Ward Assessment - Endovenous Catheters - Medication - Infections - Thromboembolic Events - Anemia - Early Ambulation - Fall Risk - Hydration & Nutrition - Sleep Hygiene - Sensory Impairment | Delirium reduction CG: 31 (29.2), IG: 23 (11.3) p < 0.001 Geriatric Syndromes diagnosis * CG: 28 (26.2), IG: 21(10.3) p < 0.001 Blood transfusions reduction CG: 24 (22.4); IG: 18 (8.9) p = 0.001 |
Ramirez-Martín et al., 2020 [85] | 175 CG: 122 IG: 53 | ≥80 | Single-center before-after cohort study | Emergency Surgery Inpatients - In-Hospital Collaborative Management Elective CRC Surgery - Preoperative CGA & Intervention - In-Hospital Collaborative Management | Preoperative CGA - Not Specified In-Hospital Management - Daily Ward Monitoring - Clinical Management Collaboration - Discharge Planning | LOS (days) Emergency Admissions CG: 27.2 (18.1), IG: 16.6 (10.7) p < 0.01 Elective Surgery (CRC) CG: 19.1 (13.4), IG: 10.6 (9.3) p < 0.01 |
Indrakusuma et al., 2015 [87] | 100 ** CG: 50 IG: 50 | ≥70 CG: 75 (71–78) IG: 81 (79–85) | Single-center retrospective cohort and match-control study | Preoperative CGA & Intervention Elective CRC surgery | Preoperative CGA & Intervention - Full Medical Study - Social Circumstances - Review of Systems - Functional Capacity - Family History - Full Physical Examination - Laboratory Tests - Cognitive Function - Depression Assessment - Nutritional Status | Mortality No significant differences Postoperative Delirium No significant differences Postoperative Complications No significant differences Length of Stay No significant differences |
Ommundsen et al., 2017 [70] | 114 CG: 62 IG: 52 | >65 CG: 79 ± 8 IG: 78 ± 7 | Multi-center randomized controlled trial | Preoperative CGA & Intervention Elective CRC Surgery - Frail Subjects | Preoperative CGA - Activities of Daily Living - Use of Medication - Comorbidity - Nutritional Status - Cognitive Function - Depression Assessment | Mild Postop. Complications Mentioned. No specific data provided Postop. Complications (Clav. I–V) No significant differences Postop. Complications (Clav. II–V) No significant differences 30-Day Mortality No significant differences 3-Month Mortality No significant differences Length of Stay No significant differences |
Author, yr. | Sample (n) | Age yr. (mean) | Duration | Features | Programs Analyzed | Principal and Other Outcomes and Results | Adherence |
---|---|---|---|---|---|---|---|
Prehabilitation Programs | |||||||
Dronkers et al., 2010 [97] | 42 | 70 | 2–4 w. | Supervised vs unsupervised home-based exercise program. | Short-term intensive program Group: 2x/w. for 60 min per session. Resistance training, inspiratory muscle training, moderate aerobic training, and training functional activities. Daily 30 min walk and inspiratory muscle training. | Postoperative complications: NSD; LOS: NSD. Functional capacity (TUG): NSD; Strength (CRT): NSD; (Hand grip): NSD. Inspiratory muscle endurance (RMA): SD. Physical activity (LASA): NSD. Fatigue (AFQ): NSD. Quality of life (EORTC-QLQ-C30): NSD. | Supervised training: 97%; Unsupervised training: Non- reported. |
Home-based exercise group: Daily activation for minimally 30 min with a pedometer. Measurements: baseline and postsurgery. | |||||||
Carli et al., 2010 [96] | 112 | 60 | 4 w. | In-hospital supervised exercise program. | Bike/strengthening Group: 7x/w. 20–30 min of moderate intensity aerobic training and 3x/w. for 10–15 min of resistance training. | Functional capacity (6MWT): NSD. Anxiety and Depression (HADS): NSD. | 16% |
Walk/breathing Group: 7x/w. training for 40–45 min per session. Walking and breathing exercises. | |||||||
Measurements: baseline, 1-week presurgery, 2- and 4-month postsurgery. | |||||||
Minnella et al., 2020 [98] | 42 | 67 | 4 w. | Prehabilitation Unit-based supervised exercise program. | High-Intensity Interval Training (HIIT) Group: 3x/w. for 40 min per session. High intensity aerobic training on a bicycle and resistance training. | 30-day complications (Clav.): NSD. LOS: NSD. Functional capacity (6MWT): NSD; (CPET): SD. | HIIT/MICT: Exercise: 89%/93%, Nutrition: 97%/99%, Loss of patients at follow-up: presurgery 19%/5% 1 month postsurgery 33%/38%, and 2 months postsurgery. 38%/48%. |
Nutrition: Balanced macronutrient composition and protein. | |||||||
Anxiety: Relaxation techniques and breathing exercises. | |||||||
Moderate Intensity Continuous Training (MICT) group: 3x/w. for 50 min per session. Moderate intensity aerobic training on a bicycle and resistance training. | |||||||
Nutrition: Balanced macronutrient composition and protein Anxiety: Relaxation techniques and breathing exercises. Measurements: baseline, presurgery, 1- and 2-month postsurgery | |||||||
Berkel et al., 2021 [95] | 57 | 74 | 3 w. | Community-based supervised exercise program. | Intervention group: 3x/w. for 60 min per session. | 30-day postoperative complications (Clav.): SD. LOS: NSD. Readmissions: NSD. Functional capacity- Aerobic fitness (V02): NSD. | Non- reported. |
Moderate to high intensity aerobic training on a cycle ergometer and resistance training. | |||||||
Control group (usual care): ERAS protocol. Nutritional counseling and advice on smoking cessation. Measurements: 30-day postsurgery. | |||||||
Chia et al., 2015 [100] | 117 | 80 | PREHAB: 2w. and REHAB: 2–6 w. | Supervised exercise or unsupervised home-based exercise depending of patient situation. | Intervention group (STF): Cardiovascular strengthening, mobilizing and muscle strengthening. Nutrition: Individual attention. | Postoperative complications (Clav.): NSD. LOS: SD. 30-day mortality: NSD. Recovery functional capacity (Barthel): NSD. | 80% |
Control group (GSS): quality reviews and a patient-centered culture. Nutrition: Individual attention. | |||||||
Measurements: 30-day mortality and 6-week postsurgery. | |||||||
Awasthi et al., 2018 [99] | 140 | 68 | PREHAB: 4 w. and REHAB: 8 w. | Supervised exercise and unsupervised home-based exercise program. | Group 1: unsupervised exercise (Gillis et al. 2014) 3x/w. for 50 min per session: moderate intensity aerobic exercise and moderate intensity resistance training. Nutrition: Nutritional assessment and protein supplementation. Anxiety: Relaxation techniques. | LOS: NSD Functional capacity (6MWT): SD. Muscle strength (Hand grip): SD. Anxiety and depression (HADS): NSD. Quality of life (SF36): SD. | Supervised exercise: 98% |
Group 2: supervised training (Bousquet-Dion et al., 2018) 1x/w. at hospital exercise laboratory for 65 min per session: moderate aerobic exercise and resistance exercise. 3 to 4x/w. at home for 30 min of moderate intensity aerobic training and resistance training. | |||||||
Nutrition: Nutritional assessment and protein supplementation. | |||||||
Anxiety: Relaxation techniques. | |||||||
Measurements: baseline, before surgery, 4- and 8-week postsurgery. | |||||||
Souwer et al. 2018 [101] | 86 | 81 | PREHAB: 4 w. and REHAB: 4–6 w. | In-hospital supervised exercise and home-based exercise program. | Intervention Group: 2x/w. for 30–45 min per session. PREHAB: Resistance and endurance training, and home exercise and breathing. REHAB; Physical training. Nutrition: Protein supplementation, dietary support. Anxiety: Cognitive and emotional guidance. | 30-day postoperative complications. Only cardiac: SD. LOS: SD. 1-year mortality: NSD. | 63% |
Control group: usual care (previous cohort). | |||||||
Measurements: 30-day and 1-year postsurgery. | |||||||
Gillis et al., 2014 [104] | 77 | 66 | PREHAB: 4 w. vs REHAB: 8 w. | Unsupervised home-based exercise program. | PREHAB: 3x/w. for 50 min per session. Moderate intensity aerobic exercise and moderate resistance training. Nutrition: Protein intake. Anxiety: 60 min of relaxation techniques and breathing exercises. | 30-day complications (Clav.): NSD. Functional capacity (6MWT): SD. Health status (SF-36): NSD. Anxiety and depression (HADS): NSD. | PREHAB = 78%; 4 w.: 53%; 8w.: 53% REHAB = 4 w.: 31% 8w.: 40% |
REHAB Group: 3x/w. for 50 min per session. Moderate intensity aerobic exercise and moderate resistance training. Nutrition: Protein intake. Anxiety: 60 min of relaxation techniques and breathing exercises. | |||||||
Measurements: baseline, presurgery, 4- and 8-week postsurgery. | |||||||
Minnella et al., 2017 [105] | 185 | 68 | PREHAB: 4 w. vs REHAB: 8 w. | Unsupervised home-based exercise and supervised exercise program. | PREHAB Group: 3x/w. for 20–30 min per session of endurance training and 2x/w. of resistance training. Nutrition: Dietary changes and protein supplementation. Anxiety: Relaxation techniques. Plus ERAS protocol. | Postoperative complications (Clav.): NDS. LOS: NSD. Functional capacity (6MWT): SD. Physical fitness (CHAMPS): SD. | PREHAB = 70–98% REHAB = 4w.:53–72% 8 w.: 53–82% |
REHAB Group: 3x/w. for 20–30 min per session of endurance training and 2x/w. of resistance training. Nutrition: Dietary changes and protein supplementation. Anxiety: Relaxation techniques. Plus ERAS protocol. | |||||||
Measurements: baseline, presurgery, 4- and 8-week postsurgery. | |||||||
Bousquet-Dion et al., 2018 [102] | 80 | 73 | PREHAB: 4 w. vs REHAB: 8 w. | In-hospital supervised and unsupervised home-based exercise program. | PREHAB Group: At hospital: 1x/w. for 65 min per session. Moderate aerobic exercise and resistance exercise. At home: 3 to 4x/w. for 30 min of moderate intensity aerobic training and resistance training. Nutrition: Protein supplementation. Anxiety: 60 min of relaxation techniques and breathing exercises. Plus ERAS protocol. | LOS: NSD. Functional capacity (6MWT): NSD. Physical activity (CHAMPS): NSD. | Supervised exercise; PREHAB 98% REHAB = 4 w. 70% 8 w.: 75% |
REHAB Group: At hospital: 1x/w. for 65 min per session. Moderate aerobic exercise and resistance exercise. At home: 3 to 4x/w. for 30 min of moderate intensity aerobic training and resistance training. Nutrition: Protein supplementation. Anxiety: 60 min of relaxation techniques and breathing exercises. Plus ERAS protocol. Measurements: baseline, presurgery, 4- and 8-week postsurgery. | |||||||
Carli et al., 2020 [103] | 110 | 78 | PREHAB: 4 w. vs REHAB: 4 w | Unsupervised home-based multimodal program with 1 session /w. supervised at hospital (similar for PREHAB and REHAB). | PREHAB group: 1x/w. for 60 min per session. Supervised moderate aerobic exercises and resistance exercises at hospital and moderate intensity aerobic activities (walking) and resistance training at home. Nutrition: Protein intake. Anxiety: Relaxation techniques and breathing exercises. | 30-day postoperative complications (CCI and Clav.): NSD. LOS: NSD. Functional capacity (6MWT): NSD. Readmissions: NSD. | PREHAB = 68% REHAB = 14%. General exercise and nutrition: PREHAB 80%, REHAB 30%. |
REHAB group: 3x/w. for 30 min per session. Supervised moderate aerobic exercises and resistance exercises at hospital and moderate-intensity aerobic activities (walking) and resistance training at home. Nutrition: Protein intake. Anxiety: Relaxation techniques and breathing exercises. Measurements: 4-week postsurgery. |
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations. |
© 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
González-Senac, N.M.; Mayordomo-Cava, J.; Macías-Valle, A.; Aldama-Marín, P.; Majuelos González, S.; Cruz Arnés, M.L.; Jiménez-Gómez, L.M.; Vidán-Astiz, M.T.; Serra-Rexach, J.A. Colorectal Cancer in Elderly Patients with Surgical Indication: State of the Art, Current Management, Role of Frailty and Benefits of a Geriatric Liaison. Int. J. Environ. Res. Public Health 2021, 18, 6072. https://doi.org/10.3390/ijerph18116072
González-Senac NM, Mayordomo-Cava J, Macías-Valle A, Aldama-Marín P, Majuelos González S, Cruz Arnés ML, Jiménez-Gómez LM, Vidán-Astiz MT, Serra-Rexach JA. Colorectal Cancer in Elderly Patients with Surgical Indication: State of the Art, Current Management, Role of Frailty and Benefits of a Geriatric Liaison. International Journal of Environmental Research and Public Health. 2021; 18(11):6072. https://doi.org/10.3390/ijerph18116072
Chicago/Turabian StyleGonzález-Senac, Nicolás M., Jennifer Mayordomo-Cava, Angela Macías-Valle, Paula Aldama-Marín, Sara Majuelos González, María Luisa Cruz Arnés, Luis M. Jiménez-Gómez, María T. Vidán-Astiz, and José Antonio Serra-Rexach. 2021. "Colorectal Cancer in Elderly Patients with Surgical Indication: State of the Art, Current Management, Role of Frailty and Benefits of a Geriatric Liaison" International Journal of Environmental Research and Public Health 18, no. 11: 6072. https://doi.org/10.3390/ijerph18116072
APA StyleGonzález-Senac, N. M., Mayordomo-Cava, J., Macías-Valle, A., Aldama-Marín, P., Majuelos González, S., Cruz Arnés, M. L., Jiménez-Gómez, L. M., Vidán-Astiz, M. T., & Serra-Rexach, J. A. (2021). Colorectal Cancer in Elderly Patients with Surgical Indication: State of the Art, Current Management, Role of Frailty and Benefits of a Geriatric Liaison. International Journal of Environmental Research and Public Health, 18(11), 6072. https://doi.org/10.3390/ijerph18116072