References
- Siegel RL, Miller KD, Jemal A. Cancer statistics, 2020. CA Cancer J Clin. 2020;70(1):7–30. doi:https://doi.org/10.3322/caac.21590
- Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, Bray F. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2021;71(3):209–49. doi:https://doi.org/10.3322/caac.21660
- Lheureux S, Gourley C, Vergote I, Oza AM. Epithelial ovarian cancer. Lancet (London, England). 2019;393(10177):1240–53. doi:https://doi.org/10.1016/S0140-6736(18)32552-2
- Jelovac D, Armstrong DK. Recent progress in the diagnosis and treatment of ovarian cancer. CA Cancer J Clin. 2011;61(3):183–203. doi:https://doi.org/10.3322/caac.20113
- Lheureux S, Braunstein M, Oza AM. Epithelial ovarian cancer: Evolution of management in the era of precision medicine. CA Cancer J Clin. 2019;69(4):280–304. doi:https://doi.org/10.3322/caac.21559
- El-Sherif A, El-Sherif S, Taylor AH, Ayakannu T. Ovarian cancer: lifestyle, diet and nutrition. Nutr Cancer. 2021;73(7):1092–16. doi:https://doi.org/10.1080/01635581.2020.1792948
- Sehouli J, Mueller K, Richter R, Anker M, Woopen H, Rasch J, et al. Effects of sarcopenia and malnutrition on morbidity and mortality in gynecologic cancer surgery: results of a prospective study. 2021;12(2):393–402.
- Hilal Z, Rezniczek GA, Klenke R, Dogan A, Tempfer CB. Nutritional status, cachexia, and anorexia in women with peritoneal metastasis and intraperitoneal chemotherapy: a longitudinal analysis. J Gynecol Oncol. 2017;28(6):e80. doi:https://doi.org/10.3802/jgo.2017.28.e80
- Yim GW, Eoh KJ, Kim SW, Nam EJ, Kim YT. Malnutrition identified by the nutritional risk index and poor prognosis in advanced epithelial ovarian carcinoma. Nutr Cancer. 2016;68(5):772–9. doi:https://doi.org/10.1080/01635581.2016.1159702
- Horowitz M, Neeman E, Sharon E, Ben-Eliyahu S. Exploiting the critical perioperative period to improve long-term cancer outcomes. Nat Rev Clin Oncol. 2015;12(4):213–26. doi:https://doi.org/10.1038/nrclinonc.2014.224
- Huhmann M, August D, Nutrition E. Perioperative nutrition support in cancer patients. Nutr Clin Pract. 2012;27(5):586–92. doi:https://doi.org/10.1177/0884533612455203
- Laky B, Janda M, Kondalsamy-Chennakesavan S, Cleghorn G, Obermair A. Pretreatment malnutrition and quality of life - association with prolonged length of hospital stay among patients with gynecological cancer: a cohort study. BMC Cancer. 2010;10:232. doi:https://doi.org/10.1186/1471-2407-10-232
- Gupta D, Lis CG, Vashi PG, Lammersfeld CA. Impact of improved nutritional status on survival in ovarian cancer. Supp Care Cancer. 2010;18(3):373–81. doi:https://doi.org/10.1007/s00520-009-0670-y
- Gupta D, Lammersfeld CA, Vashi PG, Dahlk SL, Lis CG. Can subjective global assessment of nutritional status predict survival in ovarian cancer?J Ovarian Res. 2008;1(1):5. doi:https://doi.org/10.1186/1757-2215-1-5
- Bauer J, Capra S, Ferguson M. Use of the scored patient-generated subjective global assessment (PG-SGA) as a nutrition assessment tool in patients with cancer. Eur J Clin Nutr. 2002;56(8):779–85. doi:https://doi.org/10.1038/sj.ejcn.1601412
- Laky B, Janda M, Cleghorn G, Obermair A. Comparison of different nutritional assessments and body-composition measurements in detecting malnutrition among gynecologic cancer patients. Am J Clin Nutr. 2008;87(6):1678–85. doi:https://doi.org/10.1093/ajcn/87.6.1678
- Feng Z, Wen H, Ju X, Bi R, Chen X, Yang W, Wu X. The preoperative prognostic nutritional index is a predictive and prognostic factor of high-grade serous ovarian cancer. BMC Cancer. 2018;18(1):883. doi:https://doi.org/10.1186/s12885-018-4732-8
- Zhang W, Ye B, Liang W, Ren Y. Preoperative prognostic nutritional index is a powerful predictor of prognosis in patients with stage III ovarian cancer. Sci Rep. 2017;7(1):9548. doi:https://doi.org/10.1038/s41598-017-10328-8
- Li Y, Zhang C, Ji R, Lu H, Zhang W, Li L-L, Liu R, Qian H, He A. Prognostic significance of the controlling nutritional status (CONUT) score in epithelial ovarian cancer. Int J Gynecol Cancer. 2020;30(1):74–82. doi:https://doi.org/10.1136/ijgc-2019-000865
- Arends J, Bachmann P, Baracos V, Barthelemy N, Bertz H, Bozzetti F, Fearon K, Hütterer E, Isenring E, Kaasa S, et al. ESPEN guidelines on nutrition in cancer patients. Clin Nutr. 2017;36(1):11–48. doi:https://doi.org/10.1016/j.clnu.2016.07.015
- Ravasco P, Monteiro-Grillo I, Vidal PM, Camilo ME. Dietary counseling improves patient outcomes: a prospective, randomized, controlled trial in colorectal cancer patients undergoing radiotherapy. JCO. 2005;23(7):1431–8. doi:https://doi.org/10.1200/JCO.2005.02.054
- Cawood AL, Elia M, Stratton RJ. Systematic review and meta-analysis of the effects of high protein oral nutritional supplements. Ageing Res Rev. 2012;11(2):278–96. doi:https://doi.org/10.1016/j.arr.2011.12.008
- Weimann A, Braga M, Harsanyi L, Laviano A, Ljungqvist O, Soeters P, Jauch KW, Kemen M, Hiesmayr JM, Horbach T, et al. ESPEN guidelines on enteral nutrition: surgery including organ transplantation. Clin Nutr. 2006;25(2):224–44. doi:https://doi.org/10.1016/j.clnu.2006.01.015
- Madhok BM, Yeluri S, Haigh K, Burton A, Broadhead T, Jayne DG. Parenteral nutrition for patients with advanced ovarian malignancy. J Hum Nutr Diet. 2011;24(2):187–91. doi:https://doi.org/10.1111/j.1365-277X.2010.01127.x
- Mendivil AA, Rettenmaier MA, Abaid LN, Brown JV, 3rd, Mori KM, Goldstein BH. The impact of total parenteral nutrition on postoperative recovery in patients treated for advanced stage ovarian cancer. Arch Gynecol Obstet. 2017;295(2):439–44. doi:https://doi.org/10.1007/s00404-016-4227-2
- Birmingham CL. Total parenteral nutrition in the critically ill patient. Lancet (London, England). 1999;353(9159):1116–7. doi:https://doi.org/10.1016/S0140-6736(99)00006-9
- Sowerbutts AM, Lal S, Sremanakova J, Clamp AR, Jayson GC, Hardy L, Sutton E, Raftery A-M, Teubner A, Burden S, et al. Dealing with loss: food and eating in women with ovarian cancer on parenteral nutrition. J Hum Nutr Diet. 2020;33(4):550–6. doi:https://doi.org/10.1111/jhn.12738
- Sowerbutts AM, Lal S, Sremanakova J, Clamp AR, Jayson GC, Teubner A, Hardy L, Todd C, Raftery A-M, Sutton E, et al. Palliative home parenteral nutrition in patients with ovarian cancer and malignant bowel obstruction: experiences of women and family caregivers. BMC Palliat Care. 2019;18(1):120. doi:https://doi.org/10.1186/s12904-019-0507-5
- Sowerbutts AM, Lal S, Sremanakova J, Clamp AR, Jayson GC, Teubner A, Hardy L, Todd C, Raftery A-M, Sutton E, et al. Discharging women with advanced ovarian cancer on home parenteral nutrition: making and implementing the decision. Nutrients. 2020;12(1):166. doi:https://doi.org/10.3390/nu12010166
- Knott A, Pathak S, McGrath J, Kennedy R, Horgan A, Mythen M, et al. Consensus views on implementation and measurement of enhanced recovery after surgery in England: Delphi study. BMJ Open. 2012;2(6):e001878.
- Kimball SR, Farrell PA, Jefferson LS. Invited review: Role of insulin in translational control of protein synthesis in skeletal muscle by amino acids or exercise. J Appl Physiol (1985). 2002;93(3):1168–80. doi:https://doi.org/10.1152/japplphysiol.00221.2002
- Marquini GV, Pinheiro FES, Vieira AUC, Pinto RMC, Uyeda M, Girão M, et al. Effects of preoperative fasting abbreviation with carbohydrate and protein solution on postoperative symptoms of gynecological surgeries: double-blind randomized controlled clinical trial. Revist Colegio Brasileiro Cirurgioes. 2020;46(5):e20192295.
- Marquini GV, da Silva Pinheiro FE, da Costa Vieira AU, da Costa Pinto RM, Kuster Uyeda MGB, Girão MJBC, Sartori MGF. Preoperative fasting abbreviation (Enhanced Recovery After Surgery protocol) and effects on the metabolism of patients undergoing gynecological surgeries under spinal anesthesia: A randomized clinical trial. Nutrition. 2020;77:110790. doi:https://doi.org/10.1016/j.nut.2020.110790
- Okabayashi T, Nishimori I, Yamashita K, Sugimoto T, Namikawa T, Maeda H, Yatabe T, Hanazaki K. Preoperative oral supplementation with carbohydrate and branched-chain amino acid-enriched nutrient improves insulin resistance in patients undergoing a hepatectomy: a randomized clinical trial using an artificial pancreas. Amino Acids. 2010;38(3):901–7. doi:https://doi.org/10.1007/s00726-009-0297-9
- Shi M, Hu Z, Yang D, Cai Q, Zhu Z. Preoperative oral carbohydrate reduces postoperative insulin resistance by activating AMP-activated protein kinase after colorectal surgery. Dig Surg. 2020;37(5):368–75. doi:https://doi.org/10.1159/000505515
- Wongyingsinn M, Luangchan S, Tungsongsawat S, Trakarnsanga A, Lohsiriwat V. A randomized controlled trial of preoperative carbohydrate drinks on postoperative walking capacity in elective colorectal surgery. Asia Pac J Clin Nutr. 2019;28(4):727–33. doi:https://doi.org/10.6133/apjcn.201912_28(4).0008
- Yi H, Ibrahim Z, A, Zaid Z, Mat Daud Z, Md Yusop N, Omar J, et al. Impact of enhanced recovery after surgery with preoperative whey protein-infused carbohydrate loading and postoperative early oral feeding among surgical gynecologic cancer patients: an open-labelled randomized controlled trial. Nutrients. 2020;12(1):264.
- Charoenkwan K, Matovinovic E. Early versus delayed oral fluids and food for reducing complications after major abdominal gynaecologic surgery. Cochran Database Syst Rev. 2014;2014(12):Cd004508.
- Minig L, Biffi R, Zanagnolo V, Attanasio A, Beltrami C, Bocciolone L, Botteri E, Colombo N, Iodice S, Landoni F, et al. Early oral versus "traditional" postoperative feeding in gynecologic oncology patients undergoing intestinal resection: a randomized controlled trial. Ann Surg Oncol. 2009;16(6):1660–8. doi:https://doi.org/10.1245/s10434-009-0444-2
- Bisch SP, Wells T, Gramlich L, Faris P, Wang X, Tran DT, Thanh NX, Glaze S, Chu P, Ghatage P, et al. Enhanced Recovery After Surgery (ERAS) in gynecologic oncology: System-wide implementation and audit leads to improved value and patient outcomes. Gynecol Oncol. 2018;151(1):117–23. doi:https://doi.org/10.1016/j.ygyno.2018.08.007
- Minig L, Biffi R, Zanagnolo V, Attanasio A, Beltrami C, Bocciolone L, Botteri E, Colombo N, Iodice S, Landoni F, et al. Reduction of postoperative complication rate with the use of early oral feeding in gynecologic oncologic patients undergoing a major surgery: a randomized controlled trial. Ann Surg Oncol. 2009;16(11):3101–10. doi:https://doi.org/10.1245/s10434-009-0681-4
- Feo CV, Romanini B, Sortini D, Ragazzi R, Zamboni P, Pansini GC, Liboni A. Early oral feeding after colorectal resection: a randomized controlled study. ANZ J Surg. 2004;74(5):298–301. doi:https://doi.org/10.1111/j.1445-1433.2004.02985.x
- Lassen K, Kjaeve J, Fetveit T, Tranø G, Sigurdsson HK, Horn A, Revhaug A. Allowing normal food at will after major upper gastrointestinal surgery does not increase morbidity: a randomized multicenter trial. Ann Surg. 2008;247(5):721–9. doi:https://doi.org/10.1097/SLA.0b013e31815cca68
- Cohen CW, Fontaine KR, Arend RC, Alvarez RD, Leath Iii CA, Huh WK, Bevis KS, Kim KH, Straughn JM, Gower BA, et al. A ketogenic diet reduces central obesity and serum insulin in women with ovarian or endometrial cancer. J Nutr. 2018;148(8):1253–60. doi:https://doi.org/10.1093/jn/nxy119
- Fine EJ, Miller A, Quadros EV, Sequeira JM, Feinman RD. Acetoacetate reduces growth and ATP concentration in cancer cell lines which over-express uncoupling protein 2. Cancer Cell Int. 2009;9(1):14. doi:https://doi.org/10.1186/1475-2867-9-14
- Petersen MC, Shulman GI. Mechanisms of insulin action and insulin resistance. Physiol Rev. 2018;98(4):2133–223. doi:https://doi.org/10.1152/physrev.00063.2017
- Wischmeyer PE, Carli F, Evans DC, Guilbert S, Kozar R, Pryor A, Thiele RH, Everett S, Grocott M, Gan TJ, Perioperative Quality Initiative (POQI) 2 Workgroup, et al. American Society for Enhanced recovery and perioperative quality initiative joint consensus statement on nutrition screening and therapy within a surgical enhanced recovery pathway. Anesth Analg. 2018;126(6):1883–95. doi:https://doi.org/10.1213/ANE.0000000000002743
- Cao D-x, Wu G-h, Zhang B, Quan Y-j, Wei J, Jin H, Jiang Y, Yang Z-a. Resting energy expenditure and body composition in patients with newly detected cancer. Clin Nutr. 2010;29(1):72–7. doi:https://doi.org/10.1016/j.clnu.2009.07.001
- Rock CL, Doyle C, Demark-Wahnefried W, Meyerhardt J, Courneya KS, Schwartz AL, Bandera EV, Hamilton KK, Grant B, McCullough M, et al. Nutrition and physical activity guidelines for cancer survivors. CA Cancer J Clin. 2012;62(4):243–74. doi:https://doi.org/10.3322/caac.21142
- Maurer T, von Grundherr J, Patra S, Jaeger A, Becher H, Schmalfeldt B, Zyriax B-C, Chang-Claude J. An exercise and nutrition intervention for ovarian cancer patients during and after first-line chemotherapy (BENITA study): a randomized controlled pilot trial. Int J Gynecol Cancer. 2020;30(4):541–5. doi:https://doi.org/10.1136/ijgc-2019-000585
- Albaugh VL, Pinzon-Guzman C, Barbul A. Arginine-dual roles as an onconutrient and immunonutrient. J Surg Oncol. 2017;115(3):273–80. doi:https://doi.org/10.1002/jso.24490
- Cetinbas F, Yelken B, Gulbas Z. Role of glutamine administration on cellular immunity after total parenteral nutrition enriched with glutamine in patients with systemic inflammatory response syndrome. J Crit Care. 2010;25(4):661.e1–661.e6. doi:https://doi.org/10.1016/j.jcrc.2010.03.011
- Calder PC. Polyunsaturated fatty acids and inflammation. Prostaglandin Leukot Essent Fatty Acid. 2006;75(3):197–202. doi:https://doi.org/10.1016/j.plefa.2006.05.012
- Braga M, Gianotti L, Vignali A, Carlo VD. Preoperative oral arginine and n-3 fatty acid supplementation improves the immunometabolic host response and outcome after colorectal resection for cancer. Surgery. 2002;132(5):805–14. doi:https://doi.org/10.1067/msy.2002.128350
- McCarthy MS, Martindale RG. Immunonutrition in critical illness: what is the role?Nutr Clin Pract. 2018;33(3):348–58. doi:https://doi.org/10.1002/ncp.10102
- Shuvayeva G, Bobak Y, Igumentseva N, Titone R, Morani F, Stasyk O, Isidoro C. Single amino acid arginine deprivation triggers prosurvival autophagic response in ovarian carcinoma SKOV3. Biomed Res Int. 2014;2014:505041. doi:https://doi.org/10.1155/2014/505041
- Yuan L, Sheng X, Willson AK, Roque DR, Stine JE, Guo H, Jones HM, Zhou C, Bae-Jump VL. Glutamine promotes ovarian cancer cell proliferation through the mTOR/S6 pathway. Endocr Relat Cancer. 2015;22(4):577–91. doi:https://doi.org/10.1530/ERC-15-0192
- Keshet R, Erez A. Arginine and the metabolic regulation of nitric oxide synthesis in cancer. Dis Model Mech. 2018;11(8):dmm033332. doi:https://doi.org/10.1242/dmm.033332
- Matés JM, Campos-Sandoval JA, Santos-Jiménez JL, Márquez J. Dysregulation of glutaminase and glutamine synthetase in cancer. Cancer Lett. 2019;467:29–39. doi:https://doi.org/10.1016/j.canlet.2019.09.011
- Buzquurz F, Bojesen RD, Grube C, Madsen MT, Gögenur I. Impact of oral preoperative and perioperative immunonutrition on postoperative infection and mortality in patients undergoing cancer surgery: systematic review and meta-analysis with trial sequential analysis. BJS Open. 2020;4(5):764–75. doi:https://doi.org/10.1002/bjs5.50314
- Chapman JS, Roddy E, Westhoff G, Simons E, Brooks R, Ueda S, Chen L. Post-operative enteral immunonutrition for gynecologic oncology patients undergoing laparotomy decreases wound complications. Gynecol Oncol. 2015;137(3):523–8. doi:https://doi.org/10.1016/j.ygyno.2015.04.003
- Hertlein L, Zeder-Göß C, Fürst S, Bayer D, Trillsch F, Czogalla B, Mahner S, Burges A, Rittler P. Peri-operative oral immunonutrition in malnourished ovarian cancer patients assessed by the nutritional risk screening. Arch Gynecol Obstet. 2018;297(6):1533–8. doi:https://doi.org/10.1007/s00404-018-4759-8
- Kuroki L, Guntupalli SR. Treatment of epithelial ovarian cancer. BMJ. Clinical Res. 2020;371:m3773.