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Home » Eating Disorders

Cancer Management: A Multidisciplinary Approach, 12th Edition (2009).
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Cancer Management Chapter 38: Anorexia and Cachexia

By Charles Loprinzi, MD, and Aminah Jatoi, MD | March 16, 2010

Enteral or parenteral nutrition
Despite the demonstrated efficacy of corticosteroids and progestational agents in patients with cancer anorexia and cachexia, these drugs do not have a major long-term impact on the vast majority of such patients. Consequently, other treatment approaches, such as enteral or parenteral nutritional methods, have been studied extensively. Several randomized trials failed to demonstrate that these nutritional approaches improve either quantity or quality of life. As a result, experts generally agree that the routine use of parenteral or enteral nutrition cannot be justified in patients with advanced cancer anorexia and cachexia.

There are, however, relatively rare circumstances in which parenteral nutrition may play a role in patients with advanced cancer. Such circumstances have been documented by case reports and small case series and have included patients with GI insufficiency due to surgery, radiation therapy, or abdominal carcinomatosis (without impending failure of other organs). The decision to initiate parenteral nutrition under these circumstances typically requires a multidisciplinary approach with extensive discussions between healthcare providers and family members.

Prophylactic therapy
Given the positive impact of corticosteroids and progestational agents on cancer anorexia and cachexia and the fact that many patients with advanced cancer die with, and/or of, inanition, the potential prophylactic use of these agents was evaluated. A double-blind trial was conducted in which patients with newly diagnosed, extensive-stage small-cell lung cancer were randomized to receive megestrol(Drug information on megestrol) or placebo along with standard chemoradiation therapy. This trial was unable to demonstrate any beneficial effect of megestrol on treatment response, quality of life, or survival.

Thus, patients should not be treated prophylactically for cancer anorexia and cachexia outside a clinical trial. Rather, such treatment should be reserved for patients in whom anorexia and cachexia are patient-determined, symptomatic clinical problems.

NUTRITION AS IT RELATES TO END-OF-LIFE CARE
Anorexia and cachexia are major problems for many oncology patients as they approach the final stage of life. Family members are generally more distressed than the patients if/when appetite stimulants do not provide relief. Questions commonly arise about giving enteral or parenteral nutrition or “forcing” patients to consume more calories in the belief that they would feel better, get stronger, and live longer. A small measure of appropriate education, noting that the intake of more calories does not appear to have a clinical benefit, provides substantial relief. It is worthwhile to note that patients randomized to receive total parenteral nutrition or appetite stimulants (such as megestrol) do not live any longer than do control patients and that “force-feeding” is not in the patients’ best interests.

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SUGGESTED READING

Bozzetti F, Mariani L: Defining and classifying cancer cachexia: a proposal by the SCRINIO Working Group. JPEN J Parenter Enteral Nutr In press, 2008.

Evans WJ, Morley JE, Argilés J, et al: Cachexia: a new definition. Clin Nutr 27:793–799, 2008.

Halfdanarson TR, Thordardottir E, West CP, et al: Does dietary counseling improve quality of life in cancer patients? A systematic review and meta-analysis. J Support Oncol 6:234–237, 2008.

Jatoi A, Dakhil SR, Nguyen PL, et al: A placebo-controlled double blind trial of etanercept for the cancer anorexia/weight loss syndrome: Results from N00C1 from the North Central Cancer Treatment Group. Cancer 110:1396–1403, 2007.

Jatoi A, Rowland K, Loprinzi CL, et al: An eicosapentaenoic acid supplement versus megestrol acetate versus both for patients with cancer-associated wasting: A North Central Cancer Treatment Group and National Cancer Institute of Canada collaborative effort. J Clin Oncol 22:2469–2476, 2004.

Jatoi A, Windschitl HE, Loprinzi CL, et al: Dronabinol vs megestrol acetate vs both for cancer-associated anorexia: A North Central Cancer Treatment Group Study. J Clin Oncol 20:567–573, 2002.

Loprinzi CL, Kugler JW, Sloan JA, et al: Randomized comparison of megestrol acetate versus dexamethasone versus fluoxymesterone for the treatment of cancer anorexia/cachexia. J Clin Oncol 17:3299–3306, 1999.

Lundholm K, Körner U, Bunnebo L, et al: Insulin treatment in cancer cachexia: effects on survival, metabolism, and physical functioning. Clin Cancer Res 13:2699–2706, 2007.

Mann M, Koller E, Murgo A, et al: Glucocorticoid-like activity of megestrol. Arch Intern Med 157:1651–1656, 1997.

Moertel CG, Schutt AJ, Reitemeier RJ, et al: Corticosteroid therapy of preterminal gastrointestinal cancer. Cancer 33:1607–1609, 1974.

Ravasco P, Monteiro-Grillo I, Marques Vidal P, et al: Impact of nutrition on outcome: A prospective randomized controlled trial in patients with head and neck cancer undergoing radiotherapy. Head Neck 27:659–668, 2005.

Ravasco P, Monteiro-Grillo I, Vidal PM, et al: Dietary counseling improves patient outcomes: A prospective, randomized controlled trial in colorectal cancer patients undergoing radiotherapy. J Clin Oncol 23:1431–1438, 2005.

Rock CL: Dietary counseling is beneficial for the patient with cancer. J Clin Oncol 23:1348–1349, 2005.

Strasser F, Lutz TA, Maeder MT, et al: Safety, tolerability and pharmacokinetics of intravenous ghrelin for cancer-related anorexia/cachexia: A randomised, placebo-controlled, double-blind, double-crossover study. Br J Cancer 98:300–308, 2008.

Abbreviations in this chapter
NCCTG = North Central Cancer Treatment Group; SCRINIO = Screening the Nutritional Status in Oncologic Patients


 
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