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Antiemetics: American Society of Clinical Oncology Clinical Practice Guideline Update
Author(s) -
Paul J. Hesketh,
Mark G. Kris,
Ethan Basch,
Kari Bohlke,
Sally Barbour,
Rebecca Clark-Snow,
Michael Danso,
Kristopher Dennis,
L. Lee Dupuis,
Stacie B. Dusetzina,
Cathy Eng,
Petra Feyer,
Karin Jordan,
Kimberly Noonan,
Dee Sparacio,
Mark R. Somerfield,
Gary H. Lyman
Publication year - 2017
Publication title -
journal of clinical oncology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.482
H-Index - 548
eISSN - 1527-7755
pISSN - 0732-183X
DOI - 10.1200/jco.2017.74.4789
Subject(s) - medicine , aprepitant , antiemetic , nausea , vomiting , carboplatin , chemotherapy induced nausea and vomiting , guideline , olanzapine , randomized controlled trial , chemotherapy , oncology , psychiatry , cisplatin , schizophrenia (object oriented programming) , pathology
Purpose To update the ASCO guideline for antiemetics in oncology. Methods ASCO convened an Expert Panel and conducted a systematic review of the medical literature for the period of November 2009 to June 2016. Results Forty-one publications were included in this systematic review. A phase III randomized controlled trial demonstrated that adding olanzapine to antiemetic prophylaxis reduces the likelihood of nausea among adult patients who are treated with high emetic risk antineoplastic agents. Randomized controlled trials also support an expanded role for neurokinin 1 receptor antagonists in patients who are treated with chemotherapy. Recommendation Key updates include the addition of olanzapine to antiemetic regimens for adults who receive high-emetic-risk antineoplastic agents or who experience breakthrough nausea and vomiting; a recommendation to administer dexamethasone on day 1 only for adults who receive anthracycline and cyclophosphamide chemotherapy; and the addition of a neurokinin 1 receptor antagonist for adults who receive carboplatin area under the curve ≥ 4 mg/mL per minute or high-dose chemotherapy, and for pediatric patients who receive high-emetic-risk antineoplastic agents. For radiation-induced nausea and vomiting, adjustments were made to anatomic regions, risk levels, and antiemetic administration schedules. Rescue therapy alone is now recommended for low-emetic-risk radiation therapy. The Expert Panel reiterated the importance of using the most effective antiemetic regimens that are appropriate for antineoplastic agents or radiotherapy being administered. Such regimens should be used with initial treatment, rather than first assessing the patient's emetic response with less-effective treatment. Additional information is available at www.asco.org/supportive-care-guidelines and www.asco.org/guidelineswiki .

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