2011
DOI: 10.1200/jop.2011.000397
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Antiemetics: American Society of Clinical Oncology Clinical Practice Guideline Update

Abstract: ASCO's update to its antiemetics guideline now includes an evaluation of evidence on complementary antiemetic therapy.

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Cited by 200 publications
(302 citation statements)
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“…Although no randomized study has compared the antiemetic potency of available corticosteroids, the most frequently used steroid as an antiemetic is dexamethasone. Dexamethasone is usually used in combination with serotonin (5-hydroxytryptamine 3 ) or neurokinin-1 receptor antagonists for highly or moderately emetogenic chemotherapy or as monotherapy for mildly emetogenic chemotherapy [6][7][8][9].…”
Section: Introductionmentioning
confidence: 99%
“…Although no randomized study has compared the antiemetic potency of available corticosteroids, the most frequently used steroid as an antiemetic is dexamethasone. Dexamethasone is usually used in combination with serotonin (5-hydroxytryptamine 3 ) or neurokinin-1 receptor antagonists for highly or moderately emetogenic chemotherapy or as monotherapy for mildly emetogenic chemotherapy [6][7][8][9].…”
Section: Introductionmentioning
confidence: 99%
“…At the MASCC meeting in Rome (June 2009), palonosetron was put forward as the setron of choice for MEC. [27][28][29][30] As stated before, adherence to guidelines is one of the three risk factors for patients receiving HEC or MEC. Unfortunately, it is known that adherence to and implementation of recommendations are below the optimal level.…”
Section: Clinical Guidelinesmentioning
confidence: 99%
“…Table 2 lists the actual antiemetic guidelines. [27][28][29][30] There is a strong degree of concordance between the different guidelines. Triple therapy with a setron, dexamethasone, and an NK-1 receptor antagonist is the regimen of preference for acute emesis due to HEC.…”
Section: Clinical Guidelinesmentioning
confidence: 99%
“…The oral neurokinin-1 receptor antagonist aprepitant is an antiemetic drug with a new mechanism of action that not only shows efficacy for acute CINV (within 24 hours of starting chemotherapy) but also for delayed CINV (24 hours or more after starting chemotherapy), which is poorly controlled by current therapies, and the efficacy of aprepitant against the emetic effect of singledose cisplatin has been demonstrated (Roila et al, 2010;Basch et al, 2011).…”
Section: Introductionmentioning
confidence: 99%
“…We employ a daily cisplatin regimen (FP therapy with daily administration of cisplatin at 20mg/m 2 from Day 1 to Day 4 and 5-fluorouracil (5-FU) at 400 mg/m 2 from Day 1 to Day 5) (Brizel et al, 1998) to treat patients with head and neck cancer (HNC), but there have been few studies on the efficacy of aprepitant during daily administration of cisplatin and no specific antiemetic regimen for daily cisplatin therapy has been established (Roila et al, 2010;Basch et al, 2011;Einhorn et al, 2011). When FP therapy is performed at our department, severe nausea tends to occur on or after the last day of cisplatin administration and it has a strong impact on quality of life (Sun et al, 2005).…”
Section: Introductionmentioning
confidence: 99%