Clinical guideline

Antiemetics: American Society of Clinical Oncology Clinical Practice Guideline Update

JCO · 201741 publications included in the systematic review
Hesketh PJ, Kris MG, Basch E, Bohlke K, Barbour SY, Clark-Snow RA, et al. JCO. 2017. 35:3240-3261

A newer version of this guideline has been published: Antiemetics: ASCO Guideline Update (2020)

Study type
Clinical guideline
Study name
ASCO Antiemetics 2017
Design
Clinical practice guideline update based on a systematic review of the medical literature (November 2009 to June 2016) by an ASCO expert panel
Sample size
41 publications included in the systematic review
Source
JCO · 2017

In plain words

This guideline gives updated advice on preventing and treating nausea and vomiting caused by chemotherapy and radiotherapy. It says that for many patients it is better to use the most effective combination of anti-sickness medicines from the very start, rather than first trying weaker medicines to see how the body reacts. The choice of medicines depends on the type of chemotherapy or radiotherapy and should be agreed with the treating doctor.

Key points

41 publications
Number of publications included in the systematic review
Search period: November 2009 to June 2016
Reduced likelihood of nausea in adults
Adding olanzapine to antiemetic prophylaxis for highly emetogenic agents
Based on one randomised phase 3 trial
Expanded role in patients receiving chemotherapy
Role of neurokinin 1 (NK1) receptor antagonists
Based on randomised trials

Key guideline recommendations

  1. Olanzapine should be added to antiemetic regimens for adults who receive highly emetogenic antineoplastic agents or who have breakthrough nausea and vomiting.

  2. For adults who receive anthracycline and cyclophosphamide chemotherapy, dexamethasone should be given on day 1 only.

  3. A neurokinin 1 receptor antagonist should be added for adults who receive carboplatin AUC ≥ 4 mg/mL per minute or high-dose chemotherapy, and for paediatric patients who receive highly emetogenic antineoplastic agents.

  4. For radiation-induced nausea and vomiting, the anatomic regions, risk levels and antiemetic dosing schedules were revised; for radiotherapy with low emetic risk, rescue therapy only is recommended.

  5. The most effective antiemetic regimens appropriate for the antineoplastic agent or radiotherapy should be used from the start of treatment, rather than first assessing the patient's emetic response with less effective treatment.

Study population

Adults and children treated with anticancer agents (chemotherapy and other antineoplastic agents) and patients undergoing radiotherapy who are at risk of treatment-induced nausea and vomiting.

Endpoints

This guideline is an update of the recommendations for the prevention and treatment of chemotherapy-‎ and radiotherapy-induced nausea and vomiting. Details of the endpoints of the included studies are not given in the abstract and appear in the full text.

Safety and side effects

The abstract gives no detailed information on adverse events; see the full guideline for drug safety details.

Clinical significance and place in guidelines

This update added olanzapine to antiemetic regimens for highly emetogenic agents and for breakthrough nausea and vomiting, expanded the role of NK1 receptor antagonists (carboplatin AUC ≥ 4, high-dose chemotherapy and high-risk children) and limited dexamethasone to day 1 in anthracycline plus cyclophosphamide regimens. For low-risk radiotherapy, rescue therapy only is recommended. This guideline was published in 2017; the current status of the recommendations and later updates should be checked.

Limitations

The abstract does not address the guideline's limitations or the level of evidence and strength of each recommendation; these should be checked in the full text. The systematic review covers only publications from November 2009 to June 2016.

This summary was prepared by the editorial team from the published paper; the original paper is the final reference. Read the original abstract on PubMed.