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Published on: June 21, 2024
Emetic risk classification and evaluation of the emetogenicity of antineoplastic agents-updated MASCC/ESMO consensus
Karin Jordan1,2, Alexandre Chan3, Richard J Gralla4
1Department of Hematology, Oncology and Palliative Medicine, Ernst von Bergmann Hospital Potsdam, Charlottenstraße 72, 14467, Potsdam, Germany. karin.jordan@med.uni-heidelberg.de.
Purpose:
Our goal was to identify new anticancer agents approved by the US Food and Drug Administration (FDA) and the European Medical Agency (EMA) since the 2016 MASCC/ESMO antiemetic update and classify their emetic potential.
Methods:
The MASCC/ESMO Expert Panel classified the emetogenicity of the identified new antineoplastic agents based on nonsystematic reviews of randomized controlled trials, analysis of product labeling, and evaluation of emetic classification in other international guidelines and informal consensus. The emetogenic classification system for oral anticancer agents was revised into two emetic risk categories (minimal-low; moderate-high) to be consistent with the system reported by ASCO (American Society of Clinical Oncology) in their 2017 guideline update. The previously employed four emetic risk classification categories for intravenously administered antineoplastic agents were retained for this update.
Results:
From June 2015 to January 2023, 107 new antineoplastic agents (44 intravenously administered and 63 orally administered agents) were identified. The reported incidence of vomiting varied significantly across studies for many agents, especially for oral anticancer agents.
Conclusion:
The MASCC/ESMO Expert Panel acknowledges the limitations of our efforts to classify the emetic potential of anticancer agents, especially the imprecision associated with oral agents. However, we have attempted to provide a reasonable approximation of the emetic risk associated with new antineoplastic agents by searching the available literature and reviewing other available international antiemetic guidelines.
Insights
This study identified 107 new anticancer agents and classified their emetic potential, revising risk categories for oral agents to improve antiemetic guideline accuracy.
Area of Science:
- Oncology
- Pharmacology
- Clinical Pharmacy
Background:
- Antiemetic guidelines are crucial for managing chemotherapy-induced nausea and vomiting (CINV).
- Recent advancements in oncology have led to numerous new anticancer agents requiring updated emetic potential classification.
- The Multinational Association of Supportive Care in Cancer (MASCC) and European Society for Medical Oncology (ESMO) previously updated antiemetic guidelines in 2016.
Purpose of the Study:
- To identify new anticancer agents approved by the US Food and Drug Administration (FDA) and European Medical Agency (EMA) since the 2016 MASCC/ESMO antiemetic update.
- To classify the emetic potential of these newly approved antineoplastic agents.
- To provide updated information for antiemetic guideline development and clinical practice.
Main Methods:
- The MASCC/ESMO Expert Panel reviewed randomized controlled trials, product labeling, and international guidelines.
- A revised emetogenic classification system was developed for oral anticancer agents, with two categories: minimal-low and moderate-high.
- The existing four-category system for intravenously administered antineoplastic agents was maintained.
Main Results:
- A total of 107 new antineoplastic agents were identified between June 2015 and January 2023.
- Of these, 44 were administered intravenously and 63 orally.
- Significant variability in reported vomiting incidence was observed across studies, particularly for oral agents.
Conclusions:
- The study provides an updated classification of the emetic potential for new anticancer agents.
- Limitations include imprecision in classifying the emetic risk of oral agents due to data variability.
- The findings offer a reasonable approximation of emetic risk to inform antiemetic guidelines and patient care.
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