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.

Abstract

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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