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Neurokinin 1 (NK1) receptors are distributed across the GI tract, vagal afferents, and key CNS regions including the central vomiting center and chemoreceptor trigger zone (CTZ) Chemotherapy agents stimulate enterochromaffin cells in the gastrointestinal (GI) tract to release large amounts of substance P (SP). SP is a neuropeptide released by specific sensory nerves in response to many different stressors, including those in the GI mucosa affected by chemotherapy.  SP binds and activates...
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5-HT3 receptor antagonists, such as dolasetron, granisetron (Kytril), ondansetron (Zofran), and palonosetron (Axoli), are crucial in managing chemotherapy-induced nausea and vomiting (CINV) and postoperative nausea. These drugs selectively block 5-HT3 receptors in the visceral vagal and spinal afferent nerves, chemoreceptor trigger zone, and the vomiting center. They have a rapid onset of action and can be given as a single dose before chemotherapy. Ondansetron and granisetron, in particular,...
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Tetrahydrocannabinol (THC) is a phytocannabinoid that primarily interacts with the CB1 receptor, a type of G protein-coupled receptor (GPCR) predominantly in and around the chemoreceptor trigger zone (CTZ) and emetic center. THC also blocks the serotonin receptor activity in the dorsal vagal complex (DVC) by inhibiting serotonin release. THC exerts its anti-emetic effects through these interactions, which are beneficial for patients undergoing chemotherapy.
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Updated: Jan 9, 2026

Acupoint Application Combined with Acupressure as an Adjunctive Therapy for Chemotherapy-Induced Nausea and Vomiting
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Delayed Chemotherapy-Induced Nausea - A Nurse-Led International Observational Study in Routine Oncology Practice

Ramona Engst1, Agnes Glaus2, Ulrike Moessner3

  • 1School of Health, OST Eastern Switzerland University of Applied Sciences, St.Gallen, Switzerland.

SAGE Open Nursing
|December 8, 2025
PubMed
Summary

Delayed chemotherapy-induced nausea (dCIN) affects nearly 19% of patients receiving low emetogenic chemotherapy (LEC). This highlights the need for better symptom management strategies beyond current risk classifications for cancer patients.

Keywords:
Delayed chemotherapy-induced nauseaoncology nursingprevalencesupportive caresurvey

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Area of Science:

  • Oncology
  • Clinical Pharmacology
  • Patient Quality of Life

Background:

  • Chemotherapy-induced nausea and vomiting (CINV) significantly impacts patient quality of life and treatment adherence.
  • Delayed CINV (dCIN) is commonly associated with moderate/high emetogenic chemotherapy but can occur with low (LEC) and minimal (MinEC) regimens.
  • Real-world data on dCIN occurrence, particularly with LEC and MinEC, is crucial for optimizing supportive care.

Purpose of the Study:

  • To assess the incidence and characteristics of delayed chemotherapy-induced nausea (dCIN) in patients undergoing systemic antitumour therapy.
  • To specifically evaluate dCIN occurrence in patients receiving low (LEC) and minimally emetogenic chemotherapy (MinEC).
  • To identify risk factors associated with dCIN in a real-world clinical setting.

Main Methods:

  • Prospective, multicentre, international, cross-sectional study.
  • Adult oncology outpatients receiving systemic antitumour therapy were enrolled.
  • Delayed CINV intensity was self-rated daily using a 0-100 visual analogue scale (VAS) for five consecutive days.

Main Results:

  • Delayed chemotherapy-induced nausea (dCIN) occurred in 18.5% of patients receiving low emetogenic chemotherapy (LEC) and 3% receiving minimally emetogenic chemotherapy (MinEC).
  • Vomiting was infrequent (1.7%).
  • Independent risk factors for dCIN included younger age and gastrointestinal tumours; emetogenicity, fear, and prior vomiting were not significant predictors in the final model.

Conclusions:

  • A substantial proportion of patients receiving low emetogenic chemotherapy (LEC) experience delayed chemotherapy-induced nausea (dCIN) in clinical practice.
  • Current emetogenic risk classifications may not fully capture the risk of dCIN.
  • Improved symptom management and tailored interventions are necessary for patients experiencing dCIN, irrespective of chemotherapy emetogenicity.