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Chemotherapy-Related Nausea & Vomiting
Author Bio
Introduction
What Causes Nausea & Vomiting?
Automatic Nervous System
Chemotherapy Induced NV
NV Control
Issues in Research Design
Case Study 1
Currently selected section: Case Study 2
Summary

 


Chapter 11: Chemotherapy-Related Nausea & Vomiting: Case Study 2
         In this case study, the outstanding question is, "What treatment works best for controlling delayed nausea?" (Note: This is a current research concern and a protocol designed to answer this question was submitted to the National Cancer Institute in October, 2000, by the author of this chapter, and is described below.)

Background

The control of treatment-induced delayed nausea is a high priority for oncologists, but they are hampered in this endeavor by a lack of information as to what the optimal pharmaceutical treatment is, especially for highly emetogenic chemotherapy regimens, such as those containing anthracyclines. While there are well-accepted published guidelines (Gandara et al., 1998; Gralla et al., 1999) on what to give patients on the day of treatment for the control of acute nausea and emesis from highly emetogenic chemotherapy (i.e. a 5-HT3 receptor antagonist antiemetic with a corticosteroid), there are no such guidelines for the prophylactic control of delayed nausea. The lack of published guidelines on what is the most efficacious antiemetic to give patients on days 2 - 4 following highly emetogenic chemotherapy is reflected in survey results from 27 oncologists who are affiliated with the URCC CCOP research base.

We queried these physicians on what antiemetic regimen they give new patients with breast cancer scheduled to receive a first treatment of cyclophosphamide and doxorubicin therapy. Their responses illustrated the problems in this area.

  • Not surprisingly, the large majority, 25 of 27 respondents, follow the American Society of Clinical Oncology guidelines (ASCO) (Gralla et al., 1999), reporting that they give a 5-HT3 receptor antagonist antiemetic with a corticosteroid on the day of treatment.

  • No consensus emerged, however, for the prophylactic control of nausea and emesis on days 2 - 4 following treatment. There were nine different antiemetic regimens used, none of which were endorsed by more than eight respondents. Eighteen of the oncologists prescribed prochlorperazine (Compazine), either alone or in combination with other drugs, while 14 respondents prescribed a 5-HT3 receptor antagonist; again, either alone or in combination with other drugs.

  • In addition to the differences in the medication or medications prescribed, there was also no consensus as to whether the medications should be taken regardless of symptoms in order to prevent nausea from developing or to take the medications only on an as-needed basis (p.r.n.).


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