TY - JOUR
T1 - Consensus proposal for 5HT3 antagonists in the prevention of acute emesis related to highly emetogenic chemotherapy. Dose, schedule, and route of administration
AU - Gandara, David R.
AU - Roila, Fausto
AU - Warr, David
AU - Edelman, Martin J.
AU - Perez, Edith A.
AU - Gralla, Richard J.
PY - 1998/4
Y1 - 1998/4
N2 - Selective antagonists to the Type 3 serotonin receptor (5HT3) in combination with corticosteroids are now considered the standard of care for the prevention of emesis from moderately to highly emetogenic chemotherapy. Here we address issues of optimal dose, schedule and route of administration of four currently available selectable 5HT3 antagonists. This paper utilizes an evidence based medicine approach to the literature regarding this class of drugs, emphasizing the results large, randomized, controlled trials to make formal recommendations concerning optimal use of this important new class of anti-emetic agents. We conclude that for each drug there is a plateau in therapeutic efficacy at a definable dose level above which further dose escalation does not improve outcome. Furthermore, a single dose is as effective as multiple doses or continuous infusion, and finally, emerging data demonstrate that the oral route is equally efficacious as the intravenous route of administration, even with highly emetogenic chemotherapy.
AB - Selective antagonists to the Type 3 serotonin receptor (5HT3) in combination with corticosteroids are now considered the standard of care for the prevention of emesis from moderately to highly emetogenic chemotherapy. Here we address issues of optimal dose, schedule and route of administration of four currently available selectable 5HT3 antagonists. This paper utilizes an evidence based medicine approach to the literature regarding this class of drugs, emphasizing the results large, randomized, controlled trials to make formal recommendations concerning optimal use of this important new class of anti-emetic agents. We conclude that for each drug there is a plateau in therapeutic efficacy at a definable dose level above which further dose escalation does not improve outcome. Furthermore, a single dose is as effective as multiple doses or continuous infusion, and finally, emerging data demonstrate that the oral route is equally efficacious as the intravenous route of administration, even with highly emetogenic chemotherapy.
KW - Antiemetics/administration & dosage
KW - Antineoplastic Agents/adverse effects
KW - Dose-Response Relationship, Drug
KW - Drug Administration Routes
KW - Drug Administration Schedule
KW - Evidence-Based Medicine
KW - Humans
KW - Neoplasms/drug therapy
KW - Palliative Care
KW - Randomized Controlled Trials as Topic
KW - Receptors, Serotonin, 5-HT3
KW - Receptors, Serotonin/drug effects
KW - Serotonin Antagonists/administration & dosage
KW - Treatment Outcome
KW - Vomiting/chemically induced
UR - http://www.scopus.com/inward/record.url?scp=0031596456&partnerID=8YFLogxK
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=purepublist2023&SrcAuth=WosAPI&KeyUT=WOS:000073617100010&DestLinkType=FullRecord&DestApp=WOS
U2 - 10.1007/s005200050160
DO - 10.1007/s005200050160
M3 - Review article
C2 - 9629876
SN - 0941-4355
VL - 6
SP - 237
EP - 243
JO - Supportive Care in Cancer
JF - Supportive Care in Cancer
IS - 3
ER -