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Cited by 214Nausea and vomiting managementPregnancy and Medication ImpactCancer survivorship and care

The DOI matches its Crossref record; 24 of the 24 references it cites were found in a registry or an index.

Efficacy of dronabinol alone and in combination with ondansetron versus ondansetron alone for delayed chemotherapy-induced nausea and vomiting

Meiri, Eyal, Jhangiani, Haresh, Vredenburgh, James J., Barbato, Luigi M., Carter, Frederick J., Yang, Hwa-Ming, Baranowski, Vickie·2007·Current Medical Research and Opinion
DOI 10.1185/030079907x167525
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Abstract

OBJECTIVE: To compare the efficacy and tolerability of dronabinol, ondansetron, or the combination for delayed chemotherapy-induced nausea and vomiting (CINV) in a 5-day, double-blind, placebo-controlled study. RESEARCH DESIGN AND METHODS: Patients receiving moderately to highly emetogenic chemotherapy received dexamethasone (20 mg PO), ondansetron (16 mg IV) and either placebo or dronabinol (2.5 mg) prechemotherapy on day 1. Patients randomized to active treatment (dronabinol and/or ondansetron) also received dronabinol (2.5 mg) after chemotherapy on day 1. On day 2, fixed doses of placebo, dronabinol (10 mg), ondansetron (16 mg), or combination therapy were administered. On days 3-5, patients received placebo, flexible doses of dronabinol (10-20 mg), ondansetron (8-16 mg), or dronabinol and ondansetron (10-20 mg dronabinol, 8-16 mg ondansetron). MAIN OUTCOME MEASURES: Total response (TR = nausea intensity <5 mm on visual analog scale, no vomiting/retching, no rescue antiemetic), nausea (occurrence and intensity) and vomiting/retching episodes. RESULTS: Sixty-four patients were randomized; 61 analyzed for efficacy. TR was similar with dronabinol (54%), ondansetron (58%), and combination therapy (47%) versus placebo (20%). Nausea absence was significantly greater in active treatment groups (dronabinol, 71%; ondansetron, 64%; combination therapy, 53%) versus placebo (15%; p < 0.05 vs. placebo for all). Nausea intensity and vomiting/retching were lowest in patients treated with dronabinol. Active treatments were well tolerated. The low number of patients due to slow enrollment limits the interpretation of these data. CONCLUSIONS: Dronabinol or ondansetron was similarly effective for the treatment of CINV. Combination therapy with dronabinol and ondansetron was not more effective than either agent alone. Active treatments were well tolerated.

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Research works printed but not linked: 3

  1. Gandara DR, 1992, Semin Oncol, 19, 67
  2. Navari RM, 2003, J Support Oncol, 1, 89
  3. Prevention of chemotherapy- and radiotherapy-induced emesis, 1998, Antiemetic Subcommittee of the Multinational Association of Supportive Care in Cancer (MASCC). Ann Oncol, 9, 811

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Metadata

Authors
Meiri, E., Jhangiani, H., Vredenburgh, J. J., Barbato, L. M., Carter, F. J., Yang, H.-M., & Baranowski, V.
Affiliations
  • Bethesda Hospital East (US)
  • Compassionate Cancer Care (US)
  • Duke Medical Center (US)
  • Solvay (United States) (US)
Corresponding author
Meiri, Eyal
ORCID
Vredenburgh, James J.
Venue
Current Medical Research and Opinion
Publisher
Informa Healthcare
Published
2007-02-01
Volume
23
Issue
3
Pages
533-543
ISSN
  • 0300-7995 (ISSN-L)
  • 1473-4877
DOI
10.1185/030079907x167525
OpenAlex
W2053215778
Cited by
214
References
24
Citations by year
2025: 10 · 2024: 17 · 2023: 9 · 2022: 21 · 2021: 16 · 2020: 15 · 2019: 18 · 2018: 18 · 2017: 12 · 2016: 15 · 2015: 13 · 2014: 7 · 2013: 8 · 2012: 8
FWCI
7.97
Type
journal article
Language
en
Open access
closed
Locations
  • Current Medical Research and Opinion (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Surgery › Nausea and vomiting management
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Pregnancy and Medication Impact
  • Health Sciences › Medicine › Oncology › Cancer survivorship and care
Keywords
dronabinol, ondansetron, combination antiemetic therapy, cannabinoids, antiemetic efficacy, tolerability, dexamethasone
MeSH terms
Adolescent, Adult, Analysis of Variance, Antineoplastic Combined Chemotherapy Protocols, Dose-Response Relationship, Drug, Double-Blind Method, Drug Administration Schedule, Drug Therapy, Combination, Female, Follow-Up Studies, Humans, Male, Middle Aged, Nausea, Neoplasms, Probability, Reference Values, Dronabinol, Vomiting, Treatment Outcome, Ondansetron, Risk Assessment

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