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A phase II randomized double-blind placebo-controlled study of 6-gingerol as an anti-emetic in solid tumor patients receiving moderately to highly emetogenic chemotherapy

dc.contributor.authorJ. Konmunen_US
dc.contributor.authorK. Danwilaien_US
dc.contributor.authorN. Ngamphaiboonen_US
dc.contributor.authorB. Sripanidkulchaien_US
dc.contributor.authorA. Sookpraserten_US
dc.contributor.authorS. Subongkoten_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherNaresuan Universityen_US
dc.contributor.otherKhon Kaen Universityen_US
dc.contributor.otherThe College of Pharmacotherapy of Thailanden_US
dc.date.accessioned2018-12-21T06:52:12Z
dc.date.accessioned2019-03-14T08:02:58Z
dc.date.available2018-12-21T06:52:12Z
dc.date.available2019-03-14T08:02:58Z
dc.date.issued2017-04-01en_US
dc.description.abstract© 2017, Springer Science+Business Media New York. 6-Gingerol is a natural compound extracted from ginger. Preclinical studies demonstrated that 6-gingerol has an anti-emetic activity by inhibiting neurokinin-1, serotonin, and dopamine receptors. Several clinical trials examined crude ginger powder for preventing chemotherapy-induced nausea and vomiting (CINV), but none of them was conducted with a standardized bioactive compound. Patients who received moderately to highly emetogenic adjuvant chemotherapy were randomized to receive 6-gingerol 10 mg or placebo orally twice daily for 12 weeks. Ondansetron, metoclopramide, and dexamethasone were given to all patients. The primary endpoint was complete response (CR) rate defined as no emesis or rescue treatment at any time. Eighty-eight patients were randomized to receive 6-gingerol (N = 42) or placebo (N = 46). Most patients received highly emetogenic chemotherapy (93%). Overall CR rate was significantly higher in 6-gingerol group as compared with that of the placebo (77 vs. 32%; P < 0.001). The difference in means of appetite score was significant (P = 0.001) and more noticeable over time. Mean FACT-G score indicating quality of life was significantly higher (86.21) in 6-gingerol group at 64 days as compared with that of placebo group (72.36) (P < 0.001). No toxicity related to 6-gingerol was observed. Patients treated with 6-gingerol reported significantly less grade 3 fatigue (2 vs. 20%; P = 0.020). 6-Gingerol significantly improved overall CR rate in CINV, appetite and quality of life in cancer patients receiving adjuvant chemotherapy. A phase III randomized study of 6-gingerol is warranted to confirm these results.en_US
dc.identifier.citationMedical Oncology. Vol.34, No.4 (2017)en_US
dc.identifier.doi10.1007/s12032-017-0931-4en_US
dc.identifier.issn1559131Xen_US
dc.identifier.issn13570560en_US
dc.identifier.other2-s2.0-85016330879en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/41941
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85016330879&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleA phase II randomized double-blind placebo-controlled study of 6-gingerol as an anti-emetic in solid tumor patients receiving moderately to highly emetogenic chemotherapyen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85016330879&origin=inwarden_US

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