Publication: Randomized, double-blind, placebo-controlled study of aprepitant versus two dosages of olanzapine with ondansetron plus dexamethasone for prevention of chemotherapy-induced nausea and vomiting in patients receiving high-emetogenic chemotherapy
dc.contributor.author | Suthinee Ithimakin | en_US |
dc.contributor.author | Pathra Theeratrakul | en_US |
dc.contributor.author | Apirom Laocharoenkiat | en_US |
dc.contributor.author | Akarin Nimmannit | en_US |
dc.contributor.author | Charuwan Akewanlop | en_US |
dc.contributor.author | Nopadol Soparattanapaisarn | en_US |
dc.contributor.author | Sirisopa Techawattanawanna | en_US |
dc.contributor.author | Krittiya Korphaisarn | en_US |
dc.contributor.author | Pongwut Danchaivijitr | en_US |
dc.contributor.other | Faculty of Medicine, Siriraj Hospital, Mahidol University | en_US |
dc.date.accessioned | 2020-03-26T05:01:33Z | |
dc.date.available | 2020-03-26T05:01:33Z | |
dc.date.issued | 2020-01-01 | en_US |
dc.description.abstract | © 2020, Springer-Verlag GmbH Germany, part of Springer Nature. Purpose: We assessed the efficacy of aprepitant (APR) or 10 or 5 mg OLN (OLN10 or OLN5) plus ondansetron and dexamethasone for chemotherapy-induced nausea/vomiting (CINV) prophylaxis in patients receiving high-emetogenic chemotherapy (HEC). Methods: Patients who received doxorubicin + cyclophosphamide or cisplatin were given intravenous ondansetron and dexamethasone prior to chemotherapy and oral dexamethasone on days 2–4 and randomized 1:1:1 to receive APR125 on day 1 and APR80 on days 2–3 or OLN10 or OLN5 on days 1–4. Matched placebo controls were used. The primary endpoint was no nausea in ≤ 120 h. Secondary endpoints included CINV severity, complete response (CR) rate, adverse effects (AE), and quality of life. Results: Of 141 patients, 104 received AC and 37 received cisplatin. The no-nausea rates were 33% (APR), 43.2% (OLN10; p = 0.24), and 37% (OLN5; p = 0.87). Grades 2–4 nausea were experienced by fewer patients for OLN10 than for APR (24–120 h, 8.7% vs. 27.7%, respectively; p = 0.02; overall period, 19.6% vs. 40.4%, respectively; p = 0.03). The median visual analog scale nausea score from 24 to 120 h was significantly lower for OLN10 (2.3) than for APR (1.2, p = 0.03). The degrees of vomiting, CR, and AE were similar between the APR and OLN10 groups. CINV was similar between the OLN5 and APR groups. Conclusions: Nausea was less severe for OLN10 than for APR in patients receiving HEC, but other measures were similar. CINV prevention efficacy was comparable between OLN5 and APR. | en_US |
dc.identifier.citation | Supportive Care in Cancer. (2020) | en_US |
dc.identifier.doi | 10.1007/s00520-020-05380-6 | en_US |
dc.identifier.issn | 14337339 | en_US |
dc.identifier.issn | 09414355 | en_US |
dc.identifier.other | 2-s2.0-85081034214 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/53805 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85081034214&origin=inward | en_US |
dc.subject | Medicine | en_US |
dc.title | Randomized, double-blind, placebo-controlled study of aprepitant versus two dosages of olanzapine with ondansetron plus dexamethasone for prevention of chemotherapy-induced nausea and vomiting in patients receiving high-emetogenic chemotherapy | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85081034214&origin=inward | en_US |