Efficacy, Safety And Feasibility Of Antiemetic Prophylaxis With Fosaprepitant, Granisetron And Dexamethasone In Pediatric Patients With Hemato-Oncological Malignancies
Karin Melanie Cabanillas Stanchi,1,* Martin Ebinger,1,* Ulrike Hartmann,2 Manon Queudeville,1 Judith Feucht,1 Michael Ost,1 Marie-Sarah Koch,1 Carmen Malaval,1 Markus Mezger,1 Sarah Schober,1 Simone Weber,1 Sebastian Michaelis,1 Veit Lange,1 Peter Lang,1 Rupert Handgretinger,1 Michaela Döring1 1Depa...
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Dove Medical Press,
2019-09-01T00:00:00Z.
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001 | doaj_f038ab3f48eb4bf7bdada3f3933f4ea3 | ||
042 | |a dc | ||
100 | 1 | 0 | |a Cabanillas Stanchi KM |e author |
700 | 1 | 0 | |a Ebinger M |e author |
700 | 1 | 0 | |a Hartmann U |e author |
700 | 1 | 0 | |a Queudeville M |e author |
700 | 1 | 0 | |a Feucht J |e author |
700 | 1 | 0 | |a Ost M |e author |
700 | 1 | 0 | |a Koch MS |e author |
700 | 1 | 0 | |a Malaval C |e author |
700 | 1 | 0 | |a Mezger M |e author |
700 | 1 | 0 | |a Schober S |e author |
700 | 1 | 0 | |a Weber S |e author |
700 | 1 | 0 | |a Michaelis S |e author |
700 | 1 | 0 | |a Lange V |e author |
700 | 1 | 0 | |a Lang P |e author |
700 | 1 | 0 | |a Handgretinger R |e author |
700 | 1 | 0 | |a Döring M |e author |
245 | 0 | 0 | |a Efficacy, Safety And Feasibility Of Antiemetic Prophylaxis With Fosaprepitant, Granisetron And Dexamethasone In Pediatric Patients With Hemato-Oncological Malignancies |
260 | |b Dove Medical Press, |c 2019-09-01T00:00:00Z. | ||
500 | |a 1177-8881 | ||
520 | |a Karin Melanie Cabanillas Stanchi,1,* Martin Ebinger,1,* Ulrike Hartmann,2 Manon Queudeville,1 Judith Feucht,1 Michael Ost,1 Marie-Sarah Koch,1 Carmen Malaval,1 Markus Mezger,1 Sarah Schober,1 Simone Weber,1 Sebastian Michaelis,1 Veit Lange,1 Peter Lang,1 Rupert Handgretinger,1 Michaela Döring1 1Department of General Pediatrics, Hematology/Oncology, University Children‘s Hospital Tübingen, Tübingen 72076, Germany; 2University Pharmacy, Eberhard-Karls-University of Tübingen, Tübingen 72076, Germany*These authors contributed equally to this workCorrespondence: Michaela DöringUniversity Hospital Tübingen - Children’s Hospital, Department I – General Pediatrics, Hematology/Oncology, Hoppe-Seyler-Str. 1, Tübingen 72076, GermanyTel +49-(0)7071-2981355Fax +49-(0)7071-295203Email michaela.doering@med.uni-tuebingen.deBackground: Chemotherapy-induced nausea and vomiting (CINV) are a major burden for patients undergoing emetogenic chemotherapy. International guidelines recommend an antiemetic prophylaxis with corticosteroids, 5-HT3R-antagonists and NK1R-antagonists. The NK1R-antagonist fosaprepitant has shown favorable results in pediatric and adult patients. There is little pediatric experience with fosaprepitant.Methods: This non-interventional observation study analyzed 303 chemotherapy courses administered to 83 pediatric patients with a median age of 9 years (2–17 years), who received antiemetic prophylaxis either with fosaprepitant and granisetron with or without dexamethasone (fosaprepitant group/FG; n=41), or granisetron with or without dexamethasone (control group/CG; n=42), during moderately (CINV risk 30–90%) or highly (CINV risk>90%) emetogenic chemotherapy. The two groups’ results were compared with respect to the safety and efficacy of the antiemetic prophylaxis during the acute (0-24hrs after chemotherapy), delayed (>24–120hrs after chemotherapy) and both CINV phases. Laboratory and clinical adverse events were compared between the two cohorts.Results: Adverse events were not significantly different in the two groups (p>0.05). Significantly fewer vomiting events occurred during antiemetic prophylaxis with fosaprepitant in the acute (23 vs 142 events; p<0.0001) and the delayed (71 vs 255 events; p<0.0001) CINV phase. In the control group, the percentage of chemotherapy courses with vomiting was significantly higher during the acute (24%/FG vs 45%/CG; p<0.0001) and delayed CINV phase (28%/FG vs 47%/CG; p=0.0004). Dimenhydrinate (rescue medication) was administered significantly more often in the CG, compared to the FG (114/FG vs 320/CG doses; p<0.0001). Likewise, in the control group, dimenhydrinate was administered in significantly more (p<0.0001) chemotherapy courses during the acute and delayed CINV phases (79 of 150; 52.7%), compared to the fosaprepitant group (45 of 153; 29.4%).Conclusion: Antiemetic prophylaxis with fosaprepitant and granisetron with or without dexamethasone was well tolerated, safe and effective in pediatric patients. However, larger prospective trials are needed to evaluate these findings.Keywords: fosaprepitant, granisetron, pediatric, antiemetic prophylaxis, chemotherapy induced vomiting, children | ||
546 | |a EN | ||
690 | |a Fosaprepitant | ||
690 | |a aprepitant | ||
690 | |a granisetron | ||
690 | |a pediatric | ||
690 | |a antiemetic prophylaxis | ||
690 | |a chemotherapy | ||
690 | |a CINV | ||
690 | |a chemotherapy induced nausea and vomiting | ||
690 | |a chemotherapy induced vomiting | ||
690 | |a CIV | ||
690 | |a 5-HT¬3R-antagonist | ||
690 | |a NK1R-antagonists | ||
690 | |a dexamethasone | ||
690 | |a Therapeutics. Pharmacology | ||
690 | |a RM1-950 | ||
655 | 7 | |a article |2 local | |
786 | 0 | |n Drug Design, Development and Therapy, Vol Volume 13, Pp 3439-3451 (2019) | |
787 | 0 | |n https://www.dovepress.com/efficacy-safety-and-feasibility-of-antiemetic-prophylaxis-with-fosapre-peer-reviewed-article-DDDT | |
787 | 0 | |n https://doaj.org/toc/1177-8881 | |
856 | 4 | 1 | |u https://doaj.org/article/f038ab3f48eb4bf7bdada3f3933f4ea3 |z Connect to this object online. |