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Safety Profile of HTX-019 Administered as an Intravenous Push in Cancer Patients: A Retrospective Review
INTRODUCTION: HTX-019 [CINVANTI(®) (aprepitant injectable emulsion)] is a neurokinin 1 receptor antagonist (NK-1 RA) approved as a 30-min infusion for preventing acute and delayed chemotherapy-induced nausea and vomiting. HTX-019 has been generally well tolerated when administered as a 30-min infusi...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Healthcare
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824338/ https://www.ncbi.nlm.nih.gov/pubmed/30706408 http://dx.doi.org/10.1007/s12325-019-0877-3 |
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author | Walton, Gary D. |
author_facet | Walton, Gary D. |
author_sort | Walton, Gary D. |
collection | PubMed |
description | INTRODUCTION: HTX-019 [CINVANTI(®) (aprepitant injectable emulsion)] is a neurokinin 1 receptor antagonist (NK-1 RA) approved as a 30-min infusion for preventing acute and delayed chemotherapy-induced nausea and vomiting. HTX-019 has been generally well tolerated when administered as a 30-min infusion or 2-min injection [intravenous (IV) push] in healthy subjects. This real-world analysis assesses safety of HTX-019 via IV push in patients with cancer and addresses a recent IV bag shortage. METHODS: This retrospective review involved six sites in Alabama, USA. Analyzed patients were 18–94 years old with an Eastern Cooperative Oncology Group performance status ranging from 0 to 4. Seventy-six chemotherapy regimens were utilized (emetogenicity high, n = 35; moderate, n = 35; low, n = 6) and patients received HTX-019 130 mg only or switched from fosaprepitant 150 mg to HTX-019 130 mg within a three-drug antiemetic regimen with a 5-hydroxytryptamine type 3 RA and dexamethasone. HTX-019 was administered via IV push. Electronic medical records of patients receiving HTX-019 were queried for nursing and medical documentation associated with infusion-site adverse events (ISAEs). The detailed notes were also reviewed for any discontinuation of HTX-019 or substitution of HTX-019 with another NK-1 RA. RESULTS: The HTX-019 safety profile was analyzed on the basis of 2066 IV push administrations in 591 cancer patients (most common diagnoses: lung, n = 107; breast, n = 100; colon, n = 92). No clinically significant ISAEs or adverse events associated with HTX-019 were reported. Also, no patients discontinued HTX-019 treatment, and none switched from HTX-019 to another NK-1 RA. CONCLUSION: This is the first study to demonstrate that HTX-019 can be safely administered via IV push in patients with cancer receiving emetogenic chemotherapy while negating the need for fluid bags, which are scarce. FUNDING: Heron Therapeutics, Inc., San Diego, CA, USA. PLAIN LANGUAGE SUMMARY: Plain language summary available for this article. |
format | Online Article Text |
id | pubmed-6824338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Springer Healthcare |
record_format | MEDLINE/PubMed |
spelling | pubmed-68243382019-11-06 Safety Profile of HTX-019 Administered as an Intravenous Push in Cancer Patients: A Retrospective Review Walton, Gary D. Adv Ther Original Research INTRODUCTION: HTX-019 [CINVANTI(®) (aprepitant injectable emulsion)] is a neurokinin 1 receptor antagonist (NK-1 RA) approved as a 30-min infusion for preventing acute and delayed chemotherapy-induced nausea and vomiting. HTX-019 has been generally well tolerated when administered as a 30-min infusion or 2-min injection [intravenous (IV) push] in healthy subjects. This real-world analysis assesses safety of HTX-019 via IV push in patients with cancer and addresses a recent IV bag shortage. METHODS: This retrospective review involved six sites in Alabama, USA. Analyzed patients were 18–94 years old with an Eastern Cooperative Oncology Group performance status ranging from 0 to 4. Seventy-six chemotherapy regimens were utilized (emetogenicity high, n = 35; moderate, n = 35; low, n = 6) and patients received HTX-019 130 mg only or switched from fosaprepitant 150 mg to HTX-019 130 mg within a three-drug antiemetic regimen with a 5-hydroxytryptamine type 3 RA and dexamethasone. HTX-019 was administered via IV push. Electronic medical records of patients receiving HTX-019 were queried for nursing and medical documentation associated with infusion-site adverse events (ISAEs). The detailed notes were also reviewed for any discontinuation of HTX-019 or substitution of HTX-019 with another NK-1 RA. RESULTS: The HTX-019 safety profile was analyzed on the basis of 2066 IV push administrations in 591 cancer patients (most common diagnoses: lung, n = 107; breast, n = 100; colon, n = 92). No clinically significant ISAEs or adverse events associated with HTX-019 were reported. Also, no patients discontinued HTX-019 treatment, and none switched from HTX-019 to another NK-1 RA. CONCLUSION: This is the first study to demonstrate that HTX-019 can be safely administered via IV push in patients with cancer receiving emetogenic chemotherapy while negating the need for fluid bags, which are scarce. FUNDING: Heron Therapeutics, Inc., San Diego, CA, USA. PLAIN LANGUAGE SUMMARY: Plain language summary available for this article. Springer Healthcare 2019-01-31 2019 /pmc/articles/PMC6824338/ /pubmed/30706408 http://dx.doi.org/10.1007/s12325-019-0877-3 Text en © The Author(s) 2019 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits any noncommercial use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Research Walton, Gary D. Safety Profile of HTX-019 Administered as an Intravenous Push in Cancer Patients: A Retrospective Review |
title | Safety Profile of HTX-019 Administered as an Intravenous Push in Cancer Patients: A Retrospective Review |
title_full | Safety Profile of HTX-019 Administered as an Intravenous Push in Cancer Patients: A Retrospective Review |
title_fullStr | Safety Profile of HTX-019 Administered as an Intravenous Push in Cancer Patients: A Retrospective Review |
title_full_unstemmed | Safety Profile of HTX-019 Administered as an Intravenous Push in Cancer Patients: A Retrospective Review |
title_short | Safety Profile of HTX-019 Administered as an Intravenous Push in Cancer Patients: A Retrospective Review |
title_sort | safety profile of htx-019 administered as an intravenous push in cancer patients: a retrospective review |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6824338/ https://www.ncbi.nlm.nih.gov/pubmed/30706408 http://dx.doi.org/10.1007/s12325-019-0877-3 |
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