Comparison of an extended-release formulation of granisetron (APF530) versus palonosetron for the prevention of chemotherapy-induced nausea and vomiting associated with moderately or highly emetogenic chemotherapy: results of a prospective, randomized, double-blind, noninferiority phase 3 trial

被引:35
|
作者
Raftopoulos, Harry [1 ]
Cooper, William [2 ]
O'Boyle, Erin [3 ]
Gabrail, Nashat [4 ]
Boccia, Ralph [5 ]
Gralla, Richard J. [6 ]
机构
[1] Hofstra North Shore LIJ Sch Med, Lake Success, NY 11042 USA
[2] TFS Int, Flemington, NJ 08822 USA
[3] FibroGen Inc, San Francisco, CA 94158 USA
[4] Gabrail Canc Ctr, Canton, OH 44718 USA
[5] Ctr Canc & Blood Disorders, Bethesda, MD 20819 USA
[6] Albert Einstein Coll Med, Jacobi Med Ctr, Bronx, NY 10461 USA
关键词
Cancer; Chemotherapy-induced nausea and vomiting (CINV); Extended-release; Granisetron; Subcutaneous; APF530; 5-HT3 RECEPTOR ANTAGONIST; GUIDELINE UPDATE; DELAYED EMESIS; ONDANSETRON; ANTIEMETICS;
D O I
10.1007/s00520-014-2400-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Subcutaneous APF530 provides controlled sustained release of granisetron to prevent acute (0-24 h) and delayed (24-120 h) chemotherapy-induced nausea and vomiting (CINV). This randomized, double-blind phase 3 trial compared APF530 and palonosetron in preventing acute and delayed CINV after moderately (MEC) or highly emetogenic chemotherapy (HEC). Patients receiving single-day MEC or HEC received single-dose APF530 250 or 500 mg subcutaneously (SC) (granisetron 5 or 10 mg) or intravenous palonosetron 0.25 mg. Primary objectives were to establish APF530 noninferiority to palonosetron for preventing acute CINV following MEC or HEC and delayed CINV following MEC and to determine APF530 superiority to palonosetron for preventing delayed CINV following HEC. The primary efficacy end point was complete response (CR [using CI difference for APF530 -aEuro parts per thousand palonosetron]). A lower confidence bound greater than -15 % indicated noninferiority. In the modified intent-to-treat population (MEC = 634; HEC = 707), both APF530 doses were noninferior to palonosetron in preventing acute CINV after MEC (CRs 74.8 % [-9.8, 9.3] and 76.9 % [-7.5, 11.4], respectively, vs. 75.0 % palonosetron) and after HEC (CRs 77.7 % [-11.5, 5.5] and 81.3 % [-7.7, 8.7], respectively, vs. 80.7 % palonosetron). APF530 500 mg was noninferior to palonosetron in preventing delayed CINV after MEC (CR 58.5 % [-9.5, 12.1] vs. 57.2 % palonosetron) but not superior in preventing delayed CINV after HEC. Adverse events were generally mild and unrelated to treatment, the most common (excluding injection-site reactions) being constipation. A single subcutaneous APF530 injection offers a convenient alternative to palonosetron for preventing acute and delayed CINV after MEC or HEC.
引用
收藏
页码:723 / 732
页数:10
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