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PubMed:20307224 JSONTXT

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PubmedHPO

Id Subject Object Predicate Lexical cue
T1 403-409 HP_0002018 denotes nausea
T2 414-422 HP_0002013 denotes vomiting

Allie

Id Subject Object Predicate Lexical cue
SS1_20307224_2_0 190-232 expanded denotes 5-hydroxytryptamine 3 receptor antagonists
SS2_20307224_2_0 234-242 abbr denotes 5-HT3RAs
SS1_20307224_3_0 382-422 expanded denotes chemotherapy-induced nausea and vomiting
SS2_20307224_3_0 424-428 abbr denotes CINV
SS1_20307224_3_1 509-542 expanded denotes neurokinin-1 receptor antagonists
SS2_20307224_3_1 544-550 abbr denotes NK-1RA
AE1_20307224_2_0 SS1_20307224_2_0 SS2_20307224_2_0 abbreviatedTo 5-hydroxytryptamine 3 receptor antagonists,5-HT3RAs
AE1_20307224_3_0 SS1_20307224_3_0 SS2_20307224_3_0 abbreviatedTo chemotherapy-induced nausea and vomiting,CINV
AE1_20307224_3_1 SS1_20307224_3_1 SS2_20307224_3_1 abbreviatedTo neurokinin-1 receptor antagonists,NK-1RA

PubMed_Structured_Abstracts

Id Subject Object Predicate Lexical cue
T1 166-861 BACKGROUND denotes Since the advent of the 5-hydroxytryptamine 3 receptor antagonists (5-HT3RAs) in the 1990s, dramatic improvements have been achieved in the field of antiemetic therapy. The enhanced prevention of delayed and overall chemotherapy-induced nausea and vomiting (CINV) offered by palonosetron, a second-generation 5-HT3RA and aprepitant, the first neurokinin-1 receptor antagonists (NK-1RA) represent the only significant treatment advances in the past decade. While initial trials of single-dose palonosetron indicated a potential benefit over first-generation 5-HT3RAs, only recently have new data become available, increasing the weight of evidence distinguishing it as a new 5-HT3RA in the class.
T2 892-1048 METHODS denotes History of antiemetics and palonosetron, including clinical trials and pharmacological research, and literature published between 1981 and 2010 are covered.
T3 1076-1382 RESULTS denotes Unique pharmacological characteristics of palonosetron exhibiting prolonged half-life, high receptor affinity, allosteric interactions and positive cooperativity with 5-HT3 receptor resulting in long-term alteration and internalization of this receptor may explain the clinical observation of palonosetron.
T4 1402-1613 CONCLUSIONS denotes This review of recent progress in antiemetic therapy focuses on the newest data on palonosetron and discusses future trials and implications for clinical practice, with the overall goal of learning from history.