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PubMed:21542674 JSONTXT

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PubmedHPO

Id Subject Object Predicate Lexical cue
T1 324-330 HP_0002018 denotes nausea
T2 335-343 HP_0002013 denotes vomiting
T3 508-516 HP_0002665 denotes lymphoma
T4 521-529 HP_0001909 denotes leukemia

Allie

Id Subject Object Predicate Lexical cue
SS1_21542674_2_0 303-343 expanded denotes chemotherapy-induced nausea and vomiting
SS2_21542674_2_0 345-349 abbr denotes CINV
SS1_21542674_2_1 428-448 expanded denotes receptor antagonists
SS2_21542674_2_1 450-453 abbr denotes RAs
SS1_21542674_2_2 545-575 expanded denotes highly emetogenic chemotherapy
SS2_21542674_2_2 577-580 abbr denotes HEC
SS1_21542674_2_3 585-619 expanded denotes moderately emetogenic chemotherapy
SS2_21542674_2_3 621-624 abbr denotes MEC
AE1_21542674_2_0 SS1_21542674_2_0 SS2_21542674_2_0 abbreviatedTo chemotherapy-induced nausea and vomiting,CINV
AE1_21542674_2_1 SS1_21542674_2_1 SS2_21542674_2_1 abbreviatedTo receptor antagonists,RAs
AE1_21542674_2_2 SS1_21542674_2_2 SS2_21542674_2_2 abbreviatedTo highly emetogenic chemotherapy,HEC
AE1_21542674_2_3 SS1_21542674_2_3 SS2_21542674_2_3 abbreviatedTo moderately emetogenic chemotherapy,MEC

PubMed_Structured_Abstracts

Id Subject Object Predicate Lexical cue
T1 257-659 OBJECTIVE denotes This study evaluated the rate of uncontrolled chemotherapy-induced nausea and vomiting (CINV) after initiating antiemetic prophylaxis with palonosetron versus other 5-HT₃ receptor antagonists (RAs) in patients diagnosed with hematologic malignancies (lymphoma and leukemia) and receiving highly emetogenic chemotherapy (HEC) or moderately emetogenic chemotherapy (MEC) in a hospital outpatient setting.
T2 669-1564 METHODS denotes Patients aged ≥ 18 years and diagnosed with hematologic malignancies initiating HEC or MEC and antiemetic prophylaxis with palonosetron (Group 1) and other 5-HT₃ RAs (Group 2) for the first time in a hospital outpatient setting between 4/1/2007 and 3/31/2009 were identified from the Premier Perspective Database. Within each cycle, CINV events were identified (in the hospital outpatient, inpatient, and emergency room settings) through ICD-9 codes for nausea, vomiting, and/or volume depletion (from each CT administration day 1 until the end of the CT cycle), or use of rescue medications (day 2 until the end of the CT cycle). Negative binomial distribution generalized linear multivariate regression model estimating the CINV event rate on CT, specific CT cycles, and cancer diagnosis (leukemia/lymphoma)-matched groups in the follow-up period (first of 8 cycles or 6 months) was developed.
T3 1574-2467 RESULTS denotes Of 971 identified patients, 211 initiated palonosetron (Group 1). Group 1 patients comprised of more females [50.2 vs. 41.4%; p = 0.0226], Whites [74.4 vs. 70.4%, and Hispanics [7.6 vs. 6.3%; all races p = 0.0105], received more HEC treatments [89.6 vs. 84.2%; all CT types p = 0.0129], and had more lymphoma diagnosed patients [89.6 vs. 76.3%; all cancer types p = 0.0033] at baseline. After controlling for differences in several demographic and clinical variables, the regression model predicted a 20.4% decrease in CINV event rate per CT cycle for Group 1 versus Group 2 patients. Study limitations include potential lack of generalizability, absence of data on certain confounders including alcohol consumption and prior history of motion sickness, potential underestimation of incidence of uncontrolled CINV, and inability to draw conclusions pertaining to cause and effect relationship.
T4 2480-2856 CONCLUSIONS denotes In this retrospective hospital study, patients with hematologic malignancies treated with HEC or MEC and initiated on antiemetic prophylaxis with palonosetron in the hospital outpatient setting were more likely to experience significantly lower CINV event rates (in the hospital outpatient, inpatient, and emergency room settings) versus patients initiated on other 5-HT₃ RAs.