Literature DB >> 24065402

Antiemetic guideline consistency and incidence of chemotherapy-induced nausea and vomiting in US community oncology practice: INSPIRE Study.

James W Gilmore1, Nancy W Peacock, Anna Gu, Stephen Szabo, Melissa Rammage, Joyce Sharpe, Sally T Haislip, Toni Perry, Tim L Boozan, Katherine Meador, Xiting Cao, Thomas A Burke.   

Abstract

PURPOSE: Consensus guidelines for preventing chemotherapy-induced nausea and vomiting (CINV) are variably implemented in practice. The purpose of this study was to evaluate the impact of guideline-consistent/guideline-inconsistent CINV prophylaxis (GCCP/GICP) on the incidence of no CINV after cycle 1 of highly or moderately emetogenic chemotherapy (HEC or MEC). PATIENTS AND METHODS: This prospective observational study enrolled chemotherapy-naive adult outpatients who received single-day HEC or MEC at four oncology practice networks, all using electronic health record (EHR) systems, in Georgia, Tennessee, and Florida. Results from the Multinational Association of Supportive Care in Cancer Antiemesis Tool, a validated tool to measure CINV, administered 5 to 8 days postchemotherapy, were merged with EHR data. The primary end point, no CINV, defined as no emesis and no clinically significant nausea (score < 3 on 0-10 scale), was compared between cohorts using logistic regression.
RESULTS: A total of 1,295 patients were enrolled (mean age, 59.3 years; 70.0% female; 35.5% HEC). The overall prevalence of GCCP was 57.3%. When corticosteroids were prescribed on days 2 to 4 after all HEC, GCCP for HEC increased from 28.7% to 89.8%; when NK1-receptor antagonists were prescribed after all MEC, GCCP for MEC increased from 73.1% to 97.8%. Over 5 days postchemotherapy, the incidence of no CINV was significantly higher in the GCCP cohort than the GICP cohort (53.4% v 43.8%; P < .001). The adjusted odds of no CINV with GCCP was 1.31 (95% CI, 1.07 to 1.69; P = .037).
CONCLUSION: Increased adherence to antiemetic guidelines could significantly reduce the incidence of CINV after HEC and MEC.

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Year:  2013        PMID: 24065402     DOI: 10.1200/JOP.2012.000816

Source DB:  PubMed          Journal:  J Oncol Pract        ISSN: 1554-7477            Impact factor:   3.840


  62 in total

1.  Gaps exist between patients' experience and clinicians' awareness of symptoms after chemotherapy: CINV and accompanying symptoms.

Authors:  Sun Young Rha; Su Kyung Song; Chung Eun Lee; Yeonhee Park; Jiyeon Lee
Journal:  Support Care Cancer       Date:  2016-06-08       Impact factor: 3.603

2.  Chemotherapy-induced nausea and vomiting control in pediatric patients receiving ifosfamide plus etoposide: a prospective, observational study.

Authors:  Priya Patel; Sara R Lavoratore; Jacqueline Flank; Meaghan Kemp; Ashlee Vennettilli; Helen Vol; Tracey Taylor; Elyse Zelunka; Anne Marie Maloney; Paul C Nathan; L Lee Dupuis
Journal:  Support Care Cancer       Date:  2019-06-08       Impact factor: 3.603

3.  Patient-reported outcome performance measures in oncology.

Authors:  Ethan Basch; Claire Snyder; Kristen McNiff; Rebecca Brown; Suzanne Maddux; Mary Lou Smith; Thomas M Atkinson; Doris Howell; Anne Chiang; William Wood; Nathan Levitan; Albert W Wu; Monika Krzyzanowska
Journal:  J Oncol Pract       Date:  2014-04-22       Impact factor: 3.840

4.  Evaluation of antiemetic practices for prevention of chemotherapy-induced nausea and vomiting (CINV): results of a European oncology nurse survey.

Authors:  Pascale Dielenseger; Sussanne Börjeson; Cheryl Vidall; Annie Young; Patrick Jahn
Journal:  Support Care Cancer       Date:  2019-02-19       Impact factor: 3.603

5.  A phase 1 pharmacokinetic study of oral NEPA, the fixed combination of netupitant and palonosetron, in Chinese healthy volunteers.

Authors:  Rui Chen; Hongyun Wang; Wen Zhong; Salvatore Chessari; Corinna Lanzarotti; Alberto Bernareggi; Pei Hu
Journal:  Cancer Chemother Pharmacol       Date:  2021-01-02       Impact factor: 3.333

Review 6.  ASCO, NCCN, MASCC/ESMO: a comparison of antiemetic guidelines for the treatment of chemotherapy-induced nausea and vomiting in adult patients.

Authors:  Yasmeen Razvi; Stephanie Chan; Thomas McFarlane; Erin McKenzie; Pearl Zaki; Carlo DeAngelis; William Pidduck; Ahmad Bushehri; Edward Chow; Katarzyna Joanna Jerzak
Journal:  Support Care Cancer       Date:  2018-10-03       Impact factor: 3.603

7.  Impact of CINV in earlier cycles on CINV and chemotherapy regimen modification in subsequent cycles in Asia Pacific clinical practice.

Authors:  Hoon-Kyo Kim; RueyKuen Hsieh; Alexandre Chan; Shiying Yu; Baohui Han; Yunong Gao; Ana Baños; Xiaoyan Ying; Thomas A Burke; Dorothy M K Keefe
Journal:  Support Care Cancer       Date:  2014-08-21       Impact factor: 3.603

8.  Resource Utilization for Chemotherapy-Induced Nausea and Vomiting Events in Patients with Solid Tumors Treated with Antiemetic Regimens.

Authors:  Lee Schwartzberg; Brooke Harrow; Lincy S Lal; Janna Radtchenko; Gary H Lyman
Journal:  Am Health Drug Benefits       Date:  2015 Jul-Aug

9.  Patterns of antiemetic prophylaxis for chemotherapy-induced nausea and vomiting in China.

Authors:  Xianglong Zong; Jie Zhang; Xin Ji; Jie Gao; Jiafu Ji
Journal:  Chin J Cancer Res       Date:  2016-04       Impact factor: 5.087

Review 10.  The Impact of 5-HT3RA Use on Cost and Utilization in Patients with Chemotherapy-Induced Nausea and Vomiting: Systematic Review of the Literature.

Authors:  Michael S Broder; Claudio Faria; Annette Powers; Jehangeer Sunderji; Dasha Cherepanov
Journal:  Am Health Drug Benefits       Date:  2014-05
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