Antiemetic Control with Palonosetron in Patients with Gastrointestinal Cancer Receiving a Fluoropyrimidine-Based Regimen in Addition to Either Irinotecan or Oxaliplatin: A Retrospective Study

被引:2
作者
Blazer, Marlo [1 ,2 ]
Phillips, Gary
Reardon, Joshua
Efries, David
Smith, Yahna
Weatherby, Lynn
Juergens, Kim
Rose, Jeffrey
Griffith, Niesha
Bekaii-Saab, Tanios
机构
[1] Ohio State Univ, Arthur G James Canc Hosp, Columbus, OH 43212 USA
[2] Ohio State Univ, Richard J Solove Res Inst, Columbus, OH 43212 USA
关键词
Palonosetron; Chemotherapy-induced nausea and vomiting; Gastrointestinal cancer; Fluoropyrimidine regimen; MODERATELY EMETOGENIC CHEMOTHERAPY; INDUCED NAUSEA; DELAYED EMESIS; POSTCHEMOTHERAPY NAUSEA; RECEPTOR ANTAGONISTS; PHASE-III; DEXAMETHASONE; ONDANSETRON; PROPHYLAXIS; PREVENTION;
D O I
10.1159/000339145
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: For moderately emetogenic chemotherapy, palonosetron (PALO) is reported to provide complete control of chemotherapy-induced nausea and vomiting (CINV) in 69% of patients. Prior to August 2009, our gastrointestinal (GI) cancer patients receiving the moderately emetogenic compounds oxaliplatin or irinotecan plus a fluoropyrimidine regimen received ondansetron and dexamethasone orally on day 1 of chemotherapy for CINV prevention. Beginning in August of 2009, ondansetron was replaced by PALO 0.25 mg (intravenous push). Methods: This is a single-institution retrospective study of GI cancer patients who received oxaliplatin or irinotecan plus a fluoropyrimidine. Failure of an antiemetic regimen was defined as grade >= 1 vomiting or grade >= 2 nausea (Common Terminology Criteria for Adverse Events, version 3) on days 1 through 5 following chemotherapy. Patients were divided for analysis into pre-PALO and post-PALO cohorts. Fisher's exact test compared cohort differences. Results: A total of 305 patients were included in the study, with 157 patients in the pre-PALO cohort and 148 in the post-PALO cohort. For all patients, the risk of antiemetic failure was reduced from 50.3% [95% confidence interval (CI) 42.2-58.4%] to 28.4% (95% CI 21.3-36.4%) with PALO. This reduction in the relative risk of antiemetic failure was observed in all subgroups. Conclusion: The addition of PALO may provide increased control of CINV for the moderately emetogenic regimens of oxaliplatin or irinotecan plus a fluoropyrimidine in GI cancer patients. Copyright (C) 2012 S. Karger AG, Basel
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页码:135 / 140
页数:6
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