Evaluation of palonosetron and dexamethasone with or without aprepitant to prevent carboplatin-induced nausea and vomiting in patients with advanced non-small-cell lung cancer. Issue 3 (December 2015)
- Record Type:
- Journal Article
- Title:
- Evaluation of palonosetron and dexamethasone with or without aprepitant to prevent carboplatin-induced nausea and vomiting in patients with advanced non-small-cell lung cancer. Issue 3 (December 2015)
- Main Title:
- Evaluation of palonosetron and dexamethasone with or without aprepitant to prevent carboplatin-induced nausea and vomiting in patients with advanced non-small-cell lung cancer
- Authors:
- Kusagaya, Hideki
Inui, Naoki
Karayama, Masato
Fujisawa, Tomoyuki
Enomoto, Noriyuki
Kuroishi, Shigeki
Nakamura, Yutaro
Matsuda, Hiroyuki
Yokomura, Koshi
Koshimizu, Naoki
Toyoshima, Mikio
Imokawa, Shiro
Yamada, Takashi
Shirai, Toshihiro
Hayakawa, Hiroshi
Suda, Takafumi - Abstract:
- Highlights: Carboplatin-based chemotherapy show relatively strong emetic properties. We assess the efficacy of add-on aprepitant to palonosetron and dexamethasone. Add-on aprepitant provided no improvement in carboplatin-induced emesis. Abstract: Objectives: Although antiemetic management has improved, better control of chemotherapy-induced nausea and vomiting (CINV), particularly during the delayed phase, is needed. The benefit of combination therapy using dexamethasone and the second-generation 5-hydroxytryptamine-3 receptor antagonist palonosetron compared with that of other such receptor antagonists in carboplatin-based chemotherapy is unclear. The effectiveness of adding aprepitant for CINV treatment in moderate emetogenic chemotherapy is also unknown. We compared the efficacy and safety of triple antiemetic therapy using aprepitant, palonosetron, and dexamethasone with that of double antiemetic therapy using palonosetron and dexamethasone in patients with advanced non-small-cell lung cancer receiving carboplatin-containing chemotherapy. Methods: Chemotherapy-naïve patients with non-small-cell lung cancer were enrolled in this prospective controlled study. Eighty patients were randomly assigned to groups receiving either double antiemetic therapy with palonosetron and dexamethasone, or triple antiemetic therapy with aprepitant, palonosetron, and dexamethasone. Complete response rate (no vomiting episode and no rescue therapy) was evaluated as the primary endpoint duringHighlights: Carboplatin-based chemotherapy show relatively strong emetic properties. We assess the efficacy of add-on aprepitant to palonosetron and dexamethasone. Add-on aprepitant provided no improvement in carboplatin-induced emesis. Abstract: Objectives: Although antiemetic management has improved, better control of chemotherapy-induced nausea and vomiting (CINV), particularly during the delayed phase, is needed. The benefit of combination therapy using dexamethasone and the second-generation 5-hydroxytryptamine-3 receptor antagonist palonosetron compared with that of other such receptor antagonists in carboplatin-based chemotherapy is unclear. The effectiveness of adding aprepitant for CINV treatment in moderate emetogenic chemotherapy is also unknown. We compared the efficacy and safety of triple antiemetic therapy using aprepitant, palonosetron, and dexamethasone with that of double antiemetic therapy using palonosetron and dexamethasone in patients with advanced non-small-cell lung cancer receiving carboplatin-containing chemotherapy. Methods: Chemotherapy-naïve patients with non-small-cell lung cancer were enrolled in this prospective controlled study. Eighty patients were randomly assigned to groups receiving either double antiemetic therapy with palonosetron and dexamethasone, or triple antiemetic therapy with aprepitant, palonosetron, and dexamethasone. Complete response rate (no vomiting episode and no rescue therapy) was evaluated as the primary endpoint during the 5-day post-chemotherapy period. Results: The aprepitant add-on and double therapy groups showed overall complete response rates of 80.5% (95% confidence interval [CI]: 68.4–92.6%) and 76.9% (95% CI: 63.7–90.1%; odds ratio [OR]: 0.81; 95% CI; 0.27–2.36; p = 0.788), respectively. Complete responses in the acute and delayed phases and overall incidences of treatment-related adverse events were similar between groups. Conclusion: According to the selection design, triple antiemetic therapy with aprepitant, palonosetron, and dexamethasone was not considered as an option for further studies. … (more)
- Is Part Of:
- Lung cancer. Volume 90:Issue 3(2015:Dec.)
- Journal:
- Lung cancer
- Issue:
- Volume 90:Issue 3(2015:Dec.)
- Issue Display:
- Volume 90, Issue 3 (2015)
- Year:
- 2015
- Volume:
- 90
- Issue:
- 3
- Issue Sort Value:
- 2015-0090-0003-0000
- Page Start:
- 410
- Page End:
- 416
- Publication Date:
- 2015-12
- Subjects:
- AUC area under the curve -- CINV chemotherapy-induced nausea and vomiting -- ECOG Eastern Cooperative Oncology Group -- HEC highly emetogenic chemotherapy -- 5-HT3 5-hydroxytryptamine-3 -- MEC moderately emetogenic chemotherapy -- NK-1 neurokinin-1 -- NSCLC non-small-cell lung cancer -- QOL quality of life
Antiemetic -- Aprepitant -- Carboplatin -- Chemotherapy-induced nausea and vomiting -- Non-small-cell lung cancer -- Palonosetron
Lungs -- Cancer -- Periodicals
Lung Neoplasms -- Abstracts
Lung Neoplasms -- Periodicals
Poumons -- Cancer -- Périodiques
Lungs -- Cancer
Periodicals
Electronic journals
Electronic journals
616.99424 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01695002 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/01695002 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/01695002 ↗
http://www.lungcancerjournal.info/issues ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.lungcan.2015.11.009 ↗
- Languages:
- English
- ISSNs:
- 0169-5002
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - 5307.245000
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