Addition of the Oral NK 1 Antagonist Aprepitant to Standard Antiemetics Provides Protection Against Nausea and Vomiting During Multiple Cycles of Cisplatin-Based Chemotherapy
Purpose: This analysis evaluated whether the antiemetic efficacy of the NK 1 receptor antagonist aprepitant (EMEND ™ , Merck, Whitehouse Station, NJ) plus standard antiemetics could be sustained for up to six cycles of cisplatin-based chemotherapy. Patients and Methods: Patients receiving cisplatin...
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Published in: | Journal of clinical oncology Vol. 21; no. 22; pp. 4105 - 4111 |
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Main Authors: | , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
15-11-2003
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Abstract | Purpose: This analysis evaluated whether the antiemetic efficacy of the NK
1
receptor antagonist aprepitant (EMEND
™
, Merck, Whitehouse Station, NJ) plus standard antiemetics could be sustained for up to six cycles of cisplatin-based chemotherapy.
Patients and Methods: Patients receiving cisplatin ≥ 70 mg/m
2
were blindly assigned to receive one of the following three regimens: (1) aprepitant 375 mg 1 hour before cisplatin on day 1 and aprepitant 250 mg on days 2 to 5 (n = 35); (2) aprepitant 125 mg before cisplatin and aprepitant 80 mg on days 2 to 5 (n = 81); or (3) placebo before cisplatin on days 2 to 5 (n = 86). All groups received ondansetron 32 mg and dexamethasone 20 mg before cisplatin, and dexamethasone 8 mg on days 2 to 5. The primary end point was complete response (no emesis and no rescue therapy) over 5 days following cisplatin in up to six cycles. A cumulative probability analysis using a model for transitional probabilities was used to analyze the data. The aprepitant 375/250-mg regimen was discontinued early in light of new pharmacokinetic data.
Results: In the first cycle, 64% of patients in the aprepitant group and 49% in the standard therapy group had a complete response. Thereafter, complete response rates for the aprepitant group were still 59% by cycle 6, but decreased to 34% by cycle 6 for the standard therapy group. Reasons for discontinuation were similar across treatment groups.
Conclusion: Compared with patients who received standard therapy, those who received only the aprepitant regimen had better and more sustained protection against chemotherapy-induced nausea and vomiting over multiple cycles. |
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AbstractList | Purpose: This analysis evaluated whether the antiemetic efficacy of the NK
1
receptor antagonist aprepitant (EMEND
™
, Merck, Whitehouse Station, NJ) plus standard antiemetics could be sustained for up to six cycles of cisplatin-based chemotherapy.
Patients and Methods: Patients receiving cisplatin ≥ 70 mg/m
2
were blindly assigned to receive one of the following three regimens: (1) aprepitant 375 mg 1 hour before cisplatin on day 1 and aprepitant 250 mg on days 2 to 5 (n = 35); (2) aprepitant 125 mg before cisplatin and aprepitant 80 mg on days 2 to 5 (n = 81); or (3) placebo before cisplatin on days 2 to 5 (n = 86). All groups received ondansetron 32 mg and dexamethasone 20 mg before cisplatin, and dexamethasone 8 mg on days 2 to 5. The primary end point was complete response (no emesis and no rescue therapy) over 5 days following cisplatin in up to six cycles. A cumulative probability analysis using a model for transitional probabilities was used to analyze the data. The aprepitant 375/250-mg regimen was discontinued early in light of new pharmacokinetic data.
Results: In the first cycle, 64% of patients in the aprepitant group and 49% in the standard therapy group had a complete response. Thereafter, complete response rates for the aprepitant group were still 59% by cycle 6, but decreased to 34% by cycle 6 for the standard therapy group. Reasons for discontinuation were similar across treatment groups.
Conclusion: Compared with patients who received standard therapy, those who received only the aprepitant regimen had better and more sustained protection against chemotherapy-induced nausea and vomiting over multiple cycles. |
Author | Schmidt, C. Horgan, K.J. de Wit, R. Elmer, M. Evans, J.K. Herrstedt, J. Rapoport, B. Carides, G. Carides, A.D. |
Author_xml | – sequence: 1 givenname: R. surname: de Wit fullname: de Wit, R. organization: From the Rotterdam Cancer Institute, Rotterdam, The Netherlands; Copenhagen University Hospital, Herlev, Denmark; The Medical Oncology Centre of Rosebank, Johannesburg, S Africa; and Merck Research Laboratories, West Point, PA – sequence: 2 givenname: J. surname: Herrstedt fullname: Herrstedt, J. organization: From the Rotterdam Cancer Institute, Rotterdam, The Netherlands; Copenhagen University Hospital, Herlev, Denmark; The Medical Oncology Centre of Rosebank, Johannesburg, S Africa; and Merck Research Laboratories, West Point, PA – sequence: 3 givenname: B. surname: Rapoport fullname: Rapoport, B. organization: From the Rotterdam Cancer Institute, Rotterdam, The Netherlands; Copenhagen University Hospital, Herlev, Denmark; The Medical Oncology Centre of Rosebank, Johannesburg, S Africa; and Merck Research Laboratories, West Point, PA – sequence: 4 givenname: A.D. surname: Carides fullname: Carides, A.D. organization: From the Rotterdam Cancer Institute, Rotterdam, The Netherlands; Copenhagen University Hospital, Herlev, Denmark; The Medical Oncology Centre of Rosebank, Johannesburg, S Africa; and Merck Research Laboratories, West Point, PA – sequence: 5 givenname: G. surname: Carides fullname: Carides, G. organization: From the Rotterdam Cancer Institute, Rotterdam, The Netherlands; Copenhagen University Hospital, Herlev, Denmark; The Medical Oncology Centre of Rosebank, Johannesburg, S Africa; and Merck Research Laboratories, West Point, PA – sequence: 6 givenname: M. surname: Elmer fullname: Elmer, M. organization: From the Rotterdam Cancer Institute, Rotterdam, The Netherlands; Copenhagen University Hospital, Herlev, Denmark; The Medical Oncology Centre of Rosebank, Johannesburg, S Africa; and Merck Research Laboratories, West Point, PA – sequence: 7 givenname: C. surname: Schmidt fullname: Schmidt, C. organization: From the Rotterdam Cancer Institute, Rotterdam, The Netherlands; Copenhagen University Hospital, Herlev, Denmark; The Medical Oncology Centre of Rosebank, Johannesburg, S Africa; and Merck Research Laboratories, West Point, PA – sequence: 8 givenname: J.K. surname: Evans fullname: Evans, J.K. organization: From the Rotterdam Cancer Institute, Rotterdam, The Netherlands; Copenhagen University Hospital, Herlev, Denmark; The Medical Oncology Centre of Rosebank, Johannesburg, S Africa; and Merck Research Laboratories, West Point, PA – sequence: 9 givenname: K.J. surname: Horgan fullname: Horgan, K.J. organization: From the Rotterdam Cancer Institute, Rotterdam, The Netherlands; Copenhagen University Hospital, Herlev, Denmark; The Medical Oncology Centre of Rosebank, Johannesburg, S Africa; and Merck Research Laboratories, West Point, PA |
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Cites_doi | 10.1007/BF00365579 10.1002/cncr.11320 10.1200/JCO.2001.19.7.2091 10.2165/00003495-199652050-00002 10.1200/JCO.1996.14.2.644 10.1038/bjc.1997.507 10.1200/JCO.1997.15.1.103 10.1016/S0959-8049(02)00674-3 10.1200/JCO.2001.19.6.1759 10.1200/JCO.2003.01.095 10.1007/s005200050161 10.1200/JCO.1999.17.9.2971 10.1038/bjc.1998.244 10.1093/oxfordjournals.annonc.a010548 10.1002/cncr.11433 10.1056/NEJM199901213400304 |
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Snippet | Purpose: This analysis evaluated whether the antiemetic efficacy of the NK
1
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™
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Title | Addition of the Oral NK 1 Antagonist Aprepitant to Standard Antiemetics Provides Protection Against Nausea and Vomiting During Multiple Cycles of Cisplatin-Based Chemotherapy |
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