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
Main Authors: de Wit, R., Herrstedt, J., Rapoport, B., Carides, A.D., Carides, G., Elmer, M., Schmidt, C., Evans, J.K., Horgan, K.J.
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.
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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