Aprepitant for Chemotherapy Induced Nausea and Vomiting in Chinese Advanced Non-small Cell Lung Cancers
Primary Purpose
Carcinoma, Non-small Cell Lung
Status
Completed
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
Aprepitant
placebo
Sponsored by

About this trial
This is an interventional treatment trial for Carcinoma, Non-small Cell Lung focused on measuring aprepitant, non-small cell lung cancer
Eligibility Criteria
Inclusion Criteria:
- patients pathologic diagnosed of advanced non-small cell lung cancer
- according to NCCN non-small cell lung cancer guide line(2014 V2), patients are suitable for platinum based chemotherapy.
Exclusion Criteria:
- patients could not receive platinum based chemotherapy judged by clinical doctors
- pregnancy or breast-feeding women
- any serious disease which could not be controled
- urine protein≥++, or 24h urine protein>1g
- less than 18 years old or more than 75 years old
Sites / Locations
- Hunan Cancer hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
aprepitant group
placebo
Arm Description
Patients assigned to aprepitant group should receive aprepitant for the control of CINV, aprepitant 125 mg for day1, 80mg for day2 and day3.
Patients assigned to placebo group should receive placebo for the control of CINV compared with aprepitant group.
Outcomes
Primary Outcome Measures
complete response rate of CINV
complete response rate of CINV should be recorded when platinum based chemotherapy begun, during inhospital treatment, up to 6 months
Secondary Outcome Measures
adverse event
Full Information
NCT ID
NCT02161991
First Posted
June 2, 2014
Last Updated
March 25, 2020
Sponsor
Hunan Province Tumor Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02161991
Brief Title
Aprepitant for Chemotherapy Induced Nausea and Vomiting in Chinese Advanced Non-small Cell Lung Cancers
Official Title
Randomized Phase 3 Study of Aprepitant Versus Placebo in Chinese Advanced Non-small Cell Lung Cancer Who Received Highly Emetogenic Chemotherapy
Study Type
Interventional
2. Study Status
Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
February 1, 2014 (Actual)
Primary Completion Date
February 1, 2017 (Actual)
Study Completion Date
January 31, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hunan Province Tumor Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Aprepitant is an oral neurokinin-1(NK-1) antagonist which is widely used for the prevention of chemotherapy-induced nausea and vomiting(CINV), it is metabolized by CYP34A, however, up to now it was still unknown the CINV control rate of aprepitant in Chinese non-small cell lung cancer(NSCLC) patients, we hypothesis that CYP3A4 and NK-1 polymorphism would influence aprepitant plasma concentration, which may lead to the individual difference of CINV control rate.
Detailed Description
Patients pathologic diagnosed of advanced non-small cell lung cancer, according to NCCN non-small cell lung cancer guide line(2014 V2),the patient should receive standard platinum based chemotherapy, are randomized divided into two groups, aprepitant group and placebo group. In aprepitant group, patients would receive aprepitant 125 mg at day1, then 80 mg at day2 and day3. In placebo group, patients would receive placebo from day1 to day3. In both group, dexamethasone and 5-HT inhibitor palonosetron were give at the same dose. During the treatment, any grade of nausea and vomiting should be recorded in order to evaluate the complete response rate of CINV, other side-effects should be recorded. In aprepitant group, plasma should be taken for the analyze of plasma concentration, gene polymorphism of CYP3A4 and NK-1 should be analyzed for all the patients who received aprepitant if possible.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carcinoma, Non-small Cell Lung
Keywords
aprepitant, non-small cell lung cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
244 (Actual)
8. Arms, Groups, and Interventions
Arm Title
aprepitant group
Arm Type
Experimental
Arm Description
Patients assigned to aprepitant group should receive aprepitant for the control of CINV, aprepitant 125 mg for day1, 80mg for day2 and day3.
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
Patients assigned to placebo group should receive placebo for the control of CINV compared with aprepitant group.
Intervention Type
Drug
Intervention Name(s)
Aprepitant
Other Intervention Name(s)
Emend
Intervention Description
aprepitant should be give when patients receive platinum based chemotherapy, 125mg for day1, 80mg for day2 and day3.
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
placebo should be give when patients receive platinum based chemotherapy, 125mg for day1, 80mg for day2 and day3.
Primary Outcome Measure Information:
Title
complete response rate of CINV
Description
complete response rate of CINV should be recorded when platinum based chemotherapy begun, during inhospital treatment, up to 6 months
Time Frame
during treatment, up to 6 months
Secondary Outcome Measure Information:
Title
adverse event
Time Frame
during treatment, up to 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
patients pathologic diagnosed of advanced non-small cell lung cancer
according to NCCN non-small cell lung cancer guide line(2014 V2), patients are suitable for platinum based chemotherapy.
Exclusion Criteria:
patients could not receive platinum based chemotherapy judged by clinical doctors
pregnancy or breast-feeding women
any serious disease which could not be controled
urine protein≥++, or 24h urine protein>1g
less than 18 years old or more than 75 years old
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nong Yang, MD
Organizational Affiliation
Hunan Cancer Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hunan Cancer hospital
City
Changsha
State/Province
Hunan
Country
China
12. IPD Sharing Statement
Citations:
PubMed Identifier
24276953
Citation
Hu Z, Cheng Y, Zhang H, Zhou C, Han B, Zhang Y, Huang C, Chang J, Song X, Liang J, Liang H, Bai C, Yu S, Chen J, Wang J, Pan H, Chitkara DK, Hille DA, Zhang L. Aprepitant triple therapy for the prevention of chemotherapy-induced nausea and vomiting following high-dose cisplatin in Chinese patients: a randomized, double-blind, placebo-controlled phase III trial. Support Care Cancer. 2014 Apr;22(4):979-87. doi: 10.1007/s00520-013-2043-9. Epub 2013 Nov 26.
Results Reference
background
PubMed Identifier
23062719
Citation
Aapro MS, Schmoll HJ, Jahn F, Carides AD, Webb RT. Review of the efficacy of aprepitant for the prevention of chemotherapy-induced nausea and vomiting in a range of tumor types. Cancer Treat Rev. 2013 Feb;39(1):113-7. doi: 10.1016/j.ctrv.2012.09.002. Epub 2012 Oct 11.
Results Reference
background
PubMed Identifier
22863840
Citation
Stiff PJ, Fox-Geiman MP, Kiley K, Rychlik K, Parthasarathy M, Fletcher-Gonzalez D, Porter N, Go A, Smith SE, Rodriguez TE. Prevention of nausea and vomiting associated with stem cell transplant: results of a prospective, randomized trial of aprepitant used with highly emetogenic preparative regimens. Biol Blood Marrow Transplant. 2013 Jan;19(1):49-55.e1. doi: 10.1016/j.bbmt.2012.07.019. Epub 2012 Aug 1.
Results Reference
background
PubMed Identifier
22915652
Citation
Albany C, Brames MJ, Fausel C, Johnson CS, Picus J, Einhorn LH. Randomized, double-blind, placebo-controlled, phase III cross-over study evaluating the oral neurokinin-1 antagonist aprepitant in combination with a 5HT3 receptor antagonist and dexamethasone in patients with germ cell tumors receiving 5-day cisplatin combination chemotherapy regimens: a hoosier oncology group study. J Clin Oncol. 2012 Nov 10;30(32):3998-4003. doi: 10.1200/JCO.2011.39.5558. Epub 2012 Aug 20.
Results Reference
background
Learn more about this trial
Aprepitant for Chemotherapy Induced Nausea and Vomiting in Chinese Advanced Non-small Cell Lung Cancers
We'll reach out to this number within 24 hrs