Comparison of Antiemetic Drugs in Preventing Delayed Nausea After Chemotherapy in Patients With Cancer
Status: | Completed |
---|---|
Conditions: | Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - 120 |
Updated: | 4/21/2016 |
Start Date: | July 2001 |
End Date: | October 2004 |
Treatment of Delayed Nausea: What Works Best?
RATIONALE: Antiemetic drugs may help to reduce or prevent nausea and vomiting in patients
being treated with chemotherapy.
PURPOSE: This randomized phase III trial is comparing how well different antiemetic drugs
work in preventing delayed nausea after chemotherapy in patients who have cancer.
being treated with chemotherapy.
PURPOSE: This randomized phase III trial is comparing how well different antiemetic drugs
work in preventing delayed nausea after chemotherapy in patients who have cancer.
OBJECTIVES:
- Compare the effectiveness of a 5 hydroxytryptamine 3 (5-HT3) receptor antagonist
antiemetic vs prochlorperazine in controlling delayed nausea after chemotherapy in
patients with chemotherapy-naive cancer.
- Compare the effectiveness of prochlorperazine administered on a preventive vs as needed
basis in controlling delayed nausea after chemotherapy in these patients.
- Compare the quality of life of patients treated with a 5-HT3 receptor antagonist
antiemetic vs prochlorperazine.
- Compare the quality of life of patients treated with prochlorperazine administered on a
preventive vs as needed basis.
OUTLINE: This is a randomized, multicenter study. Patients are stratified according to
center.
Patients receive their scheduled chemotherapy regimen containing doxorubicin and their
scheduled oral 5 hydroxytryptamine 3 receptor antagonist antiemetic (ondansetron,
granisetron, tropisetron, or dolasetron mesylate) combined with dexamethasone on day 1.
Patients are then randomized to 1 of 3 antiemetic arms.
- Arm I: Patients receive oral prochlorperazine every 8 hours on days 2 and 3.
- Arm II: Patients receive oral ondansetron every 12 hours, oral granisetron every 12
hours, or oral dolasetron mesylate either once a day or every 12 hours on days 2 and 3.
- Arm III: Patients receive oral prochlorperazine as needed, up to 4 times per day, on
days 2 and 3.
Quality of life is assessed at baseline and on day 4.
PROJECTED ACCRUAL: A total of 670 patients will be accrued for this study within 3 years.
- Compare the effectiveness of a 5 hydroxytryptamine 3 (5-HT3) receptor antagonist
antiemetic vs prochlorperazine in controlling delayed nausea after chemotherapy in
patients with chemotherapy-naive cancer.
- Compare the effectiveness of prochlorperazine administered on a preventive vs as needed
basis in controlling delayed nausea after chemotherapy in these patients.
- Compare the quality of life of patients treated with a 5-HT3 receptor antagonist
antiemetic vs prochlorperazine.
- Compare the quality of life of patients treated with prochlorperazine administered on a
preventive vs as needed basis.
OUTLINE: This is a randomized, multicenter study. Patients are stratified according to
center.
Patients receive their scheduled chemotherapy regimen containing doxorubicin and their
scheduled oral 5 hydroxytryptamine 3 receptor antagonist antiemetic (ondansetron,
granisetron, tropisetron, or dolasetron mesylate) combined with dexamethasone on day 1.
Patients are then randomized to 1 of 3 antiemetic arms.
- Arm I: Patients receive oral prochlorperazine every 8 hours on days 2 and 3.
- Arm II: Patients receive oral ondansetron every 12 hours, oral granisetron every 12
hours, or oral dolasetron mesylate either once a day or every 12 hours on days 2 and 3.
- Arm III: Patients receive oral prochlorperazine as needed, up to 4 times per day, on
days 2 and 3.
Quality of life is assessed at baseline and on day 4.
PROJECTED ACCRUAL: A total of 670 patients will be accrued for this study within 3 years.
DISEASE CHARACTERISTICS:
- Diagnosis of cancer for which a chemotherapy regimen containing doxorubicin (with
adjuvant, neoadjuvant, curative, or palliative intent) is scheduled
- Scheduled chemotherapy regimen must not include any of the following:
- Multiple doses of doxorubicin, dacarbazine, hexamethylmelamine, nitrosoureas, or
streptozocin
- Doxorubicin HydroCloride liposome or cisplatin
- Scheduled chemotherapy regimen may contain agents, other than those listed above,
administered orally, IV, or IV continuously on 1 or multiple days
- Must be scheduled to receive a 5 hydroxytryptamine 3 (5-HT3) receptor antagonist
antiemetic (ondansetron, granisetron, tropisetron, or dolasetron mesylate) with
dexamethasone concurrently with doxorubicin
- No clinical evidence of an impending bowel obstruction
- No symptomatic brain metastasis
PATIENT CHARACTERISTICS:
Age:
- 18 and over
Performance status:
- Not specified
Life expectancy:
- Not specified
Hematopoietic:
- Not specified
Hepatic:
- Not specified
Renal:
- Not specified
PRIOR CONCURRENT THERAPY:
Biologic therapy:
- No concurrent interferon
Chemotherapy:
- See Disease Characteristics
- No prior chemotherapy
Endocrine therapy:
- See Disease Characteristics
Radiotherapy:
- No concurrent radiotherapy
Surgery:
- Not specified
Other:
- Concurrent rescue medications (as appropriate) for control of symptoms caused by
cancer or its treatment allowed
We found this trial at
15
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