BMT-08: A Comparative Effectiveness Study of Transdermal Granisetron to Ondansetron
Study Details
Study Description
Brief Summary
Patients undergoing either an autologous or allogeneic hematopoietic stem cell transplant (HSCT) and receiving preparative chemotherapy experience a considerable amount of chemotherapy-induced nausea and vomiting (CINV). Current strategies at reducing CINV in this patient population are suboptimal due to lack of efficacy and supportive evidence, potential for increased adverse events, and drug-drug and drug-disease contraindications.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 4 |
Detailed Description
Patients undergoing either an autologous or allogeneic hematopoietic stem cell transplant (HSCT) and receiving preparative chemotherapy experience a considerable amount of chemotherapy-induced nausea and vomiting (CINV). Current strategies at reducing CINV in this patient population are suboptimal due to lack of efficacy and supportive evidence, potential for increased adverse events, and drug-drug and drug-disease contraindications. This study will be an open-label, prospective trial randomizing patients at a 1:1 ratio, to either one of two 5-hydroxytrytamine 3 (5-HT3) antagonists, transdermal granisetron or intravenous (i.v.) ondansetron, in combination with other standard, routinely administered anti-emetic drugs (dexamethasone). Rescue antiemetics will be administered at any time during the study period for vomiting or severe nausea at the request of the patients or as recommended by the attending physicians. For the granisetron treatment arm, patients will be educated and instructed to self-administer a single transdermal granisetron patch one-two days (approximately 24-48 hours) prior to start of the preparative regimen. An additional dose of transdermal granisetron will be administered 7 days after the initial granisetron dose. For the ondansetron treatment arm, patients will receive the standard dose and schedule of intravenous ondansetron that is routinely administered for each respective preparative regimen. Use of rescue medications will be assessed daily during chemotherapy, and for 7 days after the last chemotherapy drug administration (delayed phase). Nausea, vomiting, and treatment-related side effects will be documented and followed during this same time period. A quality of life questionnaire (MDASI-BMT) will be administered at Day + 7 (7 days after day of infusion). All other aspects of patient care (i.e., chemotherapy administration, supportive care, etc.) and laboratory monitoring will adhere to the routine standard of care operating procedures for stem cell transplant patients.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: Arm 1 ARM 1 -transdermal granisetron plus intravenous dexamethasone |
Drug: Granisetron Transdermal Patch
Antiemetic
Drug: Intravenous Dexamethasone
Antiemetic
|
| Active Comparator: ARM 2 ARM 2 -intravenous ondansetron plus intravenous dexamethasone |
Drug: Intravenous Dexamethasone
Antiemetic
Drug: Ondansetron
ondansetron
|
Outcome Measures
Primary Outcome Measures
- Efficacy/Safety of Transdermal Granisetron for Prevention of CINV [2 years]
To compare between the two study arms the number of patients achieving complete response (CR, no vomiting and no use of rescue medications during the acute period (0-24 hours post-chemotherapy) for patients receiving preparative chemotherapy and HSCT.
Secondary Outcome Measures
- Efficacy/Safety of Ondansetron for Prevention of CINV [2 years]
To compare between the two study arms the number of patients achieving complete response (CR, no vomiting and no use of rescue medications during the delayed (24-120 hours post-chemotherapy) and overall periods (0-120 hours post-chemotherapy) for patients receiving preparative chemotherapy and HSCT.
- Efficacy/Safety of Ondansetron and Transdermal Granisetron for Prevention of CINV [2 years]
To compare between the two study arms the number of patients achieving complete response (CR, no vomiting and no use of rescue medications during the overall period (0-120 hours post-chemotherapy) for patients receiving preparative chemotherapy and HSCT.
- Efficacy/Safety of Ondansetron and Transdermal Granisetron for Prevention of CINV [2 years]
To compare between the two study arms, the use of rescue anti-emetic medications (during and for 7 days after the preparative regimen) for patients receiving preparative chemotherapy and HSCT.
- Efficacy/Safety of Ondansetron and Transdermal Granisetron for Prevention of CINV [2 years]
To compare between the two study arms the occurrence of CINV complete protection, defined as no emetic episode, no use of rescue medications and no nausea, during the acute, delayed, and overall phases for patients receiving preparative chemotherapy and HSCT.
- Efficacy/Safety of Ondansetron and Transdermal Granisetron for Prevention of CINV [2 years]
To compare the occurrence of treatment-related adverse events (AE) between patients receiving transdermal granisetron versus intravenous ondansetron.
- Efficacy/Safety of Ondansetron and Transdermal Granisetron for Prevention of CINV [2 years]
To compare quality of life using the M.D. Anderson Symptom Inventory (MDASI) Core Items-Bone Marrow Transplant (BMT) scale throughout the course of HSCT 7 days after stem cell infusion, between patients receiving transdermal granisetron versus intravenous ondansetron
Eligibility Criteria
Criteria
Inclusion Criteria:
-
Age 18-75 years at time of enrollment receiving either a preparative regimen and either an autologous or allogeneic stem cell transplant.
-
No vomiting ≤ 24 hours prior to registration
-
No treatment with an antipsychotic agent such as risperidone, quetiapine, clozapine, phenothiazine or butyrophenone for ≤ 30 days' prior registration or planned during protocol therapy. No patients will be removed from these treatments for study enrollment purposes.
-
No chronic phenothiazine administration as an antipsychotic agent (patients may receive prochlorperazine and other phenothiazines as rescue antiemetic therapy). No patients will be removed from these treatments for study enrollment purposes.
-
No known hypersensitivity to granisetron
Exclusion Criteria:
-
Concurrent use of amifostine
-
Known hypersensitivity to granisetron patch or ondansetron
-
Patients with a history of long QT syndrome or Torsade de Pointes
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University of Illinois Cancer Center | Chicago | Illinois | United States | 60612 |
Sponsors and Collaborators
- University of Illinois at Chicago
Investigators
- Principal Investigator: Karen Sweiss, PharmD, University of Illinois at Chicago
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 2019-0886