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Steroid-sparing Therapy (Olanzapine) Versus Dexamethasone-based Therapy for Chemotherapy-induced Nausea and Vomiting

Primary Purpose

Chemotherapy-induced Nausea and Vomiting

Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
OLA group: Olanzapine
DEX group: Dexamethasone
Sponsored by
The Guthrie Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Chemotherapy-induced Nausea and Vomiting

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 18 years and older
  • confirmed cancer diagnosis
  • starting cycle 1 of an FDA approved treatment that is categorized as high-emetogenic (nausea and vomiting inducing) chemotherapy per National Comprehensive Cancer Network® guidelines
  • Eastern Cooperative Oncology Group performance score of 0 or 1
  • appropriate renal function
  • appropriate hepatic function
  • appropriate hematologic function.

Exclusion Criteria:

  • Patients will be excluded if they experience nausea or vomiting up to 24 hours before chemotherapy,
  • currently on a glucocorticoid therapy
  • contraindication to glucocorticoid therapy
  • taking any medication that has antiemetic properties.
  • scheduled or planned to receive radiation within one week of or concurrently with chemotherapy
  • brain metastases.

Sites / Locations

  • Robert Packer HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

OLA then crossover to DEX

DEX then crossover to OLA

Arm Description

OLA group: olanzapine (Zyprexa) 10 mg oral each night after chemotherapy cycle 1 on days 1-4 after HEC (or days 1-3 after MEC). DEX group: dexamethasone (Decadron) 8 mg oral daily after chemotherapy cycle 2 on days 2-4 after HEC (or days 2-3 after MEC)

DEX group: dexamethasone (Decadron) 8 mg oral daily after chemotherapy cycle 1 on days 2-4 after HEC (or days 2-3 after MEC) OLA group: olanzapine (Zyprexa) 10 mg oral each night after chemotherapy cycle 2 on days 1-4 after HEC (or days 1-3 after MEC).

Outcomes

Primary Outcome Measures

Complete response (CR) over 120 hours following chemotherapy
Complete response (CR) over 120 hours following chemotherapy, where CR is the absence of emesis and no use of a rescue antiemetic medication, in the acute phase (<24 hours following chemotherapy), delayed phase (≥24 hours but ≤120 hours following chemotherapy) and overall (≤ 120 hours following chemotherapy).

Secondary Outcome Measures

Complete control (CC- no emesis, no rescue medication and no more than minimal nausea)
no emesis, no rescue medication and no more than minimal nausea
Total Control (TC- no emesis, no rescue medication, no nausea)
no emesis, no rescue medication, no nausea
Severity of nausea and vomiting self-reported by patient questionnaire
None, mild or greater than mild
medication side effects
medication side effects including sedation, insomnia, agitation, indigestion/heartburn, depression, anorexia, increased appetite/hunger and rash/acne

Full Information

First Posted
October 18, 2022
Last Updated
February 17, 2023
Sponsor
The Guthrie Clinic
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1. Study Identification

Unique Protocol Identification Number
NCT05590923
Brief Title
Steroid-sparing Therapy (Olanzapine) Versus Dexamethasone-based Therapy for Chemotherapy-induced Nausea and Vomiting
Official Title
The Efficacy of Steroid-Sparing Anti-Emetic Therapy in Patients Treated With High or Moderate Emetogenic Chemotherapy; Single Center Non-Inferiority Open Label Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 7, 2022 (Actual)
Primary Completion Date
November 1, 2024 (Anticipated)
Study Completion Date
November 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The Guthrie Clinic

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this research is to compare two drugs that are routinely used as standard of care for treating nausea and vomiting caused by chemotherapy. This study aims to see if the drug olanzapine is as good as the steroid drug dexamethasone for preventing nausea and vomiting after chemotherapy. Both drugs are listed as appropriate treatment options in the most recent version of National Comprehensive Cancer Network guidelines on Antiemesis.
Detailed Description
The study will include patients treated with high emetogenic chemotherapy (HEC) or moderate emetogenic chemotherapy (MEC). Emetogenic means that it may cause nausea and vomiting. Your participation will last for 2 cycles of chemotherapy. For patients given high emetogenic chemotherapy (HEC): As standard of care for nausea and vomiting after high emetogenic chemotherapy (HEC), subjects will receive fosaprepitant 150 mg IV once, palonosetron 0.25 mg IV once, dexamethasone 12 mg oral or IV once on day 1. Patients will be randomly assigned to either the DEX group to receive dexamethasone or to the OLA group to receive olanzapine for the first cycle of chemotherapy. DEX group: dexamethasone (Decadron) 8 mg oral daily on days 2-4. OLA group: olanzapine (Zyprexa)10 mg oral each night on days 1-4. For the second cycle of chemotherapy, the subject will switch to the other group. For future cycles of chemotherapy, the subject will choose the drug that worked best. For patients give moderate emetogenic chemotherapy (MEC): As standard of care for nausea and vomiting after moderate emetogenic chemotherapy (MEC), subjects will receive granisetron 2 mg oral once and, dexamethasone 12 mg oral once on day 1. Subjects will be randomly assigned to either the DEX group to receive dexamethasone or to the OLA group to receive olanzapine for the first cycle of chemotherapy. DEX group: dexamethasone (Decadron) 8 mg oral daily on days 2-3. OLA group: olanzapine (Zyprexa)10 mg oral each night on days 1-3. For the second cycle of chemotherapy, the subject will switch to the other group. For future cycles of chemotherapy, the subject will choose the drug that worked best. Subjects (both HEC and MEC) will be asked to complete a survey prior to treatment on Day 1 of cycle 1 and cycle 2 prior to treatment. On Day 2 and Day 6 a member of the study will contact subjects by phone to complete another survey on any symptoms you may be experiencing.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chemotherapy-induced Nausea and Vomiting

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Model Description
Subjects will be randomly assigned to either the DEX group to receive dexamethasone or to the OLA group to receive olanzapine for the first cycle of chemotherapy. DEX group: dexamethasone (Decadron) 8 mg oral daily on days 2-4 after HEC (days 2-3 after MEC). OLA group: olanzapine (Zyprexa)10 mg oral each night on days 1-4 after HEC (days 2-3 after MEC). For the second cycle of chemotherapy, the subject will switch to the other group. Groups: OLA then DEX; DEX then OLA
Masking
None (Open Label)
Allocation
Randomized
Enrollment
104 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
OLA then crossover to DEX
Arm Type
Experimental
Arm Description
OLA group: olanzapine (Zyprexa) 10 mg oral each night after chemotherapy cycle 1 on days 1-4 after HEC (or days 1-3 after MEC). DEX group: dexamethasone (Decadron) 8 mg oral daily after chemotherapy cycle 2 on days 2-4 after HEC (or days 2-3 after MEC)
Arm Title
DEX then crossover to OLA
Arm Type
Active Comparator
Arm Description
DEX group: dexamethasone (Decadron) 8 mg oral daily after chemotherapy cycle 1 on days 2-4 after HEC (or days 2-3 after MEC) OLA group: olanzapine (Zyprexa) 10 mg oral each night after chemotherapy cycle 2 on days 1-4 after HEC (or days 1-3 after MEC).
Intervention Type
Drug
Intervention Name(s)
OLA group: Olanzapine
Other Intervention Name(s)
Steroid-sparing therapy
Intervention Description
OLA group: olanzapine 10 mg oral each night on days 1-4 after HEC (or days 1-3 after MEC). DEX group: dexamethasone (Decadron) 8 mg oral daily on days 2-4 after HEC (or days 2-3 after MEC).
Intervention Type
Drug
Intervention Name(s)
DEX group: Dexamethasone
Other Intervention Name(s)
Steroid therapy
Intervention Description
DEX group: dexamethasone (Decadron) 8 mg oral daily on days 2-4 after HEC (or days 2-3 after MEC).. OLA group: olanzapine 10 mg oral each night on days 1-4 after HEC (or days 1-3 after MEC).
Primary Outcome Measure Information:
Title
Complete response (CR) over 120 hours following chemotherapy
Description
Complete response (CR) over 120 hours following chemotherapy, where CR is the absence of emesis and no use of a rescue antiemetic medication, in the acute phase (<24 hours following chemotherapy), delayed phase (≥24 hours but ≤120 hours following chemotherapy) and overall (≤ 120 hours following chemotherapy).
Time Frame
120 hours following chemotherapy
Secondary Outcome Measure Information:
Title
Complete control (CC- no emesis, no rescue medication and no more than minimal nausea)
Description
no emesis, no rescue medication and no more than minimal nausea
Time Frame
120 hours following chemotherapy
Title
Total Control (TC- no emesis, no rescue medication, no nausea)
Description
no emesis, no rescue medication, no nausea
Time Frame
120 hours following chemotherapy
Title
Severity of nausea and vomiting self-reported by patient questionnaire
Description
None, mild or greater than mild
Time Frame
120 hours after chemotherapy
Title
medication side effects
Description
medication side effects including sedation, insomnia, agitation, indigestion/heartburn, depression, anorexia, increased appetite/hunger and rash/acne
Time Frame
120 hours after chemotherapy

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years and older confirmed cancer diagnosis starting cycle 1 of an FDA approved treatment that is categorized as high-emetogenic (nausea and vomiting inducing) chemotherapy per National Comprehensive Cancer Network® guidelines Eastern Cooperative Oncology Group performance score of 0 or 1 appropriate renal function appropriate hepatic function appropriate hematologic function. Exclusion Criteria: Patients will be excluded if they experience nausea or vomiting up to 24 hours before chemotherapy, currently on a glucocorticoid therapy contraindication to glucocorticoid therapy taking any medication that has antiemetic properties. scheduled or planned to receive radiation within one week of or concurrently with chemotherapy brain metastases.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zane Waite, PharmD, BCOP
Phone
570-887-6072
Email
zane.waite@guthrie.org
First Name & Middle Initial & Last Name or Official Title & Degree
Kelly Wurzler, PharmD
Email
kelly.wurzler@guthrie.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nicole Ink, PharmD
Organizational Affiliation
The Guthrie Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Robert Packer Hospital
City
Sayre
State/Province
Pennsylvania
ZIP/Postal Code
18840
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zane Waite, PharmD
Email
Zane.Waite@guthrie.org

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Steroid-sparing Therapy (Olanzapine) Versus Dexamethasone-based Therapy for Chemotherapy-induced Nausea and Vomiting

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