Repeated HBO Therapy in Myeloma Patients Undergoing High-Dose Therapy and Auto-HCT
Primary Purpose
Myeloma
Status
Recruiting
Phase
Early Phase 1
Locations
United States
Study Type
Interventional
Intervention
Hyperbaric oxygen
Sponsored by
About this trial
This is an interventional treatment trial for Myeloma
Eligibility Criteria
Inclusion Criteria:
- Subjects with Multiple myeloma
- Subjects must be 18 years old
- Karnosfsky Performance of greater than 70 percent
- Adequate hepatic, cardiac and pulmonary function
- Subjects should have New York Heart Association Functional Classification of: Class 1 or Class II.
Exclusion Criteria:
- Pregnant or breastfeeding
- Severe chronic obstructive pulmonary disease requiring oxygen supplementation
- History of spontaneous pneumothorax
- Active ear/sinus infection
- Sinus surgery within the last 5 years
- Claustrophobia
- History of recurrent seizures within 5 years of study enrollment
- Evidence of pneumothorax or significant pulmonary fibrosis on chest imaging within 60 days of transplant
- Prior chest surgery involving thoracotomy or prior direct irradiation to the lungs
- Subjects who have had intrathecal chemotherapy within 2 weeks of starting preparative regimen or cranial irradiation within 4 weeks of starting preparative regimen
- Active and uncontrolled viral, fungal or bacterial infection
- Use of tobacco 72 hours prior to transplant
Sites / Locations
- James P. Wilmot Cancer Center at University of Rochester Medical CenterRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Experimental Arm:single
Arm Description
Repeated treatments with hyperbaric oxygen on Days 0, +1 and +2 of high-dose therapy melphalan and autologous transplants.
Outcomes
Primary Outcome Measures
Number of participants with a treatment-limiting toxicity
Treatment-limiting toxicities (defined as the occurrence of any of the following complications within 24 hours of HBO: Seizure disorder, pneumothorax, death, any irreversible grade Ill or any grade IV toxicity that is determined by the treating physician to be at least likely related to HBO therapy) will be assessed 24-hours post-hyperbaric oxygen therapy.
Number of participants with an AE or SAE attributed to HBO therapy.
Possible long-term effects of hyperbaric oxygen therapy treatment prior to autologous peripheral blood stem cell transplant will be assessed at day +100 post-transplant. AEs and SAEs will be graded using CTCAE version 5.
Secondary Outcome Measures
Time to neutrophil recovery
Based on the patient having achieved three consecutive days of Absolute Neutrophil Count (ANC) ≥ 500/microliter
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04862676
Brief Title
Repeated HBO Therapy in Myeloma Patients Undergoing High-Dose Therapy and Auto-HCT
Official Title
A Pilot Study to Determine the Safety and Efficacy of Repeated Hyperbaric Oxygen Therapy in Multiple Myeloma Patients Undergoing High-Dose Therapy and Autologous Stem/Progenitor Transplantation
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 22, 2022 (Actual)
Primary Completion Date
May 15, 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Rochester
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Subjects with multiple myeloma (MM) who are considered eligible for high-dose therapy and autologous stem cell transplantation by the transplant team at WCI will be enrolled in the study.
Detailed Description
Subjects with multiple myeloma (MM) who are considered eligible for high-dose therapy and autologous stem cell transplantation by the transplant team at WCI will be enrolled in the study. Subjects will receive HBO therapy on Days 0, +1 and +2 of the transplant. The treatment consists of exposure to hyperbaric oxygen at 2.5 atmospheric absolutes for a total of 90 minutes after compression to 2.5 atmosphere absolutes in a monoplace hyperbaric chamber (Model 3200/3200R, Sechrist Industries, Inc., USA), breathing 100% oxygen. Subjects will be in the chamber for a total of 120 minutes as approximately 10-15 minutes will be spent during the compression and decompression phases and subjects will have 5-10 minute room air breaks every 30 minutes of hyperbaric oxygen treatment. Subjects will be seen daily until neutrophil recovery is documented . After neutrophil recovery is documented, the subjects will be seen in clinic at least weekly through day +100. A final visit will be scheduled day +100. As part of routine care, subjects will be followed daily or as directed by the treating physician until neutrophil recovery, defined as three consecutive days of achieving a neutrophil count of >500/mm3. Laboratory testing will occur per institutional guidelines. Follow-up will continue until Day +100. Donor chimerism and disease status will be determined by bone marrow biopsy on Day +30 and day +100 post-transplant.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myeloma
7. Study Design
Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Experimental Arm:single
Arm Type
Experimental
Arm Description
Repeated treatments with hyperbaric oxygen on Days 0, +1 and +2 of high-dose therapy melphalan and autologous transplants.
Intervention Type
Drug
Intervention Name(s)
Hyperbaric oxygen
Intervention Description
The treatment consists of exposure to hyperbaric oxygen at 2.5 atmospheric absolutes (ATA) for a total of 90 minutes after compression to 2.5 atmosphere absolutes (ATA) in a monoplace hyperbaric chamber breathing 100% oxygen. The subjects will be in the chamber for a total of 120 minutes as approximately 10-15 minutes are spent during the compression and decompression phases and subjects have 5-10 minute room air breaks every 30 minutes of hyperbaric oxygen treatment.
Primary Outcome Measure Information:
Title
Number of participants with a treatment-limiting toxicity
Description
Treatment-limiting toxicities (defined as the occurrence of any of the following complications within 24 hours of HBO: Seizure disorder, pneumothorax, death, any irreversible grade Ill or any grade IV toxicity that is determined by the treating physician to be at least likely related to HBO therapy) will be assessed 24-hours post-hyperbaric oxygen therapy.
Time Frame
24 hours
Title
Number of participants with an AE or SAE attributed to HBO therapy.
Description
Possible long-term effects of hyperbaric oxygen therapy treatment prior to autologous peripheral blood stem cell transplant will be assessed at day +100 post-transplant. AEs and SAEs will be graded using CTCAE version 5.
Time Frame
100 days
Secondary Outcome Measure Information:
Title
Time to neutrophil recovery
Description
Based on the patient having achieved three consecutive days of Absolute Neutrophil Count (ANC) ≥ 500/microliter
Time Frame
100 days
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:
Subjects with Multiple myeloma
Subjects must be 18 years old
Karnosfsky Performance of greater than 70 percent
Adequate hepatic, cardiac and pulmonary function
Subjects should have New York Heart Association Functional Classification of: Class 1 or Class II.
Exclusion Criteria:
Pregnant or breastfeeding
Severe chronic obstructive pulmonary disease requiring oxygen supplementation
History of spontaneous pneumothorax
Active ear/sinus infection
Sinus surgery within the last 5 years
Claustrophobia
History of recurrent seizures within 5 years of study enrollment
Evidence of pneumothorax or significant pulmonary fibrosis on chest imaging within 60 days of transplant
Prior chest surgery involving thoracotomy or prior direct irradiation to the lungs
Subjects who have had intrathecal chemotherapy within 2 weeks of starting preparative regimen or cranial irradiation within 4 weeks of starting preparative regimen
Active and uncontrolled viral, fungal or bacterial infection
Use of tobacco 72 hours prior to transplant
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lisa Metzger
Phone
(585) 276-7078
Email
Lisa_Metzger@urmc.rochester.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Omar Aljitawi, MBBS
Phone
(585) 275-5863
Email
Omar_Aljitawi@urmc.rochester.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Omar Aljitawi, MMBS
Organizational Affiliation
University of Rochester
Official's Role
Principal Investigator
Facility Information:
Facility Name
James P. Wilmot Cancer Center at University of Rochester Medical Center
City
Rochester
State/Province
New York
ZIP/Postal Code
14642-0001
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Omar Aljitawi, MD
Email
omar_aljitawi@urmc.rochester.edu
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
All individual data collected during the trial will be shared after deidentification, including dictionaries.
IPD Sharing Time Frame
Data will be available immediately following publication. No end date.
IPD Sharing Access Criteria
Anyone who wishes to access the date for any type of analyses.
Learn more about this trial
Repeated HBO Therapy in Myeloma Patients Undergoing High-Dose Therapy and Auto-HCT
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