NCT01850563

Brief Summary

Patients with brain metastases who are candidates for treatment with stereotactic radiosurgery (SRS) are potential study participants. SRS delivers high-energy, precisely-focused radiation to each brain metastasis to shrink the tumor, and is the standard-of-care for patients with these tumors. Oxygen enhances the damaging effects of radiation on tumor cells. Hyperbaric oxygen (HBO) therapy increases oxygen levels in all kinds of tissues, including tumors. The purpose of this trial is to study whether it is feasible to treat patients with HBO just prior to receiving SRS, given the timing constraints of treating sequentially with HBO and then SRS. Patients will undergo HBO treatment followed by the placement of a Gill-Thomas-Cosman head frame then transported ,via stretcher, to receive SRS. The transfer and placement of the head frame needs to be completed within the 15minute time frame. The trial's secondary objectives are to determine whether it has any effects on outcomes and quality of life. As part of study participation patients will be asked to complete quality of life questionnaires as well as mini mental status questionnaires. These will be done prior to treatment and at follow up appointments throughout the next 3 years while participating in the study. Patients will be given the option to participate in the optional bio marker blood draw study which would require patients to have blood drawn at three time points, pre-treatment, the day after treatment and at their first follow up visit.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
22

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jul 2013

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

May 7, 2013

Completed
2 days until next milestone

First Posted

Study publicly available on registry

May 9, 2013

Completed
2 months until next milestone

Study Start

First participant enrolled

July 1, 2013

Completed
6.3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 3, 2019

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

February 28, 2020

Completed
1.4 years until next milestone

Results Posted

Study results publicly available

July 29, 2021

Completed
Last Updated

February 8, 2022

Status Verified

January 1, 2022

Enrollment Period

6.3 years

First QC Date

May 7, 2013

Results QC Date

April 27, 2021

Last Update Submit

January 19, 2022

Conditions

Keywords

Demonstrate coordination of HBO with SRS treatments is feasible.Demonstrate outcomes for patients treated with combination of HBO and SRS are non-inferior .

Outcome Measures

Primary Outcomes (1)

  • The Average Time From HBO Chamber Exit to SRS beam-on

    Time from end of HBO decompression to start of SRS treatment will be measured to determine feasibility. Feasibility is defined as having been achieved if more than 50% of the 20 evaluable patients start SRS treatment within 30 minutes of leaving the HBO tank

    Approximately 30 minutes during SRS Treatment Visit

Secondary Outcomes (6)

  • Overall Survival in Years

    5 year from treatment

  • Number of Years Until Local Recurrence

    5 year from treatment

  • Number of Years Until Local Recurrence Prior to WBRT

    5 year from treatment

  • Number of Participants Developing Intercranial Distant Recurrence

    5 year from treatment

  • Number of Months Between SRS Treatment and Whole Brain Radiation Therapy

    5 year from treatment

  • +1 more secondary outcomes

Other Outcomes (3)

  • Average Score of Quality of Life as Measured by St. Louis University Mental Status Exam (SLUMS) Mental Status Exam (SLUMS)

    Baseline, 4 to 6 weeks after treatment and then every 3 months for a minimum of 1 year, up to 5 years

  • Average Score of EORTC Global Health Status (QL2)

    Baseline, 4 to 6 weeks after treatment and then every 3 months for a minimum of 1 year, up to 5 years

  • Presence of S100 and NSE (Serum Markers for Tissue Apoptosis and for Neuronal Damage)

    24-48 hours after the SRS treatment

Study Arms (1)

HBO feasibility

OTHER
Device: Hyperbaric oxygen given at 2.4 ATA for 30 minutes immediately prior to SRS - HBOT for 30 minutes - SRS without prior HBO

Interventions

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Metastatic brain tumor referred to radiation oncology for treatment
  • Size of the presenting metastatic lesion up to 5.0 cm diameter
  • Age \> 18 years
  • Patients must give informed consent indicating they are aware of the investigational nature of this treatment
  • Karnofsky Performance Status \> 70% (Zubrod score 0 to 1)
  • Women of childbearing potential must have a negative serum or urine pregnancy test within 14 days to start of study therapy
  • CBC and CMP within 30 days to start of study therapy
  • Chest imaging (Chest Xray or Chest CT) within past 12 months, that does not show any contraindication to hyperbaric therapy (if patient has had any thoracic surgery or other significant event that might have affected the thorax such as trauma, pneumothorax, chest tube insertion, pleurodesis, or thoracentesis and has not had imaging since that event, then the imaging should be repeated).
  • Neurosurgery Consult

You may not qualify if:

  • Pregnant women or women of childbearing potential without adequate contraception. Contraception, which can include abstinence, is required since the last menstrual period until completion of SRS.
  • Evidence of pneumothorax (Untreated pneumothorax risks tension pneumothorax during ascent in HBO chamber)
  • COPD with C02 retention (Such patients can develop respiratory depression as HBO reduces their hypoxemic drive)
  • Uncontrolled seizure disorder (Note that patients on adequate antiepileptic medications may receive HBO)
  • Claustrophobia resistant to medication (Pre-medication with anxiolytics is generally sufficient for almost all anxious patients undergoing HBO treatment)
  • History of middle ear surgery
  • Failure to equalize pressure in the middle ear can cause displacement of middle ear structures with consequent hearing loss
  • To clarify: placement of a tympanostomy tube is not a contraindication to HBO, and in fact may improve tolerability of the procedure
  • History of bleomycin administration (HBO can exacerbate interstitial pneumonitis in such patients)
  • Current cis-platinum chemotherapy, i.e. therapeutic levels in the bloodstream at the time of HBO therapy. (HBO can increase cytotoxicity of cis-platinum)
  • Uncontrolled high blood pressure (HBO can increase systemic vascular resistance)
  • Unstable angina or myocardial infarction within the previous 3 months (Increased afterload due to HBO can increase myocardial workload)
  • Cardiac EF ≤ 35%
  • Pulmonary edema can arise with HBO in certain patients with severe heart failure
  • In patients with prior history of CHF, subsequent echocardiogram and ECG are required to establish EF\>35%
  • +6 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Dartmouth-Hitchcock

Lebanon, New Hampshire, 03756, United States

Location

Related Publications (1)

  • Hartford AC, Gill GS, Ravi D, Tosteson TD, Li Z, Russo G, Eskey CJ, Jarvis LA, Simmons NE, Evans LT, Williams BB, Gladstone DJ, Roberts DW, Buckey JC Jr. Sensitizing brain metastases to stereotactic radiosurgery using hyperbaric oxygen: A proof-of-principle study. Radiother Oncol. 2022 Dec;177:179-184. doi: 10.1016/j.radonc.2022.10.024. Epub 2022 Oct 28.

MeSH Terms

Conditions

Brain Neoplasms

Condition Hierarchy (Ancestors)

Central Nervous System NeoplasmsNervous System NeoplasmsNeoplasms by SiteNeoplasmsBrain DiseasesCentral Nervous System DiseasesNervous System Diseases

Results Point of Contact

Title
Alan Hartford, MD, PhD, FACR, Professor of Medicine (RadOnc) Director, Radiation Oncology
Organization
Dartmouth-Hitchcock Medical Center

Study Officials

  • Alan Hartford, MD

    Dartmouth-Hitchcock Medical Center

    PRINCIPAL INVESTIGATOR

Publication Agreements

PI is Sponsor Employee
No
Restrictive Agreement
No

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Staff Physician

Study Record Dates

First Submitted

May 7, 2013

First Posted

May 9, 2013

Study Start

July 1, 2013

Primary Completion

October 3, 2019

Study Completion

February 28, 2020

Last Updated

February 8, 2022

Results First Posted

July 29, 2021

Record last verified: 2022-01

Locations