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Accelerated Hypofractionated Intensity - Modulated Radiotherapy After Hyperbaric Oxygenation for Recurrent High Grade Glioma. (HBO-RT)

Primary Purpose

Malignant Glioma, High Grade Glioma, Recurrent Glioma

Status
Recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
HBO
RT
Sponsored by
Istituto Scientifico Romagnolo per lo Studio e la cura dei Tumori
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malignant Glioma focused on measuring Hypofractionated radiotherapy, image - guided helical tomotherapy, hyperbaric oxygen therapy, malignant glioma, high grade glioma, recurrent glioma

Eligibility Criteria

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

Inclusion Criteria:

  1. Male or Female, aged >18 years.
  2. Karnofsky Performance Scale (KPS)> 60
  3. Imaging confirmation of first tumor progression o regrowth as defined by Response Assessment in Neuro-Oncology Criteria (RANO) criteria at least 12 weeks after completion of radiotherapy, unless the recurrence is outside the radiation field or has been histologically documented
  4. Recurrence after adjuvant treatment( surgery followed by radiotherapy and chemotherapy) in patients who could receive further therapeutic interventions
  5. No more than one prior line of chemotherapy (one line of chemotherapy after concurrent and adjuvant Temozolomide (TMZ) - based chemotherapy or procarbazine/lomustine/vincristine (PCV) - Radiotherapy (RT)
  6. Patients who have undergone recent surgery for recurrent o progressive high grade gliomas are eligible provided that : surgery must have confirmed the recurrence ; a minimum of 28 days must have elapsed from the days of surgery to study . For core or needle biopsy a minimum of 7 days must have elapsed prior to study .
  7. If female and of child bearing potential , have a negative result on a pregnancy test performed a maximum of 7 days before initiation .
  8. Female participants of child bearing potential and male participants whose partner is of child bearing potential must be willing to ensure that they or their partner use effective contraception during the study and for 4 months thereafter
  9. Have adequate bone marrow function , liver function , and renal function , as measured by following laboratory assessments conducted within 7 days prior to the initiation of study treatment .
  10. Hemoglobin >9.0 g/dl
  11. Absolute neutrophil count (ANC) >1500/mm3 without transfusions or granulocyte colony stimulating factor and other hematopoietic growth factors
  12. Platelet count ≥90,000/μl
  13. White Blood Cell (WBC) >3.0 x 109/L
  14. Total bilirubin <1.5 times the upper limit of normal
  15. Serum creatinine <1.5 x upper limit of normal
  16. Participant is willing and able to give informed consent for participation in the study.

Exclusion Criteria:

  1. Radiotherapy within 12 weeks prior to the diagnosis of progression, if the lesion is in the radiation field.
  2. Patients with cardiopulmonary diseases (heart failure, bolus emphysema, pneumothorax, chronic obstructive pulmonary disease (COPD) with hypercapnia sinusitis )
  3. Closed angle-glaucoma with pressure ocular superior to 24 mmHg

Sites / Locations

  • Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST)Recruiting
  • Centro IperbaricoRecruiting
  • Neuroradiology, AUSL della Romagna - RAVENNARecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

HBO and RT

Arm Description

Hyperbaric oxygenation therapy and Accelerated Hypofractionated intensity - modulated radiotherapy

Outcomes

Primary Outcome Measures

Disease control rate (DCR)
DCR will be evaluated by performing MRI images The treatment response will be evaluated according to the RANO criteria

Secondary Outcome Measures

Incidence of adverse events
Adverse events will be graded according to the National Cancer Institute Common Terminology Criteria Events v. 4.03.
Overall survival (OS)
OS will be defined as the time from the first day of treatment to death due any cause or censored at date last known alive
Progression Free survival (PFS)
PFS will be calculated as the time from the first day of treatment to the date of the first observation of documented disease progression or death due to any cause. Patients without tumor progression at the time of analysis will be censored at their last date of tumor evaluation.
Predictive score of disease progression by DSC MRI
determining a predictive score of disease, using perfusion dynamic contrast-enhanced (DSC) permeability MRI
Radionecrosis by DSC MRI
determining radionecrosis using perfusion dynamic contrast-enhanced (DSC) permeability MRI
Pseudoprogression by DSC MRI
determining pseudoprogression using perfusion dynamic contrast-enhanced (DSC) permeability MRI
Predictive score of disease progression by DCE MRI
determining a predictive score of disease using dynamic susceptibility contrast (DCE) perfusion MRI
Radionecrosis by DCE MRI
determining radionecrosis using dynamic susceptibility contrast (DCE) perfusion MRI
pseudoprogression by DCE MRI
determining pseudoprogression using dynamic susceptibility contrast (DCE) perfusion MRI

Full Information

First Posted
January 11, 2018
Last Updated
May 26, 2023
Sponsor
Istituto Scientifico Romagnolo per lo Studio e la cura dei Tumori
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1. Study Identification

Unique Protocol Identification Number
NCT03411408
Brief Title
Accelerated Hypofractionated Intensity - Modulated Radiotherapy After Hyperbaric Oxygenation for Recurrent High Grade Glioma.
Acronym
HBO-RT
Official Title
Accelerated Hypofractionated Intensity - Modulated Radiotherapy After Hyperbaric Oxygenation for Recurrent High Grade Glioma: a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 22, 2018 (Actual)
Primary Completion Date
May 2024 (Anticipated)
Study Completion Date
May 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Istituto Scientifico Romagnolo per lo Studio e la cura dei Tumori

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is a pilot study of radiotherapy using Hypofractionated image - guided helical tomotherapy after hyperbaric oxygen HBO therapy for treatment of recurrent malignant High-grade gliomas. HBO therapy will be perform in conjunction with each RT session. The treatment scheme is: Hyperbaric oxygenation therapy (the maximum period of time from completion of decompression to RT is 60 min) followed by tomotherapy (3-5 consecutive sessions- one fraction per day , 5 Gy / die ). The trial will enroll 24 patients in 24 months with a follow-up period of 1 year.
Detailed Description
This is a pilot study to evaluate the efficacy of hypofractionated image- guided helical tomotherapy after hyperbaric oxygen therapy (HBO) for treatment of recurrent malignant high - grade gliomas The primary objective of this study is to evaluate the disease control rate (DCR) of treated patients. The secondary Objectives are: Safety assessment (acute and late toxicity). Overall Survival (OS), Progression Free Survival (PFS). Evaluation of predictive score of disease, radionecrosis and pseudoprogression using perfusion DSC and DCE MRI Patients will receive fractionated stereotactic radiotherapy using tomotherapy combined with hyperbaric oxygen (HBO) therapy. Hyperbaric oxygenation therapy (the maximum period of time from completion of decompression to RT is 60 min) followed by tomotherapy (3-5 consecutive sessions- one fraction per day, 5 Gy / die). The overall duration of treatment will be max 5 days.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malignant Glioma, High Grade Glioma, Recurrent Glioma
Keywords
Hypofractionated radiotherapy, image - guided helical tomotherapy, hyperbaric oxygen therapy, malignant glioma, high grade glioma, recurrent glioma

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
24 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
HBO and RT
Arm Type
Experimental
Arm Description
Hyperbaric oxygenation therapy and Accelerated Hypofractionated intensity - modulated radiotherapy
Intervention Type
Device
Intervention Name(s)
HBO
Intervention Description
Hyperbaric oxygen is administrated in a multiplace hyperbaric chamber according to the following schedule: Ten minutes of compression with a Fraction of inspired oxygen (FiO2) more than 90% from 152 to 253 kilopascal, 60 minutes of Fraction of inspired oxygen (FiO2) more than 90% at 253 kilopascal (three breathing cycles in oxygen for 22 minutes each, with two intervals breathing air for 2 minutes each) and 10 minutes of decompression with a Fraction of inspired oxygen (FiO2) more than 90% from 253 to 152 kilopascal.
Intervention Type
Radiation
Intervention Name(s)
RT
Intervention Description
tomotherapy (within 60 minutes from completion of decompression of hyperbaric chamber) with 3-5 consecutive sessions- one fraction per day, 5 Gy / die .
Primary Outcome Measure Information:
Title
Disease control rate (DCR)
Description
DCR will be evaluated by performing MRI images The treatment response will be evaluated according to the RANO criteria
Time Frame
up to one year
Secondary Outcome Measure Information:
Title
Incidence of adverse events
Description
Adverse events will be graded according to the National Cancer Institute Common Terminology Criteria Events v. 4.03.
Time Frame
up to 36 months
Title
Overall survival (OS)
Description
OS will be defined as the time from the first day of treatment to death due any cause or censored at date last known alive
Time Frame
up to 36 months
Title
Progression Free survival (PFS)
Description
PFS will be calculated as the time from the first day of treatment to the date of the first observation of documented disease progression or death due to any cause. Patients without tumor progression at the time of analysis will be censored at their last date of tumor evaluation.
Time Frame
up to 36 months
Title
Predictive score of disease progression by DSC MRI
Description
determining a predictive score of disease, using perfusion dynamic contrast-enhanced (DSC) permeability MRI
Time Frame
up to 36 months
Title
Radionecrosis by DSC MRI
Description
determining radionecrosis using perfusion dynamic contrast-enhanced (DSC) permeability MRI
Time Frame
up to 36 months
Title
Pseudoprogression by DSC MRI
Description
determining pseudoprogression using perfusion dynamic contrast-enhanced (DSC) permeability MRI
Time Frame
up to 36 months
Title
Predictive score of disease progression by DCE MRI
Description
determining a predictive score of disease using dynamic susceptibility contrast (DCE) perfusion MRI
Time Frame
up to 36 months
Title
Radionecrosis by DCE MRI
Description
determining radionecrosis using dynamic susceptibility contrast (DCE) perfusion MRI
Time Frame
up to 36 months
Title
pseudoprogression by DCE MRI
Description
determining pseudoprogression using dynamic susceptibility contrast (DCE) perfusion MRI
Time Frame
up to 36 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or Female, aged >18 years. Karnofsky Performance Scale (KPS)> 60 Imaging confirmation of first tumor progression o regrowth as defined by Response Assessment in Neuro-Oncology Criteria (RANO) criteria at least 12 weeks after completion of radiotherapy, unless the recurrence is outside the radiation field or has been histologically documented Recurrence after adjuvant treatment( surgery followed by radiotherapy and chemotherapy) in patients who could receive further therapeutic interventions No more than one prior line of chemotherapy (one line of chemotherapy after concurrent and adjuvant Temozolomide (TMZ) - based chemotherapy or procarbazine/lomustine/vincristine (PCV) - Radiotherapy (RT) Patients who have undergone recent surgery for recurrent o progressive high grade gliomas are eligible provided that : surgery must have confirmed the recurrence ; a minimum of 28 days must have elapsed from the days of surgery to study . For core or needle biopsy a minimum of 7 days must have elapsed prior to study . If female and of child bearing potential , have a negative result on a pregnancy test performed a maximum of 7 days before initiation . Female participants of child bearing potential and male participants whose partner is of child bearing potential must be willing to ensure that they or their partner use effective contraception during the study and for 4 months thereafter Have adequate bone marrow function , liver function , and renal function , as measured by following laboratory assessments conducted within 7 days prior to the initiation of study treatment . Hemoglobin >9.0 g/dl Absolute neutrophil count (ANC) >1500/mm3 without transfusions or granulocyte colony stimulating factor and other hematopoietic growth factors Platelet count ≥90,000/μl White Blood Cell (WBC) >3.0 x 109/L Total bilirubin <1.5 times the upper limit of normal Serum creatinine <1.5 x upper limit of normal Participant is willing and able to give informed consent for participation in the study. Exclusion Criteria: Radiotherapy within 12 weeks prior to the diagnosis of progression, if the lesion is in the radiation field. Patients with cardiopulmonary diseases (heart failure, bolus emphysema, pneumothorax, chronic obstructive pulmonary disease (COPD) with hypercapnia sinusitis ) Closed angle-glaucoma with pressure ocular superior to 24 mmHg
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Oriana Nanni
Phone
+390543739266
Email
oriana.nanni@irst.emr.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Donatella Arpa
Organizational Affiliation
IRST IRCCS
Official's Role
Principal Investigator
Facility Information:
Facility Name
Istituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori (IRST)
City
Meldola
State/Province
FC
ZIP/Postal Code
47014
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Donatella Arpa, MD
Email
donatella.arpa@irst.emr.it
Facility Name
Centro Iperbarico
City
Ravenna
State/Province
RA
ZIP/Postal Code
48121
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pasquale Longobardi, MD
Facility Name
Neuroradiology, AUSL della Romagna - RAVENNA
City
Ravenna
State/Province
RA
ZIP/Postal Code
48121
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Patrizia Cenni

12. IPD Sharing Statement

Citations:
PubMed Identifier
33859944
Citation
Arpa D, Parisi E, Ghigi G, Cortesi A, Longobardi P, Cenni P, Pieri M, Tontini L, Neri E, Micheletti S, Ghetti F, Monti M, Foca F, Tesei A, Arienti C, Sarnelli A, Martinelli G, Romeo A. Role of Hyperbaric Oxygenation Plus Hypofractionated Stereotactic Radiotherapy in Recurrent High-Grade Glioma. Front Oncol. 2021 Mar 30;11:643469. doi: 10.3389/fonc.2021.643469. eCollection 2021.
Results Reference
derived

Learn more about this trial

Accelerated Hypofractionated Intensity - Modulated Radiotherapy After Hyperbaric Oxygenation for Recurrent High Grade Glioma.

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