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Supramarginal Resection in Glioblastoma Guided by Artificial Intelligence (SupraGlio-AI)

Primary Purpose

Glioblastoma

Status
Recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
GTR surgery
AI-guided surgery
Sponsored by
Hospital del Río Hortega
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Glioblastoma

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: A suspected diagnosis of supratentorial glioblastoma by MRI. Tumor in non eloquent brain region according to the UCSF (University of California, San Francisco) classification, including the sensor motor areas (precentral and postcentral gyri), perisylvian language areas in the dominant hemisphere (superior temporal, inferior frontal, and inferior parietal gyri), basal ganglia, internal capsule, thalamus, and visual cortex around the calcarine sulcus Indication for surgical treatment and where supramarginal resection is considered possible according to the preoperative imaging. This consideration needs to be verified by two specialists in neurosurgery. This criterion needs to be verified by two senior neurosurgeons. Karnofsky Performance Score ≥ 60; Written informed consent Exclusion Criteria: Tumors in eloquent areas. Recurrent gliomas (except biopsy) MR image data not usable due to artifacts during acquisition. Inability to give written informed consent KPS < 60 Severe comorbidity.

Sites / Locations

  • Hospital Universitario de La Princesa
  • University Hospital Rio HortegaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Conventional gross total resection surgery

AI-guided resection

Arm Description

Retrospective cohort of patients who underwent conventional surgery between 2018 and 2021. Confirmed gross total resection (removal of 100 % of contrast-enhancing tumor).

Tailored supramarginal surgery guided by AI-based recurrence probability maps. Aim of supramarginal resection, where the high-risk of recurrence areas identified by the AI-based model are subsidiary to be removed as safe locations for the patient.

Outcomes

Primary Outcome Measures

Feasibility using eligibility
Among all screened patients, the proportion of patients who meet the eligibility criteria
Feasibility using the proportion of consent
Among all screened patients, the proportion of patients consenting to participate

Secondary Outcome Measures

Efficacy using overall survival
Measured in days from surgery to the time of death
Efficacy using progression-free survival
Assessment of progression-free survival based on the Modified Criteria for Radiographic Response Assessment in Glioblastoma (mRANO) criteria.
Safety using the neurological function
The National Institutes of Healt Stroke Scale (NIHSS) will be used to assess neurological function. The NIHSS is composed of 11 items, each of which scores a specific ability between a 0 and 4. For each item, a score of 0 typically indicates normal function in that specific ability, while a higher score is indicative of some level of impairment.
Safety using global disability
The modified Rankin scale (mRS ) is a measure of global disability that has been widely used to assess outcome after stroke. The scale runs from 0-6, running from perfect health without symptoms to death
Extent of resection
Volumetric measurement of contrast enhancement and T2-FLAIR signal alteration on MRI
Postoperative complication
Relevant post surgical complication that requires a second surgery or prolong the length of hospitalization (i.e. hematoma, infection)

Full Information

First Posted
February 7, 2023
Last Updated
May 26, 2023
Sponsor
Hospital del Río Hortega
Collaborators
UiT Machine Learning Group, Department of Physics and Technology, UiT The Arctic University of Norway, The PET Imaging Center, University Hospital of North Norway, Intracellular Calcium Pathophysiology Group - Institute of Biology and Molecular Genetics (IBGM) - Research Unit 093, Castilla y León, Biomedical Engineering Group (GIB) - University of Valladolid - Research Unit 060, Castilla y León, Fundación de Investigación Biomédica - Hospital Universitario de La Princesa
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1. Study Identification

Unique Protocol Identification Number
NCT05735171
Brief Title
Supramarginal Resection in Glioblastoma Guided by Artificial Intelligence
Acronym
SupraGlio-AI
Official Title
Tailored Supramarginal Resection in Glioblastoma Guided by Artificial Intelligence-based Recurrence Probability Maps. A Non-randomized Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 1, 2023 (Actual)
Primary Completion Date
December 30, 2025 (Anticipated)
Study Completion Date
June 30, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital del Río Hortega
Collaborators
UiT Machine Learning Group, Department of Physics and Technology, UiT The Arctic University of Norway, The PET Imaging Center, University Hospital of North Norway, Intracellular Calcium Pathophysiology Group - Institute of Biology and Molecular Genetics (IBGM) - Research Unit 093, Castilla y León, Biomedical Engineering Group (GIB) - University of Valladolid - Research Unit 060, Castilla y León, Fundación de Investigación Biomédica - Hospital Universitario de La Princesa

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
Glioblastomas are the most common and poorly prognostic primary brain neoplasms. Despite advances in surgical techniques and chemotherapy, the median survival time for these patients remains less than 15 months. This highlights the need for more effective treatments and improved prognostic tools. The globally accepted surgical strategy currently consists of achieving the maximum safe resection of the enhancing tumor volume. However, the non-enhancing peritumoral region contains viable cells that cause the inevitable recurrence that these patients face. Clinicians currently lack an imaging tool or modality to differentiate neoplastic infiltration in the peritumoral region from vasogenic edema. In addition, it is not always feasible to include all the T2-FLAIR signal alterations surrounding the enhancing tumor in the surgical planning due to the proximity of eloquent areas and the higher risk of postoperative deficits. However, the investigators have developed a model to predict regions of recurrence based on machine learning and MRI radiomic features that have been trained and evaluated in a multi-institutional cohort. The investigators aim to analyze whether an adjusted supramarginal resection guided by these new recurrence probability maps improves survival in selected patients with glioblastoma.
Detailed Description
The SupraGlio-AI study aims to test the feasibility of the proposed AI-guided tailored supratotal resection for glioblastomas. The study will provide preliminary data on the accuracy of the AI model in predicting recurrence and the impact of using this information in surgical planning. This information will be crucial in determining the potential for a larger, randomized controlled trial in the future. The pilot study will also allow for refinement of the study design, intervention, and data collection processes before a larger-scale study is conducted. In addition to testing the feasibility and efficacy of the AI-guided tailored supratotal resection, this pilot study also has two secondary objectives: 1) Survival Analysis: A survival analysis will be performed to compare the prospective cohort of patients undergoing the AI-guided procedure with a retrospective cohort of glioblastoma patients who underwent standard gross total resection. The survival analysis will provide insights into the impact of using the AI model on patient outcomes and help determine the potential benefits of this approach. 2) Histopathological and Transcriptomic Analysis: The study will also include a histopathological and transcriptomic analysis of the tissue samples obtained from the high-risk regions defined by the AI model. This analysis will provide information on the molecular and cellular changes occurring in these regions and may offer insights into the underlying biology of glioblastoma recurrence. These data will inform the development of future studies aimed at improving patient outcomes. By incorporating these secondary objectives, this pilot study will contribute to a more comprehensive understanding of the potential benefits of using AI in guiding tailored supratotal resection for glioblastomas. The results will inform future research and potentially lead to the development of improved treatment approaches for patients with this type of brain tumor.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioblastoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Conventional gross total resection surgery
Arm Type
Active Comparator
Arm Description
Retrospective cohort of patients who underwent conventional surgery between 2018 and 2021. Confirmed gross total resection (removal of 100 % of contrast-enhancing tumor).
Arm Title
AI-guided resection
Arm Type
Experimental
Arm Description
Tailored supramarginal surgery guided by AI-based recurrence probability maps. Aim of supramarginal resection, where the high-risk of recurrence areas identified by the AI-based model are subsidiary to be removed as safe locations for the patient.
Intervention Type
Procedure
Intervention Name(s)
GTR surgery
Intervention Description
Gross total resection of the enhancing tumor volume
Intervention Type
Procedure
Intervention Name(s)
AI-guided surgery
Intervention Description
Supramarginal resection including high-risk areas of recurrence
Primary Outcome Measure Information:
Title
Feasibility using eligibility
Description
Among all screened patients, the proportion of patients who meet the eligibility criteria
Time Frame
Screening/Enrollment
Title
Feasibility using the proportion of consent
Description
Among all screened patients, the proportion of patients consenting to participate
Time Frame
Screening/Enrollment
Secondary Outcome Measure Information:
Title
Efficacy using overall survival
Description
Measured in days from surgery to the time of death
Time Frame
From date of surgery until the date of death from any cause, assessed up to 36 months
Title
Efficacy using progression-free survival
Description
Assessment of progression-free survival based on the Modified Criteria for Radiographic Response Assessment in Glioblastoma (mRANO) criteria.
Time Frame
From date of surgery until the date of first documented progression, assessed up to 36 months
Title
Safety using the neurological function
Description
The National Institutes of Healt Stroke Scale (NIHSS) will be used to assess neurological function. The NIHSS is composed of 11 items, each of which scores a specific ability between a 0 and 4. For each item, a score of 0 typically indicates normal function in that specific ability, while a higher score is indicative of some level of impairment.
Time Frame
30 days
Title
Safety using global disability
Description
The modified Rankin scale (mRS ) is a measure of global disability that has been widely used to assess outcome after stroke. The scale runs from 0-6, running from perfect health without symptoms to death
Time Frame
30 days
Title
Extent of resection
Description
Volumetric measurement of contrast enhancement and T2-FLAIR signal alteration on MRI
Time Frame
< 72 hours after surgery
Title
Postoperative complication
Description
Relevant post surgical complication that requires a second surgery or prolong the length of hospitalization (i.e. hematoma, infection)
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: A suspected diagnosis of supratentorial glioblastoma by MRI. Tumor in non eloquent brain region according to the UCSF (University of California, San Francisco) classification, including the sensor motor areas (precentral and postcentral gyri), perisylvian language areas in the dominant hemisphere (superior temporal, inferior frontal, and inferior parietal gyri), basal ganglia, internal capsule, thalamus, and visual cortex around the calcarine sulcus Indication for surgical treatment and where supramarginal resection is considered possible according to the preoperative imaging. This consideration needs to be verified by two specialists in neurosurgery. This criterion needs to be verified by two senior neurosurgeons. Karnofsky Performance Score ≥ 60; Written informed consent Exclusion Criteria: Tumors in eloquent areas. Recurrent gliomas (except biopsy) MR image data not usable due to artifacts during acquisition. Inability to give written informed consent KPS < 60 Severe comorbidity.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Santiago Cepeda, PhD
Phone
+34983420400
Ext
85954
Email
scepedac@saludcastillayleon.es
First Name & Middle Initial & Last Name or Official Title & Degree
Sergio García, PhD
Phone
+34983420400
Ext
85954
Email
segarciagarc@saludcastillayleon.es
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Santiago Cepeda, PhD
Organizational Affiliation
Hospital Río Hortega
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Universitario de La Princesa
City
Madrid
ZIP/Postal Code
28006
Country
Spain
Individual Site Status
Active, not recruiting
Facility Name
University Hospital Rio Hortega
City
Valladolid
ZIP/Postal Code
47012
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Santiago Cepeda, MD., PhD.
Phone
+34651035158
Email
scepedac@saludcastillayleon.es
First Name & Middle Initial & Last Name & Degree
Santiago Cepeda, MD., PhD.
First Name & Middle Initial & Last Name & Degree
Sergio García-García, MD., PhD.
First Name & Middle Initial & Last Name & Degree
Rosario Sarabia, MD., PhD.
First Name & Middle Initial & Last Name & Degree
Ignacio Arrese, MD., PhD.

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

Supramarginal Resection in Glioblastoma Guided by Artificial Intelligence

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