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Feasibility of Individualized, Model-guided Optimization of Proton Beam Treatment Planning in Patients With Low Grade Glioma

Prospective Phase II Trial to Assess Feasibility of Individualized, Model-guided Optimization of Proton Beam Treatment Planning in Patients With Low Grade Glioma Multicentric, Prospective Interventional, Randomized, Observer Blind Two Arm (Active Control), Parallel Group Investigator-initiated Phase II Trial

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05964569
Acronym
INDIGO
Enrollment
120
Registered
2023-07-28
Start date
2023-11-11
Completion date
2028-11-11
Last updated
2024-01-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Low Grade Glioma

Brief summary

Low-grade glioma (LGG) represent typically slowly growing primary brain tumors with world health organization (WHO) grade I or II who affect young adults around their fourth decade. Radiological feature on MRI is a predominantly T2 hyperintense signal, LGG show typically no contrast uptake. Radiotherapy plays an important role in the treatment of LGG. However, not least because of the good prognosis with long term survivorship the timing of radiotherapy has been discussed controversially. In order to avoid long term sequelae such as neurocognitive impairment, malignant transformation or secondary neoplasms initiation was often postponed as long as possible

Detailed description

Since patients with low grade glioma are expected to become long-term survivors, the prevention of long-term sequelae is particularly important. In addition to disease progression, also treatment related side effects such as decline of neurocognitive function, endocrine impairment or sensorineural deficits can have a negative impact on patient's quality of life. Owing to the biophysical properties of protons with an inverse depth dose profile compared to photons and a steep dose fall of to the normal tissue, there is a strong rationale for the use of PRT in the treatment of patients with low-grade glioma. Although data from large randomized trials are still missing there is increasing evidence from smaller prospective trials and retrospective analyses that the expected advantages indeed transform into clinical advantages. However, in about 20 % of all patients, late contrast-enhancing brain lesions (CEBL) appear on follow-up MR images 6 - 24 months after treatment. At HIT in Heidelberg and at OncoRay in Dresden, CEBLs have been observed to occur at very distinct locations in the brain and relative to the treatment field. Retrospective analysis has elucidated potential key factors that lead to CEBL occurrence. However, avoidance of CEBLs is hardly feasible using conventional treatment planning strategies. Model-aided risk avoidance denotes the use of model-based CEBL risk calculations as an auxiliary tool for clinical treatment planning: Model-based risk calculations and risk reduction via software-based optimization help the clinician to minimize risk of CEBL occurrence during treatment planning.

Interventions

OTHERmodel-guided optimization of treatment plan

original treatmant plans are optimized based on model-based NTCP

OTHERstandard treatment plan, no optimization

original treatment plans are not optimized

Sponsors

University Hospital Heidelberg
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

randomized, observer blind two arm (active control), parallel group

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age \> 18 years * histologically proven low-grade glioma * indication for definitive or adjuvant radiotherapy * ability to understand character and personal consequences of the clinical trial * written informed consent

Exclusion criteria

* previous cerebral irradiation * contraindication for contrast-enhanced MRI * neurofibromatosis * participation in another clinical trial with competing objectives

Design outcomes

Primary

MeasureTime frameDescription
incidence of contrast enhancing brain leasionsobserved within 24 months after PRT measured by quarterly contrast enhanced MRI of the brainthe cumulative incidence of contrast enhancing brain lesions

Secondary

MeasureTime frameDescription
progression-free survivalobserved within 24 months after PRT measured by quarterly contrast enhanced MRI of the brainnumber of surviving patients without tumor progression
overall survivalobserved within 24 months after Proton Beam Therapy (PRT) measured by quarterly contrast enhanced MRI of the brainnumber of surviving patients
radiation-induced brain injuriesobserved within 24 months after PRT measured by quarterly contrast enhanced MRI of the brainincidence of radiation-induced brain injuries \> CTC°II
quality of life QLQ-C30up to 24 months after completion of PRTscores on the QLQ-C30 questionare, scored 0 (absence) to 5 (fully present)
quality of life QLQ-BN20up to 24 months after completion of PRTscores on the QLQ-BN20 questionare, scored 0 (absence) to 5 (fully present)
patient reported outcomeup to 24 months after completion of radiotherapypatient reported outcome according to points on the PRO-CTCAE questionaire, scored 0/1 for absent/present)

Countries

Germany

Contacts

Primary ContactSemi Harrabi, MD
semi.harrabi@med.uni-heidelberg.de+496221 56
Backup ContactAdriane Lentz-Hommertgen, Phd
adriane.lentz-hommertgen@med.uni-heidelberg.de+496221 56

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026