Study of Adaptive Radiotherapy for High-grade Glioma Based on Interfraction MRI

NCT06201351 — Unknown, 60 participants, West China Hospital

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Study of Adaptive Radiotherapy for High-grade Glioma Based on Interfraction Magnetic Resonance Imaging (MRI)

RegistryNCT06201351
StatusUnknown
Study typeObservational
Enrollment60 (Estimated)
SponsorWest China Hospital (Other)
ConditionsHigh-grade Glioma
Interventionsadaptive radiotherapy (Device)
Datesstart 2024-01-01 (estimated), primary completion 2025-12-01 (estimated), completion 2026-09-30 (estimated), first posted 2024-01-11, last updated 2024-01-11
Locations1 site in China

Related Papers Related Patents Related Grants Related Experts
All trials for High-grade Glioma All trials of adaptive radiotherapy

-Summary

The changes of target and organs at risk in patients with high-grade glioma during concurrent chemoradiotherapy were evaluated by MRI image between radiotherapy fractions.

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+Detailed description

To prospectively evaluate the changes of target organs and risk organs in patients with high-grade glioma during concurrent chemoradiotherapy.The related factors causing this change are discussed.The relationship between changes and patient survival was analyzed.A predictive model was established to provide individualized adaptive radiotherapy for patients.

+Arms and interventions

ArmTypeInterventionsDescription
Adaptive radiotherapy groupDevice: adaptive radiotherapyMRI was performed and adaptive radiotherapy was administered at farction10 and fraction 20 during radiotherapy.
  • adaptive radiotherapy (Device), also known as ART: MRI was performed and adaptive radiotherapy was administered at farction10 and fraction 20 during radiotherapy.

+Outcome measures

Primary outcomes

  • Homogeneity index [up to 2 weeks]: HI: Homogeneity index. Dosimetric change
  • conformity index [up to 2 weeks]: CI: conformity index. Dosimetric change
  • Anatomic change [up to 2 weeks]: Dmax Volume

Secondary outcomes

  • progression-free survival (PFS) [assessed up to 12 months]: progression-free survival

+Eligibility

Sex: All, ages: 18 Years to 70 Years

Inclusion Criteria:

1. Age ≥18 years old;
2. High-grade glioma was confirmed by pathology after surgery;
3. ECOG score 0-2 points;
4. Receiving the standard STUPP regimen (i.e. 6 weeks of temozolomide concurrent chemoradiotherapy +6 cycles of temozolomide adjuvant chemotherapy);
5. Baseline data available.

Exclusion Criteria:

1. The pathological diagnosis is not clear;
2. No synchronous chemotherapy/adjuvant chemotherapy \< 6 cycles;
3. There are other malignant tumors;
4. Previously radiotherapy to the head;
5. Interruption of radiotherapy for more than 5 days;
6. Failure to collect baseline data.

+Locations (1)

FacilityCityCountryStatus
West China HospitalChengdu, SichuanChina

+Publications

  • Results publication: He S, Yu H, Yang Y, Mao Q, Wang X, Zeng Y, Wang F, Liu M, Li Y, Gao K, Peng X, Liu Y, Ai P. Study of Adaptive Radiotherapy for High-Grade Glioma Based on Interfraction MRI. Cancer Med. 2026 Sep;15(9):e72225. doi: 10.1002/cam4.72225. PMID 42675793