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Proton Beam Therapy for Chondrosarcoma

Phase II Evaluation of Proton Beam Therapy for Skull Base Chondrosarcoma

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00496522
Enrollment
15
Registered
2007-07-04
Start date
2006-04-28
Completion date
2026-08-19
Last updated
2026-03-09

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

Conditions

Chondrosarcoma

Keywords

Skull Base Chondrosarcoma, Proton Beam Therapy, Chondrosarcoma, CNS

Brief summary

The goal of this clinical research study is to learn if proton beam therapy, with or without photon beam radiation therapy, is effective in the treatment of skull base chondrosarcoma. The safety of this treatment will also be studied.

Detailed description

Patients who have skull base chondrosarcoma require complicated treatment because of its challenging location and nearness to critical structures within the brain. Pathology will be confirmed prior to discussion of the study. If you are found to be eligible to take part in this study, you will receive proton beam therapy, no sooner than 2 weeks after the last surgery to remove tumor. You will receive proton beam therapy once a day for about 35 treatments (7 weeks). Treatment will be given for 5 days in a row each week (except for Saturdays, Sundays, and holidays) at the Proton Center in Houston. The whole process should take up to 1 hour each day. If your doctor feels it is necessary, the proton beam therapy may be combined with standard photon therapy. After the proton beam, and possibly photon beam, therapy, you will be asked to come in for study follow-up visits every year, until the study is completed. At these visits, you will have magnetic resonance imaging (MRI) scans, blood draws (less than 1 teaspoon) to monitor your pituitary function, and neuropsychological testing. For the neuropsychological testing, you will be interviewed and tested by a neuropsychologist to evaluate your memory, fluency (the ability to talk and form words) complex thinking ability, planning ability, and coordination. These tests could last from 1-2 hours. You will also have eye exams performed by an ophthalmologist from MD Anderson and hearing exams. It is anticipated that it will take about 5 years to complete this study. This is an investigational study. The proton beam center and its treatment are approved by the FDA for patient use. A total of up to 15 patients will take part in this study. All will be enrolled at MD Anderson.

Interventions

A total dose of up to 70 CGE given at 2.0 CGE per daily fraction for 35 fractions.

Sponsors

M.D. Anderson Cancer Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

1. Pathologically confirmed Grade 1-3 chondrosarcoma of the skull base 2. Contrast enhanced postop MRI or CT if there is clinical contraindication for MRI of the skull base obtained with 90 days of study registration at M. D. Anderson 3. The patient has been assessed by MDACC skull base surgeons to have undergone maximal surgical debulking of disease 4. Karnofsky Performance status greater than or equal to 60 5. Signed informed consent

Exclusion criteria

1. Previous irradiation of the skull base 2. Documented evidence of disseminated metastatic disease

Design outcomes

Primary

MeasureTime frameDescription
Time to Local RecurrenceBaseline to local recurrence (evaluation every six months during estimated 5 year study)Local recurrence defined as progression on magnetic resonance imaging (MRI) or CT if MRI is contraindicated.

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORDavid Grosshans, MD,PHD

M.D. Anderson Cancer Center

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026