90Yttrium Colloid for the Treatment of Cystic Sellar/Parasellar Tumors

NCT ID: NCT02081768

Last Updated: 2025-06-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

PHASE3

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-06-30

Study Completion Date

2031-10-31

Brief Summary

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There is no consensus in the literature on the best way to treat cystic lesions of the pituitary area. Patients who are symptomatic from these tumours are rare. The cystic form of tumours present special challenges since traditional treatment modalities (surgery and/or external radiation) are often not able to completely remove or treat the cyst wall without major morbidity or even mortality.

There is no 'best practice' for the treatment of cystic tumours per se. Treatments available to patients with cystic sellar/parasellar tumours include conservative management using a 'wait and scan' approach, cyst drainage, and cyst removal via transsphenoidal and/or craniotomy approach (i.e. open surgery). Over the last 10 years we have treated approximately 8 patients with intracystic radiotherapy. All of these patients continue to be monitored clinically and radiologically and all have done well with stable regression of the cysts and no new neurological deficits. Over the past 2 years, 90yttrium colloid has been provided to CDHA through Health Canada's Special Access Program (SAP). It has only been of recent that Health Canada has requested a clinical trial to assess the benefit of intracystic radiotherapy over other available treatment options.

The experimental treatment being proposed is the stereotactic intracavitary instillation of 90yttrium colloid for treatment of cystic lesions of the pituitary (sellar) and surrounding areas (parasellar).

Detailed Description

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Surgical procedures will be performed as standard of care. The treating neurosurgeon (Dr. David B. Clarke) will determine surgical parameters based on his clinical expertise.

Conditions

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Cystic Tumors of the Sellar/Parasellar Region

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

90Yttrium colloid
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Open label

Study Groups

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90yttrium colloid

90 Yttrium colloid will be inserted into the cystic cavity. Based on clinical expertise, the treating neurosurgeon will determine the appropriate surgical procedure for each patient on an individual basis which will be reflected in the surgical consent the patient is presented and signs.

Group Type EXPERIMENTAL

90yttrium colloid

Intervention Type RADIATION

90yttrium colloid will be inserted into a sellar/parasellar cyst

Interventions

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90yttrium colloid

90yttrium colloid will be inserted into a sellar/parasellar cyst

Intervention Type RADIATION

Eligibility Criteria

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Inclusion Criteria

Patients who meet all of the following criteria are eligible for enrollment as study participants:

1. Patients 17 years of age or older.
2. Cystic sellar, suprasellar, parasellar or intrasellar masses diagnosed by histology, cytology or neuroimaging.
3. Tumour measurements and/or tumour volume can be calculated.
4. Patients who require surgical intervention as determined by the treating neurosurgeon.
5. Being a patient managed in the Halifax Neuropituitary Program surgical clinic.
6. Willingness to undergo surgery and give informed surgical consent.
7. Willingness to provide informed consent for study participation.

Exclusion Criteria

Patients who meet any of these criteria are not eligible for enrollment as study participants:

1. Neurosurgeon's assessment that surgical procedures hold unacceptable operative risk.
2. Having a solid tumour.
3. Pregnant or breast feeding at time of surgical consent and/or surgery.
4. Hypersensitivity, allergies or contraindication to the used radiopharmaceutical agent (90yttrium colloid).
Minimum Eligible Age

17 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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David Clarke

OTHER

Sponsor Role lead

Responsible Party

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David Clarke

Neurosurgeon

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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David Clarke

Role: PRINCIPAL_INVESTIGATOR

Capital District Health Auhtority

Locations

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Halifax Infirmary

Halifax, Nova Scotia, Canada

Site Status RECRUITING

Countries

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Canada

Central Contacts

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David B. Clarke, MDCM, PhD, FRCSC, DABNS, FACS

Role: CONTACT

Andrea LO Hebb, PhD, RN

Role: CONTACT

902 473-4824

Facility Contacts

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David B. Clarke, MDCM, PhD, FRCSC, DABNS, FACS

Role: primary

902-473-4591

Other Identifiers

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Yttrium2014

Identifier Type: -

Identifier Source: org_study_id

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