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Feasibility of Intraoperative Tracing of Meningioma Using [Cu64]DOTATATE

A Pilot Study to Evaluate Feasibility of Intraoperative Tracing of Meningioma Using [Cu64]DOTATATE

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06377371
Enrollment
20
Registered
2024-04-22
Start date
2024-09-11
Completion date
2027-01-01
Last updated
2026-02-27

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

Conditions

Meningioma

Brief summary

The study team hypothesizes that it is feasible to intraoperatively detect tumor following \[CU64\]DOTATATE injection using the gamma probe device.

Detailed description

Objectives: Primary objectives: The primary objective of this pilot study is to evaluate the feasibility of intraoperative tumor detection using \[Cu64\]DOTATATE. The study team further wants to validate the gamma count measurements using pre- and post-operative Positron Emission Tomography (PET) standardized uptake value (SUV) . Secondary Objectives: To correlate intraoperative tracing findings with from pathology markers ( World Health Organization grade (WHO grade), Ki-67, Somatostatin Receptor 2 expression (SSTR2A expression), Estrogen receptor expression (ER expression), Progesterone receptor expression (PR expression)) using samples obtained as part of routine surgical care. To evaluate the correlation of post resection gamma count with longitudinal PET follow up. Exploratory objectives: To establish best practices for integration of intraoperative tumor tracing using the neoprobe into the surgical workflow. To determine surgical candidates who will benefit most from intraoperative tracing based on tumor location, MRI features, etc. Overall Design: This is a single-center prospective observational pilot study to determine the feasibility of using \[Cu64\]DOTATATE for intraoperative tumor detection. 20 patients diagnosed with meningioma by conventional magnetic resonance imaging (MRI) who are candidates for surgical resection will be enrolled. Enrollment will be facilitated by colleagues in the neurosurgery department (also co- investigators on this study) with whom the PI has had several years of collaboration and an ongoing referral stream (6pprox.. 5 patients per week). Patients will subsequently undergo pre-operative \[Cu64\]DOTATATE PET/MRI 12-24 hours prior to surgery. Given that \[Cu64\]DOTATATE has a much longer half-life compared to \[Ga68\]DOTATATE, it is uniquely suited for this application, allowing the patient to be injected once with the clinically approved dose, undergo immediate Positron Emission tomography scan and magnetic resonance imaging scan (PET/MRI) or Positron Emission tomography scan and computed tomography scan (PET/CT), and undergo resection the following day with sufficient radiotracer in situ for radio-guided surgery (RGS). During the operation, the neurosurgeon will make a number of measurements using the neoprobe (available at our institution and currently in frequent routine clinical use for intraoperative sentinel node detection; commonly used for breast cancer, melanoma, oral cancer): 1. After exposing the tumor, and immediately before removal, tumor counts will be documented with the neoprobe. This count will be correlated with preoperative \[Cu64\]DOTATATE SUV to evaluate the relationship between radiographic radiotracer uptake and intraoperative radioactivity of the tumor. 2. After removing all tumor that can be removed safely, the surgeon will grade whether they feel they obtained a gross total resection (GTR) or whether tumor was left behind (subtotal resection (STR), e.g. because the surgeon had to leave behind tumor attached to critical structure). In case of STR, the neoprobe will be used to measure counts in the remaining tumor. In case of presumed GTR, the neoprobe will be used to measure counts in the resection cavity. This second count will be correlated with post-operative \[Cu64\]DOTATATE SUV to evaluate the effectiveness of this method in evaluating residual tumor. These steps will not alter the regular course of the surgery in any way. Patients will have two follow-up points after the surgery: 1) at 6 weeks to 3 months post-op and 2) at 6 months to 12 months post-op. Patients will be clinically examined and will undergo repeat \[Cu64\]DOTATATE PET/MRI or PET/CT during these follow up visits, as standard of care, with radiotracer dosage being funded by the study for the 1st follow up scan, and determined standard of care for the 2nd follow up scan.

Interventions

DIAGNOSTIC_TESTBrain Imaging with [Cu64]DOTATATE

Patients will undergo a \[Cu64\]DOTATATE PET/MRI or PET/CT before undergoing radio- guided surgery. Patients will undergo another \[Cu64\]DOTATATE PET/MRI or PET/CT 6 weeks- 3 months after their surgery, and 6 months- 12 months after surgery.

PROCEDURERadio-guided Surgery With Neoprobe Utilization

After the subjects undergo the preoperative \[Cu64\]DOTATATE PET/MRI, subjects will undergo radio-guided surgery in which the surgeon will utilize a standard intraoperative gamma probe (Neoprobe Gamma Detection System ®) to assess primary/residual tumor detection.

Sponsors

Weill Medical College of Cornell University
Lead SponsorOTHER
Curium US LLC
CollaboratorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* High suspicion of meningioma necessitating surgical resection based on conventional MRI criteria, or diagnosis of meningioma based on pathology reports from prior resection with radiographic findings of suspected recurrent or residual tumor necessitating repeat surgery.

Exclusion criteria

* Pregnant or breastfeeding * Patients undergoing endoscopic endonasal resection, eyebrow incision surgery, or any surgical procedure in which the neoprobe cannot be employed * Patients with hypersensitivity to somatostatin analogs * Patients with contraindications to conventional MRI * Patients with prior history of cranial radiation therapy * Patients currently enrolled in other therapeutic clinical trials related to meningioma will be excluded

Design outcomes

Primary

MeasureTime frameDescription
Preoperative [Cu64]DOTATATE PET SUVAt time of enrollmentpreoperative lesion \[Cu64\]DOTATATE PET SUV
1st Post-operative [Cu64]DOTATATE PET SUV3 months6 weeks to 3 months follow up post operative \[Cu64\]DOTATATE PET SUV
2nd Post-operative [Cu64]DOTATATE PET SUV1 year6 months to 12 months follow up post operative \[Cu64\]DOTATATE PET SUV
MRI Size MeasurementsAt time of enrollmentpreoperative size measurements based on Response Assessment in Neuro-Oncology (RANO) guidelines
GTR vs STR Assessment6 weeks- 3 monthspostoperative MRI-based assessment of GTR versus STR by a neuroradiologist, as determined by the presence or absence of nodular dural-based enhancement on post contrast 3D T1-weighted MR imaging and direct comparison to preoperative MRI.
MRI Progression Assessment6-12 monthsfollow-up MRI assessment of progression based on RANO guidelines
Target Lesion Neoprobe CountAt time of enrollmentNeoprobe count of the target lesion prior to resection.
Subtotal Neoprobe CountAt time of enrollmentNeoprobe count of the subtotally resected tumor or the resection cavity in case of presumed GTR post resection.
Reference Background Neoprobe CountAt time of enrollmentNeoprobe count of the reference background measured at least 1 cm away from the tumor (measured in at least two locations depending on the operative field)

Secondary

MeasureTime frameDescription
SSTR2 expressionAt time of clinical neuropathological evaluation of resected tumor tissue (Immediate postoperative setting).immunohistochemistry analysis of SSTR2 expression in the resected tumor
WHO gradeAt time of clinical neuropathological evaluation of resected tumor tissue (Immediate postoperative setting).determined histomorphologically based on pathologist's assessment of resected tumor tissue.
Ki67 Proliferation IndexAt time of clinical neuropathological evaluation of resected tumor tissue (Immediate postoperative setting).Ki67 Proliferation Index (percentage of positively stained tumor cells among the total number of malignant cells assessed).
ER/PR expressionAt time of clinical neuropathological evaluation of resected tumor tissue (Immediate postoperative setting).determined based on pathologist's assessment of resected tumor tissue.

Countries

United States

Contacts

CONTACTJana Ivanidze, MD/PhD
jai9018@med.cornell.edu212-746-4587
CONTACTAlexis Watson
alw4020@med.cornell.edu646-962-2347
PRINCIPAL_INVESTIGATORJana Ivanidze, MD/PhD

Weill Medical College of Cornell University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026