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68Ga-DOTATATE PET/CT in Oncogenic Osteomalacia

Primary Purpose

Oncogenic Osteomalacia, Mesenchymal Tumor

Status
Unknown status
Phase
Early Phase 1
Locations
China
Study Type
Interventional
Intervention
68Ga-DOTATATE
Sponsored by
Peking Union Medical College Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Oncogenic Osteomalacia focused on measuring Oncogenic osteomalacia, mesenchymal tumor, Somatostatin receptor, 68Ga-DOTATATE, PET/CT

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • In suspicion of oncogenic osteomalacia according to the clinical features such as hyperphosphaturia, hypophosphatemia, low serum vitamin D3 levels, and osteomalacia. Or prior oncogenic osteomalacia patients in suspicion of relapse or with residual tumor
  • At least 18 years old
  • Able to provide informed consent

Exclusion Criteria:

  • Females planning to bear a child recently or with childbearing potential
  • Renal function: serum creatinine >3.0 mg/dL (270 μM/L)
  • Liver function: any hepatic enzyme level more than 5 times upper limit of normal.
  • Known severe allergy or hypersensitivity to IV radiographic contrast.
  • Patients not able to enter the bore of the PET/CT scanner.
  • Inability to lie still for the entire imaging time because of cough, pain, etc.
  • Inability to complete the needed examinations due to severe claustrophobia, radiation phobia, etc.
  • Any other medical condition that, in the opinion of the Investigator, may significantly interfere with study compliance.

Sites / Locations

  • Department of Nuclear Medicine, Peking Union Medical College HopitalRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

68Ga-DOTATATE, PET/CT scan

Arm Description

We will perform 68Ga-DOTATATE PET/CT scanning on subjects

Outcomes

Primary Outcome Measures

Number and location of lesions detected by 68GA-DOTATATE PET/CT compared to 99mTc-HYNIC-TOC SPECT/CT and/or 18F-FDG PET/CT
Determine if the 68Ga-DOTATATE PET/CT changes care plans compared to conventional imaging/diagnostic techniques (99mTc-HYNIC-TOC SPECT/CT, and/or 18F-FDG PET/CT, MRI, CT, ultrasonography).

Secondary Outcome Measures

Number of participants and kinds of adverse events as a measure of safety
Determine if any adverse effects are associated with the scan and the number of patients that experience them.

Full Information

First Posted
January 29, 2012
Last Updated
April 5, 2017
Sponsor
Peking Union Medical College Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01524016
Brief Title
68Ga-DOTATATE PET/CT in Oncogenic Osteomalacia
Official Title
68Ga-DOTATATE PET/CT for Detection and Evaluation of the Causative Tumor of Oncogenic Osteomalacia
Study Type
Interventional

2. Study Status

Record Verification Date
July 2014
Overall Recruitment Status
Unknown status
Study Start Date
December 2011 (undefined)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Peking Union Medical College Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Oncogenic osteomalacia is rare disease predominantly caused by a small, somatostatin receptor positive mesenchymal tumor, which is frequently hidden in an unusual anatomical site and often goes undetected by conventional imaging. A permanent cure of the disease relies on exactly localizing the tumor and completely removing it. 68Ga-DOTATATE PET/CT is a novel scan that might have improved sensitivity and resolution specifically for somatostatin receptor positive tumors. The investigators will scan the suspicious and confirmed patients of oncogenic osteomalacia and compare it to 99mTc-HYNIC-TOC SPECT/CT and 18F-FDG PET/CT to see if it improves patient care.
Detailed Description
Oncogenic osteomalacia, or tumor-induced osteomalacia, is a rare, serious paraneoplastic syndrome. It is predominantly driven by a small, benign mesenchymal tumor. The disease is readily prompted by the clinical features such as hyperphosphaturia, hypophosphatemia, low serum vitamin D3 levels, elevated serum fibroblast growth factor 23 levels, and osteomalacia. However, the causative tumor is frequently hidden in an unusual anatomical site and often goes undetected by conventional imaging, such as computed tomography (CT), while a permanent cure of the disease will only rely on exact localization and completely removal of the tumor. Since mesenchymal tumors express somatostatin receptors (SSR), molecular imaging using radiolabeled somatostatin analogs may be one of the best ways to detect the small, occult tumors. 111In- and 99mTc-labeled octreotide and analogs have been proved useful to detect mesenchymal tumor and other SSR-positive tumors. However, the scintigraphy is insufficient to provide high-resolution images and precise anatomical information. In this study, a novel approach was proposed for exact localization of mesenchymal tumors through positron emission tomography (PET) imaging with 68Ga-DOTATATE and co-registration with CT. 68Ga-DOTATATE PET/CT is a novel method that might have improved sensitivity and resolution specifically for SSR-positive tumors, including the causative tumor of oncogenic osteomalacia. The investigators will scan the patients in suspicion of oncogenic osteomalacia and the confirmed oncogenic osteomalacia patients in suspicion of relapse or with residual tumor after surgery, and compare it to 99mTc-HYNIC-TOC SPECT/CT and 18F-FDG PET/CT of the same patients. The aim of the study was to see if 68Ga-DOTATATE PET/CT can detect more tumors with higher resolution and more exact localization, and then help to develop optimal treatment strategy and improves patient care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Oncogenic Osteomalacia, Mesenchymal Tumor
Keywords
Oncogenic osteomalacia, mesenchymal tumor, Somatostatin receptor, 68Ga-DOTATATE, PET/CT

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Early Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
68Ga-DOTATATE, PET/CT scan
Arm Type
Experimental
Arm Description
We will perform 68Ga-DOTATATE PET/CT scanning on subjects
Intervention Type
Drug
Intervention Name(s)
68Ga-DOTATATE
Other Intervention Name(s)
(68)Ga-DOTA-d-Phe(1),Tyr(3)-octreotate
Intervention Description
Intravenous injection of one dosage of 72-185MBq (2-5 mCi) 68Ga-DOTATATE solution. Tracer doses of 68Ga-DOTATATE will be used to image tumors by Positron Emission Tomography / computed tomography (PET/CT)
Primary Outcome Measure Information:
Title
Number and location of lesions detected by 68GA-DOTATATE PET/CT compared to 99mTc-HYNIC-TOC SPECT/CT and/or 18F-FDG PET/CT
Description
Determine if the 68Ga-DOTATATE PET/CT changes care plans compared to conventional imaging/diagnostic techniques (99mTc-HYNIC-TOC SPECT/CT, and/or 18F-FDG PET/CT, MRI, CT, ultrasonography).
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Number of participants and kinds of adverse events as a measure of safety
Description
Determine if any adverse effects are associated with the scan and the number of patients that experience them.
Time Frame
One year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: In suspicion of oncogenic osteomalacia according to the clinical features such as hyperphosphaturia, hypophosphatemia, low serum vitamin D3 levels, and osteomalacia. Or prior oncogenic osteomalacia patients in suspicion of relapse or with residual tumor At least 18 years old Able to provide informed consent Exclusion Criteria: Females planning to bear a child recently or with childbearing potential Renal function: serum creatinine >3.0 mg/dL (270 μM/L) Liver function: any hepatic enzyme level more than 5 times upper limit of normal. Known severe allergy or hypersensitivity to IV radiographic contrast. Patients not able to enter the bore of the PET/CT scanner. Inability to lie still for the entire imaging time because of cough, pain, etc. Inability to complete the needed examinations due to severe claustrophobia, radiation phobia, etc. Any other medical condition that, in the opinion of the Investigator, may significantly interfere with study compliance.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Fang Li, MD
Phone
86-10-65295502
Email
lifang@pumch.cn
First Name & Middle Initial & Last Name or Official Title & Degree
Zhaohui Zhu, MD, PhD
Phone
86-10-13611093752
Email
zzh_1969@yahoo.com.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Fang Li, MD
Organizational Affiliation
Department of Nuclear Medicine, Peking Union Medical College Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Nuclear Medicine, Peking Union Medical College Hopital
City
Beijing
ZIP/Postal Code
100730
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fang Li, MD
Phone
86-10-65295502
Email
lifang@pumch.cn
First Name & Middle Initial & Last Name & Degree
Zhaohui Zhu, MD, PhD
Phone
86-10-13611093752
Email
zzh_1969@yahoo.com.cn
First Name & Middle Initial & Last Name & Degree
Fang Li, MD
First Name & Middle Initial & Last Name & Degree
Zhaohui Zhu, MD, PhD
First Name & Middle Initial & Last Name & Degree
Hongli Jing, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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68Ga-DOTATATE PET/CT in Oncogenic Osteomalacia

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