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AzTrials

Gastroenteropancreatic Neuroendocrine TumorsPhase 1/2GaINNCT02078843

Diagnostic Accuracy of Gallium-68-DOTATATE PET/CT Compared to Indium-111-pentetreotide Scintigraphy (SPECT/CT) for Gastroenteropancreatic Neuroendocrine Tumors

A Phase 1/2 study testing Gallium-68-DOTATATE PET/CT (index test) and Indium-111-Octreoscan (standard test) in people with Gastroenteropancreatic Neuroendocrine Tumors, run by Insel Gruppe AG, University Hospital Bern at 1 site in Switzerland.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

The investigators hypothesize that the new imaging method Gallium-68-DOTATATE has a higher diagnostic value in the detection of neuroendocrine tumors than the established imaging method Indium-111-Octreoscan. Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Gallium-68-DOTATATE PET/CT (index test) and Indium-111-Octreoscan (standard test)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
54 participants
Where
1 siteSwitzerland
Study dates
Mar 2014to Aug 2016
Phase
Phase 1/2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age ≥ 18 years
  • Signed written informed consent with full understanding of the study procedures and the investigational nature of the study
  • Patient referred to Indium-111-pentetreotide scintigraphy., which was performed as part of clinical routine care
  • Histologically established GEP-NET (new or recurrent)
  • Tumor mass remaining after initial biopsy or surgery
  • 5.6. Suspicion of any NET (new or recurrent) but no established diagnosis or established diagnosis of any NET (new or recurrent) but no remaining tumor mass after surgery

Who cannot join

  • Previous inclusion in the same study with the following exception: a patient may be included as case if she/he was previously included as control
  • Gastric type 2 ECL cell neuroendocrine tumors
  • Pregnant or nursing women
  • Known intolerance to any protocol required diagnostic intervention
  • Patient's lack of accountability, inability to appreciate the nature, meaning and consequences of the study and to formulate his/her own wishes correspondingly
  • Patients for whom it remains unclear whether the tumor was completely removed

Trial locations and contacts

1 site in 1 country.

Switzerland1 site
  • Nuclear Medicine, Bern University Hospital

    Bern, 3010

Other trials in Switzerland

About this study

The investigators hypothesize that the new imaging method Gallium-68-DOTATATE has a higher diagnostic value in the detection of neuroendocrine tumors than the established imaging method Indium-111-Octreoscan. Therefore, the investigators will perform both imaging procedures in patients with suspected or confirmed neuroendocrine tumors. Subsequently, the investigators will compare the diagnostic performance of both methods.

Read the detailed description

Background

Neuroendocrine tumors Neuroendocrine tumors (NET) are heterogeneous slow-growing neoplasms, occurring in 1-4/100,000 people per year. They origin from endocrine cells that derive from entodermal stem cells and are characterized by an endocrine metabolism and a typical pathologic pattern.

Slow metabolic rates of NET, small lesion size and variable anatomical localization have represented the major limits for lesions diagnosis. The diagnostic workup for NET has relied on conventional morphological imaging procedures including computed tomography (CT), ultrasound (US) and magnetic resonance imaging (MRI) combined with gamma camera functional imaging, namely whole-body somatostatin receptor scintigraphy (SRS). SRS show a higher diagnostic accuracy than CT for NET diagnosis at both the primary and metastatic site, but there is still room for improvement. Novel PET tracers specifically developed for NET may increase diagnostic accuracy considerably as outlined below.

Somatostatin receptor scintigraphy (SRS) As NET have high affinity somatostatin receptors, scintigraphic methods have been developed in the early nineties to allow in vivo imaging. SRS using Indium-111-DTPA-octreotide (Indium-111-pentetreotide scintigraphy), is the most widely used diagnostic test. Although rather sensitive and helpful for whole body staging compared to traditional imaging methods, this technique has pitfalls, one of them being the poor spatial resolution, leading to the development of PET-based imaging.

Gallium-68-DOTA-peptide PET In the past decade, several positron emitting tracers have been developed for NET imaging. 68Ga-DOTA-peptides are a group of PET tracers that specifically bind to somatostatin receptors (SSTR) over-expressed on NET cells. Gallium-68-DOTA-peptides structure can be summarized in (1) the active part binding to SSTR (TOC, NOC, TATE), (2) the chelant (DOTA) and (3) the isotope (68Ga). Indications to perform 68Ga -DOTA-peptides studies in NET patients include: staging, re-staging after therapy, identification of the site of the unknown primary tumor in patients with proven NET secondary lesions and selection of cases eligible for therapy with somatostatin analogues.

68Ga-DOTA-TOC was the first tracer to be employed in NET imaging and was reported to present a high tumor to non-tumor contrast and a higher sensitivity compared to SRS . The study with the largest patients population (84 pts with NET), reported sensitivity (97%) for DOTA-TOC PET to be superior to CT (61%) and SRS (52%) for the detection of NET lesions, especially in case of small tumors at nodal or bone level. In a comparison study of 51 patients with well differentiated NET, PET with Gallium-DOTA-TOC performed better than CT and SRS for the early detection of bone NET secondary lesions (sensitivity of 97%, specificity of 92%). 68Ga-DOTA-TATE is characterized by a very high affinity for SSTR2 with a considerably higher affinity than 111In-DTPA octreotide. In a recent study, 51 patients with established NET (35 negative and 16 equivocal for uptake on SRS) were examined by 68Ga-DOTA-TATE PET. 68Ga-DOTA-TATE PET identified significantly more lesions than SRS and changed management in 36 patients (70.6%), who were subsequently deemed suitable for peptide receptor-targeted therapy.

Rationale of the study 111In-pentetreotide scintigraphy is the current standard for the detection of NET, even though its diagnostic accuracy is less than optimal. In the past decade, several 68Ga-DOTA-peptides have been developed for NET imaging, which showed a better detection for NET than 111In-pentetreotide scintigraphy in a small number of studies. These studies had several limitations, most importantly the inclusion of rather small and heterogeneous patient populations.

The aim of this study is to prospectively compare the diagnostic accuracy of 68Ga-DOTA-TATE PET/CT with 111In-pentetreotide scintigraphy in a well-defined population of consecutive patients with established GEP-NET or patients with suspicion of NET with indication for a scintigraphy.

Objective

The objective of this study is to compare the diagnostic accuracy of Gallium-68-DOTATATE PET/CT with Indium-111-pentetreotide scintigraphy (SPECT/CT) for the diagnosis of gastroenteropancreatic neuroendocrine tumors (GEP-NET) in consecutive patients with established GEP-NET or patients with suspicion of NET with indication for a scintigraphy. The working hypothesis is that Gallium-68-DOTATATE PET/CT is superior to Indium-111-pentetreotide scintigraphy (SPECT/CT) in terms of sensitivity and specificity.

Methods

The present study is a multi-center assessor-blind diagnostic case-control study of Gallium-68-DOTATATE PET/CT compared to Indium-111-pentetreotide scintigraphy (SPECT/CT) in consecutive patients with established GEP-NET or patients with suspicion of NET with indication for a scintigraphy.

The study is conducted at the University Hospital Basel, Bern University Hospital, and CHUV Lausanne. The University Clinics of Nuclear Medicine of Basel, Bern and Lausanne, as well as Endocrinology, Diabetes and Clinical Nutrition of Bern will accrue consecutive patients with established GEP-NET or patients with suspicion of GEP-NET that meet eligibility criteria. All patients will undergo Gallium-68-DOTATATE PET/CT as index test and Indium-111-pentetreotide scintigraphy as standard test. Both results will be compared with histology and the follow-up results as diagnostic gold standards.

Being tested
Gallium-68-DOTATATE PET/CT (index test), Indium-111-Octreoscan (standard test)
Keywords
NET, Gallium-68-DOTATATE, PET/CT, Indium-111-pentetreotide scintigraphy, octreoscan, GEP-NET, gastroenteropancreatic neuroendocrine tumors
Medical subject headings
Gastro-enteropancreatic neuroendocrine tumor

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Gallium-68-DOTATATE PET/CT (index test)Drug

    Somatostatin-based imaging tracer

  • Indium-111-Octreoscan (standard test)Drug

    Somatostatin-based imaging tracer

Study groups in NCT02078843
Study groupRoleWhat they receive
All patientsOtherSubsequent performance of index test and standard test
Receives: Drug: Gallium-68-DOTATATE PET/CT (index test); Drug: Indium-111-Octreoscan (standard test)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Number of patients correctly identified as having GEP-NET by using Gallium-68-DOTATATE PET/CT and Indium-111-pentetreotide scintigraphy (SPECT/CT)

    Measured: 6 months

  2. Number of patients correctly identified as not having GEP-NET by using Gallium-68-DOTATATE PET/CT and Indium-111-pentetreotide scintigraphy (SPECT/CT)

    Measured: 6 months

Secondary outcomes (2)
  1. Patient satisfaction

    Measured by patient satisfaction questionnaire relating to Indium-111-pentetreotide scintigraphy

    Measured: 6 months

  2. Number of patients with adverse events

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Mar 2014 (estimated)
  2. Study startMar 2014
  3. Primary completionAug 2016
  4. Study completionAug 2016

Why it stopped: Superiority of one imaging method

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1/2
Primary purpose
Diagnosis
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
54 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02078843
Sponsor's protocol ID
092/11
Acronym
GaIN
Status last verified
Sep 2016
First submitted
26 Feb 2014
Last updated
7 Sep 2016
Results posted
No
Data monitoring committee
No

Publications

  • Gabriel M, Oberauer A, Dobrozemsky G, Decristoforo C, Putzer D, Kendler D, Uprimny C, Kovacs P, Bale R, Virgolini IJ. 68Ga-DOTA-Tyr3-octreotide PET for assessing response to somatostatin-receptor-mediated radionuclide therapy. J Nucl Med. 2009 Sep;50(9):1427-34. doi: 10.2967/jnumed.108.053421. Epub 2009 Aug 18.

    PubMed 19690033
  • Putzer D, Gabriel M, Henninger B, Kendler D, Uprimny C, Dobrozemsky G, Decristoforo C, Bale RJ, Jaschke W, Virgolini IJ. Bone metastases in patients with neuroendocrine tumor: 68Ga-DOTA-Tyr3-octreotide PET in comparison to CT and bone scintigraphy. J Nucl Med. 2009 Aug;50(8):1214-21. doi: 10.2967/jnumed.108.060236. Epub 2009 Jul 17.

    PubMed 19617343
  • Antunes P, Ginj M, Zhang H, Waser B, Baum RP, Reubi JC, Maecke H. Are radiogallium-labelled DOTA-conjugated somatostatin analogues superior to those labelled with other radiometals? Eur J Nucl Med Mol Imaging. 2007 Jul;34(7):982-93. doi: 10.1007/s00259-006-0317-x. Epub 2007 Jan 16.

    PubMed 17225119
  • Reubi JC, Schar JC, Waser B, Wenger S, Heppeler A, Schmitt JS, Macke HR. Affinity profiles for human somatostatin receptor subtypes SST1-SST5 of somatostatin radiotracers selected for scintigraphic and radiotherapeutic use. Eur J Nucl Med. 2000 Mar;27(3):273-82. doi: 10.1007/s002590050034.

    PubMed 10774879
  • Srirajaskanthan R, Kayani I, Quigley AM, Soh J, Caplin ME, Bomanji J. The role of 68Ga-DOTATATE PET in patients with neuroendocrine tumors and negative or equivocal findings on 111In-DTPA-octreotide scintigraphy. J Nucl Med. 2010 Jun;51(6):875-82. doi: 10.2967/jnumed.109.066134. Epub 2010 May 19.

    PubMed 20484441

Questions about this trial

What is this clinical trial studying?

A Phase 1/2 study testing Gallium-68-DOTATATE PET/CT (index test) and Indium-111-Octreoscan (standard test) in people with Gastroenteropancreatic Neuroendocrine Tumors, run by Insel Gruppe AG, University Hospital Bern at 1 site in Switzerland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 7 Sep 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this combined phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study was stopped early (reason given: Superiority of one imaging method). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Number of patients correctly identified as having GEP-NET by using Gallium-68-DOTATATE PET/CT and Indium-111-pentetreotide scintigraphy (SPECT/CT) (time frame: 6 months). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT02078843, which also lists 5 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Sep 2016.

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