We're building a better ClinicalTrials.gov. Check it out and tell us what you think!
Working…
ClinicalTrials.gov
ClinicalTrials.gov Menu

Personalized PRRT of Neuroendocrine Tumors (P-PRRT)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02754297
Recruitment Status : Recruiting
First Posted : April 28, 2016
Last Update Posted : July 17, 2020
Sponsor:
Information provided by (Responsible Party):
CHU de Quebec-Universite Laval

Study Description
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information
Brief Summary:

In this study, peptide receptor radionuclide therapy (PRRT) with 177Lu-Octreotate (LuTate) will be personalized, i.e. administered activity of LuTate will be tailored for each patient to maximize absorbed radiation dose to tumor, while limiting that to healthy organs.

The purpose of this study is to:

  • Assess the objective (radiological), symptomatic and biochemical response rates following an induction course of personalized PRRT;
  • Assess the overall, the disease-specific, and the progression-free survival following P-PRRT;
  • Correlate therapeutic response and survival with tumor absorbed radiation dose;
  • Evaluate the acute, subacute and chronic adverse events following P-PRRT;
  • Correlate toxicity (i.e. occurence and severity of adverse events) with absorbed radiation doses to organs at risk;
  • Optimize the quantitative SPECT imaging-based dosimetry methods in a subset of 20 patients (sub-study funded by the Canadian Institutes of Health Research).

This study also has a compassionate purpose, which is to provide access to PRRT to patients.


Condition or disease Intervention/treatment Phase
Neuroendocrine Tumors Carcinoid Tumor Carcinoma, Neuroendocrine Drug: 177Lu-Octreotate Phase 2

Detailed Description:

A prospective, single-center, non-comparative, open phase 2 study. In this study, personalized peptide receptor radionuclide therapy (P-PRRT) with 177Lu-Octreotate (LuTate) will be administered to patients with progressive and/or symptomatic inoperable neuroendocrine tumors (NET) of any origin expressing the somatostatin receptor.

The primary objective to assess the objective response rate at 3 months following a four-cycle induction course of P-PRRT will be assessed for at least the first 85 participants.

This study as a compassionate aim to provide access to personalized PRRT patients at CHU de Québec - Université Laval center, and therefore this study has no pre-determined recruitment period duration or limited number of participants, and may remain open as long as necessary to fulfill this aim.

The study will continue until all participants have completed a minimum follow-up of 5 years. Interim analyses will be conducted annually.

Study Design
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Layout table for study information
Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 300 participants
Allocation: N/A
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Personalized Peptide Receptor Radionuclide Therapy of Neuroendocrine Tumors: A Phase 2 Study
Actual Study Start Date : April 12, 2016
Estimated Primary Completion Date : April 2021
Estimated Study Completion Date : December 2026

Resource links provided by the National Library of Medicine


Arms and Interventions
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Arm Intervention/treatment
Experimental: Personalized PRRT (P-PRRT)

177Lu-Octreotate (LuTate) P-PRRT will be administered as follows:

  • Renal absorbed radiation dose will be prescribed for the 4-cycle induction course (23 Gy) and for each subsequent cycle (6 Gy), with a reduction in cases of impaired renal or bone marrow function, or significant toxicity from prior cycles.
  • The personalized activity to be administered at each cycle will be derived from renal dose per unit of injected activity that is predicted by patient characteristics or renal dose delivered during prior cycle(s).
  • Participants responding to the induction course of P-PRRT will be eligible to receive additional consolidation and/or maintenance cycles.
  • Participants with prior PRRT exposure outside the trial may receive less induction cycles, or only consolidation/maintenance cycle(s).
 Drug: 177Lu-Octreotate
  • The induction course will consist in 4 cycles at 8-10 weeks intervals.
  • Concomitant amino acids will be administered for renal protection.
  • Intra-arterial LuTate administration will be allowed in suitable cases.
  • Dosimetry will be based on quantitative SPECT/CT imaging.
  • In patients with hormonal symptoms, somatostatine analogues can be given between P-PRRT cycles.
Other Names:
  • LuTate
  • 177Lu-[DOTA0,Tyr3]octreotate
  • 177Lu-DOTATATE


Outcome Measures
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Primary Outcome Measures :
  1. Objective response rate (ORR) [ Time Frame: 3 months after induction course ]
    Primary efficacy endpoint is the objective response rate on contrast-enhanced CT (or MRI) by RECIST criteria (and secondarily by South Western Oncology Group (SWOG) criteria) at 3 months after the 4th induction cycle of P-PRRT, in comparison to pre-treatment scan (within 3 months before commencing P-PRRT).


Secondary Outcome Measures :
  1. Progression-free survival (PFS) [ Time Frame: Time from first cycle to date of disease progression or death, reported up to 5 years after accrual closure ]
    Progression of disease is defined as the time from first cycle to the date of first documented progression of disease or death due to any cause. Progression of disease is defined by RECIST criteria.

  2. Overall survival (OS) [ Time Frame: Time from first cycle to date of death, reported up to 5 years after accrual closure ]
  3. Symptomatic response rate [ Time Frame: 3 months after induction course ]
    Proportion of participants with improved, stable or worsened NET-related symptoms (frequency and severity), based on participant interviews at baseline and 3 months after completion of induction course.

  4. Quality of life response [ Time Frame: 3 months after induction course ]
    Proportion of participants with improved, stable or worsened quality of life score by EORTC quality of life questionnaires QLQ-C30 and QLQ-GI.NET21, administered at baseline and 3 months after induction course.

  5. Biochemical response [ Time Frame: 3 months after induction course ]
    Proportion of participants with improved (decreased by 25% or more), stable or worsened (increased by 25% or more) Chromogranin-A serum levels performed at baseline and 3 months after induction course.

  6. Safety determined by type, frequency and severity of adverse events per CTCAE version 4.03 and type, frequency and severity of laboratory toxicities per CTCAE version 4.03 [ Time Frame: From the first treatment cycle administration until 5 years after accrual closure or death, whichever came first ]

Other Outcome Measures:
  1. Tumor radiation dose-response relationship [ Time Frame: 3 months after induction course ]
    Correlation between cumulative absorbed radiation dose to tumor lesions and 3-month objective response rate, as defined above

  2. Tumor radiation dose-survival relationship [ Time Frame: At least 5 years after first cycle or until study completion, whichever came first ]
    Correlation between cumulative absorbed radiation dose to tumor lesions and survival endpoints above (PFS and OS)

  3. Renal radiation dose-chronic toxicity relationship [ Time Frame: At least 5 years after first cycle or until study completion, whichever came first ]
    Correlation between cumulative absorbed radiation dose to kidney and variations in glomerular filtration rate from baseline, reported annually for at least 5 years after first cycle or until study completion.

  4. Bone marrow radiation dose-chronic toxicity relationship [ Time Frame: At least 5 years after first cycle or until study completion, whichever came first ]
    Correlation between cumulative absorbed radiation dose to bone marrow and chronic variations of blood counts from baseline, reported annually for at least 5 years after first cycle or until study completion.

  5. Bone marrow radiation dose-subacute toxicity relationship [ Time Frame: Time of nadir blood counts values between 2 and 6 weeks after each cycle ]
    Correlation between per-cycle absorbed radiation dose to bone marrow and subacute variations (nadir values between 2 and 6 weeks) of blood counts from baseline, for each cycle.


Eligibility Criteria
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Layout table for eligibility information
Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patient suffering from a progressive and/or symptomatic NET (any site);
  • Patient ineligible to, or refusing a potentially curative treatment such as surgical resection;
  • Patient who did not respond, is intolerant or refuses other indicated and available palliative treatments;
  • Demonstration of overexpression of somatostatin receptor by tumor lesions by scintigraphic imaging (Octreoscan or 68Ga positron emission tomography.

Exclusion Criteria:

  • Pregnancy;
  • Breastfeeding;.
  • Very limited survival prognosis (i.e. less than a few weeks, because of the NET disease or any other condition) or Eastern Cooperative Oncology Group (ECOG) 4 performance status;
  • Inability to obtain informed consent of the participant.
Contacts and Locations
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02754297


Contacts
Layout table for location contacts
Contact: Jean-Mathieu Beauregard, MD,MSc,FRCPC 418-525-4444 medecine.nucleaire@mail.chudequebec.ca
Contact: Geneviève Filion 418-525-4444 medecine.nucleaire@mail.chudequebec.ca

Locations
Layout table for location information
Canada, Quebec
CHU de Québec - Université Laval Recruiting
Quebec City, Quebec, Canada, G1R 2J6
Contact: Jean-Mathieu Beauregard, MD,MSc,FRCPC    418-555-4444    medecine.nucleaire@mail.chudequebec.ca   
Sub-Investigator: François-Alexandre Buteau, MD, FRCPC         
Sponsors and Collaborators
CHU de Quebec-Universite Laval
Investigators
Layout table for investigator information
Principal Investigator: Jean-Mathieu Beauregard, MD,MSc,FRCPC CHU de Québec - Université Laval
More Information
Go to 
Top of Page Study Description Study Design Arms and Interventions Outcome Measures Eligibility Criteria Contacts and Locations More Information
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Layout table for additonal information
Responsible Party: CHU de Quebec-Universite Laval
ClinicalTrials.gov Identifier: NCT02754297    
Other Study ID Numbers: A14-11-2181
First Posted: April 28, 2016    Key Record Dates
Last Update Posted: July 17, 2020
Last Verified: July 2020
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Keywords provided by CHU de Quebec-Universite Laval:
Neuroendocrine tumors
Personalized
Peptide receptor radionuclide therapy
 PRRT
177Lu-DOTATATE
177Lu-octreotate
Additional relevant MeSH terms:
Layout table for MeSH terms
Neoplasms
Neuroendocrine Tumors
Carcinoid Tumor
Carcinoma, Neuroendocrine
Neuroectodermal Tumors
Neoplasms, Germ Cell and Embryonal
Neoplasms by Histologic Type
 Neoplasms, Nerve Tissue
Adenocarcinoma
Carcinoma
Neoplasms, Glandular and Epithelial
Lutetium Lu 177 dotatate
Radiopharmaceuticals
Molecular Mechanisms of Pharmacological Action