Study to Evaluate Safety and Dosimetry of Lutathera in Adolescent Patients With GEP-NETs and PPGLs

A Multicenter Open-label Study to Evaluate Safety and Dosimetry of Lutathera in Adolescent Patients With Somatostatin Receptor Positive Gastroenteropancreatic Neuroendocrine (GEP-NET) Tumors, Pheochromocytoma and Paragangliomas (PPGL)

This is a multicenter, open-label, single-arm study to evaluate the safety and dosimetry of Lutathera in adolescent patients 12 to <18 years old with somatostatin receptor positive GEP-NETs and PPGLs. The study will enroll at least 8 patients in the GEP-NET cohort and as many adolescents with PPGL as possible in the exploratory PPGL cohort.

Study Overview

• Status: Active, not recruiting
• Conditions: Pheochromocytoma; Paraganglioma; Gastroenteropancreatic Neuroendocrine Tumors
• Intervention / Treatment: Drug: Lutetium [177Lu] oxodotreotide/dotatate

Detailed Description

The study schedule for each patient consists of the screening period (up to 2 weeks) followed by the treatment period (4 treatment administrations at 8-week interval), and the follow-up period (5 years).

The treatment period will consist of 4 Lutathera treatments administered at 8-week intervals. Lutathera administration will occur on Week 1 Day 1 of each cycle. Each patient will receive a total of 4 doses of Lutathera (7.4 GBq/200 mCi x 4 administrations every 8 weeks; cumulative dose: 29.6 GBq/800 mCi). An infusion of 2.5% Lysine - Arginine amino acid (AA) solution will be co-administered with each Lutathera dose for renal protection according to the approved Lutathera local prescribing information. An antiemetic will be administered prior to infusion of the AA solution for prevention of infusion-related nausea and vomiting.

The dosimetry and PK assessments will be performed during the first week after the 1st Lutathera dose, i.e. one time during the study treatment period for each patient. The dosimetry analysis will allow for estimation from the 1st Lutathera administration of the cumulative absorbed radiation dose from 4 Lutathera doses and also for taking a decision on the next dose levels. In the exceptional circumstances when dosimetry cannot be performed in a particular patient after the first Lutathera dose, it should be completed as soon as feasible upon a later dose. In order to minimize risk for each study subject, an accelerated analysis of dosimetry and safety data will be performed for each patient in the study, to enable the Investigator to take a decision for the subsequent Lutathera doses. The results of dosimetry assessments (imaging and blood dosimetry) will be provided to the investigators for their evaluation prior to administration of subsequent therapeutic cycles in each patient.

A total follow-up period of 5 years (60 months) after the last Lutathera dose will take place for each patient who received at least one dose of Lutathera. This follow-up period will be comprised of a short-term follow-up of 6 months to evaluate cumulative Lutathera toxicities, followed by a long-term follow up of another 54 months.

An external Data and Safety Monitoring Board (DSMB) will also operate in the study to evaluate accumulating safety and dosimetry data, to ensure the safety of adolescents enrolled in the study, and to provide recommendations to investigators as well as to the clinical team in charge of conducting the study.

• Study Type: Interventional
• Enrollment (Actual): 11
• Phase: Phase 2

Contacts and Locations

• Study Contact: Name: Novartis Pharmaceuticals; Phone Number: 1-888-669-6682; Email: novartis.email@novartis.com
• Study Contact Backup: Name: Novartis Pharmaceuticals; Phone Number: +41613241111

Study Locations

• France
  • Lyon, France
    • Centre Leon Berard
• Poland
  • Gliwice, Poland
    • Maria Sklodowska-Curie National Research Institute of Oncology
• Spain
  • Barcelona, Spain
    • Hospital Universitari Vall d'Hebron
• United Kingdom
  • London, United Kingdom
    • University College Hospital of London
• United States
  • Kentucky
    • Lexington, Kentucky, United States, 40536
      • University of Kentucky
  • Ohio
    • Cincinnati, Ohio, United States, 45229-3039
      • Cincinnati CHildren's Hospital
  • Pennsylvania
    • Philadelphia, Pennsylvania, United States, 19104
      • Children's Hospital of Philadelphia

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 12 years to 17 years (Child)
• Accepts Healthy Volunteers: No

Description

Key Inclusion Criteria:

1. GEP-NET cohort: presence of metastasized or locally advanced, inoperable (curative intent), histologically proven, G1 or G2 (Ki-67 index =< 20%), well differentiated GEP-NET.

   or PPGL cohort: presence of metastasized or locally advanced, inoperable (curative intent), histologically proven PPGL.

2. Patients from 12 to < 18 years of age at the time of enrollment.
3. Expression of somatostatin receptors confirmed by a somatostatin receptor imaging (SRI) modality within 3 months prior to enrollment, with tumor uptake observed in the target lesions more or equal to the normal liver uptake.
4. Performance status as determined by Karnofsky score >= 50 or Lansky Play-Performance Scale score >= 50.
5. Parent's ability to understand and the willingness to sign a written informed consent document for adolescents as determined by local regulations. Adolescents will sign assent along with parental/legal guardian consent or will co-sign consent with parent/legal guardian in accordance with local regulation, prior to participation in the study.

Key Exclusion Criteria:

1. Laboratory parameters:

   1. Estimated creatinine clearance calculated by the Cockroft-Gault method < 70 mL/min
   2. Hb concentration <5.0 mmol/L (<8.0 g/dL); WBC <2x109/L; platelets <75x109/L.
   3. Total bilirubin >3 x ULN for age.
   4. Serum albumin <3.0 g/dL unless prothrombin time is within the normal range.
2. Established or suspected pregnancy.
3. Breastfeeding female patients unless they accept to discontinue breastfeeding from the 1st dose until 3 months after the last administration of study drug.
4. Female patients of child-bearing potential, unless they are using highly effective methods of contraception during treatment and for 6 months after the last dose of Lutathera.
5. Sexually active male patients, unless they agree to remain abstinent or be willing to use effective methods of contraception.
6. Patients for whom in the opinion of the investigator other therapeutic options are considered more appropriate than the therapy offered in the study, based on patient and disease characteristics.
7. Current spontaneous urinary incontinence.
8. Other known co-existing malignancies except non-melanoma skin cancer and carcinoma in situ of the uterine cervix, unless definitively treated and proven no evidence of recurrence for 5 years.
9. Hypersensitivity to the study drug active substance or to any of the excipients.
10. Patients with any other significant medical, psychiatric, or surgical condition, currently uncontrolled by treatment, which may interfere with the completion of the study.
11. Patient with known incompatibility to CT Scans with I.V. contrast due to allergic reaction or renal insufficiency. If such a patient can be imaged with MRI, then the patient would not be excluded.
12. Patients who received any investigational agent within the last 30 days.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: GEP-NET and PPGL; All eligible participants will receive Lutathera (7.4 GBq/200 mCi x 4 administrations every 8 weeks; cumulative dose: 29.6 GBq/800 mCi), with a concomitant administration of 2.5% Lysine - Arginine amino acid solution.	Drug: Lutetium [177Lu] oxodotreotide/dotatate; Radiopharmaceutical solution for infusion (7.4 GBq of Lutathera per 30 ml vial); Other Names: Lutathera

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Absorbed radiation doses in target organ	Absorbed radiation doses in target organ (e.g. kidney and bone marrow) will be evaluated when all GEP-NET patients have completed the 1st treatment of Lutathera and completed the dosimetry assessment.	Up to 8 days after the first Lutetium [Lu 177] dotatate dose
Incidence of adverse events (AEs) after the 1st treatment cycle	The distribution of adverse events will be done via the analysis of frequencies for treatment emergent Adverse Event (TEAEs), Serious Adverse Event (TESAEs) and Deaths due to AEs, through the monitoring of relevant clinical and laboratory safety parameters.	Up to 8 weeks after the first Lutetium [Lu 177] dotatate dose

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Incidence of adverse events (AEs) during the short-term follow-up	Cumulative safety of Lutathera in adolescents with SSTR-positive GEP-NETs will be assessed through the incidence of adverse events (AEs) and laboratory toxicities until 6 months after the last Lutathera dose.	Up to 6 months after the last Lutetium [Lu 177] dotatate dose
Incidence of adverse events (AEs) during the long term follow-up	Long-term safety of Lutathera in adolescents with SSTR-positive GEP-NETs will be evaluated through the incidence of AEs and laboratory abnormalities during the 5-year follow-up after the last Lutathera dose.	Up to 5 years after the last Lutetium [Lu 177] dotatate dose
Comparative assessment of organ absorbed doses in adolescents and adults	Calculated organ absorbed doses based on imaging radioactivity concentration data from adolescent with SSTR-positive GEP-NETs patients will be compared to the predicted distribution/organ absorbed doses in adult population.	Up to 8 days after the first Lutetium [Lu 177] dotatate dose
Maximum plasma concentration (Cmax) of Lutetium [Lu 177] dotatate in adolescents and adults	Venous whole blood samples will be collected for activity-based pharmacokinetics characterization. Cmax will be listed and summarized using descriptive statistics.	Day 1 (0, 2, 6 hours post infusion), Day 2 (24 hours post infusion), Day 4 (72 hours post infusion)
Time of observed drug concentration occurrence (Tmax) of Lutetium [Lu 177] dotatate in adolescents and adults	Venous whole blood samples will be collected for activity-based pharmacokinetics characterization. Tmax will be listed and summarized using descriptive statistics.	Day 1 (0, 2, 6 hours post infusion), Day 2 (24 hours post infusion), Day 4 (72 hours post infusion)
Area Under plasma concentration-time Curve from time 0 to 72 hours (AUC0-72) of Lutetium [Lu 177] dotatate in adolescents and adults	Venous whole blood samples will be collected for activity-based pharmacokinetics characterization. AUC0-72 will be listed and summarized using descriptive statistics.	Day 1 (0, 2, 6 hours post infusion), Day 2 (24 hours post infusion), Day 4 (72 hours post infusion)
Total systemic clearance for intravenous administration (CL) of Lutetium [Lu 177] dotatate in adolescents and adults	Venous whole blood samples will be collected for activity-based pharmacokinetics characterization. CL will be listed and summarized using descriptive statistics.	Day 1 (0, 2, 6 hours post infusion), Day 2 (24 hours post infusion), Day 4 (72 hours post infusion)
Volume of distribution in the central compartment (V1) of Lutetium [Lu 177] dotatate in adolescents and adults	Venous whole blood samples will be collected for activity-based pharmacokinetics characterization. V1 will be listed and summarized using descriptive statistics.	Day 1 (0, 2, 6 hours post infusion), Day 2 (24 hours post infusion), Day 4 (72 hours post infusion)
Volume of distribution in the peripheral compartment (V2) of Lutetium [Lu 177] dotatate in adolescents and adults	Venous whole blood samples will be collected for activity-based pharmacokinetics characterization. V2 will be listed and summarized using descriptive statistics.	Day 1 (0, 2, 6 hours post infusion), Day 2 (24 hours post infusion), Day 4 (72 hours post infusion)

Collaborators and Investigators

• Sponsor: Advanced Accelerator Applications
• Investigators: Study Director: Novartis Pharmaceuticals, Novartis Pharmaceuticals

Study record dates

Study Major Dates

• Study Start (Actual): August 31, 2022
• Primary Completion (Estimated): March 12, 2024
• Study Completion (Estimated): May 7, 2029

Study Registration Dates

• First Submitted: December 16, 2020
• First Submitted That Met QC Criteria: January 12, 2021
• First Posted (Actual): January 15, 2021

Study Record Updates

• Last Update Posted (Actual): February 15, 2024
• Last Update Submitted That Met QC Criteria: February 14, 2024
• Last Verified: February 1, 2024

More Information

Terms related to this study

• Keywords: pediatric; adolescents; Lutathera; Lutetium Lu 177 dotatate; PRRT; GEP-NET; PPGL; Lutetium [177Lu] oxodotreotide; Peptide Receptor Radionuclide Therapy
• Additional Relevant MeSH Terms: Neoplasms by Histologic Type; Neoplasms; Neuroectodermal Tumors; Neoplasms, Germ Cell and Embryonal; Neoplasms, Nerve Tissue; Neuroendocrine Tumors; Pheochromocytoma; Paraganglioma; Molecular Mechanisms of Pharmacological Action; Radiopharmaceuticals; Lutetium Lu 177 dotatate
• Other Study ID Numbers: CAAA601A32201; 2020-002951-39 (EudraCT Number); EMEA-002950-PIP01-20 (Other Identifier: EMA paediatric Investigation plan number(s) (PIP))

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: YES

IPD Plan Description

Novartis is committed to sharing with qualified external researchers, access to patient-level data and supporting clinical documents from eligible studies. These requests are reviewed and approved by an independent review panel on the basis of scientific merit. All data provided is anonymized to respect the privacy of patients who have participated in the trial in line with applicable laws and regulations.

This trial data availability is according to the criteria and process described on www.clinicalstudydatarequest.com

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No