Study to Evaluate the Efficacy and Safety of [177Lu]Lu-DOTA-TATE in Patients With Grade 1 and Grade 2 Advanced GEP-NET

Phase 3RecruitingNCT06784752

Novartis Pharmaceuticals240 enrolled

Overview

The purpose of the current study is to evaluate the efficacy and safety of \[177Lu\]Lu-DOTA-TATE plus octreotide long-acting release (LAR) versus octreotide LAR alone in newly diagnosed patients with somatostatin receptor positive (SSTR+), well differentiated Grade1 and Grade 2 (G1 and G2) (Ki-67 \<10%) advanced gastroenteropancreatic neuroendocrine tumors (GEP-NETs) with high disease burden

The study consists of a screening phase, a treatment phase and a follow-up phase. This study compares treatment with \[177Lu\]Lu-DOTA-TATE plus octreotide LAR and octreotide LAR only.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

NONE

Enrollment

240

Conditions

Somatostatin Receptor Positive (SSTR+)Gastroenteropancreatic Neuroendocrine Tumor (GEP-NET)

Interventions

Eligibility

Sex: ALLMin age: 12 YearsMax age: 100 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Presence of metastasized or locally advanced, unresectable (curative intent), histologically proven, well differentiated Grade 1 or Grade 2 (Ki-67 \<10%) gastroenteropancreatic neuroendocrine tumor (GEP-NET) diagnosed within 6 months prior to screening. * Participants with high disease burden in the Investigator's opinion. Following criteria should be used as the guiding principle for determining high disease burden: * Primary tumor or a metastatic lesion \> 4 cm * More than one tumor or metastatic lesions measuring \> 2 cm * Elevated alkaline phosphatase \> 2.5 X upper limit of normal (ULN) * Presence of bone metastasis * Presence of peritoneal metastasis * Symptoms due to tumor volume such as pain, fatigue, weight loss, anorexia etc. * Symptoms due to hormone excess requiring active management * Additionally, participants who, in the Investigator's opinion, have high disease burden due to their disease characteristics not specified above could also be considered eligible. * Participants ≥ 12 years of age. * RLI somatostatin receptor (SSTR) uptake on all target lesions (defined by RECIST v1.1 criteria) at least as high as normal liver uptake assessed within 3 months prior to randomization. Any of the RLI modalities as available (some examples are listed below) can be used as per local practice: * \[68Ga\]Ga-DOTA-TOC PET/CT or PET/MRI * \[68Ga\]Ga-DOTA-TATE PET/CT or PET/MRI * \[64Cu\]Cu-DOTA-TATE PET/CT or PET/MRI * Somatostatin receptor scintigraphy (SRS) (planar and/or SPECT/CT) with \[111In\]In-pentetreotide * SRS (planar and/or SPECT/CT) with \[99mTc\]Tc-octreotide. * Adequate bone marrow and organ function as defined by the following laboratory values prior to receiving the first study treatment: * White blood cell (WBC) count ≥ 2 x 109/L * Platelet count ≥ 75 x 109/L * Hemoglobin (Hb) ≥ 8 g/dL * Creatinine clearance \> 40 mL/min calculated by the Cockcroft Gault method * Total bilirubin ≤ 3 x ULN * Potassium within normal limits. Potassium level of up to 6.0 millimoles per liter (mmol/L) is acceptable at study entry if associated with creatinine clearance within normal limits calculated using Cockcroft-Gault formula. Mild decrease (grade 1) below lower limit of normal (LLN) is acceptable at study entry if considered not clinically significant by Investigator. * ECOG performance status 0-1. * Presence of at least 1 measurable site of disease. Exclusion Criteria: * Prior administration of a therapeutic radiopharmaceutical for GEP-NET at any time prior to randomization in the study. * Any previous therapy with interferons, mTOR-inhibitors, chemotherapy or other systemic therapies except somatostatin analogues (SSAs) of GEP-NET. If as per Investigator's opinion a participant is candidate for such therapies, such participant must not be enrolled. * Participant who received more than 4 cycles of prior SSAs (e.g., octreotide long-acting release) are not eligible. In addition, any participant receiving treatment with short-acting octreotide, which cannot be interrupted for 24 h before the administration of \[177Lu\]Lu-DOTA-TATE, or any participant receiving treatment with SSAs, which cannot be interrupted for at least 4 weeks before the administration of \[177Lu\]Lu-DOTA-TATE. * Documented RECIST v1.1 progression during previous SSA treatments for the current GEP-NET at any time prior to randomization. * Any previous radioembolization, chemoembolization and radiofrequency ablation for GEP-NET. * Any major surgery within 12 weeks prior to randomization in the study. * Known brain metastases. * Participant with known intolerance to CT scans with intravenous (i.v.) contrast due to allergic reaction or renal insufficiency. If such a participant can be imaged with MRI, then the participant would not be excluded. * Hypersensitivity to any somatostatin analogues, to the Investigational Medicinal Products (IMPs) active substance or to any of the excipients. * Active severe urinary incontinence, severe voiding dysfunction, or urinary obstruction requiring an indwelling/condom catheter that, in the judgment of the Investigator, could prevent adhering to radiation safety instructions. Other protocol-defined Inclusion/Exclusion criteria may apply.

Locations (61)

Mayo Clinic Arizona

Scottsdale, Arizona, United States

RECRUITING

Highlands Oncology Group

Fayetteville, Arkansas, United States

RECRUITING

Rocky Mountain Cancer Centers

Denver, Colorado, United States

RECRUITING

Hartford Hospital

Hartford, Connecticut, United States

Outcomes

Primary Outcomes

Progression Free Survival (PFS) centrally assessed by Blinded Independent Review Committee (BIRC)

PFS is defined as the time from randomization to the first occurrence of progression (centrally assessed by Blinded Independent Review Committee (BIRC) according to RECIST v1.1) or death due to any cause.

Time frame: After observing approximately 88 PFS events as per BIRC assessments, expected after approximately 33 months from study start

Secondary Outcomes

Time to Deterioration (TDD) (Key Secondary)

Time to deterioration is defined as the time from randomization to the first occurrence of a deterioration compared to the baseline scores or death from any cause for each of the following domains (tested separately) of EORTC QLQ-GI.NET21 \[gastrointestinal scale (GI scale)\] and EORTC QLQ-C30 questionnaires (fatigue, diarrhea, and global health scale).

Time frame: After observing approximately 88 PFS events as per BIRC assessment, expected after approximately 33 months from study start

Progression Free Survival (PFS)

PFS is defined as the time from randomization to the first occurrence of progression (Investigator assessed according to RECIST v1.1) or death due to any cause.

Time frame: After observing approximately 88 PFS events as per BIRC assessment, expected after approximately 33 months from study start

Objective Response Rate (ORR)

ORR: Rate of participants with best overall response (BOR) of partial response (PR) or complete response (CR) as per RECIST v1.1 (both Investigator and centrally assessed by BIRC).

Time frame: After observing approximately 88 PFS events as per BIRC assessment, expected after approximately 33 months from study start

Disease Control Rate (DCR)

DCR: Rate of participants with BOR of PR, CR or stable disease (SD) as per RECIST v1.1 (both Investigator and centrally assessed by BIRC).

Time frame: After observing approximately 88 PFS events as per BIRC assessment, expected after approximately 33 months from study start

Duration of Response (DOR)

DOR: The time from initially meeting the criteria for response (CR or PR) until the time of progression according to RECIST v1.1 or death due to underlying disease only.

Time frame: After observing approximately 88 PFS events as per BIRC assessment, expected after approximately 33 months from study start

Overall Survival (OS)

OS: Time from the randomization date until the date of death due to any cause.

Time frame: Until 60 month from randomization

Time to Deterioration (TDD)

TTD is the time from randomization to the first occurrence of a deterioration compared to the baseline scores or death from any cause for EORTC QLQ-G.I.NET21 and EORTC QLQ-C30 domains not included among key secondary endpoints.

Time frame: At the time of primary PFS analysis after observing approximately 88 PFS events per BIRC assessment

Absolute change from baseline in EORTC QLQ-G.I.NET21 domain

Quality of Life assessed by EORTC QLQ-G.I.NET21 (excluding GI scale) (domains not included as key secondary objectives)

Time frame: After observing approximately 88 PFS events as per BIRC assessment, expected after approximately 33 months from study start

Absolute change from baseline in the EQ-5D-5L index at each time point

Quality of Life assessed by EQ-5D-5L

Time frame: After observing approximately 88 PFS events as per BIRC assessment, expected after approximately 33 months from study start

Absolute change from baseline in EORTC QLQ-C30 domain

Quality of Life assessed by EORTC QLQ-C30 (domains not included as key secondary objectives)

Time frame: After observing approximately 88 PFS events as per BIRC assessment, expected after approximately 33 months from study start.

Dosimetry

Absorbed radiation dose in selected organs, tumor lesions and total body

Time frame: After observing approximately 88 PFS events as per BIRC assessment, expected after approximately 33 months from study start

Pharmacokinetic (PK) parameter: Area Under Curve (AUC) from [177Lu]Lu-DOTA-TATE blood radioactivity data

The AUC from time zero to the last measurable concentration sampling time (tlast) (mass x time x volume-1). The AUC from time zero to infinity (mass x time x volume-1)

Time frame: After observing approximately 88 PFS events as per BIRC assessment, expected after approximately 33 months from study start

PK parameter: Clearance from [177Lu]Lu-DOTA-TATE blood radioactivity data

Clearance is the total body clearance of drug from the plasma or blood (volume x time-1).

Time frame: After observing approximately 88 PFS events as per BIRC assessment, expected after approximately 33 months from study start

PK parameter: Distribution volume (Vz) from [177Lu]Lu-DOTA-TATE blood radioactivity data

The apparent volume of distribution during terminal phase (associated with λz) (volume)

Time frame: After observing approximately 88 PFS events as per BIRC assessment, expected after approximately 33 months from study start

PK parameter: half-life (T1/2) from [177Lu]Lu-DOTA-TATE blood radioactivity data

The elimination half-life associated with the terminal slope (λz) of a semi logarithmic concentration-time curve (time). Use qualifier for other half-lives

Time frame: After observing approximately 88 PFS events as per BIRC assessment, expected after approximately 33 months from study start

Central Contacts

Novartis Pharmaceuticals

CONTACT

1-888-669-6682 novartis.email@novartis.com

Novartis Pharmaceuticals

CONTACT

+41613241111