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NCT07185672From ClinicalTrials.govRecruiting

PRRT Versus PRRT Plus Chemotherapy in GEP NET (PReCedeNT Trial)

PReCedeNT Trial: Phase III Randomised Controlled Open Label Trial of Lutetium 177 PRRT Plus Chemotherapy Versus PRRT Aalone in FDG Avid Well Differentiated Gastroenteropancreatic Neuroendocrine Tumors

  • Neuroendocrine Neoplasia's (NENs)
  • Neuroendocrine Tumor GEP Grade 1-3
  • Neuroendocrine Gastroenteropancreatic Tumour

At a glance

Phase
Phase 3
Study type
Interventional
Sponsor
Tata Memorial Hospital
Enrolment target
162
Started
7 August 2019
Main results due
7 August 2027
Study sites
2
Registry updated
22 September 2025

Can you take part?

  • Aged 18 years and over.
  • Open to any sex.
  • You need the condition being studied — healthy volunteers are not accepted.

These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.

Read the full eligibility criteria
Inclusion Criteria:

* Male or female, age greater than 18 years
* Histopathological diagnosis of GEP-NET, necessarily satisfying all the the criteria below
* Well differentiated G2 (Ki67 : ≥3-20%) OR G3 (ki67- greater than 20-55%), OR
* Well-differentiated G1 (\<3%) with disease progression in last 6 months
* Positive Ga-68-DOTANOC PET/CT, Krennings score \>/=3
* Positive FDG PET imaging, grade 3 or 4 uptake
* Locally advanced/inoperable disease or metastatic disease
* Karnofsky performance-status score of at least 60 or ECOG performance status \</= 2
* Life expectancy greater than 6 months

Exclusion Criteria:

* Serum creatinine level of more than 1.6 mg/dl or a creatinine clearance of less than 50 ml/min
* Hemoglobin level of less than 8.0 g per deciliter
* Red blood cell count noty less than 300,000/cubic millimeter White cell count of less than 2000 per cubic millimeter
* Platelet count of less than 75,000 per cubic millimetre
* Total bilirubin level of more than 3 times the upper limit of the normal range
* Serum albumin level \< 3.0 g/dl
* Treatment with more than 30 mg of octreotide LAR within 4 weeks before randomisation.
* Peptide receptor radionuclide therapy at any time before randomisation
* Pregnancy and Lactation
* Patients with concurrent malignancies

What this study is about

In the sponsor’s own words, from the registry.

Neuroendocrine tumours (NETs), better defined as neoplasms (NENs), are a heterogeneous group of neoplasms that range from well-differentiated tumours to more aggressive carcinomas. Peptide receptor radionuclide therapy (PRRT) with Lutetium-177 DOTATATE is the established standard of care for patients with well-differentiated metastatic or locally advanced GEP-NETs. It has demonstrated a significant improvement in outcomes compared to Octreotide LAR, both as a first-line and second-line treatment approach, following the results of NETTER-1 and NETTER-2 trials, respectively. ENETS guidelines recommend the use of Ga-68 labeled DOTANOC/TOC/TATAE imaging only for WHO Grade 1 NET whereas FDG PET is the preferred modality for WHO Grade 3 NEN and NEC. For Grade 2 tumors (Mib index ranging from 3-20%), there are no strong recommendations for the addition of FDG PETCT in existing diagnostic algorithm. FDG PET positivity has been shown to be an independent predictor of shorter progression-free and overall survival in NET patients undergoing peptide receptor radionuclide therapy (PRRT). (8) Consequently, it is imperative to address FDG-avid tumors by integrating PRRT and chemotherapy. There are no strong recommendations for the grade wise management of GEP-NETs particularly grade 2 \& 3. Although recently published NETTER 2 trial substantiated the role of PRRT as a first line treatment for advanced grade GEP-NETs, still there is lack of evidence supporting the addition of chemotherapy in management of GEP-NETs. Given the absence of a prospective study to establish this treatment regimen, we designed a Phase 3 Randomized Controlled Trial to evaluate the combination of PRRT and CAPE-TEM-based chemotherapy in patients with FDG-positive metastatic well-differentiated NETs.

Study sites(2)

  • Tata Memorial Hospital, Mumbai, India

    Mumbai, Maharashtra, India

    Recruiting

  • Advanced Centre for Treatment, Research and Education in Cancer (ACTREC)

    Navi Mumbai, Maharashtra, India

    Recruiting

Showing 2 of 2 sites. 2 of the 2 sites on this study are recruiting right now — a site can stop enrolling while the study as a whole is still open.

Source: ClinicalTrials.gov record NCT07185672. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.

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PRRT Versus PRRT Plus Chemotherapy in GEP NET (PReCedeNT Trial) | Trialion