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NCT07890012Not yet recruiting

Real World Positioning of Tyrosine Kinase Inhibitors (TKIs) Within Systemic Treatment Strategies for Advanced Neuroendocrine Tumors (NETs)

Source: ClinicalTrials.gov · Last updated 22 Oct 2026

Brief summary (registry, in English)

Well differentiated neuroendocrine tumors (NETs) are rare and heterogeneous malignancies that frequently evolve toward advanced or metastatic disease, requiring long-term systemic treatment strategies delivered over multiple lines. Their management is complex and influenced by tumor-related factors-including primary site and grade-as well as disease burden, functional status, patient comorbidities, and access to available therapeutic options. As a result, real-world treatment pathways in advanced NETs are highly diverse. In recent years, the systemic treatment landscape of advanced NETs has expanded beyond somatostatin analogues (SSA), peptide receptor radionuclide therapy (PRRT), and chemotherapy to include targeted therapies. Among these, multitarget tyrosine kinase inhibitors (TKIs) targeting tumor angiogenesis have progressively been incorporated into clinical practice. Their use varies according to tumor subtype, disease dynamics, prior treatments, and patient-related considerations, reflecting the absence of standardized sequencing algorithms. In routine clinical practice, the choice and sequencing of TKIs are driven by individualized clinical decision-making rather than predefined treatment pathways. Their positioning within systemic treatment strategies is influenced by anticipated benefit, tolerability, prior toxicities, and practical constraints such as regulatory indications, access, and reimbursement conditions, which differ by tumor origin. Consequently, the real-world positioning of TKIs within treatment sequences remains insufficiently characterized at a national level. "SEQUENCE-NET" is an ambispective observational study designed to prospectively document how TKIs are integrated into systemic treatment strategies for advanced pancreatic and extra-pancreatic NETs in routine clinical practice within the ENDOCAN-RENATEN network.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
100 (estimated)
First submitted
16 Oct 2026
Start date
1 Jan 2027
Primary completion date
1 Jul 2028
Lead sponsor
Hospices Civils de Lyon
NCT number
NCT07890012

What you commit to

  • Study type: Observational
  • Planned participants: 100
  • From 1 Jan 2027 to the primary completion date, 1 Jul 2028
  • 18 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Participation in an ongoing phase I, II, or III interventional clinical trial evaluating an investigational systemic therapy at the time of inclusion.
  • Missing minimal required data preventing reconstruction of prior systemic treatment sequences or assessment of prospective endpoints.
    • For the ancillary study :
    • \- Patient not wanting to participate (filling in the questionnaires)

Other

  • For main study :
  • Poorly differentiated neuroendocrine carcinomas (NEC), including MiNEN with a NEC component.

Who the study is looking for

  • For main study :
  • Adult patients (≥ 18 years of age).
  • Histologically confirmed advanced (metastatic or unresectable) well-differentiated NET of grade G1, G2, or G3 according to the WHO classification.
  • Initiation of a TKI in routine clinical practice, serving as the index treatment line for prospective inclusion.
  • Patient informed about the study with documented non-opposition, in accordance with applicable regulations.
    • For the ancillary study :
    • \- Advanced/metastatic NETs (usually, ileal or lung NET, but other rare location/unknown are allowed) with clinical carcinoid syndrome and/or elevation of urinary 5HIAA\> 2 upper limit of normal (ULN) Initiation of TKI in routine clinical practice, serving as the index treatment line for prospective inclusion.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (18)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CHU Angers
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AngersFranceUnknown status
CHU de CAEN
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CaenFranceUnknown status
Hôpital Beaujon - APHP
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ClichyFranceUnknown status
Chu Dijon Bourgogne
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DijonFranceUnknown status
Chu Grenoble Alpes
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La TroncheFranceUnknown status
CHRU de Lille - Hopital Claude Huriez
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LilleFranceUnknown status
Hopital Edouard Herriot
Coordinator of this site? Confirm its status
LyonFranceUnknown status
CHU Nantes
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NantesFranceUnknown status
Hôpital Saint Antoine APHP
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ParisFranceUnknown status
Hôpital Cochin APHP
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ParisFranceUnknown status
Hôpital Européen Georges Pompidou
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ParisFranceUnknown status
Institut Curie
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ParisFranceUnknown status
CHU Bordeaux - Hopital Haut-Leveque
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PessacFranceUnknown status
CHU Poitiers
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PoitiersFranceUnknown status
CHU Reims Hopital Robert Debre
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ReimsFranceUnknown status
CHRU Strasbourg - Hôpital de Hautepierre
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StrasbourgFranceUnknown status
CHU Tours - Hôpital Trousseau
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ToursFranceUnknown status
Institut Gustave Roussy
Coordinator of this site? Confirm its status
VillejuifFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.