Actively Recruiting

Phase 1
Phase 2
Age: 18Years +
All Genders
NCT06982300

SSTR2 Imaging With [68Ga]Ga-DOTA-TOC PET/CT in NPC

Led by University Medical Center Groningen · Updated on 2025-10-03

10

Participants Needed

1

Research Sites

61 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is an investigator-initiated, single-center clinical trial designed to evaluate the feasibility of \[68Ga\]Ga-DOTA-TOC positron emission tomography (PET) scan in patients with Epstein-Barr virus (EBV) related nasopharyngeal carcinome (NPC) prior to and three weeks after the start of induction chemotherapy or concurrent chemoradiotherapy (CRT). Archival tumor tissue from the diagnostic biopsy will be used to perform somatostatin receptor 2 (SSTR2) immunohistochemistry (IHC). Blood samples will be drawn at baseline, after three weeks, after completion of induction chemotherapy if applicable, and after CRT.

CONDITIONS

Official Title

SSTR2 Imaging With [68Ga]Ga-DOTA-TOC PET/CT in NPC

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Stage IB-IVA nasopharyngeal carcinoma (NPC) confirmed EBV positive by Epstein-Barr virus-encoded RNA (EBER)
  • Planned treatment with induction chemotherapy or concurrent chemoradiotherapy without induction chemotherapy
  • Age 18 years or older
  • Signed informed consent
  • Willingness and ability to follow all study procedures
  • Negative serum pregnancy test for women able to become pregnant
  • Archival tumor tissue available or willing to have a tumor biopsy
Not Eligible

You will not qualify if you...

  • Previous chemotherapy or radiotherapy treatment for nasopharyngeal carcinoma
  • Treatment with investigational agents or participation in another therapeutic clinical trial within 28 days before [68Ga]Ga-DOTA-TOC injection
  • Other diseases or conditions that could affect study results or increase risk of complications
  • Altered mental status or psychiatric conditions preventing understanding or consent
  • Unable to lie on back for 25 minutes
  • Pregnant or breastfeeding

AI-Screening

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Trial Site Locations

Total: 1 location

1

University Medical Center Groningen

Groningen, Netherlands, 9713 GZ

Actively Recruiting

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Research Team

S

Sjoukje F. Oosting, MD, PhD

CONTACT

F

Fleur van Doorn, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

DIAGNOSTIC

Number of Arms

1

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