Summary

Eligibility
for people ages 18 years and up (full criteria)
Location
at UCSF
Dates
study started
study ends around
Principal Investigator
by Thomas Hope, MD (ucsf)
Headshot of Thomas Hope
Thomas Hope

Description

Summary

This is a multicenter, randomized, open-label, phase III study comparing standard of care use of somatostatin analogues (SSAs) to standard of care observation in patients with neuroendocrine neoplasms following treatment with Peptide Receptor Radionuclide Therapy (PRRT) (ethanol-stabilized Lu-177 dotatate).

Official Title

Somatostatin Analogues vs. Observation After Peptide Receptor Radionuclide Therapy (PRRT) in Patients With Nonfunctional Neuroendocrine Neoplasms (REMAIN Trial)

Keywords

Neuroendocrine Neoplasm, Gastroenteropancreatic Neuroendocrine Neoplasm, peptide receptor, radionuclide therapy, carcinoid tumor, octreotide, lanreotide, somatostatin analogues, Neuroendocrine Tumors, Somatostatin Analogue(s), Somatostatin Analogue (SSA)

Eligibility

You can join if…

Open to people ages 18 years and up

  • Histologically or cytologically confirmed metastatic, unresectable, well- or moderately-differentiated, nonfunctional gastrointestinal neuroendocrine tumor (GI-NETs). This includes pancreatic neuroendocrine neoplasms. Any grade (grade 1, grade 2, or grade 3) is permitted.
  • Measurable disease per RECIST 1.1.
  • Appropriate for ethanol-stabilized Lu-177 dotatate treatment, as determined by positive screening with SSTR PET/CT and/or currently having received up to 3 fractions of PRRT. (Patients will be randomized prior to the start of PRRT or during PRRT, depending on the timing of enrollment.)
  • Eligible for somatostatin analogue treatment per the treating physician.
  • At least 18 years of age.
  • ECOG performance status ≤ 2 or Karnofsky ≥ 60%
  • Patients with treated brain metastases are eligible if follow-up brain imaging after central nervous system (CNS)-directed therapy shows no evidence of progression, as determined by a repeat imaging study at least 4 weeks following the completion of treatment. Patients with treated brain metastases must also be off steroids for at least 1 month and stable.
  • The effects of ethanol-stabilized Lu-177 dotatate and SSAs on the developing human fetus at the recommended therapeutic dose are unknown. For this reason and because radionucleotides and anti-angiogenic agents are known to be teratogenic, people of childbearing potential and people able to father a child must agree to use adequate contraception prior to study entry, for the duration of study participation, and for 4 months following last administration of PRRT for males and 7 months after last administration of PRRT for females, or 4 months after last day of SSA, whichever is later.
  • Ability to understand and willingness to sign an IRB approved written informed consent document. Legally authorized representatives may sign and give informed consent on behalf of study participants.

You CAN'T join if...

  • Completed prior treatment with PRRT for non-GI-NET diagnosis (i.e. in need of salvage PRRT treatment).
  • Major surgery within 4 weeks from randomization to the trial.
  • Prior or concurrent malignancy whose natural history has the potential to interfere with the safety or efficacy assessment of the investigational regimen. Patients with prior or concurrent malignancy that does NOT meet that definition are eligible for this trial
  • Currently receiving any investigational agents.
  • A history of allergic reactions attributed to compounds of similar chemical or biologic composition to SSAs.
  • Evidence of hypersensitivity to ethanol containing compounds.
  • Uncontrolled intercurrent illness including, but not limited to: ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, or cardiac arrhythmia.
  • Pregnant and/or breastfeeding. Women of childbearing potential must have a negative pregnancy test within 15 days of study entry.

Locations

  • University of California - San Francisco
    San Francisco California 94143 United States
  • Washington University School of Medicine
    St Louis Missouri 63110 United States

Lead Scientist at University of California Health

  • Thomas Hope, MD (ucsf)
    Thomas Hope, MD, is the Vice Chair of Clinical Operations and Strategy in the Department of Radiology. He also serves as the Director of Theranostics. He serves as chair of the Cancer Center’s Molecular Imaging & Radionuclide Therapy Site Committee.

Details

Status
not yet accepting patients
Start Date
Completion Date
(estimated)
Sponsor
Washington University School of Medicine
Links
Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine
ID
NCT07842172
Phase
Phase 3 research study
Study Type
Interventional
Participants
Expecting 240 study participants
Last Updated