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NCT05610826WithdrawnPhase 1/2

Preoperative PRRT Versus Surgical Cytoreduction in Metastatic Pancreatic Neuroendocrine Tumors to the Liver

Preoperative PRRT Versus Surgical Cytoreduction Alone in Metastatic Pancreatic Neuroendocrine Tumors to the Liver: A Phase II Multi-institutional Trial

Source: ClinicalTrials.gov · Last updated 26 Oct 2024

Reason given: 0 enrollment

Brief summary (registry, in English)

Doctors and researchers leading this study hope to learn more about peptide receptor radionuclide therapy (PRRT) in combination with cytoreduction (surgically removing tumors). They hope to learn if combining PRRT in combination with cytoreduction would be more effective than cytoreduction alone. PRRT itself is approved by the U.S. Food and Drug Administration (FDA) for people with PanNETs however the combination with cytoreduction is considered experimental. Your participation in this research will last about 2 years. The purpose of this research is to gather information on the safety and effectiveness of PRRT.

Status (registry)
Withdrawn
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
0 (actual)
First submitted
2 Nov 2022
Start date
7 Mar 2023
Primary completion date
11 Sept 2024
Lead sponsor
University of Chicago
NCT number
NCT05610826

Who cannot take part

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

Prior treatment

  • Previous liver-directed therapy with Yttrium-90 (TACE/TAE allowed if performed more than 12 months prior to enrollment)
  • Systemic therapy with Capecitabine and/or Temozolamide within 12 months of enrollment.
  • For female patients of childbearing potential (defined as < 2 years after last menstruation and not surgically sterile) and male patients, who are not surgically sterile or with female partners of childbearing potential: absence of effective, non-hormonal means of contraception (intrauterine contraceptive device, barrier method of contraception in conjunction with spermicidal gel). - Prior external beam radiation therapy to more than 25% of the bone marrow.

Other illness

  • Uncontrolled congestive heart failure (NYHA II, III, IV).
  • Other known co-existing malignancies except non-melanoma skin cancer and carcinoma in situ of the uterine cervix, unless definitively treated and with no evidence of recurrence.

Lab values

  • Signs of early liver failure (T-Bilirubin >3, INR > 1.5, Albumin <3.0 g/dL unless prothrombin time is within the normal range) or cirrhosis or ascites
  • calculated by the Cockroft Gault method, eventually confirmed by measured creatinine clearance
  • (or measured glomerular filtration rate (GFR) using plasma clearance methods, not gamma
  • camera-based) <50 mL/min (the measured creatinine clearance / GFR is required only as - confirmatory exam).
  • 2. Hb concentration <5.0 mmol/L (<8.0 g/dL); WBC <2x109/L (2000/mm3); platelets <75x109/L - (75x103/mm3).
  • Uncontrolled diabetes mellitus as defined by a fasting blood glucose >2 ULN.

Other

  • Patient with G3 or poorly differentiated NET (grade 3, Ki-67 >20%)
  • No tumor uptake on 68Ga DOTATATE PET CT
  • Liver tumor burden > 50% (as defined by CT or MRI)
  • Known brain metastases, unless these metastases have been treated and stabilized.
  • Pregnancy or lactation.
  • Current spontaneous urinary incontinence making impossible the safe administration of the radioactive IMP.
  • Patients who have not provided a signed informed consent form to accept this treatment.
  • Poor renal function
  • Quality Unit language added
  • editorial changes

Who the study is looking for

  • Metastatic Pancreatic neuroendocrine tumors (PanNET) to the liver
  • Well- or moderately differentiated (grade 1 or grade 2, Ki-
  • Ability to aim for equal or greater than 90% hepatic cytoreduction surgically
  • Proof of SSTR2 expression by uptake of tumor on 68Ga DOTATATE PET CT (Krenning Score on all or a majority of lesions
  • Age older than 18 years
  • No Somatostatin Analogues (SSA) or other systemic therapy for 4 weeks prior to starting PRRT, if randomized to arm 2.

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

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
The University of Chicago Comprehensive Cancer CenterChicagoUnited StatesUnknown status

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