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Treatment for Neuroendocrine Carcinoma (NET-PRO Trial)

N/A
Waitlist Available
Led By Michael O'Rorke, PhD
Research Sponsored by University of Iowa
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 1-, 3-, and 5-year
Awards & highlights
No Placebo-Only Group

Summary

With so many therapeutic options available (i.e.: biologic therapy, liver directed therapy, radiotherapy and chemotherapy), the purpose of this project is to partner with patients on comparative effectiveness research (CER) to achieve the goal of alleviating undue toxicity, and optimizing effectiveness and sequencing of therapy for neuroendocrine tumors (NET) patients. We will conduct a study of all newly occurring GEP-NET and lung NET cases aged 18 years and older diagnosed between 01/01/2018 through 12/31/2023 across 14 sites participating in the National Patient-Centered Clinical Research Network (PCORnet), enrolling an average of 215 patients per site over the 3 year study period (\~3,000 patients total), allowing up to 60 months of follow-up for medical record outcomes. Participants will complete four online or paper surveys over 18 months; these surveys will focus on patient-reported outcomes, including questions on quality of life, treatment decisions, and experiences with cancer care. Survey data will be linked to participant medical record data to achieve study aims.

Eligible Conditions
  • Neuroendocrine Carcinoma
  • Neuroendocrine Tumors

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~1-, 3-, and 5-year
This trial's timeline: 3 weeks for screening, Varies for treatment, and 1-, 3-, and 5-year for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
European Organisation for Research and Treatment of Cancer - Quality of Life Questionnaire (EORTC QLQ-C30)
European Organisation for Research and Treatment of Cancer - Quality of Life Questionnaire - Neuroendocrine Carcinoid Module (EORTC QLQ-GI.NET21)
Renal function
+1 more
Secondary study objectives
Adverse toxicities
Experiences with cancer care (from CANCORS)
Health related Quality of Life (HRQoL) by PRRT regimen
+7 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Find a Location

Who is running the clinical trial?

University of Pittsburgh Medical CenterOTHER
70 Previous Clinical Trials
73,233 Total Patients Enrolled
Neuroendocrine Tumor Research FoundationUNKNOWN
University of Texas Southwestern Medical CenterOTHER
1,077 Previous Clinical Trials
1,053,051 Total Patients Enrolled
~1191 spots leftby Jun 2026