Actively Recruiting
MicroEnvironment Tumor Effects of Radiotherapy Comprehensive Radiobiology Assessment TRial (METEOR-CRATR) for Locally Advanced Cervical and Pancreatic Cancer
Led by Washington University School of Medicine · Updated on 2025-11-12
60
Participants Needed
1
Research Sites
468 weeks
Total Duration
On this page
Sponsors
W
Washington University School of Medicine
Lead Sponsor
N
National Cancer Institute (NCI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are conducting a prospective longitudinal study to understand the effects of chemoradiotherapy on the tumor environment in patients with locally advanced cervical and pancreatic cancers. The study aims to collect detailed treatment-related data, including imaging and clinical results, along with biospecimens such as biopsies and blood samples taken before, during, and after treatment. The study involves collecting tumor biopsies and blood samples at various time points depending on the cancer type. For cervical cancer, biopsies are collected before radiation, one week and three weeks after starting radiation, and at recurrence. For pancreatic cancer, biopsies are taken before stereotactic body radiotherapy (SBRT), 12 weeks after radiotherapy, and at recurrence. Blood samples and advanced MRI imaging are also scheduled at specific intervals throughout treatment and follow-up. Participants will undergo imaging assessments using diffusion basis spectrum imaging MRI at initial staging and during follow-up visits. The study measures changes in the tumor microenvironment over an estimated five-year follow-up period. Throughout the study, researchers collect clinical data, monitor treatment effects, and evaluate tumor biology to better understand responses to radiotherapy.
CONDITIONS
Official Title
MicroEnvironment Tumor Effects of Radiotherapy - Comprehensive Radiobiology Assessment TRial
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Confirmed intent to receive radiotherapy for cervical or pancreatic cancer
- ECOG performance status of 2 or less
- Age 18 years or older
- Able to understand and willing to sign informed consent
You will not qualify if you...
- Any medical or anatomical issue that may prevent safe collection of biospecimens as judged by the treating physician
AI-Screening
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Trial Site Locations
Total: 1 location
1
Washington University School of Medicine
St Louis, Missouri, United States, 63110
Actively Recruiting
Research Team
C
Cliff Robinson, M.D.
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
DIAGNOSTIC
Number of Arms
2
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