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Adaptive Radiation for Locally Advanced Unresectable Pancreatic Cancer

Not Applicable
Not yet recruiting
Conditions
Locally Advanced Pancreatic Ductal Adenocarcinoma (PDA)
Registration Number
NCT06984562
Lead Sponsor
Fox Chase Cancer Center
Brief Summary

The goal of this clinical trial is to learn if Adaptive Radiation Therapy (ART) is safe and effective in treating patients with locally advanced pancreatic cancer.

The main questions the study aims to answer are:

* Can ART improve how well radiation therapy targets the most aggressive cancer cells, while protecting the healthy tissue around the tumor?

* Can ART help reduce the side effects that participants may experience during treatment?

Participants will:

* Undergo CT scans to plan the exact location of the radiation treatment. During this process, 1-3 small markers may be placed in or near the tumor to help with the planning.

* Have a tumor biopsy, which involves taking a small sample of tissue from the cancer.

* Receive 5 radiation treatments every other day over a 2-week period.

* Provide blood samples before, during, and after your radiation treatment.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
16
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
The rate of acute and late grade ≥3 gastrointestinal toxicity occurring within 3 months of treatment possibly, probably or definitely related to radiation.From start of radiation to 3 months after the end of radiation treatment
Secondary Outcome Measures
NameTimeMethod
The proportion of patients experiencing local control defined as stable disease or any response at the radiation target site(s).From the start of radiation to 5 years after end of radiation treatment
Overall Survival Rate - defined as the time from the start of radiation to death or last contact. Individuals who are alive at last follow-up will be considered censored at the time of last contact.From the start of radiation to death or last contact (up to 5 years after end of treatment).
The rate of acute and late adverse events at time points prescribed in the study calendar using CTCAE version 5.0.From start of radiation to end of long-term follow up (up to 5 years)

Trial Locations

Locations (1)

Fox Chase Cancer Center

🇺🇸

Philadelphia, Pennsylvania, United States

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