Radiation Therapy for the Treatment of Metastatic Gastrointestinal Cancers
Launched by UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · Jan 6, 2020
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is exploring how effective radiation therapy is for treating advanced gastrointestinal cancers that have spread to other parts of the body. The goal is to see if combining radiation therapy with immunotherapy (a treatment that helps the immune system fight cancer) can slow down or stop the growth of these cancers. Researchers believe that treating one tumor with radiation might even help the immune system attack other tumors that are not directly treated.
To participate in this trial, patients should have a confirmed diagnosis of metastatic gastrointestinal cancer, such as esophageal, gastric, or colorectal cancer, and be currently receiving immunotherapy that is not working well. They need to have at least two tumors that are getting worse and meet specific criteria for safe radiation treatment. Participants will receive radiation therapy aimed at relieving symptoms and potentially improving their overall response to cancer treatment. It’s important for interested patients to discuss their eligibility and any concerns with their healthcare team.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Patients must have a histologically, cytologically, or radiographically confirmed metastatic gastrointestinal (GI) malignancy (esophageal, gastroesophageal, gastric, small intestine, hepatocellular, pancreaticobiliary, colorectal, or anal cancer).
- • 2. Patients must be receiving immunotherapy (checkpoint inhibitor or CTLA4 inhibitor) with overall response of progressive disease by RECIST criteria.
- • 3. Patients must have at least two metastases which are individually progressing as per RECIST criteria, one of which can be safely unirradiated as adjudicated by the treating radiation oncologist (e.g. lesions for which small increases in dimensions are unlikely to precipitate significant symptoms).
- 4. Patients must have 1-5 sites of disease meeting standard-of-care indications for palliative radiation therapy as adjudicated by the treating radiation oncologist. For example:
- • Symptomatic disease causing pain, bleeding, dyspnea, dysphagia, or nausea
- • At-risk for neurologic, respiratory, cardiovascular, gastrointestinal, musculoskeletal, or hepatobiliary compromise
- • 5. Evaluation by a radiation oncologist within 28 days of study registration.
- • 6. Must have adequate organ function to administer radiation therapy and immunotherapy as per standard of care.
- • 7. Age \>= 18 years.
- • 8. Life expectancy exceeding 6 months.
- • 9. Eastern Cooperative Oncology Group (ECOG) 0-2 or Karnofsky performance status \>= 50.
- • 10. Radiation therapy is known to be teratogenic and therefore women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control) prior to study entry and for the duration of radiation therapy. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately. Men treated or enrolled on this protocol must also agree to use adequate contraception prior to the study and for 3 months after completion of radiation therapy. Contraception requirements during the follow-up period of 6 months will be according to standard of care for immunotherapy administration.
- • a. If a woman is of child-bearing potential, a negative pregnancy test within 28 days prior to study enrollment is required.
- • 11. Ability to understand a written informed consent document, and the willingness to sign it.
- Exclusion Criteria:
- • 1. Enrollment on immunotherapy clinical trial for which radiation therapy is not permitted.
- • 2. Administration of radiation therapy within 4 weeks prior to study enrollment.
- • 3. Treatment with systemic corticosteroids or other immunosuppressive medications which would significantly diminish the effect of immunotherapy as judged by the treating physician.
- • 4. Radiation therapy is contraindicated as adjudicated by the radiation oncologist.
About University Of California, San Francisco
The University of California, San Francisco (UCSF) is a leading academic institution renowned for its commitment to advancing healthcare through innovative research and clinical trials. With a focus on translating scientific discoveries into effective therapies, UCSF collaborates with a diverse array of stakeholders, including healthcare professionals, industry partners, and patient communities. The university's research programs emphasize interdisciplinary approaches and leverage cutting-edge technology to address complex medical challenges. As a sponsor of clinical trials, UCSF is dedicated to maintaining the highest standards of ethical conduct and scientific rigor, ensuring the safety and well-being of participants while contributing to the broader medical knowledge base.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
San Francisco, California, United States
Patients applied
Trial Officials
Mary Feng, MD
Principal Investigator
University of California, San Francisco
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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