
Short-Course Radiation Therapy Effective for Endometrial Cancer Patients
Key Takeaways
- The SAVE trial assessed short-course, higher dose vaginal brachytherapy for endometrial cancer, showing similar effectiveness to standard treatment regimens.
- The study aimed to reduce treatment frequency while maintaining quality of life and disease control, benefiting patients in rural areas.
Short-course, higher dose vaginal brachytherapy for endometrial cancer had similar effectiveness to more frequent, lower dose sessions.
In a randomized clinical trial, researchers from
“There isn’t high quality-data on optimal dose and schedule for brachytherapy treatments. Because of this, practice patterns really vary,” says Suneja. “The SAVE trial sought to try to lower the number of treatments that patients were receiving but maintain short-term quality of life and disease control.”
The SAVE trial compared two groups who received different treatment doses over a varying number of sessions. The control group received the standard treatment—between three to five appointments with lower doses. The experimental group received higher doses of radiation in just two sessions.
“The study outcomes will help improve cancer care for Huntsman Cancer Institute patients across the five states of the Mountain West,” says Gita Suneja, MD, MS.
The researchers found similarly effective short-term outcomes and few acute toxicities for the patients in the experimental group.
Suneja says the study outcomes will help improve cancer care for Huntsman Cancer Institute patients across the
“It’s hard for patients to get to us, especially those in a rural and frontier environment like many of our patients at Huntsman Cancer Institute,” says Suneja. “We recognize this is an enormous burden for people to come here for treatment, on top of dealing with a difficult diagnosis. We are motivated to better serve our rural population, and the results of this study will give us a way to do that.”
“It is a big win when we can preserve good outcomes and make cancer care easier," David Gaffney, MD, PhD, FACR, FABS, FASTRO, says.
“We are very grateful for the support and the enthusiasm from our clinical colleagues at MD Anderson, Loyola, Intermountain Healthcare, and Stanford, the institutions that also participated in the SAVE trial,” says Gaffney. “We are particularly grateful for the patients that agreed to participate in the study. It is a big win when we can preserve good outcomes and make cancer care easier.”
The
The National Clinical Trial number for this trial is 03422198.



































