Adaptive Daily MR-Guided Adjuvant Pelvic Therapy-Endometrial Cancer

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-90
SponsorRutgers, The State University of New Jersey

About this trial

To evaluate the safety, tolerability, and preliminary efficacy of moderately hypofractionated (15-fraction) MR-guided adaptive pelvic IMRT in patients with endometrial cancer.

Eligibility criteria

Qualifiers

Histologically confirmed endometrial carcinoma (endometrioid, serous, clear cell, carcinosarcoma, or dedifferentiated histology).

Age

High-grade histology (grade 2-3)

Depth of myometrial invasion

Disqualifiers

Prior pelvic radiotherapy.

Contraindication to pelvic radiotherapy (e.g., active connective tissue disorder or inflammatory bowel disease).

Presence of a hip prosthesis that would compromise treatment planning or delivery.

Trial design

Treatments tested in this trial

  • MR-guided adaptive pelvic intensity-modulated radiation therapy (IMRT)

Treatment groups

30 Participants
are divided into 1 treatment group