Hypofractionated External Beam Radiotherapy With Adaptive Planning for Endometrial and Cervical Cancers (HERA Trial)
Summary
After surgery to remove the main endometrial and/or cervical tumor, most women receive radiation therapy. This study uses hypo-fractionated radiation therapy, which is a type of radiation therapy in which the total prescribed dose of radiation is delivered in fewer but larger doses than conventional or standard radiotherapy. This research study aims to determine if hypo-fractionated radiation therapy given after surgery can improve treatment tolerability (i.e., fewer treatments) with comparable side effects. Participants will be in the study for about 5 years: Radiation therapy: * 5 daily treatment sessions of MRI or CT-Guided Stereotactic Body Radiation Therapy (SBRT). * Each treatment session will occur on a weekday (typically consecutive weekdays) and will last approximately an hour. Treatment Follow-Up: * Check-up Appointment and answer questions at 3 months post RT * Check-up Appointments with physical exam every 6 months (+/- 4 weeks) for up to 5 years.
Detailed description
The investigators hypothesize that adaptive planning with either computed tomography (CT) or magnetic resonance imaging (MRI) guidance may offer improved SBRT plans for postoperative gynecological cancer patients due to issues with anatomic variation between and during fractions of radiation therapy. Treatment on an MRI-guided linear accelerator with adaptive planning capabilities has been shown to significantly improve acute toxicity in the setting of prostate SBRT compared to conventional linear accelerators.10 The investigators, therefore, propose using adaptive planning with CT- or MRI-guidance to deliver 30 Gy in 5 fraction adjuvant SBRT to the pelvis for endometrial and cervical cancer patients. Stereotactic Body Radiation Therapy (SBRT) with adaptive planning will be delivered following surgical resection of the primary tumor. Patients will receive 6.0 Gy x 5 fractions delivered once every other day. Patients will not be treated on weekends or holidays as is standard practice for radiation treatments. Patients will be seen by the radiation oncologist within the first 3 months after completion of radiation therapy. For patients who live a distance far enough away from the University of California at Los Angeles (UCLA) where travel would be challenging for the patient, a phone or telemedicine follow-up will be considered acceptable. After this, follow-up will be performed every 6 months (+/- 4 weeks) for 5 years following completion of radiotherapy. Patients will be followed clinically and/or radiographically per physician discretion. SCHEMA Diagnosis of endometrial or cervical cancer Surgical resection of primary tumor Multidisciplinary discussion and recommendation for adjuvant radiotherapy to the pelvis Patient enrollment in HERA clinical trial Simulation scans to plan post-operative radiotherapy Five fractions of radiation therapy using adaptive planning and CT or MRI guidance (6 Gy per fraction) delivered once every other day excluding weekends and holidays Follow-up within 3 months of completion of radiotherapy Follow-up every 6 months (+/- 4 weeks) until 5 years of completion of radiotherapy
Arms & interventions
- RadiationExternal beam Radiotherapy
Five fractions of radiation therapy using adaptive planning and CT or MRI guidance (6 Gy per fraction) delivered once every other day excluding weekends and holidays
Outcome measures
Primary
Evaluate acute radiation toxicity
Evaluate acute radiation toxicity according to Common Terminology Criteria for Adverse Events, Version 5.0 (CTCAE v5.0). Acute toxicity is defined as treatment-related adverse events occurring within 12 weeks of completion of radiotherapy.
Time frame: treatment to 12 weeks after completion of radiotherapy
Secondary
Evaluate patient-reported quality-of-life European Organization for Research and Treatment of Cancer Quality of Life (EORTC QLQ-C30)
Time frame: treatment to 24 weeks after completion of radiotherapy
Evaluate patient-reported quality-of-life European Organization for Research and Treatment of Cancer Quality of Life (EORTC QLQ-EN24)
Time frame: treatment to 24 weeks after completion of radiotherapy
Evaluate late toxicity
Time frame: 12 weeks after completion of radiotherapy until 5 years after completion of radiotherapy
Evaluate local control
Time frame: treatment to 5 years after completion of radiotherapy
Evaluate regional control
Time frame: treatment to 5 years after completion of radiotherapy
Evaluate distant metastasis
Time frame: treatment to 5 years after completion of radiotherapy
Evaluate progression-free survival
Time frame: treatment to 5 years after completion of radiotherapy
Eligibility criteria
Study locations (1)
University of California at Los Angeles
Los Angeles, California, 90095