Adjuvant radiotherapy (RT) plays an important role in reducing the risks of local recurrence after surgery in uterine cancers. Standard adjuvant pelvic radiation treatment targets the pelvic lymph nodes, the post-operative bed, and the upper vagina and is typically treated with intensity modulated radiation therapy (IMRT) which has been shown to improve patient reported gastrointestinal (GI) and genitourinary (GU) toxicities. Although pelvic radiation has been shown to be effective at decreasing locoregional recurrences, patient quality of life and experience can be significantly impacted as pelvic RT comprises of daily radiation for 25 daily treatments, which can be a substantial burden on patients with this disease. Hypofractionated radiotherapy to a dose of 30 Gy in 5 fractions (6 Gy given every other day) for adjuvant radiation treatment in uterine cancer is hypothesized to result in similar rates of acute gastrointestinal toxicities as conventional fractionated radiation.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
50
Dose prescribed is 45 Gy in 25 fractions (1.8 Gy per fraction) delivered daily over 5 weeks.
Dose prescribed is 30 Gy in 5 fractions (6 Gy per fraction) delivered every other day over 11 days. There will be a minimum of 36 hours and maximum of 96 hours between fractions. The entire course of treatment should be completed within no less than 10 days.
Royal Victoria Hospital
Barrie, Ontario, Canada
NOT_YET_RECRUITINGLondon Regional Cancer Program
London, Ontario, Canada
NOT_YET_RECRUITINGCredit Valley Hospital
Mississauga, Ontario, Canada
NOT_YET_RECRUITINGSunnybrook Health Sciences Centre
Toronto, Ontario, Canada
RECRUITINGPrincess Margaret Cancer Centre
Toronto, Ontario, Canada
NOT_YET_RECRUITINGAcute bowel toxicity
To compare the acute bowel toxicities associated with hypofractionated vs conventional adjuvant pelvic radiation as measured by the The Expanded Prostate Cancer Index Composite (EPIC) questionnaire.
Time frame: Baseline to 2 years following RT completion
Acute bowel toxicities
To compare the acute bowel toxicities associated with hypofractionated treatment and conventional fractionation in adjuvant pelvic radiation for endometrial cancers using the Common Terminology Criteria for Adverse Events (CTCAE v5.0) criteria.
Time frame: Baseline to 2 years following RT completion
Acute urinary toxicities through CTCAE
To compare the acute urinary toxicities associated with hypofractionated treatment and conventional fractionation in adjuvant pelvic radiation for endometrial cancers using the Common Terminology Criteria for Adverse Events (CTCAE v5.0) criteria.
Time frame: Baseline to 2 years following RT completion
Acute urinary toxicities through EPIC
To compare the acute urinary toxicities associated with hypofractionated treatment and conventional fractionation in adjuvant pelvic radiation for uterine cancer as measured by EPIC.
Time frame: Baseline to 2 years following RT completion
Local- regional failure
To compare presence of tumour through physical exam or radiologic imaging between hypofractionated treatment and conventional fractionation.
Time frame: Baseline to 2 years following RT completion
Disease-free survival
To compare disease-free survival of hypofractionated treatment and conventional fractionation
Time frame: Baseline to 2 years following RT completion
Quality of life using EORTC QLQ-30 and endometrial module (EN-24)
To compare the effect of hypofractionated treatment and conventional fractionation on quality of life using the using EORTC (European Organisation for Research and Treatment of Cancer) core questionnaire (QLQ-C30) with EN-24 companion.
Time frame: Baseline to 2 years following RT completion
Correlation of GU toxicity, EORTC, and EPIC
To measure correlations between GU toxicity and EORTC questionnaire versus GU toxicity and EPIC questionnaire.
Time frame: Baseline to 2 years following RT completion
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