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Spots Global Cancer Trial Database for Hypofractionated Intensity Modulated and Image Guided Radiotherapy for Localized Prostate Cancer

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Trial Identification

Brief Title: Hypofractionated Intensity Modulated and Image Guided Radiotherapy for Localized Prostate Cancer

Official Title: Hypofractionated Intensity Modulated and Image Guided Radiotherapy for Localized Prostate Cancer: a Prospective Cohort.

Study ID: NCT02651896

Interventions

HypoIGRT

Study Description

Brief Summary: Hypofractionated intensity modulated and image guided radiotherapy (HypoIGRT) with fewer high-fraction-size treatments would be beneficial for prostate cancer because it would deliver a larger biological-equivalent dose to the tumor than would conventional treatment in 1.8-2.0 Gy fractions, while maintaining a similar or lower incidence of late normal tissue reactions. Thus, the investigators aim to assess the hypothesis that HypoIGRT treatment for localized prostate cancer will improve the therapeutic ratio by either: 1. Reducing normal tissue, mainly genitourinary and gastrointestinal, toxicity and / or 2. Improving tumour control, mainly freedom from biochemical failure survival.

Detailed Description: The investigator chose to study a HypoIGRT regimen, in participants with prostate adenocarcinoma, tumor which is considered to present a low α / β, and therefore benefit from this approach. Primary Outcome Measures: 1. Acute and late radiation induced toxicities. Secondary Outcome Measures: 1. Freedom from prostate cancer recurrence - freedom from biochemical failure survival; 2. Cause specific and overall survival 3. Aspects of quality of life and health economics Study Design: Allocation: Prospective allocation Endpoint Classification: Feasibility Study (Toxicity assessment) Intervention Model: Single Assignment Masking: Open Label Primary Purpose: Treatment Eligibility Ages Eligible for Study: 18 Years and older Genders Eligible for Study: Both Accepts Healthy Volunteers: No Study Population: Men with localized histologically confirmed T1B-T4 N0 and M0 prostate cancer.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

Hospital Sírio-Libanes, Brasilia, DF, Brazil

Hospital Sírio-Libanes, São Paulo, SP, Brazil

Contact Details

Name: Luiz Reis, MD, PhD

Affiliation: Hospital Sírio-Libanes - Ensino e Pesquisa

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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