Abstract

BackgroundIncreasing clinical data supports a low α/β ratio for prostate adenocarcinoma, potentially lower than that of surrounding normal tissues. A hypofractionated, weekly radiation therapy (RT) schedule should result in improved tumour control, reduced acute toxicity, and similar or decreased late effects. We report the toxicity profile of such treatment.Materials and MethodsWe conducted a multi-institution phase I/II trial of three-dimensional conformal radiation therapy (3D-CRT) for favourable-risk prostate cancer (T1a-T2a, Gleason ≤ 6 and PSA < 10 ng/ml). RT consisted of 45 Gy in nine 5 Gy fractions, once weekly. Primary end-points were feasibility and late gastrointestinal (GI) toxicity (RTOG scale), while secondary end-points included acute GI toxicity, acute and late genitourinary (GU) toxicity, biochemical control, and survival.ResultsBetween 2006 and 2008, 80 patients were treated. No treatment interruptions occurred. The median follow-up is 33 months (range: 20-51). Maximal grade 1, 2, and 3 acute (< 3 months) GU toxicity was 29%, 31% and 5% respectively (no grade 4). Acute GI grade 1 toxicity was reported in 30% while grade 2 occurred in 14% (no grade 3 or 4). Crude late grade ≥ 3 toxicity rates at 31 months were 2% for both GU and GI toxicity. Cumulative late grade ≥ 3 GI toxicity at 3 years was 11%. Two patients had PSA failure according to the Phoenix definition. The three-year actuarial biochemical control rate is 97%.ConclusionsWeekly RT with 45 Gy in 9 fractions is feasible and results in comparable toxicity. Long term tumour control and survival remain to be assessed.

Highlights

  • Increasing clinical data supports a low a/b ratio for prostate adenocarcinoma, potentially lower than that of surrounding normal tissues

  • Acute GI grade 1 toxicity was reported in 30% while grade 2 occurred in 14%

  • Patient Characteristics and Treatment Delivery Between March 2006 and August 2008, 81 patients were accrued in two institutions (Centre hospitalier de l’Université de Montréal and Centre hospitalier universitaire de Québec)

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Summary

Introduction

Increasing clinical data supports a low a/b ratio for prostate adenocarcinoma, potentially lower than that of surrounding normal tissues. A hypofractionated, weekly radiation therapy (RT) schedule should result in improved tumour control, reduced acute toxicity, and similar or decreased late effects. There has been increasing interest in hypofractionated radiation therapy (RT) for prostate cancer. Using the linear-quadratic (LQ) model for the effect of RT on tumour, emerging data supports a low alpha/beta (a/b) ratio for prostatic adenocarcinoma cells. In addition to the possible radiobiological benefits, hypofractionated RT with fewer fractions allows for increased patient convenience and minimal disruption to their lives. The BED for late effects on normal tissue is 72 Gy in 2 Gy fractions assuming an a/b ratio of 3

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