Abstract

Purpose: Late gastrointestinal (GI) toxicity after radiotherapy for prostate cancer may have significant impact on the cancer survivor's quality of life. To date, little is known about local dose-effects after modern radiotherapy including hypofractionation. In the current study we related the local spatial distribution of radiation dose in the rectum to late patient-reported gastrointestinal (GI) toxicities for conventionally fractionated (CF) and hypofractionated (HF) modern radiotherapy in the randomized HYPRO trial.Material and Methods: Patients treated to 78 Gy in 2 Gy fractions (n = 298) or 64.6 Gy in 3.4 Gy fractions (n = 295) with available late toxicity questionnaires (n ≥ 2 within 1–5 years post-treatment) and available 3D planning data were eligible for this study. The majority received intensity modulated radiotherapy (IMRT). We calculated two types of dose surface maps: (1) the total delineated rectum with its central axis scaled to unity, and (2) the delineated rectum with a length of 7 cm along its central axis aligned on the prostate's half-height point (prostate-half). For each patient-reported GI symptom, dose difference maps were constructed by subtracting average co-registered EQD2 (equivalent dose in 2 Gy) dose maps of patients with and without the symptom of interest, separately for HF and CF. P-values were derived from permutation tests. We evaluated patient-reported moderate to severe GI symptoms.Results: Observed incidences of rectal bleeding and increased stool frequency were significantly higher in the HF group. For rectal bleeding (p = 0.016), mucus discharge (p = 0.015), and fecal incontinence (p = 0.001), significant local dose-effects were observed in HF patients but not in CF patients. For rectal pain, similar local dose-effects (p < 0.05) were observed in both groups. No significant local dose-effects were observed for increased stool frequency. Total rectum mapping vs. prostate-half mapping showed similar results.Conclusion: We demonstrated significant local dose-effect relationships for patient-reported late GI toxicity in patients treated with modern RT. HF patients were at higher risk for increased stool frequency and rectal bleeding, and showed the most pronounced local dose-effects in intermediate-high dose regions. These findings suggest that improvement of current treatment optimization protocols could lead to clinical benefit, in particular for HF treatment.

Highlights

  • Irradiation of tumors in the pelvic area through external beam radiotherapy comes inevitably with dose delivery to nearby organs at risk, such as the rectum

  • In the current study we explored local rectal dose distributions and their relation to GI toxicity endpoints, for both hypofractionated (HF) and conventionally fractionated (CF) treatment, using toxicity data and planning data from the HYPRO trial

  • The HYPRO protocol prescribed that the rectal volume receiving 83% of the prescribed dose should be below 50% for the total rectal volume or below 60% for the rectal wall

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Summary

Introduction

Irradiation of tumors in the pelvic area through external beam radiotherapy comes inevitably with dose delivery to nearby organs at risk, such as the rectum. The QUANTEC project (quantitative analysis of normal tissue effects in the clinic) previously summarized the available clinical data and models on acute and late radiation-induced toxicities with the goal to improve patient care by providing useful tools [2]. These models were mainly derived from traditionally fractionated 3D conformal radiotherapy (3DCRT). Shortcomings and open issues of the available models have broadly been recognized, including the uncertainty of fractionation effects, a lack of reliable models for modern radiotherapy with IMRT dose distributions and image-guidance, and a lack of knowledge concerning spatial effects [3]. This causes a number of deficits in current strategies of treatment planning optimization in the current era of IMRT, image-guidance, and hypofractionated treatment

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