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Purpose
Prostate cancer patients exhibit variability in nor
mal tissue reactions and bioche
mical failure. With the use of i
mage-guided radiotherapy (IGRT), there is a greater likelihood that the differences in nor
mal tissue and tu
mor response are due to biological rather than physical factors. We tested the hypothesis that prospectively scored acute toxicity is associated with bioche
mical failure-free rate (BFFR) in prostate cancer patients treated with IGRT.
Methods and Materials
We retrospectively analyzed BFFR in 362 patients with localized prostate cancer treated with IGRT. We compared BFFR with prospectively collected Radiation Therapy Oncology Group (RTOG) maximum acute gastrointestinal (GI) and genitourinary (GU) toxicity scores. Median follow-up for all patients was 58.3 months after total radiotherapy doses of 75.6-79.8 Gy.
Results
Patients reporting RTOG acute GU or GI toxicity scores of 鈮? were considered 鈥渟ensitive鈥?(m>nm> = 141, 39%) and patients reporting scores <2 were considered 鈥渘onsensitive鈥?(m>nm> = 221, 61%). When calculating biochemical failure (BF) using the American Society for Therapeutic Radiology and Oncology definition at 5 years, 76%(CI 70-82%) of the 鈥渘onsensitive鈥?patients were failure free, compared with only 53%(CI 43-62%) of the 鈥渟ensitive鈥?patients (log-rank test, m>pm> < 0.0001). This difference was also observed using the Phoenix definition; 鈥渘onsensitive鈥?5-year BFFR was 81%(CI 74-86%) vs. 鈥渟ensitive鈥?BFFR was 68%(CI 58-76%; log-rank test m>pm>聽= 0.0012). The difference in BF between cohorts remained significant when controlled for radiation dose (75.6 vs. 79.8 Gy), prognostic stratification (T category, prostate-specific antigen, and Gleason score), and prostate volume.
Conclusions
This study unexpectedly shows that prostate cancer patients who develop 鈮rade 2 RTOG acute toxicity during radiotherapy are less likely to remain BFF at 5 years. These results deserve further study and, if validated in other large IGRT cohorts, additional models would be required to study interaction between normal tissue and tumor biology in prostate cancer patients.