Kupelian Patrick A, Thakkar Vipul V, Khuntia Deepak, Reddy Chandana A, Klein Eric A, Mahadevan Arul
Department of Radiation Oncology, M.D. Anderson Cancer Center Orlando, Orlando, FL 32806, USA.
Int J Radiat Oncol Biol Phys. 2005 Dec 1;63(5):1463-8. doi: 10.1016/j.ijrobp.2005.05.054. Epub 2005 Sep 19.
To analyze the long-term relapse-free survival and toxicity rates in patients treated with hypofractionated intensity-modulated radiotherapy.
The study sample includes the first 100 consecutive localized prostate cancer patients treated to 70.0 Gy at 2.5 Gy per fraction. The median follow-up was 66 months (range, 3 to 75 months). Biochemical failure was the study endpoint, using both the ASTRO definition (A-bRFS) and the alternate "nadir + 2 ng/mL" definition (N-bRFS). RTOG scores were used to assess toxicity.
The 5-year A-bRFS and N-bRFS rates were 85% (95%CI, 78-93%) and 88% (95%CI, 82-95%) for all cases, respectively. For low, intermediate and high-risk disease, the 5-year A-bRFS rates were 97%, 88%, and 70%. The corresponding 5-year N-bRFS rates were 97%, 93%, and 75%, respectively. The acute rectal toxicity scores were 0 in 20, 1 in 61, and 2 in 19 patients. The acute urinary toxicity scores were 0 in 9, 1 in 76, and 2 in 15 patients. The late rectal toxicity scores were 0 in 71, 1 in 19, 2 in 7, and 3 in 3 patients. The actuarial late Grade 3 rectal toxicity rate at 5 years was 3%. A number of the toxicities observed either resolved spontaneously or were corrected. At last follow-up, the rate of combined Grades 2 and 3 late rectal toxicity at 5 years was only 5%. The late urinary toxicity scores were 0 in 75, 1 in 13, 2 in 11, and 3 in 1 patients. The actuarial late Grade 3 urinary toxicity rate at 5 years was 1%.
With a median follow-up of 66 months, the long-term results after high-dose hypofractionation are excellent. Late toxicity, urinary and rectal, has been limited. High-dose hypofractionation is an alternative dose escalation method in the treatment of localized prostate cancer.
分析接受大分割调强放疗患者的长期无复发生存率和毒性率。
研究样本包括连续100例接受2.5Gy/次、总剂量70.0Gy治疗的局限性前列腺癌患者。中位随访时间为66个月(范围3至75个月)。生化失败为研究终点,采用ASTRO定义(A-bRFS)和替代的“最低点+2ng/mL”定义(N-bRFS)。采用RTOG评分评估毒性。
所有病例的5年A-bRFS和N-bRFS率分别为85%(95%CI,78-93%)和88%(95%CI,82-95%)。对于低、中、高危疾病,5年A-bRFS率分别为97%、88%和70%。相应的5年N-bRFS率分别为97%、93%和75%。急性直肠毒性评分为0分的患者有20例,1分的有61例,2分的有19例。急性泌尿毒性评分为0分的患者有9例,1分的有76例,2分的有15例。晚期直肠毒性评分为0分的患者有71例,1分的有19例,2分的有7例,3分的有3例。5年精算晚期3级直肠毒性率为3%。观察到的一些毒性反应要么自行缓解,要么得到纠正。在最后一次随访时,5年2级和3级晚期直肠毒性合并率仅为5%。晚期泌尿毒性评分为0分的患者有75例,1分的有13例,2分的有11例,3分的有1例。5年精算晚期3级泌尿毒性率为1%。
中位随访66个月,大分割高剂量放疗后的长期结果良好。晚期泌尿和直肠毒性有限。大分割高剂量放疗是局限性前列腺癌治疗中一种替代的剂量递增方法。