Norkus Darius, Miller Albert, Kurtinaitis Juozas, Haverkamp Uwe, Popov Sergey, Prott Franz-Josef, Valuckas Konstantinas Povilas
Department of Radiotherapy, Institute of Oncology, Vilnius University, Vilnius, Lithuania.
Strahlenther Onkol. 2009 Nov;185(11):715-21. doi: 10.1007/s00066-009-1982-z. Epub 2009 Nov 10.
To compare acute gastrointestinal (GI) and genitourinary (GU) toxicity between patient groups with localized prostate adenocarcinoma, treated with conventionally fractionated (CFRT) and hypofractionated (HFRT) three-dimensional conformal external-beam radiotherapy (3D-CRT).
91 patients were enrolled into a randomized study with a minimum follow-up of 3 months. 44 men in the CFRT arm were irradiated with 74 Gy in 37 fractions at 2 Gy per fraction for 7.5 weeks. 47 men in the HFRT arm were treated with 57 Gy in 17 fractions for 3.5 weeks, given as 13 fractions of 3 Gy plus four fractions of 4.5 Gy. The clinical target volume (CTV) included the prostate and the base of seminal vesicles. The CTV-to-PTV (planning target volume) margin was 8-10 mm. Study patients had portal imaging and/or simulation performed on the first fractions and repeated at least weekly.
No acute grade 3 or 4 toxicities were observed. The grade 2 GU acute toxicity proportion was significantly lower in the HFRT arm: 19.1% versus 47.7% (chi(2)-test, p = 0.003). The grade 2 GU acute toxicity-free survival was significantly better in the HFRT arm (log-rank test, p = 0.008). The median duration of overall GI acute toxicity was shorter with HFRT: 3 compared to 6 weeks with CFRT (median test, p = 0.017).
In this first evaluation, the HFRT schedule is feasible and induces acceptable or even lower acute toxicity compared with the toxicities in the CFRT schedule. Extended follow-up is needed to justify this fractionation schedule's safety in the long term.
比较接受常规分割(CFRT)和大分割(HFRT)三维适形外照射放疗(3D-CRT)治疗的局限性前列腺腺癌患者组之间的急性胃肠道(GI)和泌尿生殖系统(GU)毒性。
91例患者纳入一项随机研究,最小随访时间为3个月。CFRT组的44名男性接受74 Gy照射,分37次,每次2 Gy,共7.5周。HFRT组的47名男性接受57 Gy照射,分17次,共3.5周,即13次3 Gy加4次4.5 Gy。临床靶区(CTV)包括前列腺和精囊基部。CTV至计划靶区(PTV)的边界为8 - 10 mm。研究患者在首次分次照射时进行了门静脉成像和/或模拟,并至少每周重复一次。
未观察到急性3级或4级毒性。HFRT组2级GU急性毒性比例显著更低:19.1% 对比47.7%(卡方检验,p = 0.003)。HFRT组2级无GU急性毒性生存期显著更好(对数秩检验,p = 0.008)。HFRT组总体GI急性毒性的中位持续时间更短:3周,而CFRT组为6周(中位检验,p = 0.017)。
在这首次评估中,HFRT方案是可行的,与CFRT方案相比,其诱导的急性毒性可接受甚至更低。需要延长随访以证实这种分割方案长期的安全性。