Department of Radiotherapy, University Hospital Würzburg, Würzburg, Germany.
Strahlenther Onkol. 2010 Oct;186(10):535-43. doi: 10.1007/s00066-010-2144-z. Epub 2010 Sep 30.
:To evaluate toxicity after dose-escalated radiotherapy for prostate cancer using intensity-modulated treatment planning (IMRT) and image-guided treatment (IGRT) delivery.
100 patients were treated with simultaneous integrated boost (SIB) IMRT for prostate cancer: doses of 76.23 Gy and 60 Gy in 33 fractions were prescribed to the prostate and the seminal vesicles, respectively, for intermediate- and high-risk patients (n = 74). The total dose was 73.91 Gy in 32 fractions for low-risk patients and after transurethral resection of the prostate (n = 26). The pelvic lymphatics were treated with 46 Gy in 25 fractions in patients with high risk of lymph node metastases using an SIB to the prostate (n = 25). IGRT was practiced with cone-beam computed tomography. Acute and late gastrointestinal (GI) and genitourinary (GU) toxicity was evaluated prospectively (CTCAE v3.0).
Treatment was completed as planned by all patients. Acute GI and GU toxicity grade ≥ 2 was observed in 12% and 42% of the patients, respectively, with 4% suffering from GU toxicity grade 3. 6 weeks after treatment, the incidence of acute toxicity grade ≥ 2 had decreased to 12%. With a median follow-up of 26 months, late GI and GU toxicity grade ≥ 2 was seen in 1.5% and 7.7% of the patients at 24 months. Four patients developed late toxicity grade 3 (GI n = 1; GU n = 3). Presence of acute GI and GU toxicity was significantly associated with late GI (p = 0.0007) and GU toxicity (p = 0.006).
High-dose radiotherapy for prostate cancer using IMRT and IGRT resulted in low rates of acute toxicity and preliminary results of late toxicity are promising.
使用调强治疗计划(IMRT)和图像引导治疗(IGRT)评估前列腺癌递增剂量放疗的毒性。
100 例前列腺癌患者接受同步整合增敏(SIB)IMRT 治疗:中危和高危患者(n=74)前列腺和精囊分别给予 76.23Gy 和 60Gy,33 分次;低危患者(n=26)在经尿道前列腺切除术(TURP)后,前列腺总剂量为 73.91Gy,32 分次。25 例高危患者在前列腺 SIB 中采用盆腔淋巴结转移的 SIB 给予 46Gy,25 分次。使用锥形束 CT 进行 IGRT。前瞻性评估急性和晚期胃肠道(GI)和泌尿生殖系统(GU)毒性(CTCAE v3.0)。
所有患者均按计划完成治疗。12%的患者出现急性 GI 毒性≥2 级,42%的患者出现急性 GU 毒性≥2 级,4%的患者出现 GU 毒性 3 级。治疗后 6 周,急性毒性≥2 级的发生率下降至 12%。中位随访 26 个月,24 个月时 1.5%和 7.7%的患者出现晚期 GI 和 GU 毒性≥2 级。4 例患者发生晚期毒性 3 级(GI 1 例;GU 3 例)。急性 GI 和 GU 毒性与晚期 GI(p=0.0007)和 GU 毒性(p=0.006)显著相关。
使用 IMRT 和 IGRT 对前列腺癌进行高剂量放疗,急性毒性发生率低,晚期毒性初步结果有希望。