Department of Radiation Oncology, Fox Chase Cancer Center, Philadelphia, PA.
Biostatistics and Bioinformatics Facility, Fox Chase Cancer Center, Philadelphia, PA.
Brachytherapy. 2024 Sep-Oct;23(5):559-568. doi: 10.1016/j.brachy.2024.06.001. Epub 2024 Jul 26.
We aim to investigate perioperative and subacute postoperative complications in patients undergoing LDR or HDR monotherapy for prostate cancer. We hypothesize a low rate of complications, and a favorable toxicity profile in patients treated with HDR compared to LDR.
A prospectively collected institutional database was queried for patients treated with HDR or LDR prostate monotherapy between 1998 and 2021. Toxicities were determined per CTCAE. Claims based billing codes were obtained to identify additional events. Events occurring within 4 months of treatment were defined as perioperative or subacute postoperative complications.
759 patients were identified, 446 received LDR with I, and 313 received HDR with Ir. HDR patients had higher risk features: 75.7% with Gleason score 7+ versus 2.4% of LDR, and 16% with initial PSA 10+ ng/mL versus 2.7% of LDR. Toxicities were mild with the most common being grade 1 GU frequency and nocturia at ∼50%. HDR patients had significantly less grade 2 dysuria (2.6% vs. 9.0%), frequency (4.8% vs. 9.4%), hematuria (1.0% vs. 5.2%), nocturia (3.8% vs. 9.4%), and urinary obstructive symptoms (7.3% vs. 11.2%), all statistically significant. 11 (1.4%) patients had infection requiring antibiotics: 8 (1.8%) from the LDR group and 3 (1%) from the HDR group. Cardiopulmonary events were low at <2% overall, without difference between HDR and LDR.
Overall toxicity rates support the safety of prostate brachytherapy. HDR monotherapy is associated with significantly less perioperative and subacute postoperative GU events when compared to LDR monotherapy. Cardiopulmonary events were equally rare in both groups.
我们旨在研究接受 LDR 或 HDR 单一疗法治疗前列腺癌的患者的围手术期和亚急性术后并发症。我们假设 HDR 治疗的患者并发症发生率较低,且毒性特征优于 LDR。
通过前瞻性收集的机构数据库,对 1998 年至 2021 年间接受 HDR 或 LDR 前列腺单一疗法治疗的患者进行了查询。根据 CTCAE 确定毒性。获得基于计费代码的索赔以识别其他事件。将治疗后 4 个月内发生的事件定义为围手术期或亚急性术后并发症。
共确定了 759 例患者,446 例接受 I 期 LDR 治疗,313 例接受 Ir 期 HDR 治疗。HDR 患者具有更高的风险特征:75.7%的患者 Gleason 评分 7+,而 LDR 组为 2.4%;16%的患者初始 PSA 为 10+ng/mL,而 LDR 组为 2.7%。毒性较轻,最常见的是 1 级 GU 频率和夜尿症,发生率约为 50%。HDR 患者的 2 级排尿困难(2.6%比 9.0%)、频率(4.8%比 9.4%)、血尿(1.0%比 5.2%)、夜尿症(3.8%比 9.4%)和尿路梗阻症状(7.3%比 11.2%)明显较少,均具有统计学意义。11 例(1.4%)患者发生感染需要抗生素治疗:LDR 组 8 例(1.8%),HDR 组 3 例(1%)。总体而言,心肺事件发生率低于 2%,HDR 和 LDR 之间无差异。
总体毒性率支持前列腺近距离放射治疗的安全性。与 LDR 单一疗法相比,HDR 单一疗法与围手术期和亚急性术后 GU 事件明显减少相关。两组的心肺事件同样罕见。