Marotte Delphine, Gal Jocelyn, Schiappa Renaud, Gautier Mathieu, Boulahssass Rabia, Chand-Fouche Marie-Eve, Hannoun-Levi Jean-Michel
Department of Radiation Oncology, Antoine Lacassagne Cancer Center, University of Côte d'Azur, 33 avenue Valombrose, 06189 Nice Cedex 2, Nice, France.
Department of Statistics, Antoine Lacassagne Cancer Center, University of Côte d'Azur, Nice, France.
Clin Transl Radiat Oncol. 2022 May 21;35:104-109. doi: 10.1016/j.ctro.2022.05.001. eCollection 2022 Jul.
To analyze the oncological outcome in elderly (>70 years) prostate cancer after high-dose rate brachytherapy (HDB) boost.
MATERIALS/METHODS: In this retrospective study, patients with intermediate (IR) and high-risk (HR) prostate cancer underwent external beam radiation therapy (EBRT) followed by HDB boost with/without androgen deprivation therapy (ADT). The impact of age (≤70y vs. > 70y) was investigated. Oncological outcome focused on biochemical relapse-free survival (bRFS), cause-specific (CSS) and overall survival (OS). Late genito-urinary (GU) and gastro-intestinal (GI) toxicities were investigated.
From 07/08 to 01/22, 518 pts received a HDB boost, and 380 were analyzed (≤70y:177pts [46.6%] vs. > 70y:203pts [53.4%]). Regarding NCCN classification, 98 pts (≤70y: 53pts; >70y: 45pts; p = 0.107) and 282 pts (≤70y: 124pts; >70y: 158pts; p = NS) were IR and HR pts respectively. Median EBRT dose was 46 Gy [37.5-46] in 23 fractions [14-25]. HDB boost delivered a single fraction of 14/15 Gy (79%). ADT was used in 302 pts (≤70y: 130pts; >70y: 172pts; p = 0.01). With MFU of 72.6 months [67-83] for the whole cohort, 5-y bRFS, 5-y CSS and 5-y OS were 88% [85-92], 99% [97-100] and 94% [92-97] respectively; there was no statistical difference between the two age groups except for 5-y CSS (p = 0.05). Late GU and GI toxicity rates were 32.4% (G ≥ 3 7.3%) and 10.1% (no G3) respectively.
For IR and HR prostate cancers, HDB boost leads to high rates of disease control with few late G ≥ 3 GU/GI toxicities. For elderly pts, HDB boost remains warranted mainly in HR pts, while competing comorbidity factors influence OS.
分析高剂量率近距离放射治疗(HDB)强化后老年(>70岁)前列腺癌的肿瘤学结局。
材料/方法:在这项回顾性研究中,中危(IR)和高危(HR)前列腺癌患者接受了外照射放疗(EBRT),随后进行有或无雄激素剥夺治疗(ADT)的HDB强化。研究了年龄(≤70岁与>70岁)的影响。肿瘤学结局重点关注无生化复发生存(bRFS)、特定病因生存(CSS)和总生存(OS)。研究了晚期泌尿生殖系统(GU)和胃肠道(GI)毒性。
从2008年7月至2022年1月,518例患者接受了HDB强化,其中380例进行了分析(≤70岁:177例[46.6%] vs.>70岁:203例[53.4%])。关于美国国立综合癌症网络(NCCN)分类,分别有98例(≤70岁:53例;>70岁:45例;p = 0.107)和282例(≤70岁:124例;>70岁:158例;p = 无统计学意义)为IR和HR患者。EBRT的中位剂量为46 Gy [37.5 - 46],分23次[14 - 25次]给予。HDB强化单次给予14/15 Gy(79%)。302例患者使用了ADT(≤70岁:130例;>70岁:172例;p = 0.01)。整个队列的中位随访时间为72.6个月[67 - 83个月],5年bRFS、5年CSS和5年OS分别为88% [85 - 92%]、99% [97 - 100%]和94% [92 - 97%];除5年CSS外,两个年龄组之间无统计学差异(p = 0.05)。晚期GU和GI毒性发生率分别为32.4%(≥3级7.3%)和10.1%(无3级)。
对于IR和HR前列腺癌,HDB强化可实现较高的疾病控制率,且晚期≥3级GU/GI毒性较少。对于老年患者,HDB强化主要适用于HR患者,而并存的合并症因素会影响OS。