Chamois J, Septans A L, Schipman B, Gross E, Blanchard N, Passerat V, Debelleix C, Hemery C G, Latorzeff I, Pointreau Y
Centre Hospitalier privé, Saint Grégoire, France.
Statistiques, Weprom, Angers, France.
Clin Transl Radiat Oncol. 2024 Mar 17;46:100762. doi: 10.1016/j.ctro.2024.100762. eCollection 2024 May.
Oligometastases are defined as a number of detectable metastases less or equal to 5. In castrate-resistant oligo metastatic prostate Cancer (CR oligoM PC), Metastases-Directed Ablative radiotherapy (MDRT) is poorly investigated. Our study retrospectively reviewed the cases of CR oligoM PC treated with MDRT in 8 French high-volume radiotherapy centers. OS and PFS are defined as the delay between the first day of MDRT and death (OS) or progression according to PCWG criteria (PFS). OS and PFS are evaluated according to Kaplan Meyer, curves are compared with log rank test. Logistic regression was used to identify predictive factors for outcome: bone versus node metastasis, ISUP grade, PSA doubling Time (PSADT) at the time of MDRT, time to castration resistance. 107 patients were included in the study, among those 197 metastases received MDRT. For the overall population, the median follow-up was 25.2 months (1,4-145). OS was 93 % at 2 years and 81,4% at 3 years. At 2 years, 100 % of patients with node-only metastasis were alive versus 88,7% among those who have bone metastases (p = 0,72). The median PFS was 12,6 months (IC 95 % [9,6; 17]), with no difference among patients with node only disease versus the rest of the cohort. The PFS was 18,2 months (10,0; 32,4) in patients with PSADT >6 months versus 10,7 months (8,9; 14,3) when PSADT was inferior to 6 months. However, this difference did not reach significant. We did not find a correlation neither between ISUP grade (1-2 versus 3-4-5) and PFS, nor between hormone-sensitivity duration and PFS. Patients receiving MDRT for CR oligoM PC have a good prognosis with 81,6% OS at 3 years. PSA DT longer than 6 months could be related to better PFS. MDRT strategy could postpone the onset of new systemic treatment with median PFS >1 year.
寡转移被定义为可检测到的转移灶数量小于或等于5个。在去势抵抗性寡转移前列腺癌(CR寡转移PC)中,转移灶定向消融放疗(MDRT)的研究较少。我们的研究回顾性分析了法国8家大型放疗中心接受MDRT治疗的CR寡转移PC病例。总生存期(OS)和无进展生存期(PFS)定义为MDRT第一天至死亡(OS)或根据PCWG标准进展(PFS)的时间间隔。OS和PFS根据Kaplan-Meier法进行评估,曲线采用对数秩检验进行比较。采用逻辑回归分析确定预后的预测因素:骨转移与淋巴结转移、ISUP分级、MDRT时的前列腺特异抗原倍增时间(PSADT)、去势抵抗时间。107例患者纳入研究,其中197个转移灶接受了MDRT。总体人群的中位随访时间为25.2个月(1.4 - 145个月)。2年时OS为93%,3年时为81.4%。2年时,仅发生淋巴结转移的患者100%存活,而有骨转移的患者为88.7%(p = 0.72)。中位PFS为12.6个月(95%置信区间[9.6;17]),仅发生淋巴结转移的患者与队列其他患者之间无差异。PSADT>6个月的患者PFS为18.2个月(10.0;32.4),而PSADT低于6个月的患者为10.7个月(8.9;14.3)。然而,这种差异未达到显著水平。我们未发现ISUP分级(1 - 2级与3 - 4 - 5级)与PFS之间、激素敏感持续时间与PFS之间存在相关性。接受MDRT治疗的CR寡转移PC患者预后良好,3年OS为81.6%。PSADT长于6个月可能与更好的PFS相关。MDRT策略可将新的全身治疗的开始时间推迟,中位PFS>1年。