Ravi Praful, Zhong Caiwei, Xie Wanling, Kelly Emma, Whelpley Bridget, Kuczmarski Katelyn, Beltran Himisha, Kilbridge Kerry L, King Martin T, McGregor Bradley A, Morgans Alicia K, Pomerantz Mark, Taplin Mary-Ellen, Tewari Alok K, Viswanathan Srinivas R, Wei Xiao X, Anh Huynh Mai, Choudhury Atish D
Dana-Farber Cancer Institute, Boston, MA, USA.
Dana-Farber Cancer Institute, Boston, MA, USA.
Eur Urol Oncol. 2025 Jun;8(3):709-715. doi: 10.1016/j.euo.2024.10.014. Epub 2024 Nov 14.
It is unclear whether "total therapy" (androgen deprivation therapy [ADT] with or without an androgen receptor pathway inhibitor [ARPI], metastasis-directed therapy, and local therapy to the prostate if de novo) may lead to long-term durable remission in oligometastatic hormone-sensitive prostate cancer (omHSPC). This study aims to evaluate the outcomes after the completion of total therapy in patients with omHSPC.
A retrospective single-institution cohort of consecutive patients with omHSPC identified on conventional or molecular imaging treated with total therapy was assembled. All patients had prostate-specific antigen ≤0.1 ng/ml at the completion of systemic therapy. Kaplan-Meier and Cox regression models were used to evaluate the key outcomes of interest: clinical progression-free survival (cPFS), eugonadal progression-free survival (PFS), and time to restart of ADT (TTrADT).
Eighty-nine patients were included, of whom 23 were with de novo omHSPC; the median number of metastases was 1, and detection of disease by molecular imaging was performed in 43 patients (48%). Forty-nine patients (55%) received ADT + ARPI doublet and 40 (45%) received ADT alone. At a median follow-up of 37 mo, there were 46 cPFS events; 3-yr cPFS rate was 45% (95% confidence interval 33-56) and the median eugonadal PFS was 12 mo. The median TTrADT was 47 mo, and 60% had not restarted ADT at 3 yr. Duration of systemic therapy ≥12 mo was the only significant predictor of better outcomes.
Of the patients receiving total therapy for omHSPC, 45% remained progression free at 3 yr after completing therapy, hinting at the potential for long-term remission and possible cure with this strategy in a subset of patients with omHSPC. Prospective trials evaluating this approach are needed.
In this report, we looked at outcomes in men who had received a fixed duration of hormonal therapy along with radiotherapy to metastatic sites (and prostate radiotherapy or surgery in those with newly diagnosed disease) for oligometastatic prostate cancer. We found that nearly half of the patients had no evidence of cancer recurrence at 3 yr after completing therapy, and 60% had not resumed any therapy at this time point.
尚不清楚“全程治疗”(雄激素剥夺治疗[ADT]联合或不联合雄激素受体通路抑制剂[ARPI]、转移灶定向治疗以及初诊时对前列腺的局部治疗)是否能使寡转移激素敏感性前列腺癌(omHSPC)患者获得长期持久缓解。本研究旨在评估omHSPC患者完成全程治疗后的结局。
收集了一个回顾性单中心队列,该队列由经传统或分子影像学检查确诊并接受全程治疗的连续omHSPC患者组成。所有患者在全身治疗结束时前列腺特异性抗原≤0.1 ng/ml。采用Kaplan-Meier法和Cox回归模型评估感兴趣的关键结局:临床无进展生存期(cPFS)、性腺功能正常无进展生存期(PFS)以及重新开始ADT的时间(TTrADT)。
纳入89例患者,其中23例为初诊omHSPC;转移灶的中位数为1个,43例患者(48%)通过分子影像学检测到疾病。49例患者(55%)接受ADT + ARPI联合治疗,40例患者(45%)仅接受ADT治疗。中位随访37个月时,发生46次cPFS事件;3年cPFS率为45%(95%置信区间33 - 56),性腺功能正常的中位PFS为12个月。中位TTrADT为47个月,60%的患者在3年时未重新开始ADT治疗。全身治疗持续时间≥12个月是预后较好的唯一显著预测因素。
在接受omHSPC全程治疗的患者中,45%在完成治疗后3年仍无疾病进展,这提示该策略可能使一部分omHSPC患者获得长期缓解甚至治愈。需要开展前瞻性试验评估这种方法。
在本报告中,我们观察了接受固定疗程激素治疗并联合转移灶放疗(初诊患者还接受前列腺放疗或手术)的寡转移前列腺癌男性患者的结局。我们发现,近一半的患者在完成治疗后3年无癌症复发证据,60%的患者在此时点未恢复任何治疗。