Mercier Carole, Claessens Marc, De Troyer Bart, Debacker Tibaut, Fransis Karen, Vandeursen Hendrik, Ost Piet, Dirix Piet
Department of Radiotherapy, Iridium Netwerk, Antwerp, Belgium.
Integrated Personalised and Precision Oncology Network, University Antwerp, Antwerp, Belgium.
Front Oncol. 2022 Apr 14;12:863609. doi: 10.3389/fonc.2022.863609. eCollection 2022.
The addition of stereotactic ablative radiotherapy (SABR) to standard of care for patients with oligometastatic prostate cancer has the potential of improving survival and delaying further metastases. The primary aim of this analysis is to report survival outcomes and pattern of recurrence of patients with hormone-sensitive (HSPC) and castrate-resistant (CRPC) oligometastatic prostate cancer treated with SABR.
This is a single-center retrospective study of patients with oligometastatic prostate cancer treated in Iridium Network between 2014 and 2018. All patients with oligometastatic (≤3 active lesions) HSPC and CRPC treated with SABR were included. Data were collected using electronic records. Patterns of first progression following SABR were reported. Kaplan-Meier methods were used to determine survival outcomes.
Eighty-seven men received SABR to 115 metastases. Nineteen patients were castrate-resistant and 68 hormone-sensitive at the time of SABR. Median follow-up was 41.6 months. In 25% of patients, no decline from baseline PSA was recorded. Median bPFS was 11.7 months (95% CI 7.6 - 18.3) for HSPC as well as CRPC (95% CI 6.4 - 24.0) (p=0.27). Median DMFS was 21.8 (95% CI 16.9 - 43.2) versus 17.6 months (95% CI 6.7 - 26.2) for HSPC versus CRPC, respectively (p=0.018). Median OS was 72.6 months (95% CI 72.6 - not reached) for HSPC and not reached for CRPC (95% CI 35.4 months - not reached) (p=0.026). For the subgroup of oligorecurrent HSPC, short-term androgen-deprivation therapy was associated with improved bPFS (median 6.0 vs. 18.3 months, HR 0.31, p<0.001) and DMFS (median 15.8 vs 29.6 months, HR 0.5, p=0.06). Information on pattern of relapse was retrieved for 79 patients: 45% (36/79) of these patients were long-term disease-free (>18 months), 28% (22/79) of patients wmere oligoprogressive (≤3 new lesions) and 27% (21/79) developed a polymetastatic relapse.
In this cohort, oligometastatic HSPC showed potential benefit from SABR with a median DMFS of 21.8 months. Well-selected patients with oligometastatic CRPC may also benefit from SABR. For patients with metachronous and repeat oligorecurrent HSPC, combining SABR with short-term androgen-deprivation therapy was associated with improved bPFS and DMFS. Overall, 36/87 (41%) of patients were still free from clinical relapse at 18 months.
对于寡转移前列腺癌患者,在标准治疗基础上增加立体定向消融放疗(SABR)有可能提高生存率并延缓进一步转移。本分析的主要目的是报告接受SABR治疗的激素敏感型(HSPC)和去势抵抗型(CRPC)寡转移前列腺癌患者的生存结果和复发模式。
这是一项对2014年至2018年在铱网络接受治疗的寡转移前列腺癌患者的单中心回顾性研究。纳入所有接受SABR治疗的寡转移(≤3个活动性病灶)HSPC和CRPC患者。使用电子记录收集数据。报告SABR后首次进展的模式。采用Kaplan-Meier方法确定生存结果。
87名男性接受了针对115处转移灶的SABR治疗。19例患者在接受SABR时为去势抵抗型,68例为激素敏感型。中位随访时间为41.6个月。25%的患者未记录到PSA较基线水平下降。HSPC患者的中位生化无进展生存期(bPFS)为11.7个月(95%CI 7.6 - 18.3),CRPC患者为11.7个月(95%CI 6.4 - 24.0)(p = 0.27)。HSPC患者的中位远处转移无进展生存期(DMFS)为21.8个月(95%CI 16.9 - 43.2),CRPC患者为17.6个月(95%CI 6.7 - 26.2)(p = 0.018)。HSPC患者的中位总生存期(OS)为72.6个月(95%CI 72.6 - 未达到),CRPC患者未达到(95%CI 35.4个月 - 未达到)(p = 0.026)。对于寡复发性HSPC亚组,短期雄激素剥夺治疗与改善bPFS(中位6.0个月对18.3个月,HR 0.31,p < 0.001)和DMFS(中位15.8个月对29.6个月,HR 0.5,p = 0.06)相关。检索到79例患者的复发模式信息:这些患者中有45%(36/79)长期无病生存(>18个月),28%(22/79)为寡进展性(≤3个新病灶),27%(21/79)发生多灶性复发。
在该队列中,寡转移HSPC患者从SABR中显示出潜在益处,中位DMFS为21.8个月。精心选择的寡转移CRPC患者也可能从SABR中获益。对于异时性和复发性寡复发性HSPC患者,将SABR与短期雄激素剥夺治疗相结合与改善bPFS和DMFS相关。总体而言,87例患者中有36/87(41%)在18个月时仍无临床复发。