Eule Corbin J, Candelario Nellowe, Nath Sameer K, Robin Tyler P
Division of Medical Oncology, Department of Medicine, University of Colorado Cancer Center, Aurora, Colorado.
Division of Hematology and Oncology, Fred Hutchison Cancer Center, University of Washington, Seattle, Washington.
Adv Radiat Oncol. 2024 Oct 20;9(12):101655. doi: 10.1016/j.adro.2024.101655. eCollection 2024 Dec.
Patients with metastatic castrate-resistant prostate cancer (CRPC) with progressive disease generally require a change or escalation in systemic therapy. For patients with limited (1-3) sites of progressive disease (oligoprogression), metastasis-directed therapy with stereotactic body radiation therapy (SBRT) may allow a longer interval before next-line systemic therapy.
This is a retrospective study of patients with oligoprogressive metastatic CRPC (mCRPC) treated with SBRT at a single center between 2011 and 2022. The primary endpoint was time to next systemic therapy (TTNST) after SBRT stratified by the presence/absence of untreated nonprogressing metastases. Secondary endpoints included TTNST of the overall cohort and median overall survival (OS) after SBRT.
Thirty-two patients with oligoprogressive mCRPC received SBRT to 38 metastases. Patients had a median age of 72.5 years (range, 50.6-84.3) and a median PSA of 6.85 ng/mL (range, 0.39-922.0) at the time of SBRT. The most commonly used SBRT regimen was 3000 cGy in 5 fractions (18 metastases, 47.4%). Sixteen patients were treated to all known sites of disease, whereas 16 patients received SBRT to oligoprogressive metastases but had at least 1 untreated nonprogressing metastasis at the time of SBRT. Patients had received a median of 1.0 prior line of androgen receptor signaling inhibitors and were predominantly (26 patients, 81.3%) chemotherapy naïve. Following SBRT, the median TTNST was 10.1 months and the median OS was 41.3 months. For patients with 0 versus ≥1 untreated nonprogressing metastasis, TTNST was 11.3 versus 8.7 months, respectively (HR, 0.67; 95% CI, 0.33-1.36, logrank = .24). There was no grade ≥3 toxicities because of SBRT.
In this cohort, patients with oligoprogressive mCRPC treated with SBRT delayed the next line of systemic therapy for a median of 10.1 months. SBRT in patients with oligoprogressive mCRPC may delay initiation of the next-line systemic therapy in well-selected patients, including those with ≥1 untreated nonprogressing metastasis.
患有转移性去势抵抗性前列腺癌(CRPC)且疾病进展的患者通常需要改变或加强全身治疗。对于疾病进展部位有限(1 - 3个)的患者(寡进展),采用立体定向体部放射治疗(SBRT)进行转移灶定向治疗可能会延长至下一线全身治疗的间隔时间。
这是一项对2011年至2022年在单一中心接受SBRT治疗的寡进展性转移性CRPC(mCRPC)患者的回顾性研究。主要终点是SBRT后至下一次全身治疗的时间(TTNST),根据有无未治疗的非进展性转移进行分层。次要终点包括整个队列的TTNST以及SBRT后的中位总生存期(OS)。
32例寡进展性mCRPC患者的38个转移灶接受了SBRT治疗。患者在接受SBRT时的中位年龄为72.5岁(范围50.6 - 84.3岁),中位前列腺特异性抗原(PSA)为6.85 ng/mL(范围0.39 - 922.0)。最常用的SBRT方案是分5次给予3000 cGy(18个转移灶,47.4%)。16例患者接受了针对所有已知疾病部位的治疗,而16例患者接受了针对寡进展性转移灶的SBRT治疗,但在接受SBRT时至少有1个未治疗的非进展性转移灶。患者之前接受雄激素受体信号抑制剂治疗的中位线数为1.0,且大多数患者(26例,81.3%)未接受过化疗。SBRT后,中位TTNST为10.1个月,中位OS为41.3个月。对于无未治疗的非进展性转移灶与有≥1个未治疗的非进展性转移灶的患者,TTNST分别为11.3个月和8.7个月(风险比[HR],0.67;95%置信区间[CI],0.33 - 1.36,对数秩检验P = 0.24)。未出现因SBRT导致的≥3级毒性反应。
在该队列中,接受SBRT治疗的寡进展性mCRPC患者将下一线全身治疗的时间中位数延迟了10.1个月。对于精心挑选的寡进展性mCRPC患者,包括那些有≥1个未治疗的非进展性转移灶的患者,SBRT可能会延迟下一线全身治疗方案的启动。