Department of Urology, Kitasato University School of Medicine, Sagamihara, Japan.
Department of Radiology and Radiation Oncology, Kitasato University School of Medicine, Sagamihara, Japan.
Prostate. 2019 Apr;79(5):506-514. doi: 10.1002/pros.23757. Epub 2018 Dec 26.
Systemic Therapy in Advancing or Metastatic Prostate Cancer: Evaluation of Drug Efficacy (STAMPEDE) trial showed the survival benefit for prostate radiotherapy in newly diagnosed prostate cancer patients with a low metastatic burden. The result raises the next question whether additional radiotherapy to metastatic sites could improve the survival in those with a low metastatic burden.
We evaluated the efficacy and safety of prostate-directed radiotherapy (PDRT) with or without metastasis-directed radiotherapy (MDRT) in newly diagnosed oligometastatic patients who underwent combination of high-dose-rate prostate brachytherapy, external beam radiotherapy, and androgen deprivation therapy. Forty patients with bone metastasis and node positive prostate cancer were retrospectively analyzed. Of these, 22 (55%), 3 (7%), and 15 (38%) patients had N1M0, M1a, and M1b, respectively. Eighteen patients (45%) received MDRT to all metastatic sites. All patients initially underwent ≧6 months of androgen deprivation therapy. Oligometastatic disease was defined as presence of five or fewer metastatic lesions. Median follow-up period was 62.5 months.
Of the 40 patients, the 5-year castration-resistant prostate cancer (CRPC)-free survival rate and cancer-specific survival was 64.4% and 87.9%, respectively. Pre- or post-treatment predictive value including prostate-specific antigen (PSA) at diagnosis ≥20 ng/mL, Gleason grade group 5, positive biopsy core rate ≥51%, PSA nadir level of ≥0.02 ng/mL after the radiotherapy, and no MDRT were significantly associated with progression to CRPC. Patients with MDRT had significantly higher probability of achieving a PSA level of <0.02 ng/mL than those without the therapy (88.8% vs 54.5%, P = 0.0354) and consequently had a better CRPC-free survival than those without the therapy (HR 0.319, 95%CI: 0.116-0.877). Comparing PDRT alone, PDRT with MDRT did not significantly increase the incidences of genitourinary and gastrointestinal toxicities.
This single-institutional study revealed the feasibility of combining prostate brachytherapy and MDRT for newly diagnosed oligometastatic prostate cancer. This combined approach has potential to prolong CRPC-free survival.
在进展期或转移性前列腺癌的系统治疗中,STAMPEDE 试验显示前列腺放疗可使低转移负担的新发前列腺癌患者获益。该结果提出了下一个问题,即对于低转移负担的患者,是否可以通过额外的转移部位放疗来改善生存。
我们评估了在接受高剂量率前列腺近距离放射治疗、外照射放射治疗和雄激素剥夺治疗联合治疗的新诊断寡转移患者中,进行前列腺定向放射治疗(PDRT)加或不加转移定向放射治疗(MDRT)的疗效和安全性。对 40 例骨转移和淋巴结阳性前列腺癌患者进行回顾性分析。其中,22 例(55%)、3 例(7%)和 15 例(38%)患者分别为 N1M0、M1a 和 M1b。18 例(45%)患者接受了所有转移部位的 MDRT。所有患者最初接受了≥6 个月的雄激素剥夺治疗。寡转移疾病定义为存在 5 个或更少的转移病灶。中位随访时间为 62.5 个月。
40 例患者中,5 年去势抵抗性前列腺癌(CRPC)无进展生存率和癌症特异性生存率分别为 64.4%和 87.9%。包括诊断时前列腺特异性抗原(PSA)≥20ng/mL、Gleason 分级组 5、阳性活检核心率≥51%、放疗后 PSA 最低水平≥0.02ng/mL 以及无 MDRT 在内的治疗前或治疗后预测值与进展为 CRPC 显著相关。接受 MDRT 的患者 PSA 水平<0.02ng/mL 的概率明显高于未接受治疗的患者(88.8%比 54.5%,P=0.0354),因此无进展生存时间也明显长于未接受治疗的患者(HR 0.319,95%CI:0.116-0.877)。与单纯 PDRT 相比,PDRT 联合 MDRT 并未显著增加泌尿生殖系统和胃肠道毒性的发生率。
这项单中心研究揭示了在新诊断的寡转移性前列腺癌中联合应用前列腺近距离放射治疗和 MDRT 的可行性。这种联合方法有可能延长 CRPC 无进展生存时间。