Outcomes of metastasis-directed therapy of bone oligometastatic prostate cancer

被引:21
作者
Rogowski, Paul [1 ]
Trapp, Christian [1 ]
von Bestenbostel, Rieke [1 ]
Schmidt-Hegemann, Nina-Sophie [1 ]
Shi, Run [1 ]
Ilhan, Harun [2 ]
Kretschmer, Alexander [3 ]
Stief, Christian [3 ]
Ganswindt, Ute [4 ]
Belka, Claus [1 ,5 ]
Li, Minglun [1 ]
机构
[1] Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Radiat Oncol, Marchioninistr 15, D-81377 Munich, Germany
[2] Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Nucl Med, Munich, Germany
[3] Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Urol, Munich, Germany
[4] Med Univ Innsbruck, Dept Therapeut Radiol & Oncol, Anichstr 35, A-6020 Innsbruck, Austria
[5] German Canc Consortium DKTK, Munich, Germany
关键词
Prostate cancer; Oligometastases; Bone metastases; Radiotherapy; SBRT; Metastasis-directed therapy; STEREOTACTIC BODY RADIOTHERAPY; SALVAGE RADIOTHERAPY; RECURRENCE; ONCOLOGY; DISEASE;
D O I
10.1186/s13014-021-01849-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background The aim of this work was to investigate the outcome of metastasis-directed radiotherapy (MDT) in prostate cancer patients with bone metastases following current ESTRO/EORTC subclassifications for oligometastatic disease. Methods Clinical data of 80 consecutive oligometastatic patients with 115 bone lesions receiving MDT between 2011 and 2019 were retrospectively evaluated. Hormone-sensitive (77.5%) and castrate-resistant (22.5%) patients were included. MDT was delivered with conventional fractionated or stereotactic body radiotherapy (SBRT) techniques. Kaplan-Meier method, log rank test, as well as Cox regression were used to calculate local control (LC) and biochemical and clinical progression-free survival (bPFS/cPFS). Results At the time of MDT 31% of patients had de-novo synchronous oligometastatic disease, 46% had de-novo metachronous oligorecurrence after primary treatment and 23% had either de-novo oligoprogressive disease, repeat oligometastatic disease or induced oligometastatic disease. The median BED3 was 93.3 Gy (range 75.8-95.3 Gy). Concomitant ADT was administered in 69% of patients. After a median follow-up of 23 months the median bPFS and cPFS were 16.5 and 21.5 months, respectively. The 2-year LC rate was 98.3%. In multivariate analysis, age <= 70 (HR = 2.60, 95% CI 1.20-5.62, p = 0.015) and concomitant ADT (HR = 0.26, 95% CI 0.12-0.58, p = 0.001) significantly correlated with cPFS. Category of oligometastatic disease and hormone-sensitivity were predictive for cPFS in univariate analysis. Of 45 patients with biochemical relapse, nineteen patients (42.2%) had repeat oligometastatic disease. Fourteen patients (31%) underwent a second course of MDT. No patients experienced grade >= 3 toxicities. Conclusions MDT is safe and offers high local control rates in bone oligometastases of prostate cancer. At 2 years after treatment, more than 2 out of 5 patients are progression-free. Trial registration Retrospectively registered.
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页数:11
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