Stereotactic body radiation therapy after radical prostatectomy: current status and future directions

被引:2
|
作者
Le Guevelou, Jennifer [1 ]
Magne, Nicolas [2 ]
Counago, Felipe [3 ]
Magsanoc, Juan Martin [4 ]
Vermeille, Matthieu [5 ]
De Crevoisier, Renaud [1 ]
Benziane-Ouaritini, Nicolas [2 ]
Ost, Piet [6 ,7 ]
Niazi, Tamim [8 ]
Supiot, Stephane [9 ]
Sargos, Paul [2 ]
机构
[1] Ctr Eugene Marquis, Radiat Oncol Dept, Rennes, France
[2] Inst Bergonie, Dept Radiotherapy, Bordeaux, France
[3] GenesisCare, Natl Chair Res & Clin Trials, San Francisco Asis & La Milagrosa Hosp, Radiat Oncol Dept, Madrid, Spain
[4] St Lukes Hosp, Radiat Oncol Dept, Quezon City, Philippines
[5] Genolier Swiss Radiooncol Network, Radiat Oncol Dept, Genolier, Switzerland
[6] Iridium Network, Radiat Oncol Dept, Antwerp, Belgium
[7] Univ Ghent, Dept Human Struct & Repair, Ghent, Belgium
[8] Jewish Gen Hosp, Dept Radiat Oncol, Montreal, PQ, Canada
[9] Inst Cancerol Ouest, Radiat Oncol Dept, Nantes, France
关键词
Prostate cancer; Stereotactic body radiation therapy; Postoperative; Macroscopic recurrence; Re-irradiation; CLINICAL TARGET VOLUME; SALVAGE RADIOTHERAPY; POSTOPERATIVE RADIOTHERAPY; ADJUVANT RADIOTHERAPY; CONSENSUS GUIDELINES; CANCER; RISK; TRIAL; DEFINITION; RECURRENCE;
D O I
10.1007/s00345-023-04605-7
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
PurposeAround 40% of men with intermediate-risk or high-risk prostate cancer will experience a biochemical recurrence after radical prostatectomy (RP). The aim of this review is to describe both toxicity and oncological outcomes following stereotactic body radiation therapy (SBRT) delivered to the prostate bed (PB).MethodIn april 2023, we performed a systematic review of studies published in MEDLINE or ClinicalTrials.gov according to Preferred Reporting Items for Systematic Reviews, using the keywords "stereotactic radiotherapy" AND "postoperative" AND "prostate cancer".ResultsA total of 14 studies assessing either adjuvant or salvage SBRT to the whole PB or macroscopic local recurrence (MLR) within the PB, and SBRT on radiorecurrent MLR within the PB were included. Doses delivered to either whole PB or MLR between 30 to 40 Gy are associated with a low rate of late grade >= 2 genitourinary (GU) toxicity, ranging from 2.2 to 15.1%. Doses above 40 Gy are associated with increased rate of late GU toxicity, raising up to 38%. Oncological outcomes should be interpreted with caution, due to both short follow-up, heterogeneous populations and androgen deprivation therapy (ADT) use.ConclusionPB or MLR SBRT delivered at doses up to 40 Gy appears safe with relatively low late severe GU toxicity rates. Caution is needed with dose-escalated RT schedules above 40 Gy. Further prospective trials are eagerly awaited in this disease setting.
引用
收藏
页码:3333 / 3344
页数:12
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