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Metastasis-Free Survival and Patterns of Distant Metastatic Disease After Prostate-Specific Membrane Antigen Positron Emission Tomography (PSMA-PET)-Guided Salvage Radiation Therapy in Recurrent or Persistent Prostate Cancer After Prostatectomy

医学 谷氨酸羧肽酶Ⅱ 前列腺癌 前列腺切除术 正电子发射断层摄影术 生化复发 雄激素剥夺疗法 放射治疗 转移 危险系数 放射科 核医学 癌症 肿瘤科 泌尿科 内科学 置信区间
作者
Constantinos Zamboglou,Iosif Strouthos,Joerg Sahlmann,Andrea Farolfi,Francesca Serani,Federica Medici,L Cavallini,Alessio G. Morganti,Christian Trapp,Stefan A. Koerber,Jan C. Peeken,Marco M. E. Vogel,Kilian Schiller,Stephanie E. Combs,Matthias Eiber,Alexis Vrachimis,Konstantinos Ferentinos,Simon Spohn,Simon Kirste,Christian Gratzke,Juri Ruf,Anca‐Ligia Grosu,Francesco Ceci,Wolfgang P. Fendler,Jonathan Miksch,Stephanie Kroeze,Matthias Gückenberger,Helena Lanzafame,Stefano Fanti,George Hruby,Thomas Wiegel,Louise Emmett,Nina Sophie Schmidt-Hegemann,Christoph Henkenberens
出处
期刊:International Journal of Radiation Oncology Biology Physics [Elsevier]
卷期号:113 (5): 1015-1024 被引量:18
标识
DOI:10.1016/j.ijrobp.2022.04.048
摘要

Prostate-specific membrane antigen positron emission tomography (PSMA-PET) is increasingly used to guide salvage radiation therapy (sRT) in patients with prostate cancer and biochemical recurrence/persistence after prostatectomy. This work examined (1) metastasis-free survival (MFS) after PSMA-PET guided sRT and (2) the metastatic patterns on PSMA-PET images after sRT.This retrospective, multicenter (9 centers, 5 countries) study included patients referred for PSMA-PET due to recurrent/persistent disease after prostatectomy. Patients with distant metastases (DM) on PSMA-PET before sRT were excluded. Cox regression was performed to assess the effect of clinical parameters on MFS. The distribution of PSMA-PET detected DM after sRT and their respective risk factors were analyzed.All (n = 815) patients received intensity modulated RT to the prostatic fossa. In the case of PET-positive pelvic lymph nodes (PLN-PET) (n = 275, 34%), pelvic lymphatics had been irradiated. Androgen deprivation therapy had been given in 251 (31%) patients. The median follow-up after sRT was 36 months. The 2-/4-year MFS after sRT were 93%/81%. In multivariate analysis, the presence of PLN-PET was a strong predictor for MFS (hazard ratio, 2.39; P < .001). After sRT, DM were detected by PSMA-PET in 128/198 (65%) patients, and 2 metastatic patterns were observed: 43% had DM in sub-diaphragmatic para-aortic LNs (abdominal-lymphatic), 45% in bones, 9% in supra-diaphragmatic LNs, and 6% in visceral organs (distant). Two distinct signatures with risk factors for each pattern were identified.MFS in our study is lower compared with previous studies, obviously due to the higher detection rate of DM in PSMA-PET after sRT. Thus, it remains unclear whether MFS is a surrogate endpoint for overall survival in PSMA PET-staged patients in the post-sRT setting. PLN-PET may be proposed as a new surrogate parameter predictive of MFS. Analysis of recurrence patterns in PET after sRT revealed risk factor signatures for 2 metastatic patterns (abdominal-lymphatic and distant), which may allow individualized sRT concepts in the future.
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