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使用 PSMA PET/CT 进行放疗前分期时阳性病变的检测水平和模式。

Detection level and pattern of positive lesions using PSMA PET/CT for staging prior to radiation therapy.

机构信息

Department of Radiation Oncology, University Hospital, LMU Munich, Munich, Germany.

Department of Nuclear Medicine, University Hospital, LMU Munich, Munich, Germany.

出版信息

Radiat Oncol. 2017 Nov 10;12(1):176. doi: 10.1186/s13014-017-0902-0.

DOI:10.1186/s13014-017-0902-0
PMID:29126446
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5681820/
Abstract

BACKGROUND

To determine the potential role of Ga-PSMA positron emission tomography/computed tomography (PET/CT) in radiotherapy (RT) planning for prostate cancer (PCa).

METHODS

One hundred twenty-nine patients (pts) with Ga-PSMA PET/CT were retrospectively analysed. Potentially influencing factors (androgen deprivation therapy, amount of Ga-PSMA-HBED-CC, PSA doubling time ≤/> 10 months, PSA before PET/CT, T-/N-category and Gleason score) were evaluated by logistic regression analysis. The detection rate of PSMA PET/CT was compared to contrast enhanced CT and its impact on RT management analysed.

RESULTS

One hundred twenty-nine patients (pts) (20 at initial diagnosis, 49 with PSA relapse and 60 with PSA persistence after radical prostatectomy) received PSMA PET/CT prior to RT. The majority of pts. (71.3%) had PET-positive findings (55.1% of pts. with PSA recurrence, 75% of pts. with PSA persistence and 100% of newly diagnosed pts). Median PSA before PET/CT in pts. with pathological findings (n = 92) was 1.90 ng/ml and without (n = 37) 0.30 ng/ml. PSA level at time of PET/CT was the only factor associated with PET-positivity. In pts. with a PSA ≤ 0.2 ng/ml, the detection rate of any lesion was 33.3%, with a PSA of 0.21-0.5 ng/ml 41.2% and with a PSA of 0.51-1.0 ng/ml 69.2%, respectively. Regarding the anatomic distribution of lesions, 42.2% and 14.7% of pts. with relapse or persistence had pelvic lymph node and distant metastases. In pts. at initial diagnosis the detection rate of pelvic lymph nodes and distant metastases was 20% and 10%. Ga-PSMA PET/CT had a high detection rate of PCa recurrence outside the prostatic fossa in pts. being considered for salvage RT (22.4% PET-positive pelvic lymph nodes and 4.1% distant metastases). Compared to CT, PSMA PET/CT had a significantly higher sensitivity in diagnosing rates of local recurrence/primary tumour (10.1% vs. 38%), lymph nodes (15.5% vs. 38.8%) and distant metastases (5.4% vs. 14.0%). This resulted in a modification of RT treatment in 56.6% of pts.

CONCLUSIONS

The detection of PCa is strongly associated with PSA level at time of Ga-PSMA PET/CT. PSMA PET/CT differentiates between local, regional and distant metastatic disease with implications for disease management. PSMA PET/CT allows for tumour detection in post-prostatectomy pts. with PSA ≤ 0.5 ng/ml considered for salvage RT.

摘要

背景

为了确定 Ga-PSMA 正电子发射断层扫描/计算机断层扫描(PET/CT)在前列腺癌(PCa)放射治疗(RT)计划中的潜在作用。

方法

回顾性分析了 129 名接受 Ga-PSMA PET/CT 检查的患者。通过逻辑回归分析评估了可能影响因素(雄激素剥夺治疗、Ga-PSMA-HBED-CC 量、PSA 倍增时间≤/> 10 个月、PET/CT 前 PSA、T-/N 分期和 Gleason 评分)。比较了 PSMA PET/CT 与对比增强 CT 的检测率,并分析了其对 RT 管理的影响。

结果

129 名患者(pts)(20 名初诊患者,49 名 PSA 复发患者,60 名根治性前列腺切除术后 PSA 持续患者)在 RT 前接受了 PSMA PET/CT 检查。大多数 pts.(71.3%)的 PET 检查结果为阳性(55.1%的 PSA 复发患者,75%的 PSA 持续患者和 100%的初诊患者)。在有病理发现的 pts.(n=92)中,PET/CT 前 PSA 中位数为 1.90ng/ml,无病理发现的 pts.(n=37)中 PSA 中位数为 0.30ng/ml。PET/CT 时的 PSA 水平是唯一与 PET 阳性相关的因素。在 PSA≤0.2ng/ml 的 pts.中,任何病变的检出率为 33.3%,PSA 为 0.21-0.5ng/ml 时为 41.2%,PSA 为 0.51-1.0ng/ml 时为 69.2%。关于病变的解剖分布,42.2%和 14.7%的复发或持续患者有盆腔淋巴结和远处转移。在初诊 pts.中,盆腔淋巴结和远处转移的检出率分别为 20%和 10%。在考虑挽救性 RT 的患者中,Ga-PSMA PET/CT 对前列腺窝外 PCa 复发的检出率较高(22.4%的 PET 阳性盆腔淋巴结和 4.1%的远处转移)。与 CT 相比,PSMA PET/CT 在诊断局部复发/原发性肿瘤(10.1%比 38%)、淋巴结(15.5%比 38.8%)和远处转移(5.4%比 14.0%)的灵敏度方面有显著提高。这导致 56.6%的 pts.改变了 RT 治疗。

结论

PCa 的检出与 Ga-PSMA PET/CT 时的 PSA 水平密切相关。PSMA PET/CT 可区分局部、区域和远处转移性疾病,对疾病管理具有重要意义。PSMA PET/CT 可在 PSA≤0.5ng/ml 的前列腺切除术后 pts.中检测肿瘤,这些 pts.被认为适合进行挽救性 RT。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e8c/5681820/194e2b073d39/13014_2017_902_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e8c/5681820/2a52af0703b3/13014_2017_902_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e8c/5681820/b5af82aff951/13014_2017_902_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e8c/5681820/dbe4899a9ec5/13014_2017_902_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e8c/5681820/194e2b073d39/13014_2017_902_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e8c/5681820/2a52af0703b3/13014_2017_902_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e8c/5681820/b5af82aff951/13014_2017_902_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e8c/5681820/dbe4899a9ec5/13014_2017_902_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e8c/5681820/194e2b073d39/13014_2017_902_Fig4_HTML.jpg

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