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镓-前列腺特异性膜抗原(Ga-PSMA)或氟-氟乙基半胱氨酸(F-FEC)PET/CT检查后对前列腺癌患者淋巴结复发进行挽救性淋巴结清扫术。

Salvage lymph node dissection after Ga-PSMA or F-FEC PET/CT for nodal recurrence in prostate cancer patients.

作者信息

Herlemann Annika, Kretschmer Alexander, Buchner Alexander, Karl Alexander, Tritschler Stefan, El-Malazi Lina, Fendler Wolfgang P, Wenter Vera, Ilhan Harun, Bartenstein Peter, Stief Christian G, Gratzke Christian

机构信息

Department of Urology, Ludwig-Maximilians-University of Munich, Munich, Germany.

Comprehensive Cancer Center, Ludwig-Maximilians-University of Munich, Munich, Germany.

出版信息

Oncotarget. 2017 Sep 21;8(48):84180-84192. doi: 10.18632/oncotarget.21118. eCollection 2017 Oct 13.

DOI:10.18632/oncotarget.21118
PMID:29137414
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5663586/
Abstract

The management of patients with biochemical recurrence (BCR) after definitive treatment for prostate cancer remains controversial. Our aim was to determine survival rates and complications of salvage lymph node dissection (sLND) in patients with recurrent prostate cancer after radical prostatectomy, while evaluating biochemical response (BR) with two different positron emission tomography/computed tomography (PET/CT) tracers used for preoperative imaging. sLND was performed in 104 patients diagnosed with isolated nodal recurrence on either F-fluoroethylcholine (F-FEC) or Ga-PSMA-HBED-CC (Ga-PSMA) PET/CT. Surgical complications, BR, clinical recurrence (CR), and cancer-specific survival (CSS) were evaluated. Logistic regression was used to determine predictors of complete BR (cBR) and CR after sLND and survival rates were assessed. Median follow-up was 39.5 months. Median patient age and prostate-specific antigen (PSA) at sLND were 64 years and 4.1 ng/mL. Median number of lymph nodes (LNs) removed was 13; median number of positive LNs was 3 per patient. Rate of Clavien-Dindo Grade III complications was low (4.8%). 29.8% of patients developed cBR (PSA < 0.2 ng/mL), and 56.7% partial BR (PSA postoperative < PSA preoperative) after sLND. Patients with LN metastases diagnosed on Ga-PSMA PET/CT showed a higher rate of cBR compared to F-FEC PET/CT (45.7 vs. 21.7%, = 0.040). PSA at sLND ( = 0.031) and choice of PET tracer ( = 0.048) were independent predictors of cBR. The 5-year BCR-free, CR-free and CSS rates were 6.2%, 26.0%, and 82.8%, respectively. While preoperative staging with Ga-PSMA seems superior, only a limited number of patients developed cBR after surgery. Most patients experienced BCR and CR during follow-up.

摘要

前列腺癌根治性治疗后生化复发(BCR)患者的管理仍存在争议。我们的目的是确定根治性前列腺切除术后复发性前列腺癌患者挽救性淋巴结清扫术(sLND)的生存率和并发症,同时使用两种不同的正电子发射断层扫描/计算机断层扫描(PET/CT)示踪剂进行术前成像来评估生化反应(BR)。对104例经F-氟乙基胆碱(F-FEC)或镓-前列腺特异性膜抗原-六氮杂环十二烷四乙酸(Ga-PSMA)PET/CT诊断为孤立性淋巴结复发的患者进行了sLND。评估了手术并发症、BR、临床复发(CR)和癌症特异性生存(CSS)情况。采用逻辑回归确定sLND后完全BR(cBR)和CR的预测因素,并评估生存率。中位随访时间为39.5个月。sLND时患者的中位年龄和前列腺特异性抗原(PSA)分别为64岁和4.1 ng/mL。切除的淋巴结(LN)中位数为13个;每位患者阳性LN的中位数为3个。Clavien-DindoⅢ级并发症发生率较低(4.8%)。sLND后,29.8%的患者出现cBR(PSA<0.2 ng/mL),56.7%的患者出现部分BR(术后PSA<术前PSA)。与F-FEC PET/CT相比,经Ga-PSMA PET/CT诊断为LN转移的患者cBR发生率更高(45.7%对21.7%,P = 0.040)。sLND时的PSA(P = 0.031)和PET示踪剂的选择(P = 0.048)是cBR的独立预测因素。5年无BCR率、无CR率和CSS率分别为6.2%、26.0%和82.8%。虽然术前使用Ga-PSMA进行分期似乎更具优势,但术后只有少数患者出现cBR。大多数患者在随访期间经历了BCR和CR。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04d7/5663586/6d8b0fdc9981/oncotarget-08-84180-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04d7/5663586/d688301f1e36/oncotarget-08-84180-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04d7/5663586/413239839aa3/oncotarget-08-84180-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04d7/5663586/b7b873dd36cc/oncotarget-08-84180-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04d7/5663586/3c2a9bf2816e/oncotarget-08-84180-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04d7/5663586/6d8b0fdc9981/oncotarget-08-84180-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04d7/5663586/d688301f1e36/oncotarget-08-84180-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04d7/5663586/413239839aa3/oncotarget-08-84180-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04d7/5663586/b7b873dd36cc/oncotarget-08-84180-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04d7/5663586/3c2a9bf2816e/oncotarget-08-84180-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04d7/5663586/6d8b0fdc9981/oncotarget-08-84180-g005.jpg

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