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临床试验/NCT03223064
NCT03223064Unknown不适用

Accuracy of Lymph Node Imaging in Prostate Cancer: A Prospective Cohort Study to Determine the Concordance Between Two Imaging Modalities, "Combidex" Magnetic Resonance Imaging (Nano MRI) and 68Ga-PSMA Positron Emission Tomography (PET)

Radboud University Medical Center5 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2016年12月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
40
试验地点
5
主要终点
Concordance between and sensitivity and specificity of PSMA PET-CT and USPIO enhanced MRI

研究概览

简要总结

Following curative intended therapy in prostate cancer patients, a high proportion of patients (approx. 25%) relapse with local and/or distant recurrence. The metastasis of a lymph node (LN) in a patient with prostate cancer means that the disease has become systemic with the increased risk of disease progression. Therefore the ability to detect the presence of LN metastasis is important in terms of disease prognosis and treatment options. In the past, patients with LN metastasis have had poor prognoses due to the scarcity of accurate staging techniques and toxic treatment regimens such as radiotherapy. For those patients with a medium to high risk of having LN metastasis, the current procedure is a bilateral pelvic lymph node dissection (PLND). This is the standard procedure prior to curative treatment with either radical prostatectomy or radiation therapy. However, the procedure is not optimal due to the frequent inability to remove all positive lymph nodes within the dissection area. 41% of metastatic LN disease is not found, due to these LN being outside the routine surgery field. As a result, some urologists will perform an extended lymphadenectomy (e-PLND), which leads to extended operating times and the risk of complications. Also, therapy of LN metastases has limitations: more than 50% of metastatic LN are outside the routine (RTOG-CTV) radiation field. Thus the effect of standard LN radiotherapy is limited. Currently used imaging techniques such as CT and conventional MRI are also not sensitive enough to detect prostate cancer metastases due to the small size of the nodes (< 8mm).

In this study, patients that undergo a pelvic lymph node dissection will be undergoing a 68Ga PSMA PET-CT and a nano-MRI prior to surgery. The results of the PSMA PET-CT and the nano-MRI will be validated using the pathology results of the (PLND).

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

性别
Male
接受健康志愿者

入选标准

  • Male, aged 18 years Prostate cancer present (Gleason ≥ 7) and/or
  • PSA ≥ 15 and/or
  • Clinical or radiological Stage T3
  • Subject will be undergoing a pelvic lymph node dissection as part of the prostate cancer treatment.
  • Subject is willing to sign and date the study Informed Consent form
  • Signed, written informed consent

排除标准

  • Patients who cannot lie still for at least 30 minutes or comply with imaging
  • Subject has medical conditions that would limit study participation (per physician discretion)
  • Subject has hemochromatosis and liver disease
  • Subject has known allergy against Fe-products or dextranes
  • Subject is enrolled in one or more concurrent studies that would confound the study results of this study as determined by the study investigators
  • Previous treatment for prostate cancer (surgery, radiotherapy, chemotherapy, hormone androgen deprivation therapy)
  • Proven bony metastatic disease, visceral metastases or lymph node metastases above the level of the aortic bifurcation
  • Patients who will not get prostatectomy or pelvic lymph node dissection for any reason
  • Patient has absolute contra-indications to undergoing MRI scanning

研究组 & 干预措施

PSMA PET-CT and USPIO MRI

Experimental

干预措施: Ferumoxtran-10 enhanced MRI; MRI contrast agent (Diagnostic Test)

PSMA PET-CT and USPIO MRI

Experimental

干预措施: 68Ga PSMA PET-CT (Diagnostic Test)

结局指标

主要结局

Concordance between and sensitivity and specificity of PSMA PET-CT and USPIO enhanced MRI

时间窗: Within 8 weeks before pelvic lymph node dissection

The sensitivity and specificity of the PSMA PET-CT and nano-MRI will be determined based upon pathological validation

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (5)

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