A Phase I Integrated Boost to the Dominant Intraprostatic Nodule Based on Ga-68 Prostate-Specific Membrane Antigen (PSMA) PET/MR Study of Stereotactic Body Radiation Therapy in Patients With Localized Prostate Cancer
试验速览
- 阶段
- 不适用
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- The Probability of Acute genitourinary (GU) , gastrointestinal (GI) toxicity and erectile dysfunction
研究概览
简要总结
The aim of this study is to test the safety and efficacy of integrated boost to the dominant intraprostatic nodule based on Ga-68 Prostate-Specific Membrane Antigen (PSMA) PET/MR in Stereotactic Body Radiation Therapy (SBRT) in localized prostate carcinoma in patients for whom the standard treatment is the irradiation of the entire prostate gland with or without seminal vesicles accompanied or not by hormonal therapy.
详细描述
Radiotherapy is considered standard of care treatment for prostate cancer. In light of the accumulating clinical evidence favoring the use of hypo fractionation, SBRT regimen might constitute a much more convenient non-invasive and highly efficient outpatient therapy. Although the proposed extreme hypofractionated radiotherapy approach was expected to provide excellent local control of the primary prostate cancer, a proportion of patients with intermediate- or high-risk disease may have recurrences with local recurrence or distant metastasis in the future, requiring strategies to minimize systemic disease. Ga-68 PSMA PET/MR has high accuracy in the diagnosis and staging of prostate cancer. In this protocol, pretreatment Ga-68 PSMA PET/MR and CT scanning were performed in all patients as well as the imaging fusion before delineating the target. This study would explore the simultaneously integrated boost or equential integrated boost to the dominant intraprostatic nodule based on Ga-68 PSMA PET/MR in SBRT.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 99 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Histologically confirmed adenocarcinoma of the prostate
- •tumor clinical stage cT1-3N0M0 according to AJCC TNM 2017
- •Without any treatment of prostate cancer including radiotherapy, ADT, chemotherapy, focal treatment, etc.
- •With the examination of Ga-68 PSMA PET/MR
- •International Prostate Symptom Score(IPSS）<15 (alpha blockers allowed), without severe urethral obstruction symptoms
- •ECOG performance status 0-2
- •Written informed consent according to ICH/GCP regulations before registration and prior to any trial specific procedures
排除标准
- •Prior pelvic RT
- •A tumor located at less than 3 mm from the urethra or rectum when measured at the MRI
- •Tumor clinical stage cT4, with metastases including bone, lymph nodes or organ metastasis
- •Histologically confirmed neuroendocrine tumor or small cell carcinoma of the prostate
- •Severe or active co-morbidity likely to impact on the advisability of SBRT like severe liver or kidney dysfunction, etc.
- •Patients with other malignancies, or acute or other severe infections, with ulcerative colitis, inflammatory bowel disease, etc.
- •Patients who have participated in other clinical trials for less than three months
- •Patients have acute prostatitis or chronic prostatitis with urinary symptoms
- •Urine routine indicates obvious urinary system infection and no significant improvement after anti-infective treatment, or conversion to recurrent urinary system infection
- •Unsuitable to participate in this clinical trial judged by the investigator
结局指标
主要结局
The Probability of Acute genitourinary (GU) , gastrointestinal (GI) toxicity and erectile dysfunction
时间窗: 90 days after the first fraction of radiotherapy treatment
Acute genitourinary (GU) , gastrointestinal (GI) toxicity and erectile dysfunction (ED) (grade 2 or more) according to the NCI CTCAE v4.0.
次要结局
- The Probability of Chronic genitourinary (GU) , gastrointestinal (GI) toxicity and erectile dysfunction (ED)(> 90 days and up to 3 years from the start of protocol treatment)
- 1-year Local Progression-Free-Survival(LPFS)(Assessment at 1-year)
- 1-year Overall Survival (OS)(Assessment at 1-year)
- 1-year Distant Metastasis Free Survival(DMFS)(Assessment at 1-year)
- 1-year Biochemical Progression-free Survival (bPFS)(Assessment at 1-year)
研究者
Zhang Huo Jun
Clinical Professor
Changhai Hospital