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临床试验/NCT06461793
NCT06461793招募中2 期

Safety of Dose Escalation in Definitive Hypofractionated Radiation Therapy and Hormone Therapy With SpaceOAR TM for Patients With High - Risk Localized Prostate Cancer (DESAR-H)

Samsung Medical Center2 个研究点 分布在 2 个国家目标入组 33 人开始时间: 2023年9月12日最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
入组人数
33
试验地点
2
主要终点
NIH-NCI Common Terminology Criteria for Adverse Events (CTCAE) V 5.0 Frequency of rectal bleeding of grade 1 or higher within 3 years

研究概览

简要总结

Dose increase after injection of biodegradable material A safety study of high-risk prostate cancer patients who underwent low-fractionation curative radiation therapy and hormone therapy

详细描述

In prostate cancer, radiation therapy for curative purposes can be used regardless of the stage if there is no distant metastasis, and radiation therapy and hormone therapy may be combined in patients with moderate or high risk factors for recurrence. Randomized prospective studies to investigate the therapeutic effect of increasing dose escalation to 70 Gy or more showed significant reductions in biochemical failure. When the dose is increased, the risk of side effects (digestive system, urinary system) in surrounding normal tissues increases, and intensity modulated radiation therapy (IMRT) or image-guided radiation therapy (IGRT) Application could reduce the probability of side effects. Prostate cancer is a carcinoma characterized by slow growth, and the estimated α/β ratio is 1.5, which is smaller than surrounding normal tissues such as the bladder (4.0) and the rectum (3.9). Therefore, efforts to obtain therapeutic gain through hypofractionated radiation therapy have been attempted using three-dimensional conformal radiotherapy (3D-CRT) and IMRT. In particular, in the CHHIP trial11 announced in 2016, normal division Radiation therapy (74 Gy, 37 splits ) and as a result of comparing low-fractionation radiation therapy (60 Gy, 20 fractions ), there was no significant difference in the 5 -year biochemical or clinical recurrence -free survival rate of low-fractionation radiation therapy, it was also reported that there was no difference in rectal and bladder side effects. However, rectal and bladder side effects of grade 2 or higher were 11.9% and 11.7 % during one-time 3 Gy low-fractionated radiotherapy, respectively. The low-fractionated radiotherapy dose is 81 Gy, which is the recommended normal fractionated radiotherapy dose when using IMRT. It can be said that there is a high possibility of showing inferior treatment results in long-term follow-up results because the biological effective dose is lower than that of 'ideal '. ( Table 1)

  • Table 1. Biological Equivalent Dose by Radiation Therapy Policy (2-Gy fraction) comparison
  • Protocol: EQD1 (Gy)(α/β=1.5)
  • Low-fraction radiation therapy (70 Gy, 28 sessions): 80.0 Gy
  • Conventional fractionation radiation therapy (74 Gy, 37 times): 74 Gy
  • CHHIP trial (60 Gy, 20 times): 77.14 Gy
  • study design dose(64 Gy, 20 times): 85.94 Gy *EQD2, equivalent dose in 2-Gy fractions

Recently , a method was devised to increase the distance between prostate and rectum by injecting hydrogel between prostate and rectum to minimize rectal dose even when performing high-dose radiotherapy to prostate. In particular , a biodegradable material ( SpaceOAR (hydrogel)) that is absorbed into the body after a certain period of time has been developed, and radical radiation therapy is performed. It is currently being used in prostate cancer patients. It is judged possible to try to increase the radiation dose because the side effects can be reduced by reducing the rectal dose during radical radiation treatment through biodegradable material injection. So far, studies evaluating the side effects of treatment according to increased radiation dose after injection of biodegradable materials are very limited. Therefore, the investigator performs biodegradable material injection before radical radiotherapy in combination with hormone therapy in high - risk prostate cancer patients. The investigator plans to conduct a phase II clinical study to evaluate the safety of high - risk prostate cancer patients who has received subdivision radical radiation therapy with hormone therapy.

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
20 Years 至 —(Adult, Older Adult)
性别
Male
接受健康志愿者

入选标准

  • Histopathologically confirmed prostate adenocarcinoma within 6 months of study enrollment
  • Patients with prostate cancer at high risk or above (c T3a-T4 or grade group 4-5 or PSA > 20 n g/mL) )
  • Patients who have undergone or are scheduled to undergo hormone therapy for high-risk prostate cancer
  • Adults over 20 years of age
  • Whole body performance ECOG 0-1
  • SpaceOAR Patients who consented to the procedure and study

排除标准

  • prostate removal surgery, Patients with a history of lower pelvic surgery including rectal cancer surgery
  • primary cancer Patients with posterior extracapsular extension
  • Medically biodegradable substances such as bleeding predisposition Patients for whom infusion is not appropriate
  • Patients with a history of previous pelvic radiation therapy
  • Patients with lymph node metastasis or distant metastasis

结局指标

主要结局

NIH-NCI Common Terminology Criteria for Adverse Events (CTCAE) V 5.0 Frequency of rectal bleeding of grade 1 or higher within 3 years

时间窗: 3 years after radiation therapy of each participant

Adverse Event within three years after the radiation therapy

次要结局

  • biochemical recurrence-free survival(5 years after radiation therapy of each participant)
  • Radiation therapy-related side effects other than rectal bleeding(up to 2 years afte radiation therapy on each participant)
  • quality of life on high-risk prostate cancer patients by using EPIC questionnaire(up to 5 years after radiation therapy of each participant)
  • Side effects related to biodegradable material injection(each participant finished with radiation therapy and see after 3-6 months for acute adverse events, 1-5 years for chronic adverse events)
  • progression-free survival(up to 5 years after radiation therapy of each participant)
  • overall survival(up to 5 years after radiation therapy of each participant)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Won Park

Won Park, M.D., Ph.D.

Samsung Medical Center

研究点 (2)

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