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RecruitingNCT06461793DESAR-HUpdated Jun 21, 2024

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)

A Phase 2 interventional study of Dose increase after injection of biodegradable material A safety study of high-risk prostate cancer patients in High Risk Prostate Carcinoma, sponsored by Samsung Medical Center. Recruiting at 1 site in South Korea. Open to male participants aged 20 Years and older. Per ClinicalTrials.gov, last updated 2024-06-21.

Sponsored by Samsung Medical Center · Phase 2, Interventional, and Treatment

From the registry’s dates

  • Registered 8 months after the study started (first participant enrolled Sep 2023, registered Jun 2024).
  • Started Sep 2023; still recruiting 3 years 1 month later.
Phase
Phase 2
Study type
Interventional
Enrollment
33
Allocation
Not applicable
Ages
20 Years and older
Sex
Male
01

Study summary

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

Read the detailed description

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.

02

Conditions studied

  • High Risk Prostate Carcinoma
03

In context

Lead sponsor

Samsung Medical Center is the lead sponsor of 1,005 studies on the registry; 148 are open to participants now.

Of its 7 completed or terminated interventional studies of FDA-regulated products, 1 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years and older
Sexes eligible
Male
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  1. prostate removal surgery, Patients with a history of lower pelvic surgery including rectal cancer surgery
  2. primary cancer Patients with posterior extracapsular extension
  3. Medically biodegradable substances such as bleeding predisposition Patients for whom infusion is not appropriate
  4. Patients with a history of previous pelvic radiation therapy
  5. Patients with lymph node metastasis or distant metastasis
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
33 participants (estimated)

Study arms

  • Experimental
    Prostate cancer patient, candidate of definitive radiation treatment

    A single institution with a single group, a phase II study, we plan to evaluate grade 1 or higher rectal bleeding within 3 years in high-risk prostate cancer patients who received biodegradable substance injection followed by curative radiotherapy in combination with hormone therapy.

    Radiation: Dose increase after injection of biodegradable material A safety study of high-risk prostate cancer patients

Interventions

  • RadiationDose increase after injection of biodegradable material A safety study of high-risk prostate cancer patients

    this researcher performed biodegradable material injection during radical radiotherapy in combination with hormone therapy in high - risk prostate cancer patients. after subdivision radical received radiation therapy We plan to conduct a phase II clinical study to evaluate the safety of prostate cancer patients.

06

What researchers measure

Primary outcomes

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

    Adverse Event within three years after the radiation therapy

    Time frame: 3 years after radiation therapy of each participant

Secondary outcomes

  1. Radiation therapy-related side effects other than rectal bleeding

    Sigmoi doscopy is performed once a year for up to 2 years after the end of radiation therapy,

    Time frame: up to 2 years afte radiation therapy on each participant

  2. Side effects related to biodegradable material injection

    Time frame: each participant finished with radiation therapy and see after 3-6 months for acute adverse events, 1-5 years for chronic adverse events

  3. biochemical recurrence-free survival

    Biochemical recurrence is defined as PSA nadir + 2.0ng/ml according to the Phoenix definition, or when hormone therapy is discontinued, when hormone therapy is newly started, or when hormone therapy is in progress, when the treatment is changed.

    Time frame: 5 years after radiation therapy of each participant

  4. progression-free survival

    check on each participant by CT scan, MRI, Bone scan for any progressive disease

    Time frame: up to 5 years after radiation therapy of each participant

  5. overall survival

    overall survival of participants till the end of the study(death)

    Time frame: up to 5 years after radiation therapy of each participant

  6. quality of life on high-risk prostate cancer patients by using EPIC questionnaire

    EPIC (Extended Prostate Cancer Index Composite), Korean version

    Time frame: up to 5 years after radiation therapy of each participant

07

Study locations

1 of 1 sites recruiting
  • Samsung Medical Center
    Seoul, 06351, South Korea
    Recruiting
08

References and documents

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Sep 2023 (actual). Primary completion is estimated for Dec 2033, 123 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Jun 11, 2024
First posted
Jun 17, 2024
StartActual
Sep 12, 2023
Primary completionEst.
Dec 31, 2033
CompletionEst.
Dec 31, 2033
Last update
Jun 21, 2024
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Jun 21, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06461793
Responsible party
Won Park (Won Park, M.D., Ph.D., Samsung Medical Center) — Principal investigator
First posted
Jun 17, 2024
Start date
Sep 12, 2023
Primary completion
Dec 31, 2033 (estimated)
Completion
Dec 31, 2033 (estimated)
Last update
Jun 21, 2024

Study contacts

Won Park, M.D., Ph.D.
Contact
wonro.park@samsung.com
+82-2-3410-2616

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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