- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07699705
Prospective Study of Ultrahypofractionated Proton Beam Therapy for Localized Prostate Cancer
Prospective Cohort Study for Identifying Factors Predicting Long-term Outcomes of Prostate Cancer Patients Who Received Ultrahypofractionated Proton Beam Therapy
The goal of this prospective observational cohort study is to evaluate the long-term efficacy and safety of ultrahypofractionated proton beam therapy in patients with localized prostate cancer and to identify clinical and treatment-related factors associated with oncologic outcomes and treatment-related toxicity.
The main questions it aims to answer are:
What are the long-term biochemical recurrence-free survival, clinical progression-free survival, overall survival, and acute and late treatment-related toxicity outcomes following ultrahypofractionated proton beam therapy? Which clinical characteristics, treatment planning parameters, and patient-reported outcomes are predictive of long-term oncologic outcomes and treatment-related toxicity?
Participants will:
Receive protocol-based ultrahypofractionated proton beam therapy (35-40 Gy[RBE] in 5 fractions).
Undergo routine clinical evaluation, laboratory testing including prostate-specific antigen (PSA), and imaging studies according to the institutional follow-up schedule.
Complete patient-reported outcome questionnaires (EPIC-CP and Visual Analog Scale [VAS]) before treatment and during follow-up.
Be followed prospectively to assess biochemical recurrence, clinical progression, survival outcomes, and acute and late treatment-related toxicities.
연구 개요
상세 설명
Localized prostate cancer can be effectively treated with external beam radiotherapy (EBRT). Ultrahypofractionated radiotherapy has become an established treatment option because of its favorable radiobiological characteristics, shorter treatment duration, and improved patient convenience. Owing to the low alpha/beta ratio of prostate cancer, delivery of larger doses per fraction may provide radiobiological advantages while maintaining excellent tumor control.
Proton beam therapy (PBT) offers unique dosimetric advantages over photon radiotherapy by reducing unnecessary radiation exposure to surrounding normal tissues through the Bragg peak effect. These characteristics may be particularly beneficial for ultrahypofractionated treatment, especially in patients with intermediate- or high-risk disease who require treatment of larger target volumes, including the seminal vesicles or pelvic lymph nodes. However, prospective data regarding the long-term efficacy, safety, patient-reported outcomes, and predictive factors associated with ultrahypofractionated proton beam therapy remain limited.
This is a prospective, single-center observational cohort study conducted at the National Cancer Center, Republic of Korea. Approximately 50 adult patients with histologically confirmed localized prostate adenocarcinoma who are scheduled to undergo definitive ultrahypofractionated proton beam therapy will be prospectively enrolled after providing written informed consent.
All participants will receive protocol-based ultrahypofractionated proton beam therapy consisting of 35-40 Gy(RBE) delivered in five fractions using image-guided proton therapy. Androgen deprivation therapy will be administered according to contemporary clinical guidelines and physician discretion when indicated.
The primary objective of this study is to evaluate the long-term efficacy and safety of ultrahypofractionated proton beam therapy for localized prostate cancer. Secondary objectives include evaluation of biochemical recurrence-free survival, clinical progression-free survival, overall survival, acute and late treatment-related toxicity, and patient-reported quality of life. In addition, the study will prospectively investigate clinical characteristics, treatment planning parameters, dosimetric variables, and patient-reported outcome measures to identify factors associated with oncologic outcomes and treatment-related toxicity.
Clinical information, treatment planning data, physician-reported adverse events, laboratory findings including prostate-specific antigen (PSA), imaging studies, and patient-reported outcome measures using the Expanded Prostate Cancer Index Composite for Clinical Practice (EPIC-CP) and the Visual Analog Scale (VAS) will be prospectively collected. Patients will be followed every three months during the first two years, every six months during years three and four, and annually thereafter according to institutional follow-up practice.
The findings from this prospective cohort study are expected to provide high-quality evidence regarding the clinical effectiveness and safety of ultrahypofractionated proton beam therapy and to facilitate the development of individualized treatment strategies for patients with localized prostate cancer by identifying predictors of long-term oncologic outcomes and treatment-related toxicity.
연구 유형
등록 (추정된)
단계
- 해당 없음
연락처 및 위치
연구 연락처
- 이름: Hyuna Park Clinical Research Coordinator, BS
- 전화번호: 0491 82-31-920-0491
- 이메일: 77313@ncc.re.kr
연구 장소
-
-
Gyeonggi-do
-
Goyang-si, Gyeonggi-do, 대한민국, 10408
- 모병
- National Cancer Center, Korea
-
연락하다:
- Sung Uk Lee, M.D., Ph.D.
- 전화번호: 82-31-920-1720
- 이메일: sulee126@ncc.re.kr
-
-
참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
Inclusion Criteria:
- Histologically confirmed localized adenocarcinoma of the prostate.
- No evidence of distant metastasis (M0).
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.
- Eligible to receive definitive image-guided ultrahypofractionated pencil beam scanning proton beam therapy according to the study protocol.
- Ability to complete study questionnaires and comply with scheduled follow-up assessments.
- Provision of written informed consent before study enrollment.
Exclusion Criteria:
- Residual or recurrent prostate cancer following prior radical prostatectomy.
- Previous pelvic radiotherapy.
- Evidence of distant metastatic disease.
- Active malignancy within the previous 1 year, except adequately treated basal cell carcinoma or squamous cell carcinoma of the skin, carcinoma in situ of the cervix, or completely resected T1N0M0 malignancies.
- Uncontrolled psychiatric illness, severe traumatic brain injury, chronic alcohol or substance dependence, or other medical conditions that, in the investigator's judgment, would preclude safe participation or adequate follow-up.
- Inability or unwillingness to provide written informed consent or comply with study procedures.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 해당 없음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: ultrahypofractionated proton beam therapy
Participants receive definitive ultrahypofractionated proton beam therapy (35-40 Gy[RBE] in 5 fractions) for localized prostate adenocarcinoma using image-guided proton therapy.
Participants are prospectively followed for oncologic outcomes, treatment-related toxicity, and patient-reported quality of life.
|
Ultrahypofractionated proton beam therapy is delivered using pencil beam scanning (PBS) with image-guided proton therapy.
Before treatment planning, all participants undergo placement of an absorbable rectal hydrogel spacer and two intraprostatic gold fiducial markers.
Treatment planning is performed using CT simulation with MRI fusion after hydrogel stabilization.
Daily cone-beam CT (CBCT) with fiducial marker matching is used for image guidance and patient positioning.
A total dose of 36.25-40.0
Gy(RBE) is delivered in 5 fractions over approximately 1-2 weeks.
Unlike conventional proton beam therapy using opposed right and left lateral beam arrangements, this protocol employs four oblique beam angles (right anterior oblique, right posterior oblique, left posterior oblique, and left anterior oblique) to optimize dose conformity while minimizing radiation exposure to adjacent normal tissues.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Biochemical recurrence-free survival
기간: Up to 5 years after completion of proton beam therapy
|
Biochemical recurrence is defined according to the Phoenix definition (PSA nadir + 2 ng/mL).
Biochemical recurrence-free survival is measured from completion of proton beam therapy to biochemical recurrence or last follow-up.
|
Up to 5 years after completion of proton beam therapy
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Patient-reported quality of life
기간: baseline, postRT 1 month, 4 months, 7 months and 1 year
|
Patient-reported quality of life will be assessed using the Expanded Prostate Cancer Index Composite for Clinical Practice (EPIC-CP).
Scores range from 0 to 100, with higher scores indicating better urinary quality of life.
|
baseline, postRT 1 month, 4 months, 7 months and 1 year
|
|
Clinical recurrence-free survival
기간: Up to 5 years after completion of proton beam therapy
|
Time from radiotherapy completion to first occurrence of any clinical recurrence (local, regional, or distant) or death.
Recurrence will be confirmed by imaging studies and/or histopathological findings when available.
|
Up to 5 years after completion of proton beam therapy
|
|
Overall survival
기간: From completion of proton beam therapy to 5 years after treatment
|
Time from completion of ultrahypofractionated proton beam therapy to death from any cause.
Participants who are alive at the time of analysis will be censored at the date of the last follow-up.
|
From completion of proton beam therapy to 5 years after treatment
|
|
Treatment-related genitourinary toxicity
기간: Up to 5 years after completion of proton beam therapy
|
Treatment-related genitourinary (GU) toxicity will be assessed according to the Common Terminology Criteria for Adverse Events (CTCAE) version 4.03.
Acute toxicity is defined as adverse events occurring within 90 days after completion of proton beam therapy, and late toxicity as events occurring more than 90 days after treatment completion.
|
Up to 5 years after completion of proton beam therapy
|
|
Treatment-related gastrointestinal toxicity
기간: Up to 5 years after completion of proton beam therapy
|
Treatment-related gastrointestinal (GI) toxicity will be assessed according to the Common Terminology Criteria for Adverse Events (CTCAE) version 4.03.
Acute toxicity is defined as adverse events occurring within 90 days after completion of proton beam therapy, and late toxicity as events occurring more than 90 days after treatment completion.
|
Up to 5 years after completion of proton beam therapy
|
공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- NCC2024-0253
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
미국에서 제조되어 미국에서 수출되는 제품
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
전립선 신생물에 대한 임상 시험
-
Weill Medical College of Cornell UniversityMillennium Pharmaceuticals, Inc.완전한신경내분비성 전립선암 | 소세포 전립선암 | Prostate Adenocarcinoma Plus > 신경내분비 표지자에 대한 50% 면역조직화학적 염색미국
Ultrahypofractionated Proton Beam Therapy에 대한 임상 시험
-
Massachusetts General HospitalGenentech, Inc.모집하지 않고 적극적으로