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임상시험 NCT06902311 (H-ASSIST)은(는) 유방암, 초기 유방암, 제자리 관암종, DCIS에 대해 모집중 상태입니다. 모든 세부 정보를 보려면 임상시험 레이더 카드 뷰와 AI 발견 도구를 확인하거나 여기에서 무엇이든 물어보세요.
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Ultra Hypo-fractionated Adjuvant Whole Breast Radiation Therapy With Simultaneous Integrated Boost for Early-Stage Breast Cancer (H-ASSIST) 2상 90

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임상시험 NCT06902311 (H-ASSIST)은(는) 치료을(를) 알아보기 위한 연구입니다. 이 연구는 유방암, 초기 유방암, 제자리 관암종, DCIS에 대해 진행되며, 2상 중재연구으로 현재 상태는 모집중입니다. 연구는 2025년 2월 19일에 시작되어 90명의 참여자를 모집하고 있습니다. UNC Lineberger Comprehensive Cancer Center이(가) 진행하며, 2028년 2월 1일까지 완료될 예정입니다. ClinicalTrials.gov의 가장 최근 정보는 2026년 3월 30일에 갱신되었습니다.
간단한 개요
This study evaluates the rates of radiation-specific toxicity, quality of life, and oncologic outcomes for early-stage breast cancer and ductal carcinoma in situ treated with 5-fraction whole breast irradiation (WBI) with a simultaneous integrated tumor bed boost (SIB). SIB refers to the technique tumor bed boost given at the same time as standard radiation therapy.

The FAST-Forward trial previously showed that a 1-...

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상세한 설명
Multiple recent studies demonstrate the noninferiority of a simultaneous integrated boost (SIB) approach. This study will include women aged 50 years and older who are recommended to receive whole breast irradiation with a standard dose boost and without regional nodal irradiation.

Radiation therapy will consist of 5 fractions delivered every other day (excluding weekends), with a total dose of 26 Gy to the whole br...

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공식 제목

Ultra Hypo-fractionated Adjuvant Whole Breast Radiation Therapy With Simultaneous Integrated Boost for Early-Stage Breast Cancer (H-ASSIST)

질환명
유방암초기 유방암제자리 관암종DCIS
기타 연구 식별자
  • H-ASSIST
  • LCCC2404
NCT 번호
실제 연구 시작일
2025-02-19
최신 업데이트 게시
2026-03-30
예상 연구 완료일
2028-02
계획된 등록 인원
90
연구종류
중재연구
단계/상
2상
상태
모집중
키워드
whole breast irradiation
WBI
simultaneous integrated tumor bed boost (SIB)
SIB
Concurrent boost
adverse effects
toxicity
Radiation-specific toxicity
patient reported outcome
PRO-CTCAE
주요 목적
치료
설계 할당
해당 없음
중재 모델
단일군설계
맹검 (마스킹)
없음 (오픈 라벨)
시험군 / 개입
참가자 그룹/시험군개입/치료
실험적WBI-SIB
Five-fraction whole breast irradiation (WBI) with simultaneous integrated tumor bed boost (SIB).
Breast Radiotherapy
The tumor bed boost when given at the same time (called a simultaneous integrated boost, SIB) with whole breast irradiation (WBI).
주요결과변수
결과변수측정값 설명시간 범위
Rate of any moderate-marked adverse effects
The rate of moderate to marked adverse effects in the breast or chest wall at 1 year will be measured using a questionnaire called the Clinician Assessment of Radiation-Specific Toxicity by clinican. This will be compared against historical controls. The questionnaire includes 10 items: 4 Likert-type questions and 6 yes/no questions. Items are rated from 0 to 4, with higher scores indicating more adverse effects. A "yes" response indicates the occurrence of an adverse event.
1 year
이차결과변수
결과변수측정값 설명시간 범위
In-breast tumor recurrence
In-breast tumor recurrence at 2 years is defined according to the standard definition as the time from enrollment to any of the following events: invasive ipsilateral recurrence and/or ipsilateral DCIS recurrence. Recurrence will be measured via medical record abstraction and clinical evaluation.
2 years
Quality of life at measured by European Organization for Research and Treatment of Cancer ( EORTC QLQ-C30)
Quality of life at 12 months will be measured as defined by European Organization for Research and Treatment of Cancer ( EORTC QLQ-C30). The EORTC QLQ-C30 is a cancer-specific instrument with 30 questions that incorporates 9 multi-item scales: 5 functional scales (physical, role, cognitive, emotional, and social); 9 symptom scales (fatigue, pain, nausea and vomiting, dyspnea, insomnia, appetite loss, constipation, diarrhea and financial difficulties); and a global health and quality-of-life scale. Most questions used 4 point scale (1 'Not at all' to 4 'Very much'); 2 questions used 7-point scale (1 'very poor' to 7 'Excellent'). The scores of these scales were averaged from the scores of the component items, transformed and analyzed on a 0 - 100 scale. A higher score=better level of functioning or greater degree of symptoms.
12 months
참여 도우미
적격성 기준

연령대
성인, 노인
최소 연령
50 Years
참여 가능한 성별
여성
In order to participate in this study a subject must meet all of the eligibility criteria outlined below.
  • Willing and able to provide written informed consent obtained to participate in the study and HIPAA authorization for release of personal health information.
  • Women ≥ 50 years of age with confirmed de novo invasive carcinoma of breast or ductal carcinoma in situ.
  • Subjects with completed breast-conserving surgery (BCS) with or without sentinel lymph node biopsy (SLNB) or axillary lymph node dissection (ALND).
  • Subjects planned to receive either SOC whole breast 3D conformal radiation therapy (3D CRT) or SOC whole breast intensity modulated radiation therapy (IMRT) with standard dose tumor bed boost.
  • Subjects with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial, per the discretion of the treating radiation oncologist.
  • Enrollment in another clinical trial is allowed if there is no interference with interventions on this trial per discretion of the Principal Investigator.

  • Receipt of concurrent breast reduction involving tissue rearrangement in the lumpectomy cavity (so that boost cannot be accurately targeted).
  • Synchronous bilateral breast cancer requiring bilateral radiation therapy.
  • Clinical or imaging evidence of distant metastases.
  • Prior ipsilateral breast or thoracic radiation.
  • Autoimmune conditions
  • Collagen Vascular Disease (such as systemic lupus erythematosus, scleroderma, dermatomyositis, among others)
  • Patients with pT4 tumors.
  • Patients recommended to receive regional nodal irradiation with associated radiation risks
UNC Lineberger Comprehensive Cancer Center logoUNC Lineberger Comprehensive Cancer Center
연구 대표 연락처
연락처: Jessica Buddenbaum, 919-966-4432, [email protected]
연락처: Cory Grreenwood, 919-445-4929, [email protected]
1 1개국에 임상시험 장소

North Carolina

University of North Carolina, Chapel Hill, North Carolina, 27599, United States
Jessica Buddenbaum, 연락처, 919-966-4432, [email protected]
Dana Casey, MD, 책임연구자
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