Prospective Evaluation of a Once Per Day Regimen of Accelerated Partial Breast Irradiation in Low-Risk, Hormone-Responsive Breast Cancer
试验速览
- 阶段
- 2 期
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 48
- 试验地点
- 1
- 主要终点
- Proportion of women that rate the cosmetic appearance of the breast as acceptable ("excellent" or "good")
研究概览
简要总结
This phase II trial tests how well accelerated partial breast irradiation (APBI) delivered once per day works in ensuring an acceptable breast appearance in patients with low risk, hormone responsive breast cancer. APBI uses precise radiation beams to kill cancerous cells in a smaller area of the breast (partial breast) instead of the whole breast or chest area as in standard therapy. Additionally, APBI is given in a shorter course of treatment than whole breast radiation therapy, over fewer days instead of several weeks, with a lower total dose of radiation. APBI is currently given every other business day for a total of 5 treatments with excellent results; however, a shorter treatment duration could have similar or even better results. Undergoing APBI every day on consecutive business days for 5 treatments may result in an improved breast appearance for patients with low risk hormone responsive breast cancer.
详细描述
PRIMARY OBJECTIVES:
I. To establish that APBI delivered once per day (APBI QD) for low-risk breast cancer patients results in acceptable patient-reported cosmetic appearance of the breast at 1 year after completion of APBI QD.
SECONDARY OBJECTIVES:
I. To determine the long-term patient-reported cosmetic appearance of the breast in patients treated with APBI QD.
II. To determine the short-term and long-term physician reported cosmetic appearance of the breast in patients treated with APBI QD.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Supportive Care
- 盲法
- None
盲法说明
Cosmetic outcome assessed by blinded medical doctor review.
入排标准
- 年龄范围
- 40 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Documented informed consent of the participant and/or legally authorized representative
- •Age: >= 40 years
- •Ability to read and understand English or Spanish for questionnaires
- •Anatomic pathologic stage 0 (ductal carcinoma in situ [DCIS]) or stage IA (invasive) breast cancer
- •Malignancy must be epithelial. Non-epithelial breast malignancies such as lymphoma or sarcoma are not allowed
- •Tissue from core biopsy or resection must show hormone sensitive receptors. Hormone sensitive receptors are defined as the following:
- •- DCIS: Estrogen receptor (ER) positive (>= 60%)
- •Invasive breast cancer:
- •Oncotype DX =< 25 (if performed) OR
- •If Oncotype DX is not performed an Allred score of 7 or
- •The following combinations of proportion of ER positive cells and staining intensity are allowed:
- •ER positive (34-66% of cells) and staining intensity is strong (Allred 7)
- •ER positive (>= 67% of cells) and staining intensity is intermediate (Allred 7)
- •ER positive (>= 67% of cells) and staining intensity is strong (Allred 8)
- •Tissue from core biopsy or resection must be HER2 negative by current American Society of Clinical Oncology (ASCO)/College of American Pathologists (CAP) guidelines
- •Patients must have undergone breast conserving surgery with resulting negative surgical margins (no tumor on ink). Re-excision for negative margins is allowed. Patients with pathologically involved surgical margins are excluded
- •Patients must have pathologic Tis or T1 disease
- •Patients with invasive breast cancer, including patients with microinvasion, must have undergone surgical staging of the axilla (sentinel lymph node biopsy or axillary lymph node dissection) and have pathologically confirmed uninvolved lymph nodes. All lymph nodes must be pathologically negative (pN0[i-]). pN0(i+), pN1mic, pN1-pN3 axillary lymph nodes are not allowed Although an axillary lymph node dissection is not anticipated for low-risk ER positive breast cancers, axillary lymph node dissection is permissible
- •Patient must have physician-reported "excellent" or "good" cosmesis post-lumpectomy and prior to radiation therapy based on the 4-point Global Cosmetic Score
- •Women of childbearing potential (WOCBP): Negative urine or serum pregnancy test.
- •If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required
- •Agreement by females of childbearing potential* to use an effective method of birth control or abstain from heterosexual activity for the course of the study through at least 1 month after the last dose of protocol therapy
- •Childbearing potential is defined as not being surgically sterilized or have not been free from menses for > 1 year
排除标准
- •Any prior treatment with radiation therapy, anti-endocrine/hormone therapy, chemotherapy or biologic therapy for the currently diagnosed breast cancer PRIOR to surgical resection
- •Prior radiation to the region of the involved breast that in the opinion of the investigator would preclude partial breast irradiation
- •Clinically significant uncontrolled illness
- •Diagnosis of Paget's disease of the nipple
- •Other prior or active malignancy. Patients 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
- •Pregnant or breastfeeding
- •Prospective participants who, in the opinion of the investigator, may not be able to comply with all study procedures (including compliance issues related to feasibility/logistics)
研究组 & 干预措施
Supportive care (APBI)
Patients undergo APBI QD on consecutive business days for 5 treatments.
干预措施: Accelerated Partial Breast Irradiation (Radiation)
结局指标
主要结局
Proportion of women that rate the cosmetic appearance of the breast as acceptable ("excellent" or "good")
时间窗: At 1 year post accelerated partial breast irradiation once daily (APBI QD)
Measured by the 4-point Global Cosmetic Score (GCS). The exact test will be used to test the hypothesis that the rate of cosmesis is \>= 90% versus the null hypothesis that cosmesis is 74% or lower, at the 5% significance level.
次要结局
- Cosmetic outcome assessed by the physician post-APBI QD(Over time at baseline, day 5, 1 month, 6 months 1 year, 2 years and 3 years)
- Distant metastases(Up to 5 years post-APBI QD)
- Disease-free survival(Up to 5 years post-APBI QD)
- Regional recurrence(Up to 5 years post-APBI QD)
- Incidence of adverse events-patients reported(Up to 3 years post-APBI)
- In-breast recurrence(Up to 5 years post-APBI QD)
- Overall survival(Up to 5 years post-APBI QD)
- Cosmetic outcome by the patient post-APBI QD(Over time at baseline, day 5, 1 month, 6 months, 1 year, 2 years and 3 years)
- Incidence of adverse events-treatment team reported(Up to 3 years post-APBI)
- Cosmetic outcome assessed by the physician post-APBI QD(At 1 year)