Prophylactic Irradiation to the Contralateral Breast for BCAs Patients
NCT ID: NCT04960839
Last Updated: 2021-07-14
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
323 participants
INTERVENTIONAL
2023-01-01
2029-12-01
Brief Summary
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Besides the increased breast cancer risk for the inherited mutation carriers, the risk of subsequent contralateral breast cancer for the mutation carriers with breast cancer was also significantly increased. Contralateral prophylactic mastectomy was usually recommended to the breast cancer patients with BRCA mutation. However, many breast cancer patients refused the contralateral prophylactic mastectomy, due to the surgical injury, potential surgical complications, deleteriously affected body image and sexuality.
Solid evidence validated that radiotherapy after surgery resulted in a reduced local recurrence for three times lower than surgery alone. It is thought that radiation would eliminate the microscopic tumors which may already exist in the breast. Thus, we proposed that for the breast cancer patients with BRCA1, BRCA2 or PALB2 deleterious germline mutations, prophylactic irradiation to the contralateral breast may reduce the risk of subsequent contralateral breast cancer. And we would like to further compare the effect of prophylactic irradiation to the published data from traditional prophylactic contralateral mastectomy.
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Detailed Description
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About 5% to 10% of breast cancers are hereditary. Most inherited cases of breast cancer are associated with germline mutations in two genes: BRCA1 (BRCA1 DNA repair associated) and BRCA2 (BRCA2 DNA repair associated). The cumulative breast cancer risk for BRCA1 or BRCA2 mutation carriers at age 70 years reached as high as 50% in US population and 37% in Chinese population. Benefiting from the next generation sequencing technology, more inherited gene mutations were discovered. Among these new discovered susceptibility genes, PALB2 (Partner and localizer of BRCA2) was associated with high increased risks of breast cancer in both Chinese and US population.
Besides the increased breast cancer risk for the inherited mutation carriers, the risk of subsequent contralateral breast cancer for the mutation carriers with breast cancer was also significantly increased. For contralateral breast cancer in BRCA mutation carriers, the cumulative risk for 10 years after breast cancer diagnosis was as high as 25% and for 20 years reached to 40%, as compared 3% and 12% respectively in non-carriers. Contralateral prophylactic mastectomy was usually recommended to the breast cancer patients with BRCA mutation, as it can absolutely reduce the risk of contralateral primary cancer. However, many breast cancer patients refused the contralateral prophylactic mastectomy, due to the surgical injury, potential surgical complications, deleteriously affected body image and sexuality.
Solid evidence validated that radiotherapy after surgery resulted in a reduced local recurrence for three times lower than surgery alone. It is thought that radiation would eliminate the microscopic tumors which may already exist in the breast. Thus, we proposed that for the breast cancer patients with BRCA1, BRCA2 or PALB2 deleterious germline mutations, prophylactic irradiation to the contralateral breast may reduce the risk of subsequent contralateral breast cancer. And we would like to further compare the effect of prophylactic irradiation to the published data from traditional prophylactic contralateral mastectomy.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
TRIPLE
Study Groups
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Standard group
Standard loco-regional treatment without prophylactic contralateral breast irradiation
No interventions assigned to this group
Prophylactic irradiation group
Standard loco-regional treatment with prophylactic contralateral breast irradiation
Prophylactic contralateral breast irradiation
The whole contralateral breast will be irradiated once daily, 5 days a week, for 5-6 weeks, using 1.8-2 Gy/fx to a total dose of 45-50 Gy.
Interventions
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Prophylactic contralateral breast irradiation
The whole contralateral breast will be irradiated once daily, 5 days a week, for 5-6 weeks, using 1.8-2 Gy/fx to a total dose of 45-50 Gy.
Eligibility Criteria
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Inclusion Criteria
* Patients with a deleterious germline mutation of BRCA 1/2 or PALB2.
* The patients with no contraindictation for irradiation.
* The patients consent for prophylactic irradiation to the contralateral breast.
* The patient may receive any regimen of adjuvant, neoadjuvant chemotherapy, according to the treating physician. The radiation therapy should start at least 2 weeks after the completion of all the chemotherapy cycles.
* The patient may receive endocrine therapy before, during or after study entry.
* The patient may receive target therapy (Trastuzumab) before, during or after study entry.
* The patient must be eligible for MRI examination of the contralateral breast.
* The patient refused prophylactic contralateral mastectomy and oophorectomy.
Exclusion Criteria
* Past history of other cancer besides breast cancer
* Previous irradiation of the breast or chest wall, but not for breast cancer treatment
* Synchronous bilateral breast cancer
* Patients with active connective tissue diseases, pneumonia are excluded due to the potential risk of significant radiotherapeutic toxicity.
30 Years
70 Years
FEMALE
No
Sponsors
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Second Affiliated Hospital, School of Medicine, Zhejiang University
OTHER
Responsible Party
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Principal Investigators
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Peifen Fu, M.D.
Role: PRINCIPAL_INVESTIGATOR
Department of Breast Surgery, The First Affiliated Hospital, College of Medicine, Zhejiang University
Wenjun Chen, M.D.
Role: PRINCIPAL_INVESTIGATOR
Department of Surgical Oncology, Sir Run Run Shaw Hospital, Zhejiang University
Kejin Wu, M.D.
Role: PRINCIPAL_INVESTIGATOR
Department of Breast Surgery, Obsterics and Gynecology Hospital of Fudan University
Xiaowen Ding, M.D.
Role: PRINCIPAL_INVESTIGATOR
Department of Breast Surgery, Cancer Hospital of University of Chinese Academy of Sciences
Zhengkui Sun
Role: PRINCIPAL_INVESTIGATOR
Department of Breast Surgery, Jiangxi Provincial Cancer Hospital
Mikael Hartman
Role: PRINCIPAL_INVESTIGATOR
Department of Surgery, Yong Loo Lin School of Medicine, National University of Singapore
Yiding Chen
Role: PRINCIPAL_INVESTIGATOR
Department of Breast Surgery, The Second Affiliated Hospital, Zhejiang University School of Medicine
Jiaojiao Zhou
Role: PRINCIPAL_INVESTIGATOR
Departmen of Breast Surgery, The Second Affiliated Hospital, Zhejiang University School of Medicine
Kun Zhang
Role: PRINCIPAL_INVESTIGATOR
Departmen of Breast Surgery, The Second Affiliated Hospital, Zhejiang University School of Medicine
Wenhong Xu
Role: PRINCIPAL_INVESTIGATOR
Departmen of Radiology, The Second Affiliated Hospital, Zhejiang University School of Medicine
Zhibing Wu
Role: PRINCIPAL_INVESTIGATOR
Department of Oncology, Zhejiang Hospital
Locations
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Department of Breast Surgery, Jiangxi Provincial Cancer Hospital
Jiangxi, Jiangxi, China
Department of Breast Surgery, Obestrics and Gynecology Hospital of Fudan University
Shanghai, Shanghai Municipality, China
Department of Breast Surgery, Cancer Hospital of University of Chinese Academy of Sciences
Hangzhou, Zhejiang, China
Department of Breast Surgery, the First Affiliated Hospital, College of Medicine, Zhejiang University
Hangzhou, Zhejiang, China
Department of Breast Surgery, the Second Affiliated Hospital, Zhejiang University School of Medicine
Hangzhou, Zhejiang, China
Department of Surgical Oncology, Sir Run Run Shaw Hospital, Zhejiang University
Hangzhou, Zhejiang, China
Department of Oncology, Zhejiang Hospital
Hangzhou, Zhejiang, China
Department of Breast Surgery, Yong Loo Lin School of Medicine, National University of Singapore
Singapore, , Singapore
Countries
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Central Contacts
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Facility Contacts
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Zhengkui Sun, M.D.
Role: primary
Kejin Wu, M.D.
Role: primary
Xiaowen Ding, M.D.
Role: primary
Peifen Fu, M.D.
Role: primary
Yiding Chen, M.D.
Role: primary
Weijun Cjen, M.D.
Role: primary
Zhibing Wu
Role: primary
Mikael Hartman
Role: primary
Other Identifiers
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2019-228
Identifier Type: -
Identifier Source: org_study_id
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