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Prospective Study of Particle Radiotherapy for Breast Cancer With Different Arm Position

Prospective Phase II Randomized Clinical Study of the Accuracy of Multi-modal Guided Particle Radiotherapy for Postoperative Breast Cancer With Different Arm Position

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05878678
Enrollment
200
Registered
2023-05-26
Start date
2023-05-15
Completion date
2024-07-30
Last updated
2023-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

immobilization positions, breast cancer, particle radiotherapy, dosimetry, multi-modal guided radiotherapy

Brief summary

The optical body surface image (C-RAD) was used to guide and track the change of positions, and multimodal images (including 2D X-ray images, CT images and PET-CT images) were used to verify the treatment positions. In order to explore the accuracy of breast cancer patients' treatment positions and its impact on dose of the new fixation device in two different fixed positions of arm up and arm down, optimize the position fixed equipment and methods of particle radiotherapy for breast cancer, and then establish the precision process of particle radiotherapy for breast cancer under the guidance of multimodal images. In a word, this is a dosimetry and prospective Phase II randomized clinical study of the accuracy of multi-modal guided particle radiotherapy for postoperative breast cancer with different arm position.

Detailed description

PET-CT: Positron Emission Tomography - Computed Tomography CT: Computed Tomography

Interventions

DEVICEFixed positions of arm down and arm up

In order to explore the accuracy of breast cancer patients' treatment positions and its impact on dose of the new fixation device in two different fixed positions of arm up and arm down, optimize the position fixed equipment and methods of particle radiotherapy for breast cancer, and then establish the precision process of particle radiotherapy for breast cancer under the guidance of multimodal images.

Sponsors

Shanghai Proton and Heavy Ion Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Patients with pathologically (cytological or histological) confirmed breast cancer with positive lymph nodes and postoperative adjuvant radiotherapy 2. Exclude distant metastasis 3. No ipsilateral breast and breast radiation therapy 4. Exclude patients requiring axillary irradiation 5. Age 18-80 years old 6. General good health (Eastern Cooperative Oncology Group, ECOG 0-2) 7. No complications such as severe pulmonary hypertension, cardiovascular disease, peripheral vascular disease, or severe chronic heart disease that may affect radiotherapy. 8. Non-pregnant (confirmed by serum or urine β-HCG test) or lactating women 9. Patients must sign informed consent to receive radiotherapy.

Exclusion criteria

1. Pathology unapproved breast cancer 2. With distant metastasis 3. The ipsilateral breast or breast has received radiation therapy 4. Patients requiring axillary irradiation 5. The dose limit of organs at risk cannot reach the preset safe dose limit 6. Pregnancy (confirmed by serum or urine β-HCG test) or lactation 7. Poor general health, Karnofsky Performance Status (KPS)\<70,or ECOG\>2 8. Severe complications that may affect radiotherapy, including: a) Unstable angina pectoris, congestive heart failure, myocardial infarction requiring hospitalization in the past 6 months, b) acute bacterial or systemic fungal infection, c) hospitalization for exacerbations of chronic obstructive pulmonary disease (COPD) or other respiratory diseases 9. Unable to understand the purpose of treatment or unwilling to sign the treatment consent

Design outcomes

Primary

MeasureTime frameDescription
The accuracy of multi-modal guided particle radiotherapy for postoperative breast cancer with different immobilization positionwithin 3 months after radiotherapyThe optical body surface image (C-RAD) was used to guide and track the change of positions, and multimodal images (including 2D X-ray images, CT images and PET-CT images) were used to verify the treatment positions. In order to explore the accuracy of breast cancer patients' treatment positions and its impact on dose of the new fixation device in two different fixed positions of arm up and arm down, optimize the position fixed equipment and methods of particle radiotherapy for breast cancer, and then establish the precision process of particle radiotherapy for breast cancer under the guidance of multimodal images.

Secondary

MeasureTime frameDescription
Acute toxicitieswithin 3 months after radiotherapyAcute toxicities assessed by Common Terminology Criteria for Adverse Events (CTCAE) Version 4.03
Late toxicities> 3 months after radiotherapyLate toxicities assessed by Toxicity criteria of the Radiation Therapy Oncology Group (RTOG) and the European organization for research and treatment of cancer (EORTC)
Tumor local control rateat 5 years post radiotherapy
Overall survival rateat 5 years post radiotherapy
Progression free survival rateat 5 years post radiotherapy

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026