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Protocol for the postoperative radiotherapy in N1 breast cancer patients (PORT-N1) trial, a prospective multicenter, randomized, controlled, non-inferiority trial of patients receiving breast-conserving surgery or mastectomy

Authors
 Tae Hoon Lee  ;  Ji Hyun Chang  ;  Bum-Sup Jang  ;  Jae Sik Kim  ;  Tae Hyun Kim  ;  Won Park  ;  Yong Bae Kim  ;  Su Ssan Kim  ;  Wonshik Han  ;  Han-Byoel Lee  ;  Kyung Hwan Shin 
Citation
 BMC CANCER, Vol.22(1) : 1179, 2022-11 
Journal Title
BMC CANCER
Issue Date
2022-11
MeSH
Breast Neoplasms* / radiotherapy ; Breast Neoplasms* / surgery ; Clinical Trials, Phase III as Topic ; Female ; Humans ; Lymph Node Excision ; Mastectomy / methods ; Mastectomy, Segmental* / methods ; Multicenter Studies as Topic ; Prospective Studies ; Randomized Controlled Trials as Topic
Keywords
Adjuvant radiotherapy ; Breast cancer ; Lumpectomy ; Mastectomy ; pN1
Abstract
Background: Postoperative radiotherapy (PORT) could be useful for pN1 breast cancer patients who have undergone breast-conserving surgery (BCS) or mastectomy. However, the value of regional nodal irradiation (RNI) for BCS patients, and the indications for post-mastectomy radiotherapy (PMRT) for pN1 breast cancer mastectomy patients, have recently been challenged due to the absence of relevant trials in the era of modern systemic therapy. "PORT de-escalation" should be assessed in patients with pN1 breast cancer.

Methods: The PORT-N1 trial is a multicenter, randomized, phase 3 clinical trial for patients with pN1 breast cancer that compares the outcomes of control [whole-breast irradiation (WBI) and RNI/PMRT] and experimental (WBI alone/no PMRT) groups. PORT-N1 aims to demonstrate non-inferiority of the experimental group by comparing 7-year disease-free survival rates with the control group. Female breast cancer patients with pT1-3 N1 status after BCS or mastectomy are eligible. Participants will be randomly assigned to the two groups in a 1:1 ratio. Randomization will be stratified by surgery type (BCS vs. mastectomy) and histologic subtype (triple-negative vs. non-triple-negative). In patients who receive mastectomy, dissection of ≥5 nodes is required when there is one positive node, and axillary lymph node dissection when there are two or three positive nodes. Patients receiving neoadjuvant chemotherapy are not eligible. RNI includes a "high-tangent" or wider irradiation field. This study will aim to recruit 1106 patients.

Discussion: The PORT-N1 trial aims to verify that PORT de-escalation after BCS or mastectomy is safe for pN1 breast cancer patients in terms of oncologic outcomes and capable of reducing toxicity rates. This trial will provide information crucial for designing PORT de-escalation strategies for patients with pN1 breast cancer.

Trial registration: This trial was registered at ClinicalTrials.gov (NCT05440149) on June 30, 2022.
Files in This Item:
T9992022554.pdf Download
DOI
10.1186/s12885-022-10285-0
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Radiation Oncology (방사선종양학교실) > 1. Journal Papers
Yonsei Authors
Kim, Yong Bae(김용배) ORCID logo https://orcid.org/0000-0001-7573-6862
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/193325
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