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NCT Number: NCT06830083

Hypofractionated Radiation Fractionation in Breast Cancer Patients With Implant-Based Reconstruction

It is a randomized trial to assess the safety and efficacy between hypofractionation radiation and conventional radiation in women who have undergone mastectomy and immediate breast reconstruction. The investigators will evaluate reconstruction complication, radiotherapy side effects, cosmetic and oncologic outcomes.

Recruiting

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Key information

Age range

18 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Jiangsu Province People's Hospital/The First Affiliated with Nanjing Medical University

Nanjing, Jiangsu, 210029, China

Location status: Recruiting

Location contact

About this study

Patients with breast cancer frequently have requirement for breast reconstruction after mastectomy. For patients with limited autologous tissue availability, implant-based reconstruction remains an effective alternative. Due to the absence of high-level evidence, collaborative efforts between surgical and radiation oncology teams are advised to determine the optimal sequencing and techniques for integrating reconstruction surgery with radiotherapy. The ongoing Alliance A221505 and FABREC phase III randomized controlled trials are comparing the incidence of reconstructive complications following hypofractionated and conventional fractionation radiotherapy. FABREC trial recently showed the hypofractionated regimen did not significantly improve change in physical well-being(PWB), domain of the Functional Assessment of Cancer Therapy-Breast (FACT-B) quality-of-life assessment tool, compared with the conventional fractionation radiotherapy. This trial added to the increasing experience with HF PMRT in patients with implant-based reconstruction.

In 2019, the European Society for Radiotherapy and Oncology (ESTRO) provided guidelines for target delineation based on the position of the implant in breast reconstruction to minimize the irradiation of normal tissues. Existing studies on the risk of complications from irradiating expanders and implants have yielded inconsistent conclusions, with each approach having its own advantages and disadvantages.

Our study aims to compare the incidence of reconstructive complications between hypofractionated and conventional fractionation radiotherapy after implant-based reconstruction surgery to provide high-level evidence for medium-dose hypofractionated radiotherapy after immediate implant-based reconstructive surgery.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Pathological diagnosis of stage I-III breast cancer (non-T4), >18 years old; 2. Complete breast cancer resection (including skin-sparing and nipple-sparing total resection) 3. According to the guidelines of the Chinese Anticancer Society, postoperative adjuvant radiotherapy is required; 4. Undergo immediate reconstructive surgery (tissue dilator or permanent implant)

Exclusion criteria

  • Auto-reconstruction surgery
  • Clinical or pathological T4
  • Both sides need radiotherapy
  • Have a history of chest radiotherapy
  • Pregnancy/lactation
  • Participate in other drug clinical trials

Treatment and study plan

Hypofractionated Radiation Therapy

Radiation

Hypofractionation regimen: Total dose to the chest wall and the regional lymph nodes is 4050 cGy, and each fraction consists of 270 cGy per day(daily, Monday through Friday )

Other names: HF

Conventional fraction radiotherapy

Radiation

Total dose of plan tumor volume is 5000 cGy,and each fraction will consist of 200 cGy per day. 25 fractions(daily, Monday through Friday) to the chest wall and to the supraclavicular (with or without axillary) lymph nodes.

Other names: CF

Primary outcomes

  1. Major complication

    Time frame: From enrollment to the end of treatment at 24 months

    implant related complications requiring reoperation such as severe necrosis,severe infections, severe capsular contracture, implant rupture and implant exposure.

Secondary outcomes

  1. Any breast-related complications

    Time frame: From enrollment to the end of treatment at 24 months

    Complications included infections, wound dehiscence, skin flap necrosis, implant exposure, capsular contracture, seroma, and hematoma.

  2. Absolute reconstruction failure

    Time frame: From enrollment to the end of treatment at 24 months

  3. Oncologic outcomes

    Time frame: From enrollment to the end of treatment at 5 years

    local-regional recurrence free survival

  4. Cosmetic outcomes

    Time frame: From enrollment to the end of treatment at 24 months

    satisfaction with breast and physical and psychosocial well-bing after radiotherapy will be assessed from baseline to 24 months by trained physicians using Breast-Q Version 2.0© Reconstruction Module Scales Chinese (CN) Version .

Study contacts

Contact information is provided by the study sponsor or research team.

Jiangsu Province People's Hospital

CONTACT

[email protected]

86-025-68307676

Sponsors and collaborators

Lead sponsor

The First Affiliated Hospital with Nanjing Medical University

Other

Collaborators

  • Hunan Cancer Hospital
  • Jiangsu Taizhou People's Hospital

Registry information

Acronym: HFIBR

Important dates

Study start
2025
Primary completion
2030
Study completion
2033
First posted
Feb 17, 2025
Registry last updated
Feb 17, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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