Neoadjuvant Radiotherapy and Immediate Implant-Based Breast Reconstruction

Sponsor
Hubei Cancer Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05992870
Collaborator
(none)
40
1
1
27.8
1.4

Study Details

Study Description

Brief Summary

Neoadjuvant radiotherapy(NART) followed by mastectomy and immediate DIEP flap reconstruction is feasible and technically safe. However, reports of NACT followed immediate implant-based breast reconstruction are rare. Some studies have shown that NART followed immediate implant-based breast reconstruction seems feasible and can be safely attempted. It's well known that radiotherapy after implant-based breast reconstruction have negative effects on implant and cosmetic results. So, investigators conducted a polit study to learn about acute post-surgical complications following skin-sparing mastectomy and immediate implant-based breast reconstruction after NART.

Condition or Disease Intervention/Treatment Phase
  • Radiation: Neoadjuvant radiotherapy
N/A

Detailed Description

Radiotherapy after implant-based breast reconstruction have negative effects on implant and cosmetic results, including severe capsular contracture, mastectomy flap necrosis ,reoperation and so on. Postmastectomy radiotherapy( PMRT )is associated with implant reconstruction failure. PRADA study has shown neoadjuvant radiotherapy followed by skin-sparing mastectomy and immediate DIEP flap reconstruction is feasible and technically safe. The investigators assume that neoadjuvant radiotherapy can avoid the negative effects of PMRT on an implant and the capsule of an implant and would lead to better cosmetic results and less complications compared to PMRT. Furthermore, some studies have shown that NART could potentially result in shorter time between diagnosis and treatment completion. So, investigators conducted a polit study to learn about acute post-surgical complications following skin-sparing mastectomy and immediate implant-based breast reconstruction after NART.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
40 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Neoadjuvant Radiotherapy and Immediate Implant-Based Breast Reconstruction
Actual Study Start Date :
Jul 8, 2023
Anticipated Primary Completion Date :
Jul 8, 2025
Anticipated Study Completion Date :
Oct 31, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Neoadjuvant radiotherapy group

Radiotherapy followed by skin-sparing mastectomy and immediate implant-based reconstruction in HBCH

Radiation: Neoadjuvant radiotherapy
In case of neoadjuvant chemotherapy, RT will start 3-4 weeks after the last course of chemotherapy. A dose of 15 x 2.67 Gy 5 fractions or 16 x 2.67Gy 5 fractions per week. A skin-sparing mastectomy and a immediate implant-based breast reconstruction will be performed, approximately 2-6 weeks after latest radiotherapy treatment.

Outcome Measures

Primary Outcome Measures

  1. Postoperative complications at 3 months following skin-sparing mastectomy and immediate implant-based breast reconstruction after NART [3 months following skin-sparing mastectomy and immediate breast reconstruction]

    Surgical complications are defined as any complication requiring surgical intervention necessary within a period up to three months after the final reconstruction. Including Infection, hematoma , loss of implant or flap, fat necrosis, wound breakdown,defined and scored using the C-DC37.

Secondary Outcome Measures

  1. Number of participants with treatment-related adverse events as assessed by CTCAE v4.0 . [Within 3 months after both breast reconstruction and radiotherapy]

    Other adverse events following NART or surgery other than described in the primary outcome measure.

  2. Number of participants with removal of implant. [6 months after surgery]

    Implant are removed for postoperative complications.

  3. Patient satisfaction. [3 months and 12 months after surgery]

    Patient satisfaction (as measured using the BREAST-Q reconstruction module) before, 3 months after, and 12 months after surgery.

  4. Pathological complete response (pCR) assessed in skin-sparing mastectomy specimen [Within 2 weeks after skin-sparing mastectomy]

    A pCR was defined as absence of invasive and in situ carcinoma in the breast, irrespective of nodal status (ypT0).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 75 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
Women >18 years with histopathologically-confirmed breast cancer, who:
  • require mastectomy for any reason

  • a known indication for (adjuvant) radiotherapy

  • require implant-based breast reconstruction

Exclusion Criteria:
  • Inability to give informed consent

  • MDT unable to make recommendation for radiotherapy based on pre-operative histopathological and imaging findings

  • Previous history of breast cancer or another malignancy for which radiotherapy of the breast or axilla

  • Pregnant or lactating

  • inflammatory breast cancer

Contacts and Locations

Locations

Site City State Country Postal Code
1 Xinhong Wu Wuhan Hubei China 430079

Sponsors and Collaborators

  • Hubei Cancer Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Xinhong Wu, vice-president, Hubei Cancer Hospital
ClinicalTrials.gov Identifier:
NCT05992870
Other Study ID Numbers:
  • NeoRTIBR
First Posted:
Aug 15, 2023
Last Update Posted:
Aug 15, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Xinhong Wu, vice-president, Hubei Cancer Hospital

Study Results

No Results Posted as of Aug 15, 2023