Effect of Total Breast Reconstruction With Autologous Fat Transfer Using an Expansion Device vs Implants on Quality of Life Among Patients With Breast Cancer

Author:

Piatkowski Andrzej A.123,Wederfoort Jamilla L. M.12,Hommes Juliette E.12,Schop Sander S. J.12,Krastev Todor K.1,van Kuijk Sander M. J.4,van der Hulst René R. W. J.12,Piatkowski Andrzej5,Wederfoort Jamilla LM5,Hommes Juliette E5,Schop Sander SJ5,Krastev Todor K5,van Kuijk Sander MJ5,van der Hulst René RWJ5,Derks Danielle5,Larsen Mikko5,Rakhorst Hinne5,Schmidbauer Ute5,Smit Jan Maerten5,Tan Liang T5,Wehrens Kim M E5,de Wit Thijs5,

Affiliation:

1. Department of Plastic, Reconstructive, and Hand Surgery, Maastricht University Medical Centre+, Maastricht, the Netherlands

2. NUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, the Netherlands

3. Department of Plastic, Reconstructive, and Hand Surgery, VieCuri Medical Center, Venlo, the Netherlands

4. Department of Clinical Epidemiology and Medical Technology Assessment (KEMTA), Maastricht University Medical Centre+, Maastricht, the Netherlands

5. for the Breast Reconstruction With External Preexpansion & Autologous Fat Transfer vs Standard Therapy (BREAST) Trial Investigators

Abstract

ImportanceThere is a need for a new, less invasive breast reconstruction option for patients who undergo mastectomy in their breast cancer treatment.ObjectiveTo investigate quality of life (QoL) among patients undergoing a new breast reconstruction technique, autologous fat transfer (AFT), compared with that among patients undergoing implant-based reconstruction (IBR).Design, Setting, and ParticipantsThe BREAST trial was a randomized clinical trial conducted between November 2, 2015, and October 31, 2021, performed in 7 hospitals across the Netherlands. Follow-up was 12 months. Referrals could be obtained from general practitioners and all departments from participating or nonparticipating hospitals. The patients with breast cancer who had undergone mastectomy and were seeking breast reconstruction were screened for eligibility (radiotherapy history and physique) by participating plastic surgeons. Patients receiving postmastectomy radiotherapy were excluded.InterventionsBreast reconstruction with AFT plus expansion or 2-phased IBR. Randomization was done in a 1:1 ratio.Main Outcomes and MeasuresThe statistical analysis was performed per protocol. The predefined primary outcome was QoL at 12 months after final surgery. This was measured by the BREAST-Q questionnaire, a validated breast reconstruction surgery questionnaire. Questions on the BREAST-Q questionnaire are scored from 0 to 100, with a higher score indicating greater satisfaction or better QoL (depending on the scale). Secondary outcomes were breast volume and the safety and efficacy of the techniques.ResultsA total of 193 female patients (mean [SD] age, 49.2 [10.6] years) 18 years or older who desired breast reconstruction were included, of whom 91 patients in the AFT group (mean [SD] age, 49.3 [10.3] years) and 80 in the IBR group (mean age, 49.1 [11.0] years) received the allocated intervention. In total, 64 women in the AFT group and 68 women in the IBR group completed follow-up. In the IBR group, 18 patients dropped out mainly due to their aversion to implant use while in the AFT group 6 patients ended their treatment prematurely because of the burden (that is, the treatment being too heavy or tiring). The BREAST-Q scores were higher in the AFT group in all 5 domains and significantly higher in 3: satisfaction with breasts (difference, 9.9; P = .002), physical well-being: chest (difference; 7.6; P = .007), and satisfaction with outcome (difference, 7.6; P = .04). Linear mixed-effects regression analysis showed that QoL change over time was dependent on the treatment group in favor of AFT. The mean (SD) breast volume achieved differed between the groups (AFT: 300.3 [111.4] mL; IBR: 384.1 [86.6] mL). No differences in oncological serious adverse events were found.Conclusions and RelevanceThis randomized clinical trial found higher QoL and an increase in QoL scores over time in the AFT group compared with the IBR group. No evidence was found that AFT was unsafe. This is encouraging news since it provides a third, less invasive reconstruction option for patients with breast cancer.Trial RegistrationClinicalTrials.gov Identifier: NCT02339779

Publisher

American Medical Association (AMA)

Subject

Surgery

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