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Immediate DIEP flap breast reconstruction following neoadjuvant therapy: Histopathological assessment of vascular integrity in internal mammary and deep inferior epigastric arteries

dc.contributor.authorGuray, Seyda
dc.contributor.authorErdem, Ilhan
dc.contributor.authorAre, Nursah
dc.contributor.authorAytekin, Bugra Mert
dc.contributor.authorDogan, Zeynep Deniz Akdeniz
dc.contributor.authorUgurlu, Mustafa Umit
dc.contributor.authorCinel, Leyla
dc.contributor.authorSacak, Bulent
dc.date.accessioned2026-11-05T11:00:55Z
dc.date.issued2026
dc.description.abstractBackground: The impact of neoadjuvant chemotherapy (CT) and radiotherapy (RT) on the microvasculature critical for autologous breast reconstruction remains unclear. The internal mammary artery (IMA) and deep inferior epigastric artery (DIEA) are key conduits in deep inferior epigastric perforator (DIEP) free flap surgery. Prior studies suggest that radiation and chemotherapeutic agents may induce vascular injury; however, the clinical relevance of such alterations in flap viability is debated. We aimed to evaluate whether neoadjuvant CT or combined CT+RT induce histopathological changes in the IMA and DIEA that could affect microvascular anastomosis or DIEP flap outcomes. Methods: This single-center retrospective cohort study included 83 female patients with breast cancer who underwent nipple-sparing mastectomy followed by immediate DIEP flap reconstruction between 2019 and 2023. Patients were divided into three groups: no neoadjuvant therapy (Group 1), CT only (Group 2), and CT+RT (Group 3). Arterial segments from IMA and DIEA were histologically examined for tunica media thickness, lumen area, atherosclerosis, calcification, and elastic fiber fragmentation. Clinical parameters including anastomosis time and flap loss were also analyzed. Statistical analyzes were performed using ANOVA, Kruskal-Wallis, chi-square, or Fishers's exact tests, as appropriate. Results: No significant differences were observed among the groups in terms of tunica media thickness (IMA, p = 0.230; DIEA, p = 0.327), lumen area (IMA, p = 0.061; DIEA, p = 0.134), atherosclerosis scores, or calcification. Elastic fiber fragmentation in the IMA also did not differ significantly (p = 0.627). Flap loss occurred in 5 of 83 patients (6%) and was comparable across the groups (p = 0.131). Mean anastomosis times were 60.7 +/- 13.3, 55.1 +/- 11.7, and 66.1 +/- 14.8 in groups 1, 2, and 3, respectively (p = 0.011). Conclusion: Neoadjuvant CT and RT do not appear to cause significant histopathological deterioration of the IMA or DIEA. Immediate DIEP flap reconstruction performed at the time of mastectomy after neoadjuvant therapy appears to be microsurgically feasible and clinically safe. (c) 2026 British Association of Plastic, Reconstructive and Aesthetic Surgeons. Published by Elsevier Ltd. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
dc.description.pages91-98
dc.description.volume122
dc.identifier.doi10.1016/j.bjps.2026.08.031
dc.identifier.issn1748-6815
dc.identifier.issn1878-0539
dc.identifier.urihttps://doi.org/10.1016/j.bjps.2026.08.031
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/10597
dc.identifier.wosWOS:001872151900001
dc.language.isoen
dc.publisherELSEVIER SCI LTD
dc.relation.hasversion10.1016/j.bjps.2026.08.031
dc.relation.ispartofJOURNAL OF PLASTIC RECONSTRUCTIVE AND AESTHETIC SURGERY
dc.subjectAutologous reconstruction
dc.subjectBreast cancer
dc.subjectDIEP flap
dc.subjectInternal mammary artery
dc.subjectMicrovascular surgery
dc.subjectNeoadjuvant therapy
dc.subjectHEART-DISEASE
dc.subjectRADIATION
dc.subjectCOMPLICATIONS
dc.subjectCHEMOTHERAPY
dc.subjectTOXICITY
dc.subjectSurgery
dc.titleImmediate DIEP flap breast reconstruction following neoadjuvant therapy: Histopathological assessment of vascular integrity in internal mammary and deep inferior epigastric arteries
dc.typeArticle
oaire.citation.editionScience Citation Index Expanded (SCI-EXPANDED)
oaire.citation.endPage98
oaire.citation.startPage91
oaire.citation.volume122
person.identifier.ridPHN-6739-2026
person.identifier.ridLWK-8341-2024
person.identifier.ridABB-6668-2020

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