Evidence map›Paper›PMID 42192428›Full record

ArticleWorld journal of surgical oncology2026

Exploring the impacts of docetaxel and paclitaxel based neoadjuvant therapies on early postoperative complications in HER2-positive breast cancer patients.

Mehmet Furkan Sagdic, Emre Tunc, Seher Kaya, Mahmut Onur Kulturoglu, Özgen Ahmet Yıldırım, Lutfı Dogan

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Article in World journal of surgical oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Mehmet Furkan SagdicDepartment of Surgical Oncology, Ankara Etlik City Hospital, Ankara, Turkey. m.f.sagdic@gmail.com.ORCID http://orcid.org/0000-0002-3598-1625
Emre TuncDepartment of Surgical Oncology, Mehmet Akif İnan Training and Research Hospital, Şanlıurfa, Turkey.ORCID http://orcid.org/0000-0003-2177-7065
Seher KayaDepartment of Medical Oncology, Ankara Etlik City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0001-5418-507X
Mahmut Onur KulturogluDepartment of Surgical Oncology, Ankara Etlik City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0003-2293-7139
Özgen Ahmet YıldırımDepartment of Medical Oncology, Ankara Etlik City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0002-4139-067X
Lutfı DoganDepartment of Surgical Oncology, Ankara Etlik City Hospital, Ankara, Turkey.ORCID http://orcid.org/0000-0002-3834-0911

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHER2-positive breast cancer accounts for 15-20% of all breast cancer cases. Anti-HER2-based neoadjuvant therapy combined with taxanes, particularly docetaxel and paclitaxel, constitutes the standard treatment approach. Although these regimens are widely used, most studies have focused on systemic adverse effects, with limited data addressing their impact on postoperative surgical complications. This study aimed to evaluate the association between docetaxel- and paclitaxel-based neoadjuvant regimens and early wound complications in HER2-positive breast cancer patients.

methodWe retrospectively analyzed 139 patients with HER2-positive breast cancer who underwent breast-conserving surgery following neoadjuvant therapy at Ankara Etlik City Hospital between October 2022 and January 2025. Patients were grouped according to the taxane received (docetaxel, n = 95; paclitaxel, n = 44). Demographic, clinicopathologic characteristics, and early postoperative wound complications were compared. Major complications were defined as major wound dehiscence and skin necrosis. Associations between variables and major complications were evaluated using univariate analysis.

resultsMajor complications were significantly more frequent in the docetaxel group compared to the paclitaxel group (9.5% vs. 0%, p = 0.022), while no significant difference was observed in minor complications (p = 0.704). In subgroup analysis excluding patients who underwent axillary lymph node dissection, this association remained significant (11.1% vs. 0%, p = 0.034).

conclusionsDocetaxel-based neoadjuvant therapy was associated with a higher rate of major postoperative wound complications compared with paclitaxel-based regimens in patients with HER2-positive breast cancer. This association persisted after excluding patients who underwent axillary lymph node dissection. These findings should be interpreted with caution due to the retrospective design and limited number of events.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBreast NeoplasmsMastectomy, SegmentalNeoadjuvant TherapyPostoperative ComplicationsAdultAgedDocetaxelErb-b2 Receptor Tyrosine KinasesFemaleFollow-Up StudiesHumansMiddle AgedPaclitaxelPrognosisRetrospective StudiesDocetaxelERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesPaclitaxelBreast cancerDocetaxelHER2-positiveNeoadjuvant therapyPaclitaxelPostoperative complications

Identifiers

PMID42192428
PMCPMC13393861

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.