Evidence map›Paper›PMID 41847206›Full record

ArticleQatar medical journal2026

The impact of neoadjuvant chemotherapy on immunohistochemistry and molecular subtype in breast cancer: A retrospective analysis from Oman.

Mustafa Talib Al-Ani, Asila Rashid Al Ismaili, Nahad Al-Mahrouqi, Hasan Al-Sayegh, Khalid Al Baimani, Hind Saif Ali Alshahi, Arti Trehan, Zaid Al-Ishaq, Marwa Youssef, Asma Naaz Nadaf and 1 more

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Article in Qatar medical journal, 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

11 authors.

Mustafa Talib Al-AniDepartment of Surgery, Sultan Qaboos Comprehensive Cancer Care and Research Centre, University Medical City, Oman.
Asila Rashid Al IsmailiDepartment of Surgery, Sultan Qaboos Comprehensive Cancer Care and Research Centre, University Medical City, Oman.
Nahad Al-MahrouqiResearch Laboratories Department, Sultan Qaboos Comprehensive Cancer Care and Research Centre, University Medical City, Oman.
Hasan Al-SayeghResearch Laboratories Department, Sultan Qaboos Comprehensive Cancer Care and Research Centre, University Medical City, Oman.
Khalid Al BaimaniDepartment of Medicine, Sultan Qaboos Comprehensive Cancer Care and Research Centre, University Medical City, Oman.
Hind Saif Ali AlshahiDepartment of Surgery, Sultan Qaboos Comprehensive Cancer Care and Research Centre, University Medical City, Oman.
Arti TrehanDepartment of Pathology, Sultan Qaboos Comprehensive Cancer Care and Research Centre, University Medical City, Oman *Email: mustafa.talib.2@gmail.com.
Zaid Al-IshaqDepartment of Surgery, Sultan Qaboos Comprehensive Cancer Care and Research Centre, University Medical City, Oman.
Marwa YoussefDepartment of Surgery, Sultan Qaboos Comprehensive Cancer Care and Research Centre, University Medical City, Oman.
Asma Naaz NadafDepartment of Pathology, Sultan Qaboos Comprehensive Cancer Care and Research Centre, University Medical City, Oman *Email: mustafa.talib.2@gmail.com.
Adil Aljarrah AlajmiDepartment of Surgery, Sultan Qaboos Comprehensive Cancer Care and Research Centre, University Medical City, Oman.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Neoadjuvant chemotherapy (NACT) is used in breast cancer (BC) to downsize and downstage the tumor before surgery. Different studies were conducted looking into the alterations in the immunohistochemistry after NACT, which may alter the adjuvant treatment. Our study aimed to assess the changes in immunohistochemistry biomarker status (estrogen receptor [ER], progesterone receptor [PR], and human epidermal growth factor receptor 2 [HER2]) in BC cells after administration of NACT at a single institution in Oman. Methods: We conducted a retrospective cross-sectional study on patients with BC with residual disease post-NACT in a single institution and studied immunohistochemistry status changes before and after NACT. We used the McNemar test to evaluate the receptor changes, and logistic regression to assess the effect of risk factors on receptor status change. Results: All biomarkers changed after NACT, with a tendency for BC cells to lose PR and HER2 expression and gain ER expression. The immunohistochemistry changes were 36/114 (31.6%) in PR, 7/114 (6.1%) in ER, and 11/114 (9.6%) in HER2. BC subtypes changed in 4/114 (3.5%) of HER2+ve, 10/114 (8.8%) of hormone positive (ER or PR) with HER2 overexpression (HER2+ve/HR+ve), 3/114 (2.6%) in hormone positive with HER2 negative (HR+ve), and 3/114 (2.6%) triple-negative BCs. These changes resulted in adjuvant treatment adjustments in 9/110 (8.18%) patients with residual disease. Conclusion: Changes in the expression of all immunohistochemistry biomarkers and BC subtypes occurred after NACT, which led to changes in adjuvant treatment in specific cases.

Indexed as

breast neoplasmsErbB-2 receptorsEstrogen receptorsNeoadjuvant therapyProgesterone receptors

Identifiers

PMID41847206
PMCPMC12969371

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