Evidence map›Paper›PMID 42286385›Full record

ArticleBreast cancer (Tokyo, Japan)2026

Changes in CD8-positive lymphocytes following chemotherapy with concomitant bevacizumab in HER2-negative breast cancer.

Eriko Narusawa, Ayaka Katayama, Yukio Koibuchi, Daisuke Takata, Chikako Kanno Honda, Sayaka Obayashi, Sasagu Kurozumi, Daisuke Takahari, Ken Shirabe

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Article in Breast cancer (Tokyo, Japan), 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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5 · Who and what money

Authors and funding

9 authors.

Eriko NarusawaDepartment of Breast and Endocrine Surgery, National Hospital Organization Takasaki General Medical Center, Takasaki, Gunma, Japan.
Ayaka KatayamaDivision of Pathology, Shizuoka Cancer Center, Shizuoka, Japan.
Yukio KoibuchiDepartment of Breast and Endocrine Surgery, National Hospital Organization Takasaki General Medical Center, Takasaki, Gunma, Japan.
Daisuke TakataDepartment of Breast and Endocrine Surgery, National Hospital Organization Takasaki General Medical Center, Takasaki, Gunma, Japan.
Chikako Kanno HondaDepartment of Breast and Endocrine Surgery, National Hospital Organization Takasaki General Medical Center, Takasaki, Gunma, Japan.
Sayaka ObayashiDepartment of General Surgical Science, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan.
Sasagu KurozumiDepartment of Breast and Endocrine Surgery, National Hospital Organization Takasaki General Medical Center, Takasaki, Gunma, Japan. skurozumi@gunma-u.ac.jp.ORCID http://orcid.org/0000-0002-0418-5466
Daisuke TakahariDepartment of Medical Oncology, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan.
Ken ShirabeDepartment of General Surgical Science, Gunma University Graduate School of Medicine, Maebashi, Gunma, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBevacizumab is an anti-angiogenic agent that inhibits tumor vascularization and thereby suppresses tumor growth. Tumor-infiltrating lymphocytes (TILs), particularly CD8-positive TILs, play a critical role in the antitumor immune response. However, little is known about the effect of bevacizumab-containing chemotherapy on CD8-positive TIL dynamics. This study aimed to evaluate changes in CD8-positive TILs before and after treatment in patients with advanced breast cancer receiving bevacizumab in combination with chemotherapy.

methodsThirty patients with initially inoperable advanced breast cancer who responded to first-line bevacizumab-containing chemotherapy and subsequently became eligible for surgery were included. CD8-positive TILs were assessed by immunohistochemistry in biopsy samples obtained before treatment and in surgical specimens collected after treatment. Stromal CD8-positive TILs were classified as low, intermediate, or high, based on their proportion among total stromal TILs.

resultsOf the 30 patients, 20 had luminal-like breast cancer and 10 had triple-negative breast cancer. Before treatment, CD8-positive TIL expression was low in 16 patients (64.0%), intermediate in 6 (24.0%), and high in 3 (12.0%). After treatment, 10 patients (33.3%) showed low expression, 11 (36.7%) had intermediate expression, and 9 (30.0%) had high expression, indicating an increase in CD8-positive TIL levels. The high pathological response (a pathological response grade of 2 or higher) rate was 36.7%, and patients with increased CD8-positive TILs tended to show higher pathological response and better overall survival, although these differences did not reach statistical significance. In contrast, the ypT stage was significantly lower in cases with high post-treatment CD8-positive TIL expression, suggesting that immune activation after bevacizumab may contribute to local tumor regression.

conclusionsBevacizumab-containing chemotherapy appears to enhance CD8-positive TIL infiltration in primary breast tumors, which may contribute to improved local tumor regression and better therapeutic outcomes.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBevacizumabBreast NeoplasmsCD8-Positive T-LymphocytesLymphocytes, Tumor-InfiltratingAdultAgedErb-b2 Receptor Tyrosine KinasesFemaleHumansMiddle AgedBevacizumabERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesBevacizumabCD8HER2 negative breast cancerTumor-infiltrating lymphocytes

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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.