Evidence map›Paper›PMID 42775277›Full record

ArticleInternational journal of women's health2026

Expression of CXCL10 and CXCL16 in Triple-Negative Breast Cancer and Their Association with Immunotherapy Efficacy and Prognosis.

Qian Zhang, Fei Li, Dongdong Du, Jingyan Feng, Jing Li

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Article in International journal of women's health, 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

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5 authors.

Qian ZhangDepartment of Breast, Xuzhou Cancer Hospital, Xuzhou City, Jiangsu Province, People's Republic of China.
Fei LiDepartment of Pathology, Xuzhou Cancer Hospital, Xuzhou City, Jiangsu Province, People's Republic of China.
Dongdong DuDepartment of Breast, Xuzhou Cancer Hospital, Xuzhou City, Jiangsu Province, People's Republic of China.
Jingyan FengDepartment of Breast, Xuzhou Cancer Hospital, Xuzhou City, Jiangsu Province, People's Republic of China.
Jing LiDepartment of Breast, Xuzhou Cancer Hospital, Xuzhou City, Jiangsu Province, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Triple-negative breast cancer (TNBC) represents the most aggressive breast cancer subtype with limited therapeutic options. This study investigated the expression patterns of chemokines CXCL10 and CXCL16 in TNBC and their association with immunotherapy response and clinical outcomes. Methods: We retrospectively analyzed 128 TNBC patients treated at our institution between 2019-2023. CXCL10 and CXCL16 expressions were assessed by immunohistochemistry. Sixty-eight patients received immune checkpoint inhibitor (ICI)-based therapy. The primary endpoints were objective response rate (ORR), progression-free survival (PFS), and overall survival (OS). Results: High CXCL10 expression (≥50% positive cells) was observed in 72 patients (56.25%), while high CXCL16 expression was found in 65 patients (50.78%). In the immunotherapy cohort, patients with high CXCL10 expression demonstrated significantly higher ORR (44.44% vs 18.75%, p=0.024) and longer median PFS (8.62 vs 4.35 months, HR=0.467, 95% CI: 0.268-0.814, p=0.007). Combined high expression of both chemokines showed the most favorable outcomes, with ORR of 52.63% and median PFS of 10.84 months. Multivariate Cox regression confirmed CXCL10 (HR=0.512, p=0.008) and CXCL16 (HR=0.623, p=0.032) as independent prognostic factors for PFS. Conclusion: CXCL10 and CXCL16 expression levels are associated with improved immunotherapy response and favorable prognosis in TNBC and may serve as candidate predictive biomarkers. Combined assessment of both chemokines may optimize patient selection for ICI-based therapy. Prospective validation in larger cohorts is warranted.

Indexed as

biomarkersCXCL10CXCL16immunotherapyprognosistriple-negative breast cancer

Identifiers

PMID42775277
PMCPMC13596113

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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.