Role of B7-H3 in predicting response to neoadjuvant chemotherapy in muscle-invasive bladder cancer

IF 1.6 Q3 UROLOGY & NEPHROLOGY BJUI compass Pub Date : 2024-09-11 DOI:10.1002/bco2.418
Ekamjit S. Deol, Reza Nabavizadeh, Roxane R. Lavoie, Mihai G. Dumbrava, Edlira Horjeti, Prabin Thapa, John C. Cheville, Igor Frank, Fabrice Lucien
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Abstract

Background

Neoadjuvant platinum-based chemotherapy offers a modest survival advantage in muscle-invasive bladder cancer (MIBC) for patients with pathologic response. B7-H3 (CD276), an immune checkpoint overexpressed in various cancers, including urothelial-cell carcinoma (UCC), has been associated with chemoresistance and poor oncologic outcomes. We aimed to explore if B7H3 expression on bladder biopsy samples was a predictive biomarker for pathologic response to neoadjuvant platinum-based chemotherapy.

Methods

This was a retrospective cohort study among MIBC patients receiving neoadjuvant platinum-based chemotherapy followed by radical cystectomy. All patients underwent routine preoperative biopsy of their tumour. Immunohistochemistry was used to evaluate B7-H3 expression from pre-operative specimens. The primary outcome of interest was pathologic complete response (pCR). Statistical analysis included Mann–Whitney U test, Fisher's exact test, Kaplan–Meier method, and Cox regression for survival analysis.

Results

Among 87 patients analysed, high B7-H3 expression was found in 44.8% (n = 39) of patients. The median follow-up periods were similar between the high and low B7-H3 groups (high expression; 4.29 years [SD 3.04], low expression 3.94 years [SD 3.04], p = 0.60). Only 20.5% of patients with high B7-H3 expression achieved pCR, compared to 41.7% in the low expression group (p = 0.04). Cox regression showed no significant differences in recurrence-free or cancer-specific survival between the high and low B7-H3 expression groups (p > 0.05).

Conclusion

High B7-H3 expression is associated with a reduced likelihood of achieving pCR in MIBC patients undergoing neoadjuvant chemotherapy. This suggests B7-H3's potential as a predictive biomarker for chemotherapy response. Further research is needed to explore the role of B7-H3 on platinum-based chemotherapy response in urothelial cancer.

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B7-H3 在预测肌层浸润性膀胱癌新辅助化疗反应中的作用
背景:新辅助铂类化疗为病理反应的肌层浸润性膀胱癌(MIBC)患者提供了适度的生存优势。B7-H3(CD276)是一种在包括尿路上皮细胞癌(UCC)在内的多种癌症中过度表达的免疫检查点,它与化疗耐药性和不良的肿瘤预后有关。我们旨在探讨膀胱活检样本中 B7H3 的表达是否是新辅助铂类化疗病理反应的预测性生物标志物:这是一项回顾性队列研究,研究对象是接受新辅助铂类化疗后进行根治性膀胱切除术的MIBC患者。所有患者均接受了常规的术前肿瘤活检。免疫组化技术用于评估术前标本中B7-H3的表达。主要研究结果为病理完全反应(pCR)。统计分析包括 Mann-Whitney U 检验、费雪精确检验、Kaplan-Meier 法和用于生存分析的 Cox 回归法:结果:在分析的 87 例患者中,44.8%(39 例)的患者发现 B7-H3 高表达。B7-H3 高表达组和低表达组的中位随访时间相似(高表达组:4.29 年 [SD 3.04],低表达组:3.94 年 [SD 3.04],P = 0.60)。B7-H3高表达组仅有20.5%的患者达到pCR,而低表达组为41.7%(P = 0.04)。Cox回归结果显示,B7-H3高表达组和低表达组的无复发生存率或癌症特异性生存率无明显差异(P > 0.05):结论:B7-H3高表达与接受新辅助化疗的MIBC患者获得pCR的可能性降低有关。结论:B7-H3的高表达与接受新辅助化疗的MIBC患者获得pCR的可能性降低有关,这表明B7-H3有可能成为化疗反应的预测性生物标志物。还需要进一步研究B7-H3对尿路上皮癌铂类化疗反应的作用。
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