Department of Translational Medicine, Lund University, Malmö, Sweden; Department of Urology, Skåne University Hospital, Malmö, Sweden.
Department of Translational Medicine, Lund University, Malmö, Sweden; Department of Urology, Skåne University Hospital, Malmö, Sweden.
Eur Urol. 2022 May;81(5):523-532. doi: 10.1016/j.eururo.2021.10.035. Epub 2021 Nov 13.
For muscle-invasive bladder cancer (MIBC), no tissue biomarkers are available for clinical use to predict response to neoadjuvant chemotherapy.
To investigate how molecular subtypes impact pathological response and survival in patients receiving preoperative cisplatin-based chemotherapy.
DESIGN, SETTING, AND PARTICIPANTS: Classification of a retrospective cohort of 149 patients was performed by tumor transcriptomic profiling and immunostaining. A cohort treated with radical cystectomy alone and public data sets were used for comparison and external validation.
Complete pathological response in the cystectomy specimen (ypT0N0) and survival were compared in predefined molecular subtypes. Differential gene expression and chemotherapy response were explored beyond molecular subtypes.
Patients with genomically unstable (GU) and urothelial-like (Uro) tumors had higher proportions of complete pathological response (16/31 [52%] and 17/54 [31%]), versus five out of 24 (21%) with the basal/squamous (Ba/Sq) subtype following neoadjuvant chemotherapy and radical cystectomy. Molecular subtype was independently associated with improved survival for patients with GU tumors (hazard ratio [HR] 0.29, 95% confidence interval [CI]: 0.11-0.79) and UroC tumors (HR 0.37, 95% CI: 0.14-0.94) compared with Ba/Sq tumors, adjusting for clinical stage. In addition, expression of the gene coding for osteopontin (SPP1) showed a subtype-dependent effect on chemotherapy response.
Urothelial cancer of the luminal-like (GU and Uro) subtypes is more responsive to cisplatin-based neoadjuvant chemotherapy. A second-generation of subtype-specific biomarkers, for example, SPP1, may be a way forward to develop a more precision-based treatment approach for neoadjuvant chemotherapy in MIBC.
This study shows that tumor classification by gene expression profiling and molecular subtyping can identify patients who are more likely to benefit from chemotherapy before radical cystectomy for muscle-invasive bladder cancer. Together with other markers for response, molecular subtypes could have a role in selective administration of such chemotherapy.
对于肌层浸润性膀胱癌(MIBC),尚无组织生物标志物可用于临床预测新辅助化疗的反应。
研究分子亚型如何影响接受术前顺铂为基础的化疗的患者的病理反应和生存。
设计、设置和参与者:通过肿瘤转录组分析和免疫染色对 149 例回顾性队列患者进行分类。使用单独接受根治性膀胱切除术的队列和公共数据集进行比较和外部验证。
比较预定分子亚型中膀胱切除标本(ypT0N0)的完全病理缓解和生存。探索了分子亚型之外的差异基因表达和化疗反应。
基因组不稳定(GU)和尿路上皮样(Uro)肿瘤患者的完全病理缓解比例较高(16/31 [52%] 和 17/54 [31%]),而新辅助化疗和根治性膀胱切除术后基底/鳞状(Ba/Sq)亚型仅有 5 例(21%)。分子亚型与 GU 肿瘤(危险比[HR]0.29,95%置信区间[CI]:0.11-0.79)和 UroC 肿瘤(HR 0.37,95%CI:0.14-0.94)患者的生存改善独立相关,与 Ba/Sq 肿瘤相比,调整临床分期后。此外,骨桥蛋白(SPP1)基因的表达显示出对化疗反应的亚型依赖性影响。
基底样(GU 和 Uro)亚型的尿路上皮癌对顺铂为基础的新辅助化疗更敏感。例如,第二代亚型特异性生物标志物,如 SPP1,可能是为 MIBC 的新辅助化疗开发更基于精准的治疗方法的一种途径。
本研究表明,通过基因表达谱和分子分型进行肿瘤分类可以识别出在接受根治性膀胱切除术治疗肌层浸润性膀胱癌之前更有可能受益于化疗的患者。与其他反应标志物一起,分子亚型在这种化疗的选择性给药中可能具有作用。