Bansal Rani, Adeyelu Tolulope, Elliott Andrew, Tan Antoinette R, Ribeiro Jennifer R, Meisel Jane, Oberley Matthew J, Graff Stephanie L, Sledge George W, Grilley-Olson Juneko E, Sammons Sarah L, Rosenberger Laura H
Duke Cancer Institute, Duke University Hospital, Durham, NC.
Caris Life Sciences, Phoenix, AZ.
JCO Precis Oncol. 2024 Dec;8:e2400289. doi: 10.1200/PO.24.00289. Epub 2024 Dec 5.
Malignant phyllodes tumors (MPTs) are rare fibroepithelial tumors of the breast with aggressive biologic behavior and high recurrence rates. Surgery remains the primary treatment modality for these tumors; however, initial investigations suggest a potential for targeted therapies in managing this disease. Therefore, we aimed to assess the molecular landscape of MPTs to reveal possible treatment opportunities.
MPTs (n = 57) from primary and metastatic sites underwent genomic sequencing (592-gene panel or whole exome), whole-transcriptome sequencing, and immunohistochemistry (PD-L1, human epidermal growth factor receptor 2 [HER2]) at Caris Life Sciences (Phoenix, AZ). Immune cell fractions in the tumor microenvironment were estimated using quanTIseq. Mann-Whitney , chi-square, and Fisher's exact tests were used to determine significance ( < .05).
MPTs had low expression, comparable with the HER2-negative subset of a large cohort of breast adenocarcinoma samples (N = 9,926). Frequent alterations included promoter; , , and mutations; and less frequently , , and . Differences in mutation prevalences were observed between primary sites, lung metastases, and nonlung metastases. One MPT specimen harbored a pathogenic fusion, and treatment with larotrectinib for over 16 months suggested a clinical response to therapy. PD-L1+ status was observed in 15.2% of MPTs overall, with similar prevalence in primary sites and lung metastases. B cells, M2 macrophages, neutrophils, and natural killer cells had the highest median cell fractions in MPTs.
Considering the occurrence of several actionable alterations including a fusion reported herein, these results support the use of next-generation sequencing (NGS) including RNA analysis for fusion detection to identify such alterations in patients with MPTs. These findings highlight the importance of comprehensive NGS in MPT research to uncover potential targeted treatment options for these patients.
恶性叶状肿瘤(MPT)是一种罕见的乳腺纤维上皮性肿瘤,具有侵袭性生物学行为和高复发率。手术仍然是这些肿瘤的主要治疗方式;然而,初步研究表明靶向治疗在管理这种疾病方面具有潜力。因此,我们旨在评估MPT的分子特征,以揭示可能的治疗机会。
来自原发和转移部位的57例MPT在Caris生命科学公司(亚利桑那州凤凰城)进行了基因组测序(592基因panel或全外显子组)、全转录组测序和免疫组化(PD-L1、人表皮生长因子受体2 [HER2])。使用quanTIseq估计肿瘤微环境中的免疫细胞分数。采用曼-惠特尼检验、卡方检验和费舍尔精确检验确定显著性(P <.05)。
MPT的HER2表达较低,与一大组乳腺腺癌样本(N = 9926)中的HER2阴性亚组相当。常见的改变包括PIK3CA启动子;PIK3CA、AKT1和TP53突变;以及较少见的BRAF、MAP2K4和RB1改变。在原发部位、肺转移和非肺转移之间观察到突变发生率的差异。一个MPT标本存在致病性NTRK3融合,用拉罗替尼治疗超过16个月显示出临床反应。总体上15.2%的MPT观察到PD-L1阳性状态,在原发部位和肺转移中的发生率相似。B细胞、M2巨噬细胞、中性粒细胞和自然杀伤细胞在MPT中的中位细胞分数最高。
考虑到本文报道的包括NTRK3融合在内的几种可操作改变的发生情况,这些结果支持使用包括RNA分析以检测融合的下一代测序(NGS)来识别MPT患者中的此类改变。这些发现强调了全面NGS在MPT研究中的重要性,以揭示这些患者潜在的靶向治疗选择。