Wang Xiaoping, Zhao Li, Song Xingzhi, Wu Xiaogang, Krishnamurthy Savitri, Semba Takashi, Shao Shan, Knafl Mark, Coffer Larry W, Alexander Angela, Vines Anita, Bopparaju Swetha, Woodward Wendy A, Chu Randy, Zhang Jianhua, Yam Clinton, Loo Lenora W M, Nasrazadani Azadeh, Huong Le-Petross, Woodman Scott E, Futreal Andrew, Tripathy Debu, Ueno Naoto T
Morgan Welch Inflammatory Breast Cancer Research Program and Clinic, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Department of Breast Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
NPJ Precis Oncol. 2024 Nov 18;8(1):265. doi: 10.1038/s41698-024-00729-0.
Triple-negative inflammatory breast cancer (TN-IBC) is the most aggressive type of breast cancer, yet its defining genomic, molecular, and immunological features remain largely unknown. In this study, we performed the largest and most comprehensive genomic and transcriptomic analyses of prospectively collected TN-IBC patient samples from a phase II clinical trial (ClinicalTrials.gov, NCT02876107, registered on August 22, 2016) and compared them to similarly analyzed stage III TN-non-IBC patient samples (ClinicalTrials.gov, NCT02276443, registered on October 21, 2014). We found that TN-IBC tumors have distinctive genomic, molecular, and immunological characteristics, including a lower tumor mutation load than TN-non-IBC, and an association of immunosuppressive tumor-infiltrating immune components with an unfavorable response to neoadjuvant chemotherapy. To our knowledge, this is the only study in which TN-IBC and TN-non-IBC samples were collected prospectively. Our analysis improves the understanding of the molecular landscape of the most aggressive subtype of breast cancer. Further studies are needed to discover novel prognostic biomarkers and druggable targets for TN-IBC.
三阴性炎性乳腺癌(TN-IBC)是最具侵袭性的乳腺癌类型,但其明确的基因组、分子和免疫学特征在很大程度上仍不清楚。在本研究中,我们对来自一项II期临床试验(ClinicalTrials.gov,NCT02876107,于2016年8月22日注册)的前瞻性收集的TN-IBC患者样本进行了最大规模、最全面的基因组和转录组分析,并将其与经过类似分析的III期TN-非IBC患者样本(ClinicalTrials.gov,NCT02276443,于2014年10月21日注册)进行比较。我们发现,TN-IBC肿瘤具有独特的基因组、分子和免疫学特征,包括肿瘤突变负荷低于TN-非IBC,以及免疫抑制性肿瘤浸润免疫成分与新辅助化疗反应不佳相关。据我们所知,这是唯一一项前瞻性收集TN-IBC和TN-非IBC样本的研究。我们的分析增进了对最具侵袭性乳腺癌亚型分子格局的理解。需要进一步研究以发现TN-IBC的新型预后生物标志物和可成药靶点。