早期ルミナル乳がんにおけるネオアジュバント レトロゾールおよびパルボシクリブ後の分子および細胞組成の変化
Paul Cottu1, Yann Kieffer2, Jerome Lemonnier3
1Department of Medical Oncology, Institut Curie, Paris, France; Université Paris Cité, Paris, France; French Breast Cancer InterGroup UCBG, Research and Development Department, Unicancer, Paris, France; IHU Institute of Women's Cancer, Institut Curie, Paris, France.
Abstract:
The NeoPAL trial compares neoadjuvant letrozole-palbociclib (LP) with chemotherapy (CT) in 103 patients with high-risk, early luminal breast cancer. At surgery, the NanoString BC360 proliferation score and Ki67 expression are reduced in both arms, together with upregulation of immune-related signatures. Overall, there is very little difference in the changes observed with LP as compared to CT, even in signatures related to response to estrogen and CDK4/6 manipulation. Deconvolution of bulk RNA sequencing (RNA-seq) data reveals high content at baseline in cancer cells, immunosuppressive cancer-associated fibroblasts, FOXP3+ CD4+ regulatory T lymphocytes, and TREM2+ macrophages. In contrast, myoepithelial cells, normal-like fibroblasts, FOLR2+ macrophages, and SELL+ CD4+ T lymphocytes accumulate after treatment in both arms. A low ROR score is observed at surgery in 63.3% and 43.5% of patients in the LP and CT arms, respectively. No 3-year breast cancer-specific survival events are observed in these patients. These data provide a rationale for CT-sparing trials in this setting.
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