Early Stage HER2-Positive Breast Cancers Not Achieving a pCR From Neoadjuvant Trastuzumab- or Pertuzumab-Based Regimens Have an Immunosuppressive Phenotype

Approximately 30% to 40% of HER2-postivie (HER2(+)) early-stage breast cancers do not completely respond to neoadjuvant anti-HER2 therapy. We investigated immune cell-associated markers in 30 early-stage HER2(+) breast cancer tissues treated with neoadjuvant TCH (docetaxel, carboplatin, and trastuzumab) with or without pertuzumab. We identified an immunosuppressive tumor immune microenvironment in cancers with residual disease. These hypothesis-generating results should be validated in a larger cohort. Background: Stromal tumor-infiltrating lymphocytes (TILs) might predict pathologic complete response (pCR) in patients with HER2-positive (HER2(+)) breast cancer treated with trastuzumab (H). Docetaxel (T), carboplatin (C), H, and pertuzumab (P) have immune-modulating effects. Pre- and post-treatment immune biomarkers in cancers treated with neoadjuvant TCH with or without P are lacking. In this study we quantified baseline and changes in TILs, cluster of differentiation (CD) 4(+), CD8(+), FoxP3(+), and PD-L1(+) cells using immunohistochemistry (IHC) and quantified productive T-cell receptor beta (TCR beta) rearrangements and TCR beta clonality using next-generation sequencing (NGS) in 30 HER2(+) breast cancer tissues treated with neoadjuvant H with or without P regimens. Materials and Methods: Thirty pre- and post-neoadjuvant TCH (n = 4) or TCHP (n = 26) breast cancer tissues were identified. TILs were quantified manually using hematoxylin and eosin. CD4, CD8, FoxP3, and PD-L1 were stained using IHC. TCR beta was evaluated using NGS. Immune infiltrates were compared between pCR and non-pCR groups using the Wilcoxon rank sum test. Results: A pCR occurred in 15 (n = 15; 50%) cancers (TCH n = 2; TCHP, n = 13). Pretreatment TILs, CD4(+), CD8(+), FoxP3(+), and PD-L1(+) cells were not associated with response (P = .42, P = .55, P = .19, P = .66, P = .87, respectively. Pretreatment productive TCR beta and TCR beta clonality did not predict response, P = .84 and P = .40, respectively). However, post-treatment CD4(+) and FoxP3(+) cells (T-regulatory cells) were elevated in the non-pCR cohort (P = .042 and P = .082, respectively). Conclusion: An increase in regulatory T cells in non-pCR tissues suggests the development of an immunosuppressive phenotype. Further investigation in a larger cohort of samples is warranted to validate these findings. (C) 2018 Elsevier Inc. All rights reserved.