Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/188946
Title: Early on-treatment transcriptional profiling as a tool for improving pathological response prediction in HER2-positive inflammatory breast cancer
Author: Pernas, Sonia
Guerriero, Jennifer L.
Naumenko, Sergey
Goel, Shom
Regan, Meredith M.
Hu, Jiani
Harrison, Beth T.
Lynce, Filipa
Lin, Nancy U.
Partridge, Ann
Morikawa, Aki
Hutchinson, John
Mittendorf, Elizabeth A.
Sokolov, Artem
Overmoyer, Beth
Keywords: Càncer de mama
Expressió gènica
Resposta immunitària
Breast cancer
Gene expression
Immune response
Issue Date: 1-Jan-2022
Publisher: SAGE Publications
Abstract: Background: Inflammatory breast cancer (IBC) is a rare and understudied disease, with 40% of cases presenting with human epidermal growth factor receptor 2 (HER2)-positive subtype. The goals of this study were to (i) assess the pathologic complete response (pCR) rate of short-term neoadjuvant dual-HER2-blockade and paclitaxel, (ii) contrast baseline and on-treatment transcriptional profiles of IBC tumor biopsies associated with pCR, and (iii) identify biological pathways that may explain the effect of neoadjuvant therapy on tumor response. Patients and Methods: A single-arm phase II trial of neoadjuvant trastuzumab (H), pertuzumab (P), and paclitaxel for 16 weeks was completed among patients with newly diagnosed HER2-positive IBC. Fresh-frozen tumor biopsies were obtained pretreatment (D1) and 8 days later (D8), following a single dose of HP, prior to adding paclitaxel. We performed RNA-sequencing on D1 and D8 tumor biopsies, identified genes associated with pCR using differential gene expression analysis, identified pathways associated with pCR using gene set enrichment and gene expression deconvolution methods, and compared the pCR predictive value of principal components derived from gene expression profiles by calculating and area under the curve for D1 and D8 subsets. Results: Twenty-three participants were enrolled, of whom 21 completed surgery following neoadjuvant therapy. Paired longitudinal fresh-frozen tumor samples (D1 and D8) were obtained from all patients. Among the 21 patients who underwent surgery, the pCR and the 4-year disease-free survival were 48% (90% CI 0.29-0.67) and 90% (95% CI 66-97%), respectively. The transcriptional profile of D8 biopsies was found to be more predictive of pCR (AUC = 0.91, 95% CI: 0.7993-1) than the D1 biopsies (AUC = 0.79, 95% CI: 0.5905-0.9822). Conclusions: In patients with HER2-positive IBC treated with neoadjuvant HP and paclitaxel for 16 weeks, gene expression patterns of tumor biopsies measured 1 week after treatment initiation not only offered different biological information but importantly served as a better predictor of pCR than baseline transcriptional analysis.
Note: Reproducció del document publicat a: https://doi.org/10.1177/17588359221113269
It is part of: Therapeutic Advances in Medical Oncology, 2022, vol. 14, p. 175883592211132
URI: http://hdl.handle.net/2445/188946
Related resource: https://doi.org/10.1177/17588359221113269
ISSN: 1758-8340
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

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