TY - JOUR A1 - Issa-Nummer, Yasmin A1 - Darb-Esfahani, Silvia A1 - Loibl, Sibylle A1 - Kunz, Georg A1 - Nekljudova, Valentina A1 - Schrader, Iris A1 - Sinn, Bruno Valentin A1 - Ulmer, Hans-Ullrich A1 - Kronenwett, Ralf A1 - Just, Marianne A1 - Kühn, Thorsten A1 - Diebold, Kurt A1 - Untch, Michael A1 - Holms, Frank A1 - Blohmer, Jens-Uwe A1 - Habeck, Jörg-Olaf A1 - Dietel, Manfred A1 - Overkamp, Friedrich A1 - Krabisch, Petra A1 - Minckwitz, Gunter von A1 - Denkert, Carsten Michael T1 - Prospective validation of immunological infiltrate for prediction of response to neoadjuvant chemotherapy in HER2-negative breast cancer : a substudy of the neoadjuvant GeparQuinto trial T2 - PLoS One N2 - Introduction: We have recently described an increased lymphocytic infiltration rate in breast carcinoma tissue is a significant response predictor for anthracycline/taxane-based neoadjuvant chemotherapy (NACT). The aim of this study was to prospectively validate the tumor-associated lymphocyte infiltrate as predictive marker for response to anthracycline/taxane-based NACT. Patients and Methods: The immunological infiltrate was prospectively evaluated in a total of 313 core biopsies from HER2 negative patients of the multicenter PREDICT study, a substudy of the neoadjuvant GeparQuinto study. Intratumoral lymphocytes (iTuLy), stromal lymphocytes (strLy) as well as lymphocyte-predominant breast cancer (LPBC) were evaluated by histopathological assessment. Pathological complete response (pCR) rates were analyzed and compared between the defined subgroups using the exact test of Fisher. Results: Patients with lymphocyte-predominant breast cancer (LPBC) had a significantly increased pCR rate of 36.6%, compared to non-LPBC patients (14.3%, p<0.001). LPBC and stromal lymphocytes were significantly independent predictors for pCR in multivariate analysis (LPBC: OR 2.7, p = 0.003, strLy: OR 1.2, p = 0.01). The amount of intratumoral lymphocytes was significantly predictive for pCR in univariate (OR 1.2, p = 0.01) but not in multivariate logistic regression analysis (OR 1.2, p = 0.11). Conclusion: Confirming previous investigations of our group, we have prospectively validated in an independent cohort that an increased immunological infiltrate in breast tumor tissue is predictive for response to anthracycline/taxane-based NACT. Patients with LPBC and increased stromal lymphocyte infiltration have significantly increased pCR rates. The lymphocytic infiltrate is a promising additional parameter for histopathological evaluation of breast cancer core biopsies. Y1 - 2013 UR - http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/32887 UR - https://nbn-resolving.org/urn:nbn:de:hebis:30:3-328874 SN - 1932-6203 N1 - Copyright: © 2013 Issa-Nummer et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/ , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. VL - 8 IS - (12):e79775 PB - PLoS CY - Lawrence, Kan. ER -