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. 2022 Nov 17;128(2):266–274. doi: 10.1038/s41416-022-02050-8

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© The Author(s) 2022, corrected publication 2022

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Fig. 1 — On the left: the clinical cohort of our study (n = 247) in which we identified the propensity-score matched population of patients treated with anthracycline-taxane (AT) chemotherapy with or without carboplatin (AT-Cb). On the right: the translational cohort were we evaluated tumor-infiltrating lymphocytes (TILs) at baseline (n = 163) and on residual disease (RD-TILs, n = 96), assessing the delta TIL variation.