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ABSTRACT: Background
Luminal breast cancers with high proliferation (MKShi) and low ER-related signalling (ERSlo) have a poor prognosis. We investigated treatment responses and molecular features of MKShi/ERSlo tumours to inform potential therapies.Methods
Gene expression data from patients who received neoadjuvant chemotherapy (NAC) without (MDACC, N = 199) or with pembrolizumab (I-SPY2, N = 40), or endocrine therapy (NET) without (POETIC, N = 172) or with palbociclib (NeoPalAna, N = 32) were analyzed to assess treatment response by MKS/ERS-subgroups. TCGA was used to assess the mutational landscape and biomarkers associated with palbociclib-resistance (Cyclin-E, RBsig, IRPR) and immunotherapy-response (TMB, TILs, T-cell inflamed) by MKS/ERS-subgroups.Results
Compared to MKShi/ERShi tumours, MKShi/ERSlo tumours had higher pathological response rates to NAC (22% vs 8%, p = 0.06) but a higher recurrence risk (4-year metastasis-free survival 70% vs 94%, p = 0.01). MKShi/ERSlo tumours frequently harboured TP53 (34%) and PIK3CA (33%) mutations, and showed high expression of Cyclin-E, RBsig and IRPR, high TMB and elevated TIL and T-cell inflamed metagene expression. MKShi/ERSlo tumours retained high proliferation after NET with or without palbociclib but had higher pathological complete response rates when pembrolizumab was added to NAC (42% vs 21%, p = 0.07).Conclusions
MKShi/ERSlo tumours have dismal outcomes and are enriched in chemotherapy-sensitive but ET- and palbociclib-resistant tumours. Biomarker analysis and clinical data suggest a potential role for immunotherapy in this group.
SUBMITTER: Licata L
PROVIDER: S-EPMC10703787 | biostudies-literature | 2023 Nov
REPOSITORIES: biostudies-literature
Licata Luca L Barreca Marco M Galbardi Barbara B Dugo Matteo M Viale Giulia G Győrffy Balàzs B Karn Thomas T Pusztai Lajos L Gianni Luca L Callari Maurizio M Bianchini Giampaolo G
British journal of cancer 20231107 12
<h4>Background</h4>Luminal breast cancers with high proliferation (MKS<sup>hi</sup>) and low ER-related signalling (ERS<sup>lo</sup>) have a poor prognosis. We investigated treatment responses and molecular features of MKS<sup>hi</sup>/ERS<sup>lo</sup> tumours to inform potential therapies.<h4>Methods</h4>Gene expression data from patients who received neoadjuvant chemotherapy (NAC) without (MDACC, N = 199) or with pembrolizumab (I-SPY2, N = 40), or endocrine therapy (NET) without (POETIC, N = 1 ...[more]