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Biomedical subjects

Luca Malorni

Publications and source records attributed to Luca Malorni.

2 recordsLinked to original sources

Prognostic role of thymidine kinase 1 activity in hormone receptor positive metastatic breast cancer. A systematic review and meta-analysis.

INTRODUCTION: Circulating thymidine kinase 1 activity (TKa) is a potential prognostic biomarker in patients with hormone receptor-positive (HR+) metastatic breast cancer (MBC); however, results are heterogeneous. In this study we aimed to summarize the current evidence on the prognostic role of circulating TKa in women with HR+&#xa0;MBC. METHODS: We conducted a systematic review of PubMed, Embase, and Cochrane CENTRAL databases and abstracts from main international oncology meetings. Phase II-IV clinical trials and prospective observational studies in patients with MBC assessing circulating TK1 levels or TKa and reporting hazard ratios (HRs) for progression-free survival (PFS) and/or overall survival (OS) were included. HRs were pooled using random-effects models (restricted maximum likelihood with Hartung-Knapp adjustment), with heterogeneity quantified by I2 and prediction intervals. The primary study outcome was the association of baseline and on-treatment TKa with PFS and OS. Secondary analyses aimed at exploring the source of heterogeneity. RESULTS: Eighteen studies, reporting data from nearly 3000 women, were included in the systematic review and 15 studies were meta-analyzed. Patients with HR+&#xa0;MBC and high baseline TKa showed a significantly higher risk of progression (PFS: HR 1.90; 95% CI 1.57-2.30; p&#xa0;<&#xa0;0.001) and death (OS: HR 2.48; 95% CI 1.94-3.17; p&#xa0;<&#xa0;0.001) than those with low TKa. TKa at 2 and 4 weeks on-treatment was also prognostic (2 weeks, PFS: HR 2.76; 95% CI 2.34-3.26; p&#xa0;<&#xa0;0.001; 4 weeks, HR 2.26; 95% CI 1.93-2.66; p&#xa0;<&#xa0;0.001). Similar pooled effects were obtained when accounting for different cut-offs, TKa assessment, and sample-type. CONCLUSION: Pre-treatment high TKa is an adverse prognostic factor in women with HR+&#xa0;MBC. High on-treatment TKa is also associated with worse outcome, potentially serving as an early signal of treatment resistance. We provide a comprehensive summary of the currently available evidence on the prognostic value of circulating TKa.

Breast cancer

The genomic landscape of HER2 negative metastatic breast cancer with loss of estrogen and progesterone receptors.

INTRODUCTION: Loss of estrogen receptor (ER) and/or progesterone receptor (PR) might occur during the metastatic progression of ER positive and HER2 negative (ER+/HER2-) breast cancer (BC), but the underpinning molecular alterations remain elusive. We explored the genomic context of HER2- tumors with ER and/or PR loss to investigate potential drivers and actionable alterations that might help personalize treatment of ER+/HER2- BC. METHODS: We accessed data from metastatic HER2- BC included in the MSK-2018 dataset to compare outcome, tumor characteristics and genomic alterations of BC with loss of ER (ER+/-, n&#xa0;=&#xa0;66) to those maintaining ER positivity (ER+/+, n&#xa0;=&#xa0;364) or ER negativity (ER-/-, n&#xa0;=&#xa0;50). We also compared metastatic ER+/+ BC with loss of PR (PR+/-, n&#xa0;=&#xa0;111) to those maintaining PR positivity (PR+/+, n&#xa0;=&#xa0;192) or PR negativity (PR-/-, n&#xa0;=&#xa0;41). RESULTS: In line with previous reports, ER+/-&#xa0;BC was associated with aggressive clinico-pathological characteristics and poor outcome. ER+/-&#xa0;BC showed significantly higher frequency of TP53 and RB1 mutations and lower frequency of PIK3CA and GATA3 mutations compared to ER+/+. ER+/-&#xa0;or PR+/-&#xa0;status was mutually exclusive with ESR1 mutations and was associated with a significantly higher tumor mutational burden. Moreover, ER+/-&#xa0;BC were enriched in driver alterations in the genes of the Notch and Retinoblastoma pathways and showed a significantly lower frequency of level 1 actionable alterations according to OncoKB. CONCLUSIONS: Loss of ER and/or PR may identify a distinct evolutionary trajectory of ER+/HER2- metastatic progression, largely non-overlapping with ESR1-mutant endocrine resistance. Further studies on matched primary and metastatic samples are warranted.

Humans