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Masakazu Toi

Researcher at Kyoto University

Publications -  658
Citations -  28522

Masakazu Toi is an academic researcher from Kyoto University. The author has contributed to research in topics: Breast cancer & Cancer. The author has an hindex of 69, co-authored 578 publications receiving 23200 citations. Previous affiliations of Masakazu Toi include The Breast Cancer Research Foundation & Tokyo Metropolitan Komagome Hospital.

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Cryosurgery for primary breast cancers, its biological impact, and clinical outcomes.

TL;DR: Cryoablation for primary tumor may enhance the treatment effect of immune checkpoint inhibitors in patients with breast cancer and induces an immunomodulatory effect, which is an interesting topic of research in the era of immune checkpoints inhibitors.
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BOLERO-1: A randomized, phase III, double-blind, placebo-controlled multicenter trial of everolimus in combination with trastuzumab and paclitaxel as first-line therapy in women with HER2-positive (HER2+), locally advanced or metastatic breast cancer (BC).

TL;DR: Everolimus, an orally bioavailable inhibitor of mammalian target of rapamycin (mTOR), a protein kinase central to multiple protein synthesis pathways and implicated in trastuzumab resistance, and everolimus-containing regimens have shown promising results in patients with ER+, HER2– advanced BC in phase II/III trials.
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Trastuzumab: updates and future issues

TL;DR: A more precise understanding of the mechanisms of therapeutic response is needed so that trastuzumab-based therapies can be optimized more individually and the interaction between the Her-axis and the hormone-axis is investigated.
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Clinical Significance of PIK3CA and ESR1 Mutations in circulating tumor DNA: Analysis from the MONARCH 2 Study of Abemaciclib Plus Fulvestrant.

TL;DR: Abemaciclib plus fulvestrant was effective regardless of PIK3CA or ESR1 mutation status, with benefit in both PFS and OS, with a numerically greater improvement in median PFS relative to placebo plus ful vestrant for PIK1-mutant tumors compared to the respective wild-type subgroups.