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Triple negative breast cancer (TNBC) accounts for approximately 15%-20% of all breast cancers
Lacnotuzumab (MCS110) is a neutralizing human IgG1 κ monoclonal antibody that can bind to CSF1 and block CSF1-mediated receptor activation
This study is a phase II clinical trial designed to evaluate the efficacy of Lacnotuzumab in the combination of gemcitabine and carboplatin for patients with advanced TNBC
Recruiting advanced TNBC female patients with high levels of tumor-related macrophages who are not suitable for surgery or radiotherapy for curative treatment, are treated with gemcitabine + carboplatin with or without Lacnotuzumab until intolerable toxicity, disease progression, doctors Or the patient decides to stop treatment
Progression-free survival of the two treatment groups
Progression-free survival of the two treatment groupsA total of 49 patients were recruited, of which 34 received Lacnotuzumab + gemcitabine + carboplatin treatment, and 15 patients received gemcitabine + carboplatin treatment
The best treatment response of the two treatment groups
The best treatment response of the two treatment groupsThe median progression-free survival in the combination group and gemcitabine+carboplatin group were 5.
The median progression-free survival of the combination group and gemcitabine+carboplatin group were 5.
Lacnotuzumab + gemcitabine + carboplatin showed comparable antitumor activity to gemcitabine + carboplatin alone in advanced TNBC , but the tolerance was slightly poor.
Original source:
Sherko Kuemmel, Mario Campone, Delphine Loirat, et al.
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