Publications by authors named "M Pecoraro"

Objective: The primary aim was to determine the performance of neoadjuvant chemotherapy VI-RADS (nacVI-RADS) in predicting response to systemic therapy in patients with MIBC and to evaluate its inter-reader agreement.

Materials And Methods: Prospective study, including patients with non-metastatic muscle-invasive bladder cancer (MIBC) who underwent neoadjuvant chemotherapy before radical cystectomy (RC). Patients underwent pre- and post-treatment MRI.

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Background: In the phase 3 randomized controlled study, ATTRibute-CM, acoramidis, a transthyretin (TTR) stabilizer, demonstrated significant efficacy on the primary endpoint. Participants with transthyretin amyloid cardiomyopathy (ATTR-CM) who completed ATTRibute-CM were invited to enroll in an open-label extension study (OLE). We report efficacy and safety data of acoramidis in participants who completed ATTRibute-CM and enrolled in the ongoing OLE.

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The synthesis and application of aryl-substituted pyridine(diimine) iron complexes (PDI)FeCH to the catalytic borylation of heteroarenes under thermal conditions is described. Improvements in catalyst design and performance were guided by precatalyst activation studies, where investigations into stoichiometric reactivities of iron borohydride (4- Bu- PDI)Fe(HBPin) and iron furyl (4- Bu- PDI)Fe(2-methylfuryl) complexes revealed facile C(sp)-H activation and a slower and potentially turnover-limiting C(sp)-B formation step. Formation of the flyover dimer, [(4- Bu- PDI)Fe] was identified as a catalyst deactivation pathway and formally iron(0) complexes were found to be inactive for borylation.

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Background: The role of sex in choosing between coronary artery bypass grafting (CABG) and percutaneous coronary intervention (PCI) for unprotected left main coronary artery (ULMCA) disease has gained interest.

Methods: Randomized controlled trials and adjusted observational studies comparing PCI versus CABG in ULMCA patients with outcomes by sex were included. The primary endpoint was major adverse cardiovascular events (MACE), with secondary endpoints being all-cause mortality and repeated revascularization.

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Article Synopsis
  • Experimental and computational research has highlighted the principles of redox-neutral C-H activation using iron(II) complexes, specifically through the dimethyl complex (depe)Fe(CH).
  • The C(sp)-H methylation reaction of pivalophenone was discovered to be influenced by factors such as the type of phosphine ligands, the iron center's spin state, and the nature of halide or hydrocarbyl ligands in the corresponding complexes.
  • Additional studies indicated that ketones and aldehydes are the most effective substrates for this reaction, and the research also established the significant role of orbital hybridization in enhancing selectivity in C-H activation.
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