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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11647599PMC
http://dx.doi.org/10.1016/j.jceh.2024.102455DOI Listing

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Purpose: The associations between first dose reduction or interruption by side effects and lenvatinib plasma trough concentration (C) after administration of a starting dose of 24 mg in 70 Japanese patients with thyroid cancer were evaluated.

Methods: Plasma samples were collected each week for 1 month and at the first incidence of side effects leading to dose reduction or interruption after beginning administration of 24 mg lenvatinib.

Results: The area under the receiver operating characteristic curve was 0.

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Article Synopsis
  • Nivolumab, an immune checkpoint inhibitor, was tested alongside external beam radiation therapy (EBRT) for treating hepatocellular carcinoma (HCC) with macrovascular invasion, aiming to evaluate its efficacy and safety.* -
  • In a phase II trial involving 50 patients, the median progression-free survival (PFS) was 5.6 months, and overall survival was 15.2 months, with an objective response rate of 36% and a disease control rate of 74% observed.* -
  • While 80% of patients experienced treatment-related side effects, mostly mild (like pruritus and rash), the combination therapy demonstrated promising results, indicating that it can be a viable option for managing this type
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Article Synopsis
  • * The artemis trial is a Phase II study testing a new chemotherapy regimen combining carboplatin, paclitaxel, lenvatinib, and pembrolizumab for patients with advanced or recurrent thymic carcinoma, involving 35 participants.
  • * The main goal of the trial is to measure the objective response rate, while also assessing progression-free survival and safety of the treatment options.
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Objectives Anaplastic thyroid cancer (ATC) is an aggressive disease associated with poor outcomes and resistance to therapies. Our study aim was to evaluate the activity of a combinatorial regimen of sandwich sequencing of pembrolizumab immunotherapy and hypofractionated radiotherapy (RT). Methods In this case series, patients with ATC received hypofractionated RT (QUAD-shot) and intravenous pembrolizumab 200mg every 3-4 weeks.

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