Publications by authors named "P G Corrie"

Background: The multi-centre two-stage SCALOP-2 trial (ISRCTN50083238) assessed whether dose escalation of consolidative chemoradiotherapy (CRT) or concurrent sensitization using the protease inhibitor nelfinavir improve outcomes in locally advanced pancreatic cancer (LAPC) following four cycles of gemcitabine/nab-paclitaxel.

Methods: In stage 1, the maximum tolerated dose (MTD) of nelfinavir concurrent with standard-dose CRT (50.4 Gy in 28 fractions) was identified from a cohort of 27 patients.

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Little more than 10 years ago, metastatic melanoma was considered to have one of the poorest cancer outcomes, associated with a median overall survival of 6-8 months. Cytotoxic chemotherapy offered modest response rates of 20%-30%, but no clear survival benefit. Patients were routinely enrolled in clinical trials as their first-line therapy in the search for effective novel therapeutics.

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Aims: The MAPK pathway is constitutively activated in uveal melanoma (UM). Selumetinib (AZD6244, ARRY-142886), a MEK inhibitor, has shown limited activity as monotherapy in metastatic UM. Pre-clinical studies support synergistic cytotoxic activity for MEK inhibitors combined with taxanes, and here we sought to assess the clinical efficacy of combining selumetinib and paclitaxel.

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Article Synopsis
  • Mucosal (MM) and acral melanomas (AM) are rare types of melanoma that often have KIT mutations, which could be treated with targeted small-molecule inhibitors, though none are currently approved for melanoma.
  • A Phase II clinical trial (NICAM) assessed the safety and effectiveness of nilotinib in patients with KIT-mutant MM and AM; 18% of screened patients had KIT mutations, with some showing promising results.
  • The trial found that nilotinib demonstrated activity in treating these mutations, suggesting the need for further research on its use in managing KIT-mutated melanoma.
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