Publications by authors named "John Lenehan"

Article Synopsis
  • Fecal microbiota transplantation (FMT) is being explored as a way to enhance the effectiveness of immune checkpoint inhibitors in treating advanced melanoma, but its use in initial treatments was previously untested.
  • A phase I trial involving 20 untreated melanoma patients showed that FMT combined with PD-1 inhibitors (nivolumab or pembrolizumab) was safe, with no severe adverse events from FMT alone, although some patients experienced immune-related side effects.
  • The trial found a 65% objective response rate, with changes in gut microbiome observed, indicating that successful treatments were linked to beneficial bacterial changes after FMT, suggesting that this approach should be studied further in conjunction with immune therapies.
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Article Synopsis
  • This study aimed to assess the best order of systemic treatments (first-line targeted therapy vs. first-line immunotherapy) for patients with BRAF-mutated metastatic melanoma using data from the Canadian Melanoma Research Network.
  • A total of 79 patients received first-line immunotherapy (1L-IO) and 107 received first-line targeted therapy (1L-TT), with no significant differences in overall survival (OS) between the two treatment groups.
  • However, patients who started with 1L-TT followed by immunotherapy (2L-IO) experienced the longest overall survival, suggesting that the sequence of treatments may influence outcomes, while also indicating that immunotherapy is effective in advanced BRAF-mut
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Consensus guidelines exist for genotype-guided fluoropyrimidine dosing based on variation in the gene dihydropyrimidine dehydrogenase (DPYD). However, these guidelines have not been widely implemented in North America and most studies of pretreatment DPYD screening have been conducted in Europe. Given regional differences in treatment practices and rates of adverse events (AEs), we investigated the impact of pretreatment DPYD genotyping on AEs in a Canadian context.

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This is a 2-center, retrospective study which aimed to evaluate the effect of baseline corticosteroid use on immunotherapy efficacy in patients with advanced melanoma. We included all patients with advanced unresectable and metastatic melanoma on single-agent programmed cell death protein 1 (PD-1) inhibitors at the Cancer Centre of Southeastern Ontario and London Regional Cancer Program. We defined baseline corticosteroid use as prednisone-equivalent of ≥10 mg within 30 days of immunotherapy initiation.

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Neoadjuvant immunotherapy involves administering immune checkpoint inhibitors before surgical resection in high-risk resectable disease. This strategy was shown to have a high pathological response rate and prolonged relapse-free survival in randomized trials in melanoma, glioblastoma, and colon cancer with small numbers of patients. In resectable cancers, immune checkpoint inhibitors such as anti-programmed cell death-1 (PD1) and anti-cytotoxic T-lymphocyte-associated protein-4 (CTLA-4) can enhance antitumor immunity by activating antigen-specific T cells found in the primary tumor.

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Pancreatic cancer has a high mortality rate, and its incidence is increasing worldwide. The almost universal poor prognosis of pancreatic cancer is partly due to symptoms presenting only at late stages and limited effective treatments. Recently, immune checkpoint blockade inhibitors have drastically improved patient survival in metastatic and advanced settings in certain cancers.

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Purpose: Female patients with breast cancer frequently develop arthralgia when treated with aromatase inhibitors (AI). Although the mechanism of AI-induced arthralgia is unknown, potential biomarkers have been identified. The purpose of this study was to investigate the clinical and genetic predictors of AI-induced arthralgia in a prospective cohort of patients with estrogen receptor-positive breast cancer.

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Purpose: The aromatase inhibitor (AI) letrozole is a first-line drug in the adjuvant treatment of breast cancer in postmenopausal women. Adherence to AI therapy, including letrozole, remains problematic due to the development of debilitating AI-induced arthralgia. Letrozole is metabolized in the liver by CYP2A6.

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Objective: To assess women's knowledge, attitudes, and behaviours related to Human Papillomavirus (HPV) and HPV vaccination.

Methods: A self-administered questionnaire was completed by 98 women (90.7% response rate) attending a hospital-based obstetrics and gynaecology outpatient clinic in a mid-size Ontario city.

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Recently protein kinases have emerged as some of the most promising drug targets; and therefore, pharmaceutical strategies have been developed to inhibit kinases in the treatment of a variety of diseases. CK2 is a serine/threonine-protein kinase that has been implicated in a number of cellular processes, including maintenance of cell viability, protection of cells from apoptosis, and tumorigenesis. Elevated CK2 activity has been established in a number of cancers where it was shown to promote tumorigenesis via the regulation of the activity of various oncogenes and tumor suppressor proteins.

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