Introduction: There is a critical lack of surgical capacity for the growing burden of cancer care in West Africa. To address this gap, the development of a surgical oncology fellowship training program was proposed. However, given the limited data needed to inform the creation of this program, a comprehensive needs assessment and environmental scan of the current surgical oncology landscape in the West African region was conducted.
Methods: A convergent parallel mixed-methods design was employed. Stakeholders from eight flagship West African cancer centers were surveyed on the existing clinical capacity and scope of current practice. Data were supplemented by site visit observations and informal interviews with stakeholders. The American Society of Clinical Oncology resource-stratified guideline was used to comparably evaluate the clinical capacity for cancer care across institutions. The educational capacity was described and analyzed using qualitative description. Results were presented using a strengths, weaknesses, opportunities, and threats (SWOT) analysis.
Results: Thirty-seven individuals representing the eight institutions completed the needs assessment survey. Capacity within various clinical domains essential to the delivery of comprehensive cancer care was reported and compared between institutions. A comprehensive list of surgical procedures that should form the basis of surgical oncology training was produced by consensus. Educational capacity including teaching, assessment, evaluation and expansion was described. Aggregate results from all data sources were presented as a SWOT analysis.
Conclusion: This needs assessment represents a crucial first step towards establishing a robust surgical oncology fellowship program tailored to the needs and available resources in West Africa.
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http://dx.doi.org/10.1245/s10434-024-16483-3 | DOI Listing |
Patient Saf Surg
January 2025
Department of Surgery, University of Virginia, Charlottesville, Virginia, USA.
Background: While existing risk calculators focus on mortality and complications, elderly patients are concerned with how operations will affect their quality of life, especially their independence. We sought to develop a novel clinically relevant and easy-to-use score to predict elderly patients' loss of independence after gastrointestinal surgery.
Methods: This retrospective cohort study included patients age ≥ 65 years enrolled in the American College of Surgeons National Surgical Quality Improvement Program database and Geriatric Pilot Project who underwent pancreatic, colorectal, or hepatic surgery (January 1, 2014- December 31, 2018).
Ann Surg Oncol
January 2025
Department of Surgical Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Introduction: Children and young adults diagnosed with sarcoma often present with pulmonary metastases requiring wedge resection. It is important to balance the risk of pulmonary recurrence against the desire to limit resection of benign parenchyma. This study aims to determine the impact of resection margins on survival and recurrence among pediatric and young adult sarcoma patients.
View Article and Find Full Text PDFSurgery
January 2025
Melanoma Institute Australia, The University of Sydney, North Sydney, NSW, Australia; Faculty of Medicine and Health, The University of Sydney, Sydney, NSW, Australia. Electronic address: https://www.twitter.com/SerineLo.
J Geriatr Oncol
January 2025
Department of Geriatrics, Marien Hospital Herne, University Hospital, Ruhr University Bochum, Herne, Germany.
Gut
January 2025
Nuffield Department of Surgical Sciences, University of Oxford, Oxford, UK
Background: The immune suppression mechanisms in pancreatic ductal adenocarcinoma (PDAC) remain unknown, but preclinical studies have implicated macrophage-mediated immune tolerance. Hence, pathways that regulate macrophage phenotype are of strategic interest, with reprogramming strategies focusing on inhibitors of phosphoinositide 3-kinase-gamma (PI3Kγ) due to restricted immune cell expression. Inhibition of PI3Kγ alone is ineffective in PDAC, despite increased infiltration of CD8+ T cells.
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