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    Development of a pO2-Guided Fine Needle Tumor Biopsy Device

    Source: Journal of Medical Devices:;2022:;volume( 016 ):;issue: 002::page 21003-1
    Author:
    McDonald, Robert C.
    DOI: 10.1115/1.4052900
    Publisher: The American Society of Mechanical Engineers (ASME)
    Abstract: Tumor biopsies are an important aspect of oncology providing a guide for medical treatment and evaluation of disease progression. Highly heterogenous tumors have complex regions of active cancer cells interdigitated with necrotic tissue and healthy noncancerous tissue. The reliable access to tumor tissue pathology is therefore challenging and usually requires multiple needle insertions with accompanying patient discomfort and risk of infection. Oxygen levels provide a means of detecting and evaluating tumor tissue with levels reduced by 2-fold to 22-fold, depending on the type of organ. However, if the biopsy needle is placed in an area of normal tissue, there is always a chance that no diagnostic cells will be acquired for meaningful pathology and molecular analysis. While not the case in all tumors, there are cases where the in vivo oxygen levels differ with tumor cells having a value of pO2 lying between the anoxic necrotic tissue and normoxic normal tissue. The level of oxygen in tumor cells can also vary with time as related to complex biochemical pathways. The efficacy of radiation therapy is also sensitive to oxygen levels in tumors. Lower levels of oxygen present greater resistance to treatment. To address these concerns, a pO2-guided biopsy needle (OGBN) was developed to determine oxygen levels and fluctuations in highly resolved regions of tumors, in order to aide in determining the optimal region for cell sampling help in determining medical treatment options.
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      Development of a pO2-Guided Fine Needle Tumor Biopsy Device

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    contributor authorMcDonald, Robert C.
    date accessioned2022-05-08T08:28:55Z
    date available2022-05-08T08:28:55Z
    date copyright2/3/2022 12:00:00 AM
    date issued2022
    identifier issn1932-6181
    identifier othermed_016_02_021003.pdf
    identifier urihttp://yetl.yabesh.ir/yetl1/handle/yetl/4283977
    description abstractTumor biopsies are an important aspect of oncology providing a guide for medical treatment and evaluation of disease progression. Highly heterogenous tumors have complex regions of active cancer cells interdigitated with necrotic tissue and healthy noncancerous tissue. The reliable access to tumor tissue pathology is therefore challenging and usually requires multiple needle insertions with accompanying patient discomfort and risk of infection. Oxygen levels provide a means of detecting and evaluating tumor tissue with levels reduced by 2-fold to 22-fold, depending on the type of organ. However, if the biopsy needle is placed in an area of normal tissue, there is always a chance that no diagnostic cells will be acquired for meaningful pathology and molecular analysis. While not the case in all tumors, there are cases where the in vivo oxygen levels differ with tumor cells having a value of pO2 lying between the anoxic necrotic tissue and normoxic normal tissue. The level of oxygen in tumor cells can also vary with time as related to complex biochemical pathways. The efficacy of radiation therapy is also sensitive to oxygen levels in tumors. Lower levels of oxygen present greater resistance to treatment. To address these concerns, a pO2-guided biopsy needle (OGBN) was developed to determine oxygen levels and fluctuations in highly resolved regions of tumors, in order to aide in determining the optimal region for cell sampling help in determining medical treatment options.
    publisherThe American Society of Mechanical Engineers (ASME)
    titleDevelopment of a pO2-Guided Fine Needle Tumor Biopsy Device
    typeJournal Paper
    journal volume16
    journal issue2
    journal titleJournal of Medical Devices
    identifier doi10.1115/1.4052900
    journal fristpage21003-1
    journal lastpage21003-5
    page5
    treeJournal of Medical Devices:;2022:;volume( 016 ):;issue: 002
    contenttypeFulltext
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