Development of a pO2-Guided Fine Needle Tumor Biopsy DeviceSource: Journal of Medical Devices:;2022:;volume( 016 ):;issue: 002::page 21003-1Author:McDonald, Robert C.
DOI: 10.1115/1.4052900Publisher: 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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| contributor author | McDonald, Robert C. | |
| date accessioned | 2022-05-08T08:28:55Z | |
| date available | 2022-05-08T08:28:55Z | |
| date copyright | 2/3/2022 12:00:00 AM | |
| date issued | 2022 | |
| identifier issn | 1932-6181 | |
| identifier other | med_016_02_021003.pdf | |
| identifier uri | http://yetl.yabesh.ir/yetl1/handle/yetl/4283977 | |
| description 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. | |
| publisher | The American Society of Mechanical Engineers (ASME) | |
| title | Development of a pO2-Guided Fine Needle Tumor Biopsy Device | |
| type | Journal Paper | |
| journal volume | 16 | |
| journal issue | 2 | |
| journal title | Journal of Medical Devices | |
| identifier doi | 10.1115/1.4052900 | |
| journal fristpage | 21003-1 | |
| journal lastpage | 21003-5 | |
| page | 5 | |
| tree | Journal of Medical Devices:;2022:;volume( 016 ):;issue: 002 | |
| contenttype | Fulltext |