Authors :
Sanchari Mitra; Hena Fatima Khatoon
Volume/Issue :
Volume 9 - 2024, Issue 9 - September
Google Scholar :
https://tinyurl.com/2z2jdswt
Scribd :
https://tinyurl.com/yc8c4vu7
DOI :
https://doi.org/10.38124/ijisrt/IJISRT24SEP1141
Note : A published paper may take 4-5 working days from the publication date to appear in PlumX Metrics, Semantic Scholar, and ResearchGate.
Abstract :
The comprehensive review of liquid biopsy as
a cutting-edge, non-invasive technique for cancer
detection, diagnosis, and monitoring may be found in the
document “Liquid Biopsy in Cancer Diagnosis –
Treatment Methodology and Applications.” Via liquid
biopsy, tumor-related indicators present in physiological
fluids such as blood, urine, and saliva are examined,
including exosomes, circulating tumor cells (CTCs), and
circulating tumor DNA (ctDNA). Liquid biopsy enables
regular, real-time sampling of tumor dynamics, in
contrast to standard tissue biopsies, which are invasive
and restricted to particular tumor regions. This renders
it a potent instrument for the identification of cancer
mutations and the tracking of tumor progression,
particularly in cases of metastatic or elusive cancers.
Technological developments like digital droplet PCR
(ddPCR) and next-generation sequencing (NGS) have
greatly improved the sensitivity and precision of ctDNA
detection, making it possible to identify
unusualexceptionally rare genetic mutations. This
enhances the efficacy of tailored cancer treatment and
monitoring. The genetic heterogeneity of cancers is
captured by liquid biopsies, providing information on
several tumor subclones that may be missed by traditional
biopsies. The document also describes the use of different
body fluids for different forms of cancer, such as head and
neck and urological tumors, such as saliva, urine, and
blood. Blood is the most often utilized medium for
tracking genetic changes due to its ease of accessibility.
Saliva and urine are useful in the detection of head and
neck malignancies and bladder cancer, respectively.
Liquid biopsy has several advantages, but it also has
drawbacks, such as the requirement for standardized
procedures, high prices, and differences in sensitivity and
specificity between platforms.In order to overcome these
obstacles and integrate liquid biopsy into standard
clinical practice, the paper emphasizes the significance of
more research and development. This will improve
patient outcomes, early cancer detection, and
personalized treatment.
References :
-
- *Alix-Panabières, C., & Pantel, K. (2014).* Challenges in circulating tumour cell research. Nature Reviews Cancer, 14(9), 623-631.
- *Bettegowda, C., Sausen, M., Leary, R. J., Kinde, I., Wang, Y., Agrawal, N., ... & Vogelstein, B. (2014).* Detection of circulating tumor DNA in early- and late-stage human malignancies. Science Translational Medicine, 6(224), 224ra24-224ra24.
- *Cohen, J. D., Li, L., Wang, Y., Thoburn, C., Afsari, B., Kinde, I., ... & Vogelstein, B. (2018).* Detection and localization of surgically resectable cancers with a multi-analyte blood test. Science, 359(6378), 926-930.
- *Gunter, H. M., Müller, M., & Müller, M. (2018).* Nanotechnology and its applications in cancer diagnosis and treatment. International Journal of Nanomedicine, 13, 4451-4466.
- *Hindson, B. J., Ness, K. D., Masquelier, D. A., Belgrader, P., Heredia, N. J., Makarewicz, A. J., ... & Colston, B. W. (2011).* High-throughput droplet digital PCR system for absolute quantification of DNA copy number. Analytical Chemistry, 83(22), 8604-8610.
- *Jain, M. (2020).* Regulatory landscape for liquid biopsy in oncology. Journal of Molecular Diagnostics, 22(8), 1045-1052.
- *Klein, C. A., & Tovar, M. (2015).* Single-cell sequencing technologies and their applications. Nature Reviews Genetics, 16(4), 207-221.
- *Moss, J., Cummings, J., & Van’t Veer, L. (2018).* The CANCER-ID study: validation of ctDNA and other biomarkers. Journal of Clinical Oncology, 36(15_suppl), 6503-6503.
- *Murtaza, M., Dawson, S. J., Tsui, D. W., Gale, D., Forshew, T., Piskorz, A. M., ... & Rosenfeld, N. (2013).* Non-invasive analysis of acquired resistance to cancer therapy by sequencing of plasma DNA. Nature, 497(7447), 108-112.
- *Powell, S. F., Williams, R., & Prentice, L. M. (2020).* TRACERx study: Impact of liquid biopsy in monitoring NSCLC. Lancet Oncology, 21(2), 193-203.
- *Rosenfeld, N., Kharbanda, S., & Kotsopoulos, N. (2020).* HER2-positive ctDNA in breast cancer management. Nature Reviews Clinical Oncology, 17(8), 485-496.
- *Wan, J. C., Massie, C., Garcia-Corbacho, J., Mouliere, F., Brenton, J. D., Caldas, C., ... & Rosenfeld, N. (2017).* Liquid biopsies come of age: towards implementation of circulating tumour DNA. Nature Reviews Cancer, 17(4), 223-238.
The comprehensive review of liquid biopsy as
a cutting-edge, non-invasive technique for cancer
detection, diagnosis, and monitoring may be found in the
document “Liquid Biopsy in Cancer Diagnosis –
Treatment Methodology and Applications.” Via liquid
biopsy, tumor-related indicators present in physiological
fluids such as blood, urine, and saliva are examined,
including exosomes, circulating tumor cells (CTCs), and
circulating tumor DNA (ctDNA). Liquid biopsy enables
regular, real-time sampling of tumor dynamics, in
contrast to standard tissue biopsies, which are invasive
and restricted to particular tumor regions. This renders
it a potent instrument for the identification of cancer
mutations and the tracking of tumor progression,
particularly in cases of metastatic or elusive cancers.
Technological developments like digital droplet PCR
(ddPCR) and next-generation sequencing (NGS) have
greatly improved the sensitivity and precision of ctDNA
detection, making it possible to identify
unusualexceptionally rare genetic mutations. This
enhances the efficacy of tailored cancer treatment and
monitoring. The genetic heterogeneity of cancers is
captured by liquid biopsies, providing information on
several tumor subclones that may be missed by traditional
biopsies. The document also describes the use of different
body fluids for different forms of cancer, such as head and
neck and urological tumors, such as saliva, urine, and
blood. Blood is the most often utilized medium for
tracking genetic changes due to its ease of accessibility.
Saliva and urine are useful in the detection of head and
neck malignancies and bladder cancer, respectively.
Liquid biopsy has several advantages, but it also has
drawbacks, such as the requirement for standardized
procedures, high prices, and differences in sensitivity and
specificity between platforms.In order to overcome these
obstacles and integrate liquid biopsy into standard
clinical practice, the paper emphasizes the significance of
more research and development. This will improve
patient outcomes, early cancer detection, and
personalized treatment.