Harnessing Minimal Residual Disease as a Predictor for Colorectal Cancer: Promising Horizons Amidst Challenges
Minimal Residual Disease (MRD) detection has emerged as an independent factor in clinical and pathological cancer assessment offering a highly effective method for predicting recurrence in colorectal cancer (CRC). The ongoing research initiatives such as the DYNAMIC and CIRCULATE-Japan studies, have...
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| Veröffentlicht in: | Medicina (Kaunas, Lithuania) Jg. 59; H. 10; S. 1886 |
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| Abstract | Minimal Residual Disease (MRD) detection has emerged as an independent factor in clinical and pathological cancer assessment offering a highly effective method for predicting recurrence in colorectal cancer (CRC). The ongoing research initiatives such as the DYNAMIC and CIRCULATE-Japan studies, have revealed the potential of MRD detection based on circulating tumor DNA (ctDNA) to revolutionize management for CRC patients. MRD detection represents an opportunity for risk stratification, treatment guidance, and early relapse monitoring. Here we overviewed the evolving landscape of MRD technology and its promising applications through the most up-to-date research and reviews, underscoring the transformative potential of this approach. Our primary focus is to provide a point-to-point perspective and address key challenges relating to the adoption of ctDNA-based MRD detection in the clinical setting. By identifying critical areas of interest and hurdles surrounding clinical significance, detection criteria, and potential applications of basic research, this article offers insights into the advancements needed to evaluate the role of ctDNA in CRC MRD detection, contributing to favorable clinical options and improved outcomes in the management of CRC. |
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| AbstractList | Minimal Residual Disease (MRD) detection has emerged as an independent factor in clinical and pathological cancer assessment offering a highly effective method for predicting recurrence in colorectal cancer (CRC). The ongoing research initiatives such as the DYNAMIC and CIRCULATE-Japan studies, have revealed the potential of MRD detection based on circulating tumor DNA (ctDNA) to revolutionize management for CRC patients. MRD detection represents an opportunity for risk stratification, treatment guidance, and early relapse monitoring. Here we overviewed the evolving landscape of MRD technology and its promising applications through the most up-to-date research and reviews, underscoring the transformative potential of this approach. Our primary focus is to provide a point-to-point perspective and address key challenges relating to the adoption of ctDNA-based MRD detection in the clinical setting. By identifying critical areas of interest and hurdles surrounding clinical significance, detection criteria, and potential applications of basic research, this article offers insights into the advancements needed to evaluate the role of ctDNA in CRC MRD detection, contributing to favorable clinical options and improved outcomes in the management of CRC. Minimal Residual Disease (MRD) detection has emerged as an independent factor in clinical and pathological cancer assessment offering a highly effective method for predicting recurrence in colorectal cancer (CRC). The ongoing research initiatives such as the DYNAMIC and CIRCULATE-Japan studies, have revealed the potential of MRD detection based on circulating tumor DNA (ctDNA) to revolutionize management for CRC patients. MRD detection represents an opportunity for risk stratification, treatment guidance, and early relapse monitoring. Here we overviewed the evolving landscape of MRD technology and its promising applications through the most up-to-date research and reviews, underscoring the transformative potential of this approach. Our primary focus is to provide a point-to-point perspective and address key challenges relating to the adoption of ctDNA-based MRD detection in the clinical setting. By identifying critical areas of interest and hurdles surrounding clinical significance, detection criteria, and potential applications of basic research, this article offers insights into the advancements needed to evaluate the role of ctDNA in CRC MRD detection, contributing to favorable clinical options and improved outcomes in the management of CRC.Minimal Residual Disease (MRD) detection has emerged as an independent factor in clinical and pathological cancer assessment offering a highly effective method for predicting recurrence in colorectal cancer (CRC). The ongoing research initiatives such as the DYNAMIC and CIRCULATE-Japan studies, have revealed the potential of MRD detection based on circulating tumor DNA (ctDNA) to revolutionize management for CRC patients. MRD detection represents an opportunity for risk stratification, treatment guidance, and early relapse monitoring. Here we overviewed the evolving landscape of MRD technology and its promising applications through the most up-to-date research and reviews, underscoring the transformative potential of this approach. Our primary focus is to provide a point-to-point perspective and address key challenges relating to the adoption of ctDNA-based MRD detection in the clinical setting. By identifying critical areas of interest and hurdles surrounding clinical significance, detection criteria, and potential applications of basic research, this article offers insights into the advancements needed to evaluate the role of ctDNA in CRC MRD detection, contributing to favorable clinical options and improved outcomes in the management of CRC. |
| Audience | Academic |
| Author | Wen, Xiaofen Massidda, Matteo Rallo, Vincenzo Shen, Jiaxin Carru, Ciriaco Muroni, Maria Rosaria Coradduzza, Donatella De Miglio, Maria Rosaria Scanu, Antonio Mario Angius, Andrea |
| AuthorAffiliation | 3 Department of Hematology, The First Affiliated Hospital of Shantou University Medical College, Shantou 515041, China 2 Department of Medical Oncology, Cancer Hospital of Shantou University Medical College, Shantou 515041, China 4 Department of Medicine, Surgery and Pharmacy, University of Sassari, 07100 Sassari, Italy; scanu@uniss.it (A.M.S.); mrmuroni@uniss.it (M.R.M.); mmassidda@uniss.it (M.M.) 5 Istituto di Ricerca Genetica e Biomedica (IRGB), Consiglio Nazionale delle Ricerche, CNR, Cittadella Universitaria di Cagliari, Monserrato, 09042 Cagliari, Italy; vincenzo.rallo@irgb.cnr.it (V.R.); andrea.angius@irgb.cnr.it (A.A.) 1 Department of Biomedical Sciences, University of Sassari, 07100 Sassari, Italy; x.wen@studenti.uniss.it (X.W.); dcoradduzza@uniss.it (D.C.); j.shen@studenti.uniss.it (J.S.); carru@uniss.it (C.C.) |
| AuthorAffiliation_xml | – name: 1 Department of Biomedical Sciences, University of Sassari, 07100 Sassari, Italy; x.wen@studenti.uniss.it (X.W.); dcoradduzza@uniss.it (D.C.); j.shen@studenti.uniss.it (J.S.); carru@uniss.it (C.C.) – name: 3 Department of Hematology, The First Affiliated Hospital of Shantou University Medical College, Shantou 515041, China – name: 4 Department of Medicine, Surgery and Pharmacy, University of Sassari, 07100 Sassari, Italy; scanu@uniss.it (A.M.S.); mrmuroni@uniss.it (M.R.M.); mmassidda@uniss.it (M.M.) – name: 5 Istituto di Ricerca Genetica e Biomedica (IRGB), Consiglio Nazionale delle Ricerche, CNR, Cittadella Universitaria di Cagliari, Monserrato, 09042 Cagliari, Italy; vincenzo.rallo@irgb.cnr.it (V.R.); andrea.angius@irgb.cnr.it (A.A.) – name: 2 Department of Medical Oncology, Cancer Hospital of Shantou University Medical College, Shantou 515041, China |
| Author_xml | – sequence: 1 givenname: Xiaofen surname: Wen fullname: Wen, Xiaofen – sequence: 2 givenname: Donatella orcidid: 0000-0002-8978-0490 surname: Coradduzza fullname: Coradduzza, Donatella – sequence: 3 givenname: Jiaxin orcidid: 0000-0003-0146-8863 surname: Shen fullname: Shen, Jiaxin – sequence: 4 givenname: Antonio Mario orcidid: 0000-0001-7878-1167 surname: Scanu fullname: Scanu, Antonio Mario – sequence: 5 givenname: Maria Rosaria surname: Muroni fullname: Muroni, Maria Rosaria – sequence: 6 givenname: Matteo orcidid: 0000-0002-5246-5585 surname: Massidda fullname: Massidda, Matteo – sequence: 7 givenname: Vincenzo orcidid: 0000-0002-8938-5650 surname: Rallo fullname: Rallo, Vincenzo – sequence: 8 givenname: Ciriaco orcidid: 0000-0002-6985-4907 surname: Carru fullname: Carru, Ciriaco – sequence: 9 givenname: Andrea orcidid: 0000-0003-2596-6461 surname: Angius fullname: Angius, Andrea – sequence: 10 givenname: Maria Rosaria orcidid: 0000-0002-9393-3234 surname: De Miglio fullname: De Miglio, Maria Rosaria |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/37893604$$D View this record in MEDLINE/PubMed |
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| Keywords | colorectal cancer (CRC) Minimal Residual Disease (MRD) MRD techniques MRD clinical application in CRC |
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