Monitoring Chronic Myeloid Leukemia: How Molecular Tools May Drive Therapeutic Approaches
More than 15 years ago, imatinib entered into the clinical practice as a “magic bullet”; from that point on, the prognosis of patients affected by chronic myeloid leukemia (CML) became comparable to that of aged-matched healthy subjects. The aims of treatment with tyrosine kinase inhibitors (TKIs) a...
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doaj-0e66519f3aa548d0a3066924eda54e1d2020-11-25T00:54:18ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2019-09-01910.3389/fonc.2019.00833458509Monitoring Chronic Myeloid Leukemia: How Molecular Tools May Drive Therapeutic ApproachesBarbara Izzo0Enrico Marco Gottardi1Santa Errichiello2Filomena Daraio3Claudia Baratè4Sara Galimberti5Department of Clinical Medicine and Surgery, Molecular Biology, University Federico II, Naples, ItalyDepartment of Clinical and Biological Sciences, University of Turin, Turin, ItalyDepartment of Clinical Medicine and Surgery, Molecular Biology, University Federico II, Naples, ItalyDepartment of Clinical and Biological Sciences, University of Turin, Turin, ItalySection of Hematology, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, ItalySection of Hematology, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, ItalyMore than 15 years ago, imatinib entered into the clinical practice as a “magic bullet”; from that point on, the prognosis of patients affected by chronic myeloid leukemia (CML) became comparable to that of aged-matched healthy subjects. The aims of treatment with tyrosine kinase inhibitors (TKIs) are for complete hematological response after 3 months of treatment, complete cytogenetic response after 6 months, and a reduction of the molecular disease of at least 3 logs after 12 months. Patients who do not reach their goal can switch to another TKI. Thus, the molecular monitoring of response is the main consideration of management of CML patients. Moreover, cases in deep and persistent molecular response can tempt the physician to interrupt treatment, and this “dream” is possible due to the quantitative PCR. After great international effort, today the BCR-ABL1 expression obtained in each laboratory is standardized and expressed as “international scale.” This aim has been reached after the establishment of the EUTOS program (in Europe) and the LabNet network (in Italy), the platforms where biologists meet clinicians. In the field of quantitative PCR, the digital PCR is now a new and promising, sensitive and accurate tool. Some authors reported that digital PCR is able to better classify patients in precise “molecular classes,” which could lead to a better identification of those cases that will benefit from the interruption of therapy. In addition, digital PCR can be used to identify a point mutation in the ABL1 domain, mutations that are often responsible for the TKI resistance. In the field of resistance, a prominent role is played by the NGS that enables identification of any mutation in ABL1 domain, even at sub-clonal levels. This manuscript reviews how the molecular tools can lead the management of CML patients, focusing on the more recent technical advances.https://www.frontiersin.org/article/10.3389/fonc.2019.00833/fullCMLchronic myeloid leukemiadigital PCRreal-time PCRNGSmutations |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Barbara Izzo Enrico Marco Gottardi Santa Errichiello Filomena Daraio Claudia Baratè Sara Galimberti |
spellingShingle |
Barbara Izzo Enrico Marco Gottardi Santa Errichiello Filomena Daraio Claudia Baratè Sara Galimberti Monitoring Chronic Myeloid Leukemia: How Molecular Tools May Drive Therapeutic Approaches Frontiers in Oncology CML chronic myeloid leukemia digital PCR real-time PCR NGS mutations |
author_facet |
Barbara Izzo Enrico Marco Gottardi Santa Errichiello Filomena Daraio Claudia Baratè Sara Galimberti |
author_sort |
Barbara Izzo |
title |
Monitoring Chronic Myeloid Leukemia: How Molecular Tools May Drive Therapeutic Approaches |
title_short |
Monitoring Chronic Myeloid Leukemia: How Molecular Tools May Drive Therapeutic Approaches |
title_full |
Monitoring Chronic Myeloid Leukemia: How Molecular Tools May Drive Therapeutic Approaches |
title_fullStr |
Monitoring Chronic Myeloid Leukemia: How Molecular Tools May Drive Therapeutic Approaches |
title_full_unstemmed |
Monitoring Chronic Myeloid Leukemia: How Molecular Tools May Drive Therapeutic Approaches |
title_sort |
monitoring chronic myeloid leukemia: how molecular tools may drive therapeutic approaches |
publisher |
Frontiers Media S.A. |
series |
Frontiers in Oncology |
issn |
2234-943X |
publishDate |
2019-09-01 |
description |
More than 15 years ago, imatinib entered into the clinical practice as a “magic bullet”; from that point on, the prognosis of patients affected by chronic myeloid leukemia (CML) became comparable to that of aged-matched healthy subjects. The aims of treatment with tyrosine kinase inhibitors (TKIs) are for complete hematological response after 3 months of treatment, complete cytogenetic response after 6 months, and a reduction of the molecular disease of at least 3 logs after 12 months. Patients who do not reach their goal can switch to another TKI. Thus, the molecular monitoring of response is the main consideration of management of CML patients. Moreover, cases in deep and persistent molecular response can tempt the physician to interrupt treatment, and this “dream” is possible due to the quantitative PCR. After great international effort, today the BCR-ABL1 expression obtained in each laboratory is standardized and expressed as “international scale.” This aim has been reached after the establishment of the EUTOS program (in Europe) and the LabNet network (in Italy), the platforms where biologists meet clinicians. In the field of quantitative PCR, the digital PCR is now a new and promising, sensitive and accurate tool. Some authors reported that digital PCR is able to better classify patients in precise “molecular classes,” which could lead to a better identification of those cases that will benefit from the interruption of therapy. In addition, digital PCR can be used to identify a point mutation in the ABL1 domain, mutations that are often responsible for the TKI resistance. In the field of resistance, a prominent role is played by the NGS that enables identification of any mutation in ABL1 domain, even at sub-clonal levels. This manuscript reviews how the molecular tools can lead the management of CML patients, focusing on the more recent technical advances. |
topic |
CML chronic myeloid leukemia digital PCR real-time PCR NGS mutations |
url |
https://www.frontiersin.org/article/10.3389/fonc.2019.00833/full |
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