Treatment and monitoring of Philadelphia chromosome-positive leukemia patients: recent advances and remaining challenges.

Acute lymphoblastic leukemia Allogeneic stem cell transplantation BCR-ABL1 Chemotherapy Chronic myeloid leukemia Minimal residual disease Next-generation sequencing Tyrosine kinase inhibitors

Journal

Journal of hematology & oncology
ISSN: 1756-8722
Titre abrégé: J Hematol Oncol
Pays: England
ID NLM: 101468937

Informations de publication

Date de publication:
23 04 2019
Historique:
received: 16 02 2019
accepted: 02 04 2019
entrez: 25 4 2019
pubmed: 25 4 2019
medline: 16 5 2020
Statut: epublish

Résumé

The Philadelphia (Ph) chromosome, resulting from the t(9;22)(q34;q11) translocation, can be found in chronic myeloid leukemia (CML) as well as in a subset of acute lymphoblastic leukemias (ALL). The deregulated BCR-ABL1 tyrosine kinase encoded by the fusion gene resulting from the translocation is considered the pathogenetic driver and can be therapeutically targeted. In both CML and Ph-positive (Ph+) ALL, tyrosine kinase inhibitors (TKIs) have significantly improved outcomes. In the TKI era, testing for BCR-ABL1 transcript levels by real-time quantitative polymerase chain reaction (RQ-PCR) has become the gold standard to monitor patient response, anticipate relapse, and guide therapeutic decisions. In CML, key molecular response milestones have been defined that draw the ideal trajectory towards optimal long-term outcomes. Treatment discontinuation (treatment-free remission, TFR) has proven feasible in a proportion of patients, and clinical efforts are now focused on how to increase this proportion and how to best select TFR candidates. In Ph+ ALL, results of trials with second- and third-generation TKIs are challenging the role of intensive chemotherapy and even that of allogeneic stem cell transplantation. Additional weapons are offered by the recently introduced monoclonal antibodies. In patients harboring mutations in the BCR-ABL1 kinase domain, prompt therapeutic reassessment and individualization based on mutation status are important to regain response and prevent disease progression. Next-generation sequencing is likely to become a precious tool for mutation testing because of the greater sensitivity and the possibility to discriminate between compound and polyclonal mutations. In this review, we discuss the latest advances in treatment and monitoring of CML and Ph+ ALL and the issues that still need to be addressed to make the best use of the therapeutic armamentarium and molecular testing technologies currently at our disposal.

Identifiants

pubmed: 31014376
doi: 10.1186/s13045-019-0729-2
pii: 10.1186/s13045-019-0729-2
pmc: PMC6480772
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

39

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Auteurs

Simona Soverini (S)

Hematology/Oncology 'L. e A. Seràgnoli', Department of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Via Massarenti 9, 40138, Bologna, Italy. simona.soverini@unibo.it.

Renato Bassan (R)

Division of Hematology, Ospedale dell'Angelo, Mestre, Venice, Italy.

Thomas Lion (T)

Children's Cancer Research Institute (CCRI) and Medical University of Vienna, Vienna, Austria.

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