2018
DOI: 10.5935/1676-2444.20180015
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The role of cytogenetics and molecular biology in the diagnosis, treatment and monitoring of patients with chronic myeloid leukemia

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Cited by 11 publications
(16 citation statements)
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“…The presence of the Ph chromosome should be monitored by conventional cytogenetic analysis to obtain complete cytogenetic response (CCR) or molecular response (MR) by analysis of transcription levels of BCR-ABL1 by RT-PCR and can correlate with prognosis[ 32 , 69 , 70 ]. The FISH is recommended for diagnosis in cases where the Ph chromosome is not detected by classical cytogenetics.…”
Section: Diagnosismentioning
confidence: 99%
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“…The presence of the Ph chromosome should be monitored by conventional cytogenetic analysis to obtain complete cytogenetic response (CCR) or molecular response (MR) by analysis of transcription levels of BCR-ABL1 by RT-PCR and can correlate with prognosis[ 32 , 69 , 70 ]. The FISH is recommended for diagnosis in cases where the Ph chromosome is not detected by classical cytogenetics.…”
Section: Diagnosismentioning
confidence: 99%
“…Considering that FISH can quantify proliferating neoplastic cells in metaphase and non-proliferating cells in interphase, it used to be used for diagnosis and to analyze response to therapy using either peripheral blood or BM[ 72 ]. However, this technique has been replaced and it can only substitute chromosomal analysis in CML monitoring if BM cells are not obtained and/or for the definition of complete cytogenetic remission (CCyR)[ 69 ]. In addition, in patients with atypical transcripts, its use may be necessary for monitoring disease progression[ 41 ].…”
Section: Diagnosismentioning
confidence: 99%
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“…O conhecimento sobre a LMC adveio conjuntamente ao avanço de técnicas analíticas em citogenética humana, já que nesta leucemia se encontra a primeira mutação cromossômica ligada ao câncer, o cromossomo Ph, o qual é utilizado como marcador de LMC (DORFMAN et al, 2018).…”
Section: Citogenéticaunclassified
“…Estas variantes simples incluem um ou mais cromossomos além do 9 e 22, mas sempre modificando o cromossomo 22. Alterações secundárias ou outros rearranjos cromossômicos crípticos complexos em BCR-ABL1 podem ser vistos em pacientes com LMC com cariótipo normal (DORFMAN et al, 2018).…”
Section: Simões 2008)unclassified