"Double-Hit" Chronic Lymphocytic Leukemia, Involving the TP53 and MYC Genes
Although the 17p deletion [del(17p)] is rare in cases of treatment-naive chronic lymphocytic leukemia (CLL), its frequency is higher in refractory/relapsed CLL - particularly in patients undergoing chemo(immuno)therapy. disruption (deletion and/or mutation) is the strongest prognostic factor for ref...
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Veröffentlicht in: | Frontiers in oncology 2022-01, Vol.11, p.826245-826245 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Although the 17p deletion [del(17p)] is rare in cases of treatment-naive chronic lymphocytic leukemia (CLL), its frequency is higher in refractory/relapsed CLL - particularly in patients undergoing chemo(immuno)therapy.
disruption (deletion and/or mutation) is the strongest prognostic factor for refractoriness to chemotherapy; the use of Bruton tyrosine kinase inhibitors and BCL2 inhibitors is then indicated. Rare cases of CLL can also harbor translocation or gain of the
oncogene. "Double-hit CLL" (with del(17p) and
gain) is associated with a very poor prognosis. The prognostic impact of
disruption with
aberrations in patients receiving targeted therapies must now be evaluated. |
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ISSN: | 2234-943X 2234-943X |
DOI: | 10.3389/fonc.2021.826245 |