Rapid decline of Philadelphia‑positive metaphases after nilotinib treatment in a cml patient expressing a rare e14a3 bcr‑abl1 fusion transcript: A case report
Author(s) -
Michele Massimino,
Stefania Stella,
Elena Tirr�,
Maria Letizia Consoli,
Maria Stella Pennisi,
Adriana Puma,
Silvia Rita Vitale,
Chiara Romano,
Valentina Zammit,
Fabio Stagno,
Francesco Di Raimondo,
Livia Manzella
Publication year - 2019
Publication title -
oncology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.766
H-Index - 54
eISSN - 1792-1082
pISSN - 1792-1074
DOI - 10.3892/ol.2019.10558
Subject(s) - nilotinib , fusion transcript , cancer research , oncogene , philadelphia chromosome , cell cycle , medicine , fusion gene , cancer , oncology , biology , chromosomal translocation , imatinib , genetics , gene , myeloid leukemia
We report a case of chronic myeloid leukemia in a 52-year-old male expressing a rare e14a3 BCR-ABL1 fusion transcript. Cytogenetic analysis showed the t(9;22) translocation and multiplex RT-PCR detected an atypical fragment of approximately 230 base pairs. Using two primers recognizing exon 10 of BCR and exon 4 of ABL1 , a larger PCR product was identified, cloned, sequenced and defined as an e14a3 BCR-ABL1 rearrangement. The patient was treated with nilotinib and monitored measuring cytogenetic and hematological parameters, while BCR-ABL1 transcripts were surveyed by conventional and semi-nested PCR. The patient achieved a complete hematologic response after two months of treatment followed by a complete cytogenetic remission two months later. Furthermore, PCR and semi-nested PCR failed to detect the e14a3 BCR-ABL1 mRNA after 15 and 21 months of nilotinib, respectively.
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