Monitoring of Minimal Residual Disease and Mixed Chimerism in a Case of High-risk Tel/aml1-positive Acute Lymphocytic Leukemia

نویسندگان

  • Tiziana Clelia Storlazzi
  • Vincenzo Liso
  • Francesco Albano
  • Gianluigi Castoldi
  • Mariano Rocchi
  • Giorgina Specchia
چکیده

therapy (methotrexate, idarubicin) but we observed hematologic relapse after three months of CR; FISH analysis showed the same chromosomal abnormality. Reinduction therapy was started with the FLANG regimen. The girl died of resistant disease in December 1999. Several groups have reported a higher incidence of abnormal/complex karyotypes in AMLM0, particularly deletion -7/7q and/or -5/5q and trisomy 8, 4 and 13, which are all frequently associated with poor prognosis.1,6 To our knowledge, this t(8;13;14) is the first described in the literature.7 In this three-way translocation between chromosomes 8, 13 and 14 we also analyzed whether the regions of chromosomes 8 and 14 involved were the same as those found in the t(8;14) reciprocal translocation commonly associated with ALL L3.8,9 Our data showed that C-MYC was not involved in the rearrangement (data not shown). Larger studies are needed to clarify which chromosome abnormalities contribute to the poor prognosis of this disease.

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تاریخ انتشار 2000