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[The clinical significance of minimal residual disease of acute leukemia with t(4;11) (q21;q23)].

Abstract
Hybrid fusion genes are specific tumor markers of several leukemic subtypes. The use of reverse transcription-polymerase chain reaction (RT-PCR) to amplify chimeric cDNAs allows sensitive detection of the leukemia clone. The clinical relevance of minimal residual disease (MRD) remains controversial. In this report, an infantile acute lymphoblastic leukemia with t(4;11) (q21; q23) was analyzed after each treatment for the presence of MRD by RT-PCR amplification of the MLL/LTG4 fusion gene which became available recently. The patient soon achieved a hematological CR, after induction therapy, and underwent autologous BMT following consolidation chemotherapy for 9 months. However, he relapsed three months after the BMT. MRD was always detectable during his clinical course. These findings suggest that the detection of MRD of the MLL/LTG4 fusion transcript is a useful tool for monitoring MRD and selecting treatment.
AuthorsT Okamura, Y D Park, M Inoue, M Yasui, M Ueno, C Endo, K Yagi, K Kawa
Journal[Rinsho ketsueki] The Japanese journal of clinical hematology (Rinsho Ketsueki) Vol. 37 Issue 11 Pg. 1318-21 (Nov 1996) ISSN: 0485-1439 [Print] Japan
PMID8960669 (Publication Type: Case Reports, English Abstract, Journal Article, Research Support, Non-U.S. Gov't)
Topics
  • Child, Preschool
  • Chromosomes, Human, Pair 11
  • Chromosomes, Human, Pair 4
  • Humans
  • Male
  • Neoplasm, Residual
  • Polymerase Chain Reaction
  • Precursor Cell Lymphoblastic Leukemia-Lymphoma (genetics)
  • Translocation, Genetic

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