PMID- 15678915 OWN - NLM STAT- MEDLINE DCOM- 20050422 LR - 20071115 IS - 0485-1439 (Print) IS - 0485-1439 (Linking) VI - 45 IP - 12 DP - 2004 Dec TI - [Prognostic efficacy for measurement of real-time quantitative PCR-based major bcr/abl mRNA in patients with Philadelphia chromosome-positive leukemia]. PG - 1241-6 AB - Evaluation of minimal residual disease (MRD) provides prognostic information on various hematological malignancies. We describe here the prognostic efficacy of real-time quantitative polymerase chain reaction (RQ-PCR)-based analysis of major bcr/abl mRNA in cases of Philadelphia chromosome-positive leukemia (Ph-leukemia). Twenty-one patients with Ph-leukemia were enrolled as subjects to determine the usefulness of RQ-PCR-based measurement of bcr-abl/abl ratios. Imatinib mesylate (imatinib) was administered to seven of the 21 patients before allogeneic stem cell transplantation (SCT). Hematological relapse or failure of treatment with SCT was observed in 2 of those patients who showed bcr-abl/abl ratios of more than 0.002%, and 5 of the 7 patients showed both RQ-PCR and RT-PCR negativity immediately after SCT. All of the 5 patients who did not receive imatinib before allogeneic SCT showed RQ-PCR negativity immediately after SCT, but the results of RT-PCR were positive in 3 patients at the same time points, and those became negative after donor lymphocyte infusion or the appearance of graft-versus-host disease. Administration of imatinib before SCT was thought to induce an early remission. On the other hand, 8 patients who received imatinib without SCT showed a remarkable decrease in bcr-abl/abl ratios. The ratio gradually rose in one patient with Ph+ALL, enabling prediction of the hematological relapse preceding detection by fluorescence in situ hybridization (FISH) analysis. Standardization of RQ-PCR analysis of bcr-abl mRNA will help to predict early hematological relapse in patients with MRD. In conclusion, it is thought that measurement of RQ-PCR-based major bcr/abl mRNA in patients who were given imatinib and were treated with SCT is useful for the evaluation of MRD and in deciding additional treatment. FAU - Takahata, Mutsumi AU - Takahata M AD - Department of Gastroenterology and Hematology, Hokkaido University Graduate School of Medicine. FAU - Hashino, Satoshi AU - Hashino S FAU - Fujisawa, Fumie AU - Fujisawa F FAU - Kondo, Takeshi AU - Kondo T FAU - Ota, Syuichi AU - Ota S FAU - Kobayashi, Sumiko AU - Kobayashi S FAU - Tanaka, Junji AU - Tanaka J FAU - Imamura, Masahiro AU - Imamura M FAU - Asaka, Masahiro AU - Asaka M LA - jpn PT - English Abstract PT - Journal Article PL - Japan TA - Rinsho Ketsueki JT - [Rinsho ketsueki] The Japanese journal of clinical hematology JID - 2984782R RN - 0 (RNA, Messenger) SB - IM MH - Adult MH - Female MH - Genes, abl/*genetics MH - Humans MH - Leukemia, Myelogenous, Chronic, BCR-ABL Positive/genetics/*mortality MH - Male MH - Middle Aged MH - Polymerase Chain Reaction MH - Prognosis MH - RNA, Messenger/analysis EDAT- 2005/02/01 09:00 MHDA- 2005/04/23 09:00 CRDT- 2005/02/01 09:00 PHST- 2005/02/01 09:00 [pubmed] PHST- 2005/04/23 09:00 [medline] PHST- 2005/02/01 09:00 [entrez] PST - ppublish SO - Rinsho Ketsueki. 2004 Dec;45(12):1241-6.