Activating Mutations of FLT3 Gene in Childhood Acute Myeloid Leukemia and Their Applications for Detection of Minimal Residual Disease
Forty-two children with acute myeloid leukemia (AML) were screened for two activating mutations of the FLT3 gene, internal tandem duplication (ITD) and Asp 835 substitution (D835), using polymerase chain reaction (PCR). ITD and D835 were detected in 8 (19.0%) and 3 (7.1%) patients, respectively. Alt...
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Published in | The Japanese Journal of Pediatric Hematology Vol. 19; no. 1; pp. 19 - 24 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | Japanese |
Published |
THE JAPANESE SOCIETY OF PEDIATRIC HEMATOLOGY/ONCOLOGY
2005
特定非営利活動法人 日本小児血液・がん学会 |
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Online Access | Get full text |
ISSN | 0913-8706 1884-4723 |
DOI | 10.11412/jjph1987.19.19 |
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Abstract | Forty-two children with acute myeloid leukemia (AML) were screened for two activating mutations of the FLT3 gene, internal tandem duplication (ITD) and Asp 835 substitution (D835), using polymerase chain reaction (PCR). ITD and D835 were detected in 8 (19.0%) and 3 (7.1%) patients, respectively. Although no difference was found in the remission rate between ITD-positive and -negative patients (100% vs. 81%, p= 0.32), the relapse rate of ITD-positive patients was significantly higher than that of ITD-negative patients (87.5 ± 11.7% vs. 40.1 ± 10.5%, p = 0.0435). Interestingly, among 7 patients with t (8; 21), 3 cases were positive for ITD and all those cases experienced relapse while only one out of 4 ITD-negative cases experienced it. Thus, ITD may detect patients with poor prognosis in AML with t (8; 21). For D835-positive AML, we could not clarify the clinical significance because of its low positivity. Minimal residual leukemic cells in patients with remission could be detected effectively by PCR using the patient's ITD sequence-specific primer. The results obtained from ITD-specific PCR were closely correlated with those of reverse transcription-PCR for AML1-MTG8 or PML-RARA in patients with t (8; 21) or t (15; 17). Thus, ITD-specific PCR would be a useful method for the detection of minimal residual disease (MRD) in patients with ITD-positive AML who have no other applicable MRD targets. |
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AbstractList | Forty-two children with acute myeloid leukemia (AML) were screened for two activating mutations of the FLT3 gene, internal tandem duplication (ITD) and Asp 835 substitution (D835), using polymerase chain reaction (PCR). ITD and D835 were detected in 8 (19.0%) and 3 (7.1%) patients, respectively. Although no difference was found in the remission rate between ITD-positive and -negative patients (100% vs. 81%, p= 0.32), the relapse rate of ITD-positive patients was significantly higher than that of ITD-negative patients (87.5 ± 11.7% vs. 40.1 ± 10.5%, p = 0.0435). Interestingly, among 7 patients with t (8; 21), 3 cases were positive for ITD and all those cases experienced relapse while only one out of 4 ITD-negative cases experienced it. Thus, ITD may detect patients with poor prognosis in AML with t (8; 21). For D835-positive AML, we could not clarify the clinical significance because of its low positivity. Minimal residual leukemic cells in patients with remission could be detected effectively by PCR using the patient's ITD sequence-specific primer. The results obtained from ITD-specific PCR were closely correlated with those of reverse transcription-PCR for AML1-MTG8 or PML-RARA in patients with t (8; 21) or t (15; 17). Thus, ITD-specific PCR would be a useful method for the detection of minimal residual disease (MRD) in patients with ITD-positive AML who have no other applicable MRD targets.
小児AML42例に対し, PCRを用いてFLT3遺伝子の異常 (ITDおよびD835) の有無を検討した.ITD陽性は8例 (19.0%), D835陽性は3例 (7.1%) であった.ITDの有無による完全寛解率は, 陽性例, 陰性例でそれぞれ100%, 81% (p=0.32) と差はなかったが, 陽性例の再発率は87.5%±11.7%と陰性例 (40.1%±10.5%) と比較して有意に高く (p=0.0435), 予後不良因子と考えられた.また, t (8;21) 陽性AMLの7例中3例がITD陽性であり, 3例全例が再発した.陰性例の再発は1例のみであったことより, 予後良好とされるt (8;21) から予後不良群を抽出できる可能性があると考えられた.D835の異常にっいては, 症例数が少ないため臨床的意義は明らかにできなかった.さらに寛解期検体に対してITD特異的プライマーを用いてPCRを行い, MRDの有無を解析したところ, 融合遺伝子を指標とした結果とよく一致していた.ITD陽性AMLではMRDマーカーのない場合も多く, このような予後不良の症例では有力な指標となり得ると考えられた. Forty-two children with acute myeloid leukemia (AML) were screened for two activating mutations of the FLT3 gene, internal tandem duplication (ITD) and Asp 835 substitution (D835), using polymerase chain reaction (PCR). ITD and D835 were detected in 8 (19.0%) and 3 (7.1%) patients, respectively. Although no difference was found in the remission rate between ITD-positive and -negative patients (100% vs. 81%, p= 0.32), the relapse rate of ITD-positive patients was significantly higher than that of ITD-negative patients (87.5 ± 11.7% vs. 40.1 ± 10.5%, p = 0.0435). Interestingly, among 7 patients with t (8; 21), 3 cases were positive for ITD and all those cases experienced relapse while only one out of 4 ITD-negative cases experienced it. Thus, ITD may detect patients with poor prognosis in AML with t (8; 21). For D835-positive AML, we could not clarify the clinical significance because of its low positivity. Minimal residual leukemic cells in patients with remission could be detected effectively by PCR using the patient's ITD sequence-specific primer. The results obtained from ITD-specific PCR were closely correlated with those of reverse transcription-PCR for AML1-MTG8 or PML-RARA in patients with t (8; 21) or t (15; 17). Thus, ITD-specific PCR would be a useful method for the detection of minimal residual disease (MRD) in patients with ITD-positive AML who have no other applicable MRD targets. |
Author | OKUDA, Kumiko IKUTA, Koichiro KAI, Sumio YAMAZAKI, Sakurako KUROKI, Fumiko GOTO, Hiroaki TAKAHASHI, Hiroyuki FUJII, Hisaki |
Author_FL | 甲斐 純夫 黒木 文子 山崎 桜子 生田 孝一郎 高橋 浩之 藤井 久紀 奥田 久美子 後藤 裕明 |
Author_FL_xml | – sequence: 1 fullname: 奥田 久美子 – sequence: 2 fullname: 山崎 桜子 – sequence: 3 fullname: 甲斐 純夫 – sequence: 4 fullname: 藤井 久紀 – sequence: 5 fullname: 黒木 文子 – sequence: 6 fullname: 後藤 裕明 – sequence: 7 fullname: 生田 孝一郎 – sequence: 8 fullname: 高橋 浩之 |
Author_xml | – sequence: 1 fullname: GOTO, Hiroaki organization: Department of Pediatrics, Yokohama City University School of Medicine – sequence: 1 fullname: YAMAZAKI, Sakurako organization: Department of Pediatrics, Yokohama City University School of Medicine – sequence: 1 fullname: KAI, Sumio organization: Department of Pediatrics, Yokohama City University School of Medicine – sequence: 1 fullname: FUJII, Hisaki organization: Department of Pediatrics, Yokohama City University School of Medicine – sequence: 1 fullname: IKUTA, Koichiro organization: Department of Pediatrics, Yokohama City University School of Medicine – sequence: 1 fullname: TAKAHASHI, Hiroyuki organization: Department of Pediatrics, Yokohama City University School of Medicine – sequence: 1 fullname: KUROKI, Fumiko organization: Department of Pediatrics, Yokohama City University School of Medicine – sequence: 1 fullname: OKUDA, Kumiko organization: Department of Pediatrics, Yokohama City University School of Medicine |
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References | 7) Schnittger S, Schoch C, Dugas M, et al : Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia : Correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease. Blood 100 : 59-66, 2002 8) Deguchi K, Gilliland DG : Cooperativity between mutation in tyrosine kinases and hematopoietic transcription factor in AML. Leukemia 16 : 740-744, 2002 6) Liang DC, Shih Y, Hung IJ, et al : Clinical relevance of internal tandem duplication of the FLT3 gene in childhood acute myeloid leukemia. Cancer 94 : 3292-3298, 2002 1) Gilliland DG, Griffin JD : The roles of FLT3 in hematopoiesis and leukemia. Blood 100 : 1532-1542, 2002 3) Yamamoto Y, Kiyoi H, Nakano Y, et al : Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies. Blood 97 : 2434-2439, 2001 2) Levis M, Small D : FLT3 : ITDoes matter in leukemia. Leukemia 17 : 1738-1752, 2003 5) Zwaan CM, Meshinchi S, Radich JP, et al : FLT3 internal tandem duplication in 234 children with acute myeloid leukemia : Prognostic significance and relation to cellular drug resistance. Blood 102 : 2387-2394, 2003 9) 多和昭雄, 月本一郎 : 急性骨髄性白血病のリスク分類に基づいた層別化治療.日小血会誌18 : 200-209, 2004 10) Kiyoi H, Naoe T, Nakano S, et al : Prognostic implication of FLT3 and N-RAS gene mutations in acute myeloid leukemia. Blood 93 : 3074-3080, 1999 4) Liang DC, Shih LY, Yang CP, et al : FLT3-TKD mutation in childhood acute myeloid leukemia. Leukemia 17 : 883-886, 2003 |
References_xml | – reference: 7) Schnittger S, Schoch C, Dugas M, et al : Analysis of FLT3 length mutations in 1003 patients with acute myeloid leukemia : Correlation to cytogenetics, FAB subtype, and prognosis in the AMLCG study and usefulness as a marker for the detection of minimal residual disease. Blood 100 : 59-66, 2002 – reference: 4) Liang DC, Shih LY, Yang CP, et al : FLT3-TKD mutation in childhood acute myeloid leukemia. Leukemia 17 : 883-886, 2003 – reference: 8) Deguchi K, Gilliland DG : Cooperativity between mutation in tyrosine kinases and hematopoietic transcription factor in AML. Leukemia 16 : 740-744, 2002 – reference: 3) Yamamoto Y, Kiyoi H, Nakano Y, et al : Activating mutation of D835 within the activation loop of FLT3 in human hematologic malignancies. Blood 97 : 2434-2439, 2001 – reference: 6) Liang DC, Shih Y, Hung IJ, et al : Clinical relevance of internal tandem duplication of the FLT3 gene in childhood acute myeloid leukemia. Cancer 94 : 3292-3298, 2002 – reference: 1) Gilliland DG, Griffin JD : The roles of FLT3 in hematopoiesis and leukemia. Blood 100 : 1532-1542, 2002 – reference: 2) Levis M, Small D : FLT3 : ITDoes matter in leukemia. Leukemia 17 : 1738-1752, 2003 – reference: 5) Zwaan CM, Meshinchi S, Radich JP, et al : FLT3 internal tandem duplication in 234 children with acute myeloid leukemia : Prognostic significance and relation to cellular drug resistance. Blood 102 : 2387-2394, 2003 – reference: 9) 多和昭雄, 月本一郎 : 急性骨髄性白血病のリスク分類に基づいた層別化治療.日小血会誌18 : 200-209, 2004 – reference: 10) Kiyoi H, Naoe T, Nakano S, et al : Prognostic implication of FLT3 and N-RAS gene mutations in acute myeloid leukemia. Blood 93 : 3074-3080, 1999 |
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Title | Activating Mutations of FLT3 Gene in Childhood Acute Myeloid Leukemia and Their Applications for Detection of Minimal Residual Disease |
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