V.成人急性リンパ性白血病(ALL)―診断と治療の目覚ましい進歩

・フィラデルフィア染色体(Philadelphia chromosome:Ph)陽性急性リンパ性白血病(acute lymphoblastic leukemia:ALL)とPh陰性ALLでは大きく治療方針が異なり,ALLの診断後,早期にPhの有無を判定することが必要である.・Ph陰性ALLに対しては,多剤併用化学療法を行う.・思春期・若年成人ALLは,小児プロトコールで治療することが望ましい.・Ph陽性ALLは,60歳以上の高齢者でも,チロシンキナーゼ阻害薬(tyrosine kinase inhibitor:TKI)を使用することにより,高率に完全寛解に導入できる....

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Published in日本内科学会雑誌 Vol. 107; no. 7; pp. 1301 - 1308
Main Author 長藤, 宏司
Format Journal Article
LanguageJapanese
Published 一般社団法人 日本内科学会 10.07.2018
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ISSN0021-5384
1883-2083
DOI10.2169/naika.107.1301

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Abstract ・フィラデルフィア染色体(Philadelphia chromosome:Ph)陽性急性リンパ性白血病(acute lymphoblastic leukemia:ALL)とPh陰性ALLでは大きく治療方針が異なり,ALLの診断後,早期にPhの有無を判定することが必要である.・Ph陰性ALLに対しては,多剤併用化学療法を行う.・思春期・若年成人ALLは,小児プロトコールで治療することが望ましい.・Ph陽性ALLは,60歳以上の高齢者でも,チロシンキナーゼ阻害薬(tyrosine kinase inhibitor:TKI)を使用することにより,高率に完全寛解に導入できる.
AbstractList ・フィラデルフィア染色体(Philadelphia chromosome:Ph)陽性急性リンパ性白血病(acute lymphoblastic leukemia:ALL)とPh陰性ALLでは大きく治療方針が異なり,ALLの診断後,早期にPhの有無を判定することが必要である.・Ph陰性ALLに対しては,多剤併用化学療法を行う.・思春期・若年成人ALLは,小児プロトコールで治療することが望ましい.・Ph陽性ALLは,60歳以上の高齢者でも,チロシンキナーゼ阻害薬(tyrosine kinase inhibitor:TKI)を使用することにより,高率に完全寛解に導入できる.
Author 長藤, 宏司
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References 9) Huguet F, et al: Pediatric-inspired therapy in adults with Philadelphia chromosome-negative acute lymphoblastic leukemia: the GRAALL-2003 study. J Clin Oncol 27: 911-918, 2009.
2) Bennett JM, et al: Proposals for the classification of the acute leukaemias. French-American-British (FAB) co-operative group. Br J Haematol 33: 451-458, 1976.
13) Jabbour E, et al: Combination of hyper-CVAD with ponatinib as first-line therapy for patients with Philadelphia chromosome-positive acute lymphoblastic leukaemia: a single-centre, phase 2 study. The Lancet Oncol 16: 1547-1555. 2015.
5) Pui CH, Evans WE: Treatment of acute lymphoblastic leukemia. N Engl J Med 354: 166-178, 2006.
11) Yanada M, et al: High complete remission rate and promising outcome by combination of imatinib and chemotherapy for newly diagnosed BCR-ABL-positive acute lymphoblastic leukemia: a phase II study by the Japan Adult Leukemia Study Group. J Clin Oncol 24: 460-466, 2006.
3) Arber DA, et al: The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood 127: 2391, 2016.
10) Nagafuji K, et al: Monitoring of minimal residual disease (MRD) is useful to predict prognosis of adult patients with Ph-negative ALL: results of a prospective study (ALL MRD2002 Study). J Hematol Oncol 6: 14, 2013.
7) Stock W, et al: What determines the outcomes for adolescents and young adults with acute lymphoblastic leukemia treated on cooperative group protocols? A comparison of Children's Cancer Group and Cancer and Leukemia Group B studies. Blood 112: 1646-1654, 2008.
12) Foà R, et al: Dasatinib as first-line treatment for adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia. Blood 118: 6521-6528, 2011.
4) Iacobucci I, Mullighan CG. Genetic Basis of Acute Lymphoblastic Leukemia. J Clin Oncol 35: 975-983, 2017.
8) Hayakawa F, et al: Markedly improved outcomes and acceptable toxicity in adolescents and young adults with acute lymphoblastic leukemia following treatment with a pediatric protocol: a phase II study by the Japan Adult Leukemia Study Group. Blood Cancer J 4: e252, 2014.
6) van Dongen JJ, et al: Minimal residual disease diagnostics in acute lymphoblastic leukemia: need for sensitive, fast, and standardized technologies. Blood 125: 3996-4009, 2015.
1) Harrison CJ: Cytogenetics of paediatric and adolescent acute lymphoblastic leukaemia. Br J Haematol 144: 147-156, 2009.
References_xml – reference: 4) Iacobucci I, Mullighan CG. Genetic Basis of Acute Lymphoblastic Leukemia. J Clin Oncol 35: 975-983, 2017.
– reference: 6) van Dongen JJ, et al: Minimal residual disease diagnostics in acute lymphoblastic leukemia: need for sensitive, fast, and standardized technologies. Blood 125: 3996-4009, 2015.
– reference: 5) Pui CH, Evans WE: Treatment of acute lymphoblastic leukemia. N Engl J Med 354: 166-178, 2006.
– reference: 9) Huguet F, et al: Pediatric-inspired therapy in adults with Philadelphia chromosome-negative acute lymphoblastic leukemia: the GRAALL-2003 study. J Clin Oncol 27: 911-918, 2009.
– reference: 12) Foà R, et al: Dasatinib as first-line treatment for adult patients with Philadelphia chromosome-positive acute lymphoblastic leukemia. Blood 118: 6521-6528, 2011.
– reference: 3) Arber DA, et al: The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. Blood 127: 2391, 2016.
– reference: 1) Harrison CJ: Cytogenetics of paediatric and adolescent acute lymphoblastic leukaemia. Br J Haematol 144: 147-156, 2009.
– reference: 8) Hayakawa F, et al: Markedly improved outcomes and acceptable toxicity in adolescents and young adults with acute lymphoblastic leukemia following treatment with a pediatric protocol: a phase II study by the Japan Adult Leukemia Study Group. Blood Cancer J 4: e252, 2014.
– reference: 11) Yanada M, et al: High complete remission rate and promising outcome by combination of imatinib and chemotherapy for newly diagnosed BCR-ABL-positive acute lymphoblastic leukemia: a phase II study by the Japan Adult Leukemia Study Group. J Clin Oncol 24: 460-466, 2006.
– reference: 10) Nagafuji K, et al: Monitoring of minimal residual disease (MRD) is useful to predict prognosis of adult patients with Ph-negative ALL: results of a prospective study (ALL MRD2002 Study). J Hematol Oncol 6: 14, 2013.
– reference: 7) Stock W, et al: What determines the outcomes for adolescents and young adults with acute lymphoblastic leukemia treated on cooperative group protocols? A comparison of Children's Cancer Group and Cancer and Leukemia Group B studies. Blood 112: 1646-1654, 2008.
– reference: 13) Jabbour E, et al: Combination of hyper-CVAD with ponatinib as first-line therapy for patients with Philadelphia chromosome-positive acute lymphoblastic leukaemia: a single-centre, phase 2 study. The Lancet Oncol 16: 1547-1555. 2015.
– reference: 2) Bennett JM, et al: Proposals for the classification of the acute leukaemias. French-American-British (FAB) co-operative group. Br J Haematol 33: 451-458, 1976.
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Snippet ・フィラデルフィア染色体(Philadelphia chromosome:Ph)陽性急性リンパ性白血病(acute lymphoblastic leukemia:ALL)とPh陰性ALLでは大きく治療方針が異なり,ALLの...
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SubjectTerms チロシンキナーゼ阻害薬
フィラデルフィア染色体
微小残存病変
急性リンパ性白血病
Title V.成人急性リンパ性白血病(ALL)―診断と治療の目覚ましい進歩
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