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3 - Treatment of acute lymphoblastic leukemia (ALL) in adults

Published online by Cambridge University Press:  10 January 2011

Ryan Mattison
Affiliation:
Division of Hematology/Oncology, School of Medicine and Public Health, University of Wisconsin, Madison, WI, USA
Sarah Larson
Affiliation:
Section of Hematology-Oncology, Department of Medicine, University of Chicago Medical Center, Chicago, IL, USA
Wendy Stock
Affiliation:
Section of Hematology-Oncology, Department of Medicine, University of Chicago Medical Center, Chicago, IL, USA
Susan O'Brien
Affiliation:
University of Texas/MD Anderson Cancer Center, Houston
Julie M. Vose
Affiliation:
University of Nebraska Medical Center, Omaha
Hagop M. Kantarjian
Affiliation:
University of Texas/MD Anderson Cancer Center, Houston
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Summary

Introduction

Acute lymphoblastic leukemia (ALL) is a neoplastic clonal disorder resulting from the maturation arrest of lymphoid progenitors. While both T-cell precursors and B-cell precursors can be transformed, greater than 85% of cases are derived from precursor B cells. Accumulation of lymphoblasts within the bone marrow can result in anemia, thrombocytopenia, and neutropenia. Symptoms of fatigue, bleeding, bruising, and infection are frequent initial manifestations of the disease. There are a number of ALL subtypes that are characterized by particular morphologic, immunophenotypic, cytogenetics, and molecular findings. Treatment of ALL in the pediatric population has been a success story in hematology/oncology, with cure rates approaching 80%. Unfortunately, a majority of adult patients, approximately 65%, succumb to their disease. The use of novel agents and the introduction of risk-adapted therapies, including stem cell transplantation (SCT), the identification of new molecular targets, and the application of pediatric treatment approaches to adult patients are promising strategies that offer hope to improve treatment outcomes for adults with this heterogeneous group of diseases.

Epidemiology/etiology

Incidence

ALL comprises 20% of newly diagnosed acute leukemias in adults. Approximately 5200 new cases were diagnosed in the United States in 2007, and 1420 patients died from the disease that year. Most cases occur de novo, though prior exposure to chemotherapy, especially topoisomerase II inhibitors and alkylating agents, is a risk factor for both ALL and acute myeloid leukemia (AML). Therapy-related leukemias are strongly associated with rearrangements of the MLL (mixed-lineage leukemia) gene located on chromosome 11q23.

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Publisher: Cambridge University Press
Print publication year: 2010

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References

Jemal, A, Siegel, R, Ward, E, et al. Cancer statistics, 2007. CA Cancer J Clin 2007;57:43–66.CrossRefGoogle ScholarPubMed
Andersen, MK, Christiansen, DH, Jensen, BA, et al. Therapy-related acute lymphoblastic leukaemia with MLL rearrangements following DNA topoisomerase II inhibitors, an increasing problem: report on two new cases and review of the literature since 1992. Br J Haematol 2001;114:539–43.CrossRefGoogle ScholarPubMed
Leone, G, Voso, MT, Sica, S, et al. Therapy related leukemias: susceptibility, prevention and treatment. Leuk Lymphoma 2001;41:255–76.CrossRefGoogle Scholar
Zipursky, A, Poon, A, Doyle, J. Leukemia in Down syndrome: a review. Pediatr Hematol Oncol 1992;9:139–49.CrossRefGoogle ScholarPubMed
Gurbuxani, S, Vyas, P, Crispino, JD. Recent insights into the mechanisms of myeloid leukemogenesis in Down syndrome. Blood 2004;103:399–406.CrossRefGoogle ScholarPubMed
Shaw, MP, Eden, OB, Grace, E, et al. Acute lymphoblastic leukemia and Klinefelter's syndrome. Pediatr Hematol Oncol 1992;9:81–5.CrossRefGoogle ScholarPubMed
German, J, Bloom, D, Passarge, E, et al. Bloom's syndrome. VI. The disorder in Israel and an estimation of the gene frequency in the Ashkenazim. Am J Hum Genet 1977;29:553–62.Google ScholarPubMed
Toledano, SR, Lange, BJ. Ataxia-telangiectasia and acute lymphoblastic leukemia. Cancer 1980;45:1675–8.3.0.CO;2-D>CrossRefGoogle ScholarPubMed
Greaves, MF, Maia, AT, Wiemels, JL, et al. Leukemia in twins: lessons in natural history. Blood 2003;102:2321–33.CrossRefGoogle ScholarPubMed
Wiemels, JL, Cazzaniga, G, Daniotti, M, et al. Prenatal origin of acute lymphoblastic leukaemia in children. Lancet 1999;354:1499–503.CrossRefGoogle ScholarPubMed
Fasching, K, Panzer, S, Haas, OA, et al. Presence of clone-specific antigen receptor gene rearrangements at birth indicates an in utero origin of diverse types of early childhood acute lymphoblastic leukemia. Blood 2000;95:2722–4.Google Scholar
Mori, H, Colman, SM, Xiao, Z, et al. Chromosome translocations and covert leukemic clones are generated during normal fetal development. Proc Natl Acad Sci U S A 2002;99:8242–7.CrossRefGoogle ScholarPubMed
Preston, DL, Kusumi, S, Tomonaga, M, et al. Cancer incidence in atomic bomb survivors. Part III. Leukemia, lymphoma and multiple myeloma, 1950–1987. Radiat Res 1994;137:S68–97.CrossRefGoogle ScholarPubMed
Sandler, DP, Shore, DL, Anderson, JR, et al. Cigarette smoking and risk of acute leukemia: associations with morphology and cytogenetic abnormalities in bone marrow. J Natl Cancer Inst 1993;85:1994–2003.CrossRefGoogle ScholarPubMed
UK Childhood Cancer Study Investigators. Childhood cancer and residential proximity to power lines. Br J Cancer 2000;83:1573–80.
Jaffe, E, Harris, N, Stein, H, et al. (eds.) World Health Organization Classification of Tumours:Pathology and Genetics of Tumours of Haematopoietic and Lymphoid Tissues. Lyon, IARC Press. 2001; 111–87.Google Scholar
Thomas, DA, O'Brien, S, Jorgensen, JL, et al. Prognostic significance of CD20 expression in adults with de novo precursor B-lineage acute lymphoblastic leukemia. Blood 2009;113:6330–7.CrossRefGoogle ScholarPubMed
Faderl, S, Kantarjian, HM, Talpaz, M, et al. Clinical significance of cytogenetic abnormalities in adult acute lymphoblastic leukemia. Blood 1998;91:3995–4019.Google ScholarPubMed
Secker-Walker, LM, Prentice, HG, Durrant, J, et al. Cytogenetics adds independent prognostic information in adults with acute lymphoblastic leukaemia on MRC trial UKALL XA. MRC Adult Leukaemia Working Party. Br J Haematol 1997;96:601–10.CrossRefGoogle ScholarPubMed
Wetzler, M, Dodge, RK, Mrozek, K, et al. Prospective karyotype analysis in adult acute lymphoblastic leukemia: the cancer and leukemia Group B experience. Blood 1999;93:3983–93.Google ScholarPubMed
Skorski, T, Kanakaraj, P, Nieborowska-Skorska, M, et al. Phosphatidylinositol-3 kinase activity is regulated by BCR/ABL and is required for the growth of Philadelphia chromosome-positive cells. Blood 1995;86:726–36.Google ScholarPubMed
Ferrando, AA, Look, AT. Clinical implications of recurring chromosomal and associated molecular abnormalities in acute lymphoblastic leukemia. Semin Hematol 2000;37:381–95.CrossRefGoogle ScholarPubMed
Golub, TR, Barker, GF, Bohlander, SK, et al. Fusion of the TEL gene on 12p13 to the AML1 gene on 21q22 in acute lymphoblastic leukemia. Proc Natl Acad Sci U S A 1995;92:4917–21.CrossRefGoogle ScholarPubMed
Shurtleff, SA, Buijs, A, Behm, FG, et al. TEL/AML1 fusion resulting from a cryptic t(12;21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis. Leukemia 1995;9:1985–9.Google Scholar
Dalla-Favera, R, Bregni, M, Erikson, J, et al. Human c-myc onc gene is located on the region of chromosome 8 that is translocated in Burkitt lymphoma cells. Proc Natl Acad Sci U S A 1982;79:7824–7.CrossRefGoogle ScholarPubMed
Taub, R, Kirsch, I, Morton, C, et al. Translocation of the c-myc gene into the immunoglobulin heavy chain locus in human Burkitt lymphoma and murine plasmacytoma cells. Proc Natl Acad Sci U S A 1982;79:7837–41.CrossRefGoogle ScholarPubMed
Bertin, R, Acquaviva, C, Mirebeau, D, et al. CDKN2A, CDKN2B, and MTAP gene dosage permits precise characterization of mono- and bi-allelic 9p21 deletions in childhood acute lymphoblastic leukemia. Genes Chromosomes Cancer 2003;37:44–57.CrossRefGoogle ScholarPubMed
Sherr, CJ, Roberts, JM. CDK inhibitors: positive and negative regulators of G1-phase progression. Genes Dev 1999;13:1501–12.CrossRefGoogle ScholarPubMed
Stock, W, Tsai, T, Golden, C, et al. Cell cycle regulatory gene abnormalities are important determinants of leukemogenesis and disease biology in adult acute lymphoblastic leukemia. Blood 2000;95:2364–71.Google ScholarPubMed
Aster, JC, Pear, WS, Blacklow, SC. Notch signaling in leukemia. Annu Rev Pathol 2008;3:587–613.CrossRefGoogle ScholarPubMed
Weng, AP, Millholland, JM, Yashiro-Ohtani Y, et al. c-Myc is an important direct target of Notch1 in T-cell acute lymphoblastic leukemia/lymphoma. Genes Dev 2006;20:2096–109.CrossRefGoogle ScholarPubMed
Palomero, T, Lim, WK, Odom, DT, et al. NOTCH1 directly regulates c-MYC and activates a feed-forward-loop transcriptional network promoting leukemic cell growth. Proc Natl Acad Sci U S A 2006;103:18 261–6.CrossRefGoogle ScholarPubMed
Chan, SM, Weng, AP, Tibshirani, R, et al. Notch signals positively regulate activity of the mTOR pathway in T-cell acute lymphoblastic leukemia. Blood 2007;110:278–86.CrossRefGoogle ScholarPubMed
Palomero, T, Sulis, ML, Cortina, M, et al. Mutational loss of PTEN induces resistance to NOTCH1 inhibition in T-cell leukemia. Nat Med 2007;13:1203–10.CrossRefGoogle ScholarPubMed
Palomero, T, Dominguez, M, Ferrando, AA. The role of the PTEN/AKT pathway in NOTCH1-induced leukemia. Cell Cycle 2008;7:965–70.CrossRefGoogle ScholarPubMed
Mullighan, CG, Goorha, S, Radtke, I, et al. Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia. Nature 2007;446:758–64.CrossRefGoogle ScholarPubMed
Mullighan, CG, Miller, CB, Radtke, I, et al. BCR-ABL1 lymphoblastic leukaemia is characterized by the deletion of Ikaros. Nature 2008;453:110–14.CrossRefGoogle ScholarPubMed
Mi, S, Lu, J, Sun, M, et al. MicroRNA expression signatures accurately discriminate acute lymphoblastic leukemia from acute myeloid leukemia. Proc Natl Acad Sci U S A 2007;104:19 971–6.CrossRefGoogle ScholarPubMed
Larson, RA, Dodge, RK, Burns, CP, et al. A five-drug remission induction regimen with intensive consolidation for adults with acute lymphoblastic leukemia: cancer and leukemia group B study 8811. Blood 1995;85:2025–37.Google Scholar
Kantarjian, HM, Walters, RS, Keating, MJ, et al. Results of the vincristine, doxorubicin, and dexamethasone regimen in adults with standard- and high-risk acute lymphocytic leukemia. J Clin Oncol 1990;8:994–1004.CrossRefGoogle ScholarPubMed
Lazzarino, M, Morra, E, Alessandrino, EP, et al. Adult acute lymphoblastic leukemia. Response to therapy according to presenting features in 62 patients. Eur J Cancer Clin Oncol 1982;18:813–19.CrossRefGoogle ScholarPubMed
Hoelzer, D, Thiel, E, Loffler, H, et al. Prognostic factors in a multicenter study for treatment of acute lymphoblastic leukemia in adults. Blood 1988;71:123–31.Google Scholar
Chessells, JM, Hall, E, Prentice, HG, et al. The impact of age on outcome in lymphoblastic leukaemia; MRC UKALL X and XA compared: a report from the MRC Paediatric and Adult Working Parties. Leukemia 1998;12:463–73.CrossRefGoogle ScholarPubMed
Secker-Walker, LM, Craig, JM, Hawkins, JM, et al. Philadelphia positive acute lymphoblastic leukemia in adults: age distribution, BCR breakpoint and prognostic significance. Leukemia 1991;5:196–9.Google ScholarPubMed
Linker, CA, Levitt, LJ, O'Donnell, M, et al. Treatment of adult acute lymphoblastic leukemia with intensive cyclical chemotherapy: a follow-up report. Blood 1991;78:2814–22.Google ScholarPubMed
Hoelzer, D, Thiel, E, Ludwig, WD, et al. The German multicentre trials for treatment of acute lymphoblastic leukemia in adults. The German Adult ALL Study Group. Leukemia 1992;6 Suppl 2:175–7.Google ScholarPubMed
Faderl, S, Albitar, M. Insights into the biologic and molecular abnormalities in adult acute lymphocytic leukemia. Hematol Oncol Clin North Am 2000;14:1267–88.CrossRefGoogle ScholarPubMed
Mandelli, F, Annino, L, Rotoli, B. The GIMEMA ALL 0183 trial: analysis of 10-year follow-up. GIMEMA Cooperative Group, Italy. Br J Haematol 1996;92:665–72.CrossRefGoogle ScholarPubMed
Suggs, JL, Cruse, JM, Lewis, RE. Aberrant myeloid marker expression in precursor B-cell and T-cell leukemias. Exp Mol Pathol 2007;83:471–3.CrossRefGoogle ScholarPubMed
Matutes, E, Morilla, R, Farahat, N, et al. Definition of acute biphenotypic leukemia. Haematologica 1997;82:64–6.Google ScholarPubMed
Boldt, DH, Kopecky, KJ, Head, D, et al. Expression of myeloid antigens by blast cells in acute lymphoblastic leukemia of adults. The Southwest Oncology Group experience. Leukemia 1994;8:2118–26.Google ScholarPubMed
Pui, CH, Behm, FG, Singh, B, et al. Myeloid-associated antigen expression lacks prognostic value in childhood acute lymphoblastic leukemia treated with intensive multiagent chemotherapy. Blood 1990;75:198–202.Google ScholarPubMed
Preti, HA, Huh, YO, O'Brien, SM, et al. Myeloid markers in adult acute lymphocytic leukemia. Correlations with patient and disease characteristics and with prognosis. Cancer 1995;76:1564–70.3.0.CO;2-1>CrossRefGoogle ScholarPubMed
Gaynor, J, Chapman, D, Little, C, et al. A cause-specific hazard rate analysis of prognostic factors among 199 adults with acute lymphoblastic leukemia: the Memorial Hospital experience since 1969. J Clin Oncol 1988;6:1014–30.CrossRefGoogle ScholarPubMed
Pongers-Willemse, MJ, Seriu, T, Stolz, F, et al. Primers and protocols for standardized detection of minimal residual disease in acute lymphoblastic leukemia using immunoglobulin and T cell receptor gene rearrangements and TAL1 deletions as PCR targets: report of the BIOMED-1 CONCERTED ACTION: investigation of minimal residual disease in acute leukemia. Leukemia 1999;13:110–18.CrossRefGoogle Scholar
Gabert, J, Beillard, E, Velden, VH, et al. Standardization and quality control studies of ‘real-time’ quantitative reverse transcriptase polymerase chain reaction of fusion gene transcripts for residual disease detection in leukemia – a Europe Against Cancer program. Leukemia 2003;17:2318–57.CrossRefGoogle ScholarPubMed
Mortuza, FY, Papaioannou, M, Moreira, IM, et al. Minimal residual disease tests provide an independent predictor of clinical outcome in adult acute lymphoblastic leukemia. J Clin Oncol 2002;20:1094–104.CrossRefGoogle ScholarPubMed
Bruggemann, M, Raff, T, Flohr, T, et al. Clinical significance of minimal residual disease quantification in adult patients with standard-risk acute lymphoblastic leukemia. Blood 2006;107:1116–23.CrossRefGoogle ScholarPubMed
Vidriales, MB, San-Miguel, JF, Orfao, A, et al. Minimal residual disease monitoring by flow cytometry. Best Pract Res Clin Haematol 2003;16:599–612.CrossRefGoogle ScholarPubMed
Krampera, M, Vitale, A, Vincenzi, C, et al. Outcome prediction by immunophenotypic minimal residual disease detection in adult T-cell acute lymphoblastic leukaemia. Br J Haematol 2003;120:74–9.CrossRefGoogle ScholarPubMed
Gokbuget, N, Arnold, R, Bohme, A, et al. Improved outcome in high risk and very high risk ALL by risk adapted SCT and in standard risk ALL by intensive chemotherapy in 713 adult ALL patients treated according to the prospective GMALL study 07/2003. ASH Annual Meeting Abstracts 2007;110:12.Google Scholar
Larson, RA, Dodge, RK, Linker, CA, et al. A randomized controlled trial of filgrastim during remission induction and consolidation chemotherapy for adults with acute lymphoblastic leukemia: CALGB study 9111. Blood 1998;92:1556–64.Google ScholarPubMed
Takeuchi, J, Kyo, T, Naito, K, et al. Induction therapy by frequent administration of doxorubicin with four other drugs, followed by intensive consolidation and maintenance therapy for adult acute lymphoblastic leukemia: the JALSG-ALL93 study. Leukemia 2002;16:1259–66.CrossRefGoogle ScholarPubMed
Annino, L, Vegna, ML, Camera, A, et al. Treatment of adult acute lymphoblastic leukemia (ALL): long-term follow-up of the GIMEMA ALL 0288 randomized study. Blood 2002; 99:863–71.CrossRefGoogle ScholarPubMed
Kantarjian, H, Thomas, D, O'Brien, S, et al. Long-term follow-up results of hyperfractionated cyclophosphamide, vincristine, doxorubicin, and dexamethasone (HyperCVAD), a dose-intensive regimen, in adult acute lymphocytic leukemia. Cancer 2004;101:2788–801.CrossRefGoogle Scholar
Thomas, X, Boiron, JM, Huguet, F, et al. Outcome of treatment in adults with acute lymphoblastic leukemia: analysis of the LALA-94 trial. J Clin Oncol 2004; 22:4075–86.CrossRefGoogle ScholarPubMed
Rowe, JM, Buck, G, Burnett, AK, et al. Induction therapy for adults with acute lymphoblastic leukemia: results of more than 1500 patients from the international ALL trial: MRC UKALL XII/ECOG E2993. Blood 2005;106:3760–7.CrossRefGoogle ScholarPubMed
Hussein, KK, Dahlberg, S, Head, D, et al. Treatment of acute lymphoblastic leukemia in adults with intensive induction, consolidation, and maintenance chemotherapy. Blood 1989;73:57–63.Google ScholarPubMed
Schauer, P, Arlin, ZA, Mertelsmann, R, et al. Treatment of acute lymphoblastic leukemia in adults: results of the L-10 and L-10M protocols. J Clin Oncol 1983;1:462–70.CrossRefGoogle ScholarPubMed
Gottlieb, AJ, Weinberg, V, Ellison, RR, et al. Efficacy of daunorubicin in the therapy of adult acute lymphocytic leukemia: a prospective randomized trial by cancer and leukemia group B. Blood 1984;64:267–74.Google ScholarPubMed
Radford, JE, Burns, CP, Jones, MP, et al. Adult acute lymphoblastic leukemia: results of the Iowa HOP-L protocol. J Clin Oncol 1989;7:58–66.CrossRefGoogle ScholarPubMed
Cuttner, J, Mick, R, Budman, DR, et al. Phase III trial of brief intensive treatment of adult acute lymphocytic leukemia comparing daunorubicin and mitoxantrone: a CALGB Study. Leukemia 1991;5:425–31.Google ScholarPubMed
Hoelzer, D, Ludwig, WD, Thiel, E, et al. Improved outcome in adult B-cell acute lymphoblastic leukemia. Blood 1996;87:495–508.Google ScholarPubMed
Gokbuget, N, Hoelzer, D, Arnold, R, et al. Treatment of adult ALL according to protocols of the German Multicenter Study Group for Adult ALL (GMALL). Hematol Oncol Clin North Am 2000;14:1307–25.CrossRefGoogle Scholar
Nachman, JB, Sather, HN, Sensel, MG, et al. Augmented post-induction therapy for children with high-risk acute lymphoblastic leukemia and a slow response to initial therapy. N Engl J Med 1998;338:1663–71.CrossRefGoogle Scholar
Kantarjian, HM, O'Brien, S, Smith, TL, et al. Results of treatment with HyperCVAD, a dose-intensive regimen, in adult acute lymphocytic leukemia. J Clin Oncol 2000;18:547–61.CrossRefGoogle Scholar
Larson, RA, Fretzin, MH, Dodge, RK, et al. Hypersensitivity reactions to L-asparaginase do not impact on the remission duration of adults with acute lymphoblastic leukemia. Leukemia 1998;12:660–5.CrossRefGoogle Scholar
Dekker, AW, van't Veer, MB, Sizoo, W, et al. Intensive postremission chemotherapy without maintenance therapy in adults with acute lymphoblastic leukemia. Dutch Hemato-Oncology Research Group. J Clin Oncol 1997;15:476–82.CrossRefGoogle ScholarPubMed
Reman, O, Pigneux, A, Huguet, F, et al. Central nervous system involvement in adult acute lymphoblastic leukemia at diagnosis and/or at first relapse: results from the GET-LALA group. Leuk Res 2008;32:1741–50.CrossRefGoogle ScholarPubMed
Cortes, J, O'Brien, SM, Pierce, S, et al. The value of high-dose systemic chemotherapy and intrathecal therapy for central nervous system prophylaxis in different risk groups of adult acute lymphoblastic leukemia. Blood 1995;86:2091–7.Google ScholarPubMed
Law, IP, Blom, J. Adult acute leukemia: frequency of central system involvement in long term survivors. Cancer 1977;40:1304–6.3.0.CO;2-V>CrossRefGoogle ScholarPubMed
Omura, GA, Moffitt, S, Vogler, WR, et al. Combination chemotherapy of adult acute lymphoblastic leukemia with randomized central nervous system prophylaxis. Blood 1980;55:199–204.Google ScholarPubMed
Mastrangelo, R. The problem of “staging” in childhood acute lymphoblastic leukemia: a review. Med Pediatr Oncol 1986;14:121–3.CrossRefGoogle ScholarPubMed
Kantarjian, HM, Walters, RS, Smith, TL, et al. Identification of risk groups for development of central nervous system leukemia in adults with acute lymphocytic leukemia. Blood 1988;72:1784–9.Google ScholarPubMed
Tucker, J, Prior, PF, Green, CR, et al. Minimal neuropsychological sequelae following prophylactic treatment of the central nervous system in adult leukaemia and lymphoma. Br J Cancer 1989;60:775–80.CrossRefGoogle ScholarPubMed
Pullen, J, Boyett, J, Shuster, J, et al. Extended triple intrathecal chemotherapy trial for prevention of CNS relapse in good-risk and poor-risk patients with B-progenitor acute lymphoblastic leukemia: a Pediatric Oncology Group study. J Clin Oncol 1993;11:839–49.CrossRefGoogle ScholarPubMed
Mandelli, F, Annino, L, Vegna, ML, et al. GIMEMA ALL 0288: a multicentric study on adult acute lymphoblastic leukemia. Preliminary results. Leukemia 1992;6 Suppl 2:182–5.Google ScholarPubMed
Laver, JH, Barredo, JC, Amylon, M, et al. Effects of cranial radiation in children with high risk T cell acute lymphoblastic leukemia: a Pediatric Oncology Group report. Leukemia 2000;14:369–73.CrossRefGoogle Scholar
Storb, R, Bryant, JI, Buckner, CD, et al. Allogeneic marrow grafting for acute lymphoblastic leukemia: leukemic relapse. Transplant Proc 1973;5:923–6.Google ScholarPubMed
Weiden, PL, Flournoy, N, Thomas, ED, et al. Antileukemic effect of graft-versus-host disease in human recipients of allogeneic-marrow grafts. N Engl J Med 1979;300:1068–73.CrossRefGoogle ScholarPubMed
Oh, H, Gale, RP, Zhang, MJ, et al. Chemotherapy vs HLA-identical sibling bone marrow transplants for adults with acute lymphoblastic leukemia in first remission. Bone Marrow Transplant 1998;22:253–7.CrossRefGoogle ScholarPubMed
Hunault, M, Harousseau, JL, Delain, M, et al. Better outcome of adult acute lymphoblastic leukemia after early genoidentical allogeneic bone marrow transplantation (BMT) than after late high-dose therapy and autologous BMT: a GOELAMS trial. Blood 2004;104:3028–37.CrossRefGoogle ScholarPubMed
Ribera, JM, Oriol, A, Bethencourt, C, et al. Comparison of intensive chemotherapy, allogeneic or autologous stem cell transplantation as post-remission treatment for adult patients with high-risk acute lymphoblastic leukemia. Results of the PETHEMA ALL-93 trial. Haematologica 2005;90:1346–56.Google ScholarPubMed
Goldstone, AH, Richards, SM, Lazarus, HM, et al. In adults with standard-risk acute lymphoblastic leukemia, the greatest benefit is achieved from a matched sibling allogeneic transplantation in first complete remission, and an autologous transplantation is less effective than conventional consolidation/maintenance chemotherapy in all patients: final results of the International ALL Trial (MRC UKALL XII/ECOG E2993). Blood 2008;111:1827–33.CrossRefGoogle Scholar
Laport, GG, Alvarnas, JC, Palmer, JM, et al. Long-term remission of Philadelphia chromosome-positive acute lymphoblastic leukemia after allogeneic hematopoietic cell transplantation from matched sibling donors: a 20-year experience with the fractionated total body irradiation-etoposide regimen. Blood 2008;112:903–9.CrossRefGoogle ScholarPubMed
Witte, T, Awwad, B, Boezeman, J, et al. Role of allogenic bone marrow transplantation in adolescent or adult patients with acute lymphoblastic leukaemia or lymphoblastic lymphoma in first remission. Bone Marrow Transplant 1994;14:767–74.Google ScholarPubMed
Thiebaut, A, Vernant, JP, Degos, L, et al. Adult acute lymphocytic leukemia study testing chemotherapy and autologous and allogeneic transplantation. A follow-up report of the French protocol LALA 87. Hematol Oncol Clin North Am 2000; 14:1353–66.CrossRefGoogle ScholarPubMed
Dhedin, N, Dombret, H, Thomas, X, et al. Autologous stem cell transplantation in adults with acute lymphoblastic leukemia in first complete remission: analysis of the LALA-85, -87 and -94 trials. Leukemia 2006;20:336–44.CrossRefGoogle ScholarPubMed
Yanada, M, Matsuo, K, Suzuki, T, et al. Allogeneic hematopoietic stem cell transplantation as part of postremission therapy improves survival for adult patients with high-risk acute lymphoblastic leukemia: a metaanalysis. Cancer 2006;106:2657–63.CrossRefGoogle ScholarPubMed
Thomas, DA, Cortes, J, O'Brien, S, et al. HyperCVAD program in Burkitt's-type adult acute lymphoblastic leukemia. J Clin Oncol 1999;17:2461–70.CrossRefGoogle Scholar
Yustein, JT, Dang, CV. Biology and treatment of Burkitt's lymphoma. Curr Opin Hematol 2007;14:375–81.CrossRefGoogle ScholarPubMed
Zeller, KI, Zhao, X, Lee, CW, et al. Global mapping of c-Myc binding sites and target gene networks in human B cells. Proc Natl Acad Sci U S A 2006;103:17 834–9.CrossRefGoogle ScholarPubMed
Hummel, M, Bentink, S, Berger, H, et al. A biologic definition of Burkitt's lymphoma from transcriptional and genomic profiling. N Engl J Med 2006;354:2419–30.CrossRefGoogle ScholarPubMed
Dave, SS, Fu, K, Wright, GW, et al. Molecular diagnosis of Burkitt's lymphoma. N Engl J Med 2006;354:2431–42.CrossRefGoogle ScholarPubMed
Murphy, SB, Bowman, WP, Abromowitch, M, et al. Results of treatment of advanced-stage Burkitt's lymphoma and B cell (SIg+) acute lymphoblastic leukemia with high-dose fractionated cyclophosphamide and coordinated high-dose methotrexate and cytarabine. J Clin Oncol 1986;4:1732–9.CrossRefGoogle Scholar
Soussain, C, Patte, C, Ostronoff, M, et al. Small noncleaved cell lymphoma and leukemia in adults. A retrospective study of 65 adults treated with the LMB pediatric protocols. Blood 1995;85:664–74.Google ScholarPubMed
Thomas, DA, Faderl, S, O'Brien, S, et al. Chemoimmunotherapy with HyperCVAD plus rituximab for the treatment of adult Burkitt and Burkitt-type lymphoma or acute lymphoblastic leukemia. Cancer 2006;106:1569–80.CrossRefGoogle ScholarPubMed
Mead, GM, Sydes, MR, Walewski, J, et al. An international evaluation of CODOX-M and CODOX-M alternating with IVAC in adult Burkitt's lymphoma: results of United Kingdom Lymphoma Group LY06 study. Ann Oncol 2002;13:1264–74.CrossRefGoogle ScholarPubMed
Rizzieri, DA, Johnson, JL, Niedzwiecki, D, et al. Intensive chemotherapy with and without cranial radiation for Burkitt leukemia and lymphoma: final results of Cancer and Leukemia Group B Study 9251. Cancer 2004;100:1438–48.CrossRefGoogle ScholarPubMed
Divine, M, Casassus, P, Koscielny, S, et al. Burkitt lymphoma in adults: a prospective study of 72 patients treated with an adapted pediatric LMB protocol. Ann Oncol 2005;16:1928–35.CrossRefGoogle ScholarPubMed
Hoelzer, D, Hiddemann, W, Baumann, A, et al. High survival rate in adult Burkitt's lymphoma/leukemia and diffuse large B-cell lymphoma with mediastinal involvement. ASH Annual Meeting Abstracts 2007;110:518.Google Scholar
Gleissner, B, Gokbuget, N, Bartram, CR, et al. Leading prognostic relevance of the BCR-ABL translocation in adult acute B-lineage lymphoblastic leukemia: a prospective study of the German Multicenter Trial Group and confirmed polymerase chain reaction analysis. Blood 2002;99:1536–43.Google ScholarPubMed
Moorman, AV, Harrison, CJ, Buck, GA, et al. Karyotype is an independent prognostic factor in adult acute lymphoblastic leukemia (ALL): analysis of cytogenetic data from patients treated on the Medical Research Council (MRC) UKALLXII/Eastern Cooperative Oncology Group (ECOG) 2993 trial. Blood 2007;109:3189–97.CrossRefGoogle ScholarPubMed
Dombret, H, Gabert, J, Boiron, JM, et al. Outcome of treatment in adults with Philadelphia chromosome-positive acute lymphoblastic leukemia–results of the prospective multicenter LALA-94 trial. Blood 2002;100:2357–66.CrossRefGoogle ScholarPubMed
Thomas, DA, Faderl, S, Cortes, J, et al. Treatment of Philadelphia chromosome-positive acute lymphocytic leukemia with HyperCVAD and imatinib mesylate. Blood 2004;103:4396–407.CrossRefGoogle Scholar
Yanada, M, Takeuchi, J, Sugiura, I, 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 2006;24:460–6.CrossRefGoogle ScholarPubMed
Labarthe, A, Rousselot, P, Huguet-Rigal, F, et al. Imatinib combined with induction or consolidation chemotherapy in patients with de novo Philadelphia chromosome-positive acute lymphoblastic leukemia: results of the GRAAPH-2003 study. Blood 2007;109:1408–13.CrossRefGoogle ScholarPubMed
Ottmann, OG, Wassmann, B, Pfeifer, H, et al. Imatinib compared with chemotherapy as frontline treatment of elderly patients with Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ALL). Cancer 2007;109:2068–76.CrossRefGoogle Scholar
Vignetti, M, Fazi, P, Cimino, G, et al. Imatinib plus steroids induces complete remissions and prolonged survival in elderly Philadelphia chromosome-positive patients with acute lymphoblastic leukemia without additional chemotherapy: results of the Gruppo Italiano Malattie Ematologiche dell'Adulto (GIMEMA) LAL0201-B protocol. Blood 2007;109:3676–8.CrossRefGoogle ScholarPubMed
Lee, S, Kim, YJ, Min, CK, et al. The effect of first-line imatinib interim therapy on the outcome of allogeneic stem cell transplantation in adults with newly diagnosed Philadelphia chromosome-positive acute lymphoblastic leukemia. Blood 2005;105:3449–57.CrossRefGoogle ScholarPubMed
Schultz, KR, Bowman, WP, Slayton, W, et al. Improved early event free survival (EFS) in children with Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia (ALL) with intensive imatinib in combination with high dose chemotherapy: Children's Oncology Group (COG) Study AALL0031. ASH Annual Meeting Abstracts 2007;110:4.Google Scholar
Wassmann, B, Pfeifer, H, Goekbuget, N, et al. Alternating versus concurrent schedules of imatinib and chemotherapy as frontline therapy for Philadelphia-positive acute lymphoblastic leukemia (Ph+ ALL). Blood 2006;108:1469–77.CrossRefGoogle Scholar
Delannoy, A, Ferrant, A, Bosly, A, et al. Acute lymphoblastic leukemia in the elderly. Eur J Haematol 1990;45:90–3.CrossRefGoogle ScholarPubMed
Taylor, PR, Reid, MM, Bown, N, et al. Acute lymphoblastic leukemia in patients aged 60 years and over: a population-based study of incidence and outcome. Blood 1992;80:1813–7.Google ScholarPubMed
Ferrari, A, Annino, L, Crescenzi, S, et al. Acute lymphoblastic leukemia in the elderly: results of two different treatment approaches in 49 patients during a 25-year period. Leukemia 1995;9:1643–7.Google ScholarPubMed
Pagano, L, Mele, L, Casorelli, I, et al. Acute lymphoblastic leukemia in the elderly. A twelve-year retrospective, single center study. Haematologica 2000;85:1327–9.Google ScholarPubMed
Delannoy, A, Delabesse, E, Lheritier, V, et al. Imatinib and methylprednisolone alternated with chemotherapy improve the outcome of elderly patients with Philadelphia-positive acute lymphoblastic leukemia: results of the GRAALL AFR09 study. Leukemia 2006;20:1526–32.CrossRefGoogle ScholarPubMed
Hofmann, WK, Komor, M, Hoelzer, D, et al. Mechanisms of resistance to STI571 (Imatinib) in Philadelphia-chromosome positive acute lymphoblastic leukemia. Leuk Lymphoma 2004;45:655–60.CrossRefGoogle Scholar
Deininger, M, Buchdunger, E, Druker, BJ. The development of imatinib as a therapeutic agent for chronic myeloid leukemia. Blood 2005;105:2640–53.CrossRefGoogle ScholarPubMed
Soverini, S, Colarossi, S, Gnani, A, et al. Contribution of ABL kinase domain mutations to imatinib resistance in different subsets of Philadelphia-positive patients: by the GIMEMA Working Party on Chronic Myeloid Leukemia. Clin Cancer Res 2006;12:7374–9.CrossRefGoogle ScholarPubMed
Branford, S, Rudzki, Z, Walsh, S, et al. Detection of BCR-ABL mutations in patients with CML treated with imatinib is virtually always accompanied by clinical resistance, and mutations in the ATP phosphate-binding loop (P-loop) are associated with a poor prognosis. Blood 2003;102:276–83.CrossRefGoogle ScholarPubMed
Soverini, S, Martinelli, G, Rosti, G, et al. ABL mutations in late chronic phase chronic myeloid leukemia patients with up-front cytogenetic resistance to imatinib are associated with a greater likelihood of progression to blast crisis and shorter survival: a study by the GIMEMA Working Party on Chronic Myeloid Leukemia. J Clin Oncol 2005;23:4100–9.CrossRefGoogle ScholarPubMed
Pfeifer, H, Wassmann, B, Pavlova, A, et al. Kinase domain mutations of BCR-ABL frequently precede imatinib-based therapy and give rise to relapse in patients with de novo Philadelphia-positive acute lymphoblastic leukemia (Ph+ ALL). Blood 2007;110:727–34.CrossRefGoogle Scholar
Talpaz, M, Shah, NP, Kantarjian, H, et al. Dasatinib in imatinib-resistant Philadelphia chromosome-positive leukemias. N Engl J Med 2006;354:2531–41.CrossRefGoogle ScholarPubMed
Foa, R, Vignetti, M, Vitale, A, et al. Dasatinib as frontline monotherapy for the induction treatment of adult and elderly Ph+ acute lymphoblastic leukemia (ALL) patients: interim analysis of the GIMEMA Prospective Study LAL1205. ASH Annual Meeting Abstracts 2007;110:7.Google Scholar
Porkka, K, Koskenvesa, P, Lundan, T, et al. Dasatinib crosses the blood-brain barrier and is an efficient therapy for central nervous system Philadelphia chromosome-positive leukemia. Blood 2008;112:1005–12.CrossRefGoogle ScholarPubMed
Ravandi, R, O'Brien, S, Thomas, DA, et al. First report of phase II study of dasatinib with hyperCVAD for the frontline treatment of patients with Philadelphia chromosome-positive (Ph+) acute lymphoblastic leukemia. Blood 2010; May 13 epub.
O'Hare, T, Walters, DK, Stoffregen, EP, et al. In vitro activity of Bcr-Abl inhibitors AMN107 and BMS-354825 against clinically relevant imatinib-resistant Abl kinase domain mutants. Cancer Res 2005;65:4500–5.CrossRefGoogle ScholarPubMed
Weisberg, E, Manley, PW, Breitenstein, W, et al. Characterization of AMN107, a selective inhibitor of native and mutant Bcr-Abl. Cancer Cell 2005;7:129–41.CrossRefGoogle ScholarPubMed
Larson, R, Ottman, O, Kantarjian, H, et al. A phase II study of nilotinib administered to imatinib resistant or intolerant patients with chronic myelogenous leukemia (CML) in blast crisis (BC) or relapsed/refractory Ph+ acute lymphoblastic leukemia (ALL). J Clin Oncol (2007 ASCO Annual Meeting Proceedings Part I) 2007;25(18S):Abstract 7040.Google Scholar
Reiter, A, Schrappe, M, Ludwig, WD, et al. Chemotherapy in 998 unselected childhood acute lymphoblastic leukemia patients. Results and conclusions of the multicenter trial ALL-BFM 86. Blood 1994;84:3122–33.Google ScholarPubMed
Schrappe, M, Reiter, A, Zimmermann, M, et al. Long-term results of four consecutive trials in childhood ALL performed by the ALL-BFM study group from 1981 to 1995. Berlin-Frankfurt-Munster. Leukemia 2000;14:2205–22.CrossRefGoogle Scholar
Stock, W, La, M, Sanford, B, 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 2008;112:1646–54.CrossRefGoogle Scholar
Boissel, N, Auclerc, MF, Lheritier, V, et al. Should adolescents with acute lymphoblastic leukemia be treated as old children or young adults? Comparison of the French FRALLE-93 and LALA-94 trials. J Clin Oncol 2003;21:774–80.CrossRefGoogle ScholarPubMed
Bont, JM, Holt, B, Dekker, AW, et al. Significant difference in outcome for adolescents with acute lymphoblastic leukemia treated on pediatric vs adult protocols in the Netherlands. Leukemia 2004;18:2032–5.CrossRefGoogle ScholarPubMed
Testi, AM, Valsecchi, MG, Conter, V, et al. Difference in outcome of adolescents with acute lymphoblastic leukemia (ALL) enrolled in pediatric (AIEOP) and adult (GIMEMA) protocols. ASH Annual Meeting Abstracts 2004;104:1954.Google Scholar
Ramanujachar, R, Richards, S, Hann, I, et al. Adolescents with acute lymphoblastic leukaemia: outcome on UK national paediatric (ALL97) and adult (UKALLXII/E2993) trials. Pediatr Blood Cancer 2007;48:254–61.CrossRefGoogle ScholarPubMed
Ribera, JM, Oriol, A, Sanz, MA, et al. Comparison of the results of the treatment of adolescents and young adults with standard-risk acute lymphoblastic leukemia with the Programa Espanol de Tratamiento en Hematologia pediatric-based protocol ALL-96. J Clin Oncol 2008;26:1843–9.CrossRefGoogle Scholar
DeAngelo, DJ. The treatment of adolescents and young adults with acute lymphoblastic leukemia. Am Soc Hematol Educ Prog 2005:123–30.Google Scholar
Jeha, S. Who should be treating adolescents and young adults with acute lymphoblastic leukaemia?Eur J Cancer 2003;39:2579–83.CrossRefGoogle Scholar
Schiffer, CA. Differences in outcome in adolescents with acute lymphoblastic leukemia: a consequence of better regimens? Better doctors? Both?J Clin Oncol 2003;21:760–1.CrossRefGoogle Scholar
Barry, E, DeAngelo, DJ, Neuberg, D, et al. Favorable outcome for adolescents with acute lymphoblastic leukemia treated on Dana-Farber Cancer Institute Acute Lymphoblastic Leukemia Consortium Protocols. J Clin Oncol 2007;25:813–19.CrossRefGoogle ScholarPubMed
DeAngelo, DJ, Dahlberg, S, Silverman, LB, et al. A multicenter phase II study using a dose intensified pediatric regimen in adults with untreated acute lymphoblastic leukemia. ASH Annual Meeting Abstracts 2007;110:587.Google Scholar
Kantarjian, HM, O'Brien, S, Smith, T, et al. Acute lymphocytic leukaemia in the elderly: characteristics and outcome with the vincristine-adriamycin-dexamethasone (VAD) regimen. Br J Haematol 1994;88:94–100.CrossRefGoogle ScholarPubMed
Bassan, R, Di Bona, E, Lerede, T, et al. Age-adapted moderate-dose induction and flexible outpatient postremission therapy for elderly patients with acute lymphoblastic leukemia. Leuk Lymphoma 1996;22:295–301.CrossRefGoogle ScholarPubMed
Thomas, X, Olteanu, N, Charrin, C, et al. Acute lymphoblastic leukemia in the elderly: The Edouard Herriot Hospital experience. Am J Hematol 2001;67:73–83.CrossRefGoogle Scholar
Robak, T, Szmigielska-Kaplon, A, Wrzesien-Kus, A, et al. Acute lymphoblastic leukemia in elderly: the Polish Adult Leukemia Group (PALG) experience. Ann Hematol 2004;83:225–31.CrossRefGoogle ScholarPubMed
Sancho, JM, Ribera, JM, Xicoy, B, et al. Results of the PETHEMA ALL-96 trial in elderly patients with Philadelphia chromosome-negative acute lymphoblastic leukemia. Eur J Haematol 2007;78:102–10.Google ScholarPubMed
Spath-Schwalbe, E, Heil, G, Heimpel, H. Acute lymphoblastic leukemia in patients over 59 years of age. Experience in a single center over a 10-year period. Ann Hematol 1994;69:291–6.CrossRefGoogle Scholar
Pullarkat, V, Slovak, ML, Kopecky, KJ, et al. Impact of cytogenetics on the outcome of adult acute lymphoblastic leukemia: results of Southwest Oncology Group 9400 study. Blood 2008;111:2563–72.CrossRefGoogle Scholar
Hughes, WT, Armstrong, D, Bodey, GP, et al. 2002 guidelines for the use of antimicrobial agents in neutropenic patients with cancer. Clin Infect Dis 2002;34:730–51.CrossRefGoogle ScholarPubMed
Gafter-Gvili, A, Fraser, A, Paul, M, et al. Antibiotic prophylaxis for bacterial infections in afebrile neutropenic patients following chemotherapy. Cochrane Database Syst Rev 2005;(4):CD004386.
Bow, EJ, Laverdiere, M, Lussier, N, et al. Antifungal prophylaxis for severely neutropenic chemotherapy recipients: a meta analysis of randomized-controlled clinical trials. Cancer 2002;94:3230–46.CrossRefGoogle ScholarPubMed
Sandherr, M, Einsele, H, Hebart, H, et al. Antiviral prophylaxis in patients with haematological malignancies and solid tumours: Guidelines of the Infectious Diseases Working Party (AGIHO) of the German Society for Hematology and Oncology (DGHO). Ann Oncol 2006;17:1051–9.CrossRefGoogle Scholar
Ottmann, OG, Hoelzer, D, Gracien, E, et al. Concomitant granulocyte colony-stimulating factor and induction chemoradiotherapy in adult acute lymphoblastic leukemia: a randomized phase III trial. Blood 1995;86:444–50.Google ScholarPubMed
Geissler, K, Koller, E, Hubmann, E, et al. Granulocyte colony-stimulating factor as an adjunct to induction chemotherapy for adult acute lymphoblastic leukemia–a randomized phase-III study. Blood 1997;90:590–6.Google ScholarPubMed
Thomas, DA, O'Brien, S, Cortes, J, et al. Outcome with the HyperCVAD regimens in lymphoblastic lymphoma. Blood 2004;104:1624–30.CrossRefGoogle Scholar
Coiffier, B, Altman, A, Pui, CH, et al. Guidelines for the management of pediatric and adult tumor lysis syndrome: an evidence-based review. J Clin Oncol 2008;26:2767–78.CrossRefGoogle Scholar
Bassan, R, Lerede, T, Barbui, T. Strategies for the treatment of recurrent acute lymphoblastic leukemia in adults. Haematologica 1996;81:20–36.Google ScholarPubMed
Thomas, DA, Kantarjian, H, Smith, TL, et al. Primary refractory and relapsed adult acute lymphoblastic leukemia: characteristics, treatment results, and prognosis with salvage therapy. Cancer 1999;86:1216–30.3.0.CO;2-O>CrossRefGoogle ScholarPubMed
Fielding, AK, Richards, SM, Chopra, R, et al. Outcome of 609 adults after relapse of acute lymphoblastic leukemia (ALL); an MRC UKALL12/ECOG 2993 study. Blood 2007;109:944–50.CrossRefGoogle ScholarPubMed
Giona, F, Annino, L, Rondelli, R, et al. Treatment of adults with acute lymphoblastic leukaemia in first bone marrow relapse: results of the ALL R-87 protocol. Br J Haematol 1997;97:896–903.CrossRefGoogle ScholarPubMed
Martino, R, Brunet, S, Sureda, A, et al. Treatment of refractory and relapsed adult acute leukemia using a uniform chemotherapy protocol. Leuk Lymphoma 1993;11:393–8.CrossRefGoogle ScholarPubMed
Weiss, MA, Aliff, TB, Tallman, MS, et al. A single, high dose of idarubicin combined with cytarabine as induction therapy for adult patients with recurrent or refractory acute lymphoblastic leukemia. Cancer 2002;95:581–7.CrossRefGoogle ScholarPubMed
Tavernier, E, Boiron, JM, Huguet, F, et al. Outcome of treatment after first relapse in adults with acute lymphoblastic leukemia initially treated by the LALA-94 trial. Leukemia 2007;21:1907–14.CrossRefGoogle ScholarPubMed
DeAngelo, DJ, Yu, D, Johnson, JL, et al. Nelarabine induces complete remissions in adults with relapsed or refractory T-lineage acute lymphoblastic leukemia or lymphoblastic lymphoma: Cancer and Leukemia Group B study 19801. Blood 2007;109:5136–42.CrossRefGoogle ScholarPubMed
Weiss, MA. Treatment of adult patients with relapsed or refractory acute lymphoblastic leukemia (ALL). Leukemia 1997;11 Suppl 4:S28–30.Google Scholar
Dunsmore, K, Devidas, M, Borowitz, MJ, et al. Nelarabine in combination with intensive modified BFM AALL00P2: a pilot study for the treatment of high risk T-ALL, a report from the Children's Oncology Group. J Clin Oncol 2008 ASCO Annual Meeting Proceedings Part I 2008;26 Abstract 10002.CrossRefGoogle Scholar
Jeha, S, Gaynon, PS, Razzouk, BI, et al. Phase II study of clofarabine in pediatric patients with refractory or relapsed acute lymphoblastic leukemia. J Clin Oncol 2006;24:1917–23.CrossRefGoogle ScholarPubMed
Karp, JE, Ricklis, RM, Balakrishnan, K, et al. A phase 1 clinical-laboratory study of clofarabine followed by cyclophosphamide for adults with refractory acute leukemias. Blood 2007;110:1762–9.CrossRefGoogle ScholarPubMed
Leonetti, C, Scarsella, M, Semple, SC, et al. In vivo administration of liposomal vincristine sensitizes drug-resistant human solid tumors. Int J Cancer 2004;110:767–74.CrossRefGoogle ScholarPubMed
Thomas, DA, Sarris, AH, Cortes, J, et al. Phase II study of sphingosomal vincristine in patients with recurrent or refractory adult acute lymphocytic leukemia. Cancer 2006;106:120–7.CrossRefGoogle ScholarPubMed
Wetzler, M, Sanford, BL, Kurtzberg, J, et al. Effective asparagine depletion with pegylated asparaginase results in improved outcomes in adult acute lymphoblastic leukemia: Cancer and Leukemia Group B Study 9511. Blood 2007;109:4164–7.CrossRefGoogle Scholar
Avramis, VI, Sencer, S, Periclou, AP, et al. A randomized comparison of native Escherichia coli asparaginase and polyethylene glycol conjugated asparaginase for treatment of children with newly diagnosed standard-risk acute lymphoblastic leukemia: a Children's Cancer Group study. Blood 2002;99:1986–94.CrossRefGoogle ScholarPubMed
Golas, JM, Arndt, K, Etienne, C, et al. SKI-606, a 4-anilino-3-quinolinecarbonitrile dual inhibitor of Src and Abl kinases, is a potent antiproliferative agent against chronic myelogenous leukemia cells in culture and causes regression of K562 xenografts in nude mice. Cancer Res 2003;63:375–81.Google ScholarPubMed
Kimura, S, Naito, H, Segawa, H, et al. NS-187, a potent and selective dual Bcr-Abl/Lyn tyrosine kinase inhibitor, is a novel agent for imatinib-resistant leukemia. Blood 2005;106:3948–54.CrossRefGoogle ScholarPubMed
Naito, H, Kimura, S, Nakaya, Y, et al. In vivo antiproliferative effect of NS-187, a dual Bcr-Abl/Lyn tyrosine kinase inhibitor, on leukemic cells harbouring Abl kinase domain mutations. Leuk Res 2006;30:1443–6.CrossRefGoogle ScholarPubMed
Giles, FJ, Cortes, J, Jones, D, et al. MK-0457, a novel kinase inhibitor, is active in patients with chronic myeloid leukemia or acute lymphocytic leukemia with the T315I BCR-ABL mutation. Blood 2007;109:500–2.CrossRefGoogle ScholarPubMed
Thomas, DA, Kantarjian, H, Cortes, J, et al. Long-term outcome after HyperCVAD and rituximab chemoimmunotherapy for Burkitt (BL) or Burkitt-like (BLL) leukemia/lymphoma and mature B-cell acute lymphocytic leukemia (B-ALL). ASH Annual Meeting Abstracts 2007;110:2825.Google Scholar
Raetz, EA, Cairo, MS, Borowitz, MJ, et al. Chemoimmunotherapy reinduction with epratuzumab in children with acute lymphoblastic leukemia in marrow relapse: a Children's Oncology Group Pilot Study. J Clin Oncol 2008;26:3756–62.CrossRefGoogle ScholarPubMed
Stock, W, Yu, D, Sanford, B, et al. Incorporation of alemtuzumab into frontline therapy of adult acute lymphoblastic leukemia (ALL) is feasible: a phase I/II study from the Cancer and Leukemia Group B (CALGB 10102). ASH Annual Meeting Abstracts 2005;106:145.Google Scholar
Staal, FJ, Langerak, AW. Signaling pathways involved in the development of T-cell acute lymphoblastic leukemia. Haematologica 2008;93:493–7.CrossRefGoogle ScholarPubMed
DeAngelo, DJ, Stone, RM, Silverman, LB, et al. A phase I clinical trial of the notch inhibitor MK-0752 in patients with T-cell acute lymphoblastic leukemia/lymphoma (T-ALL) and other leukemias. J Clin Oncol (2006 ASCO Annual Meeting Proceedings Part I) 2006;24(18S) Abstract 6585.Google Scholar
Wei, G, Twomey, D, Lamb, J, et al. Gene expression-based chemical genomics identifies rapamycin as a modulator of MCL1 and glucocorticoid resistance. Cancer Cell 2006;10:331–42.CrossRefGoogle ScholarPubMed
Teachey, DT, Obzut, DA, Cooperman, J, et al. The mTOR inhibitor CCI-779 induces apoptosis and inhibits growth in preclinical models of primary adult human ALL. Blood 2006;107:1149–55.CrossRefGoogle ScholarPubMed
Avellino, R, Romano, S, Parasole, R, et al. Rapamycin stimulates apoptosis of childhood acute lymphoblastic leukemia cells. Blood 2005;106:1400–6.CrossRefGoogle ScholarPubMed
Kharas, MG, Janes, MR, Scarfone, VM, et al. Ablation of PI3K blocks BCR-ABL leukemogenesis in mice, and a dual PI3K/mTOR inhibitor prevents expansion of human BCR-ABL leukemia cells. J Clin Invest 2008;118:3038–50.CrossRefGoogle Scholar
Jackman, KM, Frye, CB, Hunger, SP. Flavopiridol displays preclinical activity in acute lymphoblastic leukemia. Pediatr Blood Cancer 2008;50:772–8.CrossRefGoogle ScholarPubMed
Karp, JE, Passaniti, A, Gojo, I, et al. Phase I and pharmacokinetic study of flavopiridol followed by 1-beta-D-arabinofuranosylcytosine and mitoxantrone in relapsed and refractory adult acute leukemias. Clin Cancer Res 2005;11:8403–12.CrossRefGoogle ScholarPubMed

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