Summary
Burkitt’s-type leukemias have specific cytologic, immunologic, and cytogenetic characteristics. Initial symptomatology frequently includes abdominal tumors and initial CNS involvement. Despite intensive treatment including high-dose cyclophosphamide, prognosis remains poor in most patients because of failures to achieve complete remission (CR) or because of early relapses, especially CNS relapses. Class III acute lymphoblastic leukemia in children is defined by the presence of two or more unfavorable parameters and recent progress has been achieved by intensive therapy. Cox’s multifactorial analysis allows improved discrimination. A phase I protocol for increased-risk leukemias, including testis preventive irradiation and monthly reinductions without continuous maintenance for the first 6 months of CR, seems promising.
This research was carried out with the aid of Contrat INSERM, Commission 8; Subvention du Comité Franco-Américain de Recherche sur le Cancer (INSERM); USPHS Research Grant, CA 13239-05 from the National Cancer Institute; Caisse Régionale d Assurances Maladies de Paris; and Formation de Recherche Associé n°42 INSERM
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© 1982 Springer-Verlag Berlin · Heidelberg
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Weil, M., Jacquillat, C., Auclerc, M.F., Schaison, G., Chastang, C., Bernard, J. (1982). Poor-Prognosis Acute Lymphoblastic Leukemias. In: Mathé, G., Bonadonna, G., Salmon, S. (eds) Adjuvant Therapies of Cancer. Recent Results in Cancer Research, vol 80. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-81685-7_7
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DOI: https://doi.org/10.1007/978-3-642-81685-7_7
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