Volume 17, Issue 2 pp. 83-91
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Treating childhood acute lymphoblastic leukaemia (ALL): Summary of ten years' experience in Italy

Prof. G. Paolucci MD

Corresponding Author

Prof. G. Paolucci MD

4th International Symposium on Therapy of Acute Leukemias 1987, Rome, Italy

Clinica Pediatrica, Ospedale S. Orsola, Via Massarenti 11, 40138, Bologna, ItalySearch for more papers by this author
G. Masera MD

G. Masera MD

4th International Symposium on Therapy of Acute Leukemias 1987, Rome, Italy

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V. Vecchi MD

V. Vecchi MD

4th International Symposium on Therapy of Acute Leukemias 1987, Rome, Italy

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S. Marsoni MD

S. Marsoni MD

4th International Symposium on Therapy of Acute Leukemias 1987, Rome, Italy

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A. Pession MD

A. Pession MD

4th International Symposium on Therapy of Acute Leukemias 1987, Rome, Italy

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M. G. Zurlo MD

M. G. Zurlo MD

4th International Symposium on Therapy of Acute Leukemias 1987, Rome, Italy

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First published: 1989
Citations: 38

Abstract

Between 1976 and 1986, 2,093 children with ALL were enrolled in three consecutive generations of trials conducted by the Associazione Italiana Ematologia Oncologia Pediatrica (AIEOP). A 50% event-free survival at 5 years was achieved overall in this population, approximately accounting for more than 50% of the entire childhood ALL population in Italy. Participation in the group protocols increased from the original seven founding centers to the current 37 institutions. Results in the standard population (non-T immunophenotype, non-FAB L3, and < 50,000 white blood cells [WBC]/ml) were considerably better with more recent, more aggressive protocols. The two major results in this population (N = 540) were a relatively low incidence (8% at 5 years) of central nervous system (CNS) relapse in the “good”-risk population (< 10,000 WBC, ages 3–6 years, and FAB L1), without the use of cranial irradiation, and a projected 4-year disease-free interval for bone-marrow relapse of 80% in the “average”-risk group, where a three-drug reinduction program was adopted after consolidation. Overall, the event-free survival of the most recent generation (protocol 82, median follow-up time of 38 months) is 66% at 4 years (95% confidence limits [CL] 61–71). Based on these 10 years of experience, the general strategy of the group for the 90s is outlined and discussed.

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