Literature DB >> 9573676

Late intensification chemotherapy has not improved the results of intensive chemotherapy in adult acute lymphoblastic leukemia. Results of a prospective multicenter randomized trial (PETHEMA ALL-89). Spanish Society of Hematology.

J M Ribera1, J J Ortega, A Oriol, M Fontanillas, J M Hernández-Rivas, S Brunet, J García-Conde, J Maldonado, J Zuazu, S Gardella, J Besalduch, P León, J Macià, A Domingo-Albós, E Feliu, J F San Miguel.   

Abstract

BACKGROUND AND
OBJECTIVE: Intensive induction and post-remission therapies have improved the prognosis in adult acute lymphoblastic leukemia (ALL). However, different from children, the impact of late intensification therapy in the overall results of treatment has not been consistently evaluated. The objective of this study was to analyze the results of a multicenter prospective protocol, PETHEMA ALL-89, in which, after intensive induction and consolidation therapy, randomization to receive delayed intensification treatment was performed. DESIGN AND METHODS: One hundred and eight adults (age > or = 15 years) diagnosed with ALL (ALL L3 excluded) in 22 Spanish hospitals from 1989 to 1994 were treated with a five-drug induction therapy, followed by four cycles of early post-remission treatment during four months, and maintenance therapy for two years. Patients in remission at the end of the first year were randomized to receive one six-week cycle of late intensification therapy. Uni- and multivariate analyses of early response to treatment, complete remission (CR), leukemia-free survival (LFS) and overall survival (OS) were performed.
RESULTS: The median (range) age of the series was 28 (15-74) years and leukocyte count 26 x 10(9)/L (1-600). ALL L1/L2 was present in 38/70 patients, early pre-B in 13, common in 53, pre-B in 12 and T in 30 cases. The CR rate was 86%, and refractory disease 9%. Median LFS was 34 months, with a 5-yr probability of 41% (95% CI, 29-53), whereas median OS was 51 months and 5-year probability 47% (34-59%). There were no differences in either LFS and OS between patients who did or did not receive delayed intensification therapy. Prognostic factors for CR attainment were advanced age and slow response to therapy. These two features were, in addition to high leukocyte counts, the parameters with negative influence in both LFS and OS. INTERPRETATION AND
CONCLUSIONS: The results of PETHEMA ALL-89 are similar to those referred in other chemotherapy-based protocols in adult ALL. Delayed intensification has not improved the length of remission and survival. Efforts to improve the prognosis of adult ALL patients must be mainly focused in early intensification treatment.

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Year:  1998        PMID: 9573676

Source DB:  PubMed          Journal:  Haematologica        ISSN: 0390-6078            Impact factor:   9.941


  4 in total

1.  Outcome after relapse of acute lymphoblastic leukemia in adult patients included in four consecutive risk-adapted trials by the PETHEMA Study Group.

Authors:  Albert Oriol; Susana Vives; Jesús-María Hernández-Rivas; Mar Tormo; Inmaculada Heras; Concepción Rivas; Concepción Bethencourt; Federico Moscardó; Javier Bueno; Carlos Grande; Eloy del Potro; Ramon Guardia; Salut Brunet; Juan Bergua; Teresa Bernal; Maria-José Moreno; Carlota Calvo; Pilar Bastida; Evarist Feliu; Josep-Maria Ribera
Journal:  Haematologica       Date:  2010-02-09       Impact factor: 9.941

Review 2.  Modern treatment programs for adults with acute lymphoblastic leukemia.

Authors:  Farhad Ravandi; Stefan Faderl; Partow Kebriaei; Hagop Kantarjian
Journal:  Curr Hematol Malig Rep       Date:  2007-07       Impact factor: 3.952

3.  Frequent and simultaneous epigenetic inactivation of TP53 pathway genes in acute lymphoblastic leukemia.

Authors:  Amaia Vilas-Zornoza; Xabier Agirre; Vanesa Martín-Palanco; José Ignacio Martín-Subero; Edurne San José-Eneriz; Leire Garate; Sara Álvarez; Estíbaliz Miranda; Paula Rodríguez-Otero; José Rifón; Antonio Torres; María José Calasanz; Juan Cruz Cigudosa; José Román-Gómez; Felipe Prósper
Journal:  PLoS One       Date:  2011-02-28       Impact factor: 3.240

4.  Transcriptional silencing of the Dickkopfs-3 (Dkk-3) gene by CpG hypermethylation in acute lymphoblastic leukaemia.

Authors:  J Roman-Gomez; A Jimenez-Velasco; X Agirre; J A Castillejo; G Navarro; M Barrios; E J Andreu; F Prosper; A Heiniger; A Torres
Journal:  Br J Cancer       Date:  2004-08-16       Impact factor: 7.640

  4 in total

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