Long-Term Results of the AIEOP-ALL-95 Trial for Childhood Acute Lymphoblastic Leukemia: Insight on the Prognostic Value of DNA Index in the Framework of Berlin-Frankfurt-Muenster–Based Chemotherapy

Author:

Aricò Maurizio1,Valsecchi Maria Grazia1,Rizzari Carmelo1,Barisone Elena1,Biondi Andrea1,Casale Fiorina1,Locatelli Franco1,Lo Nigro Luca1,Luciani Matteo1,Messina Chiara1,Micalizzi Concetta1,Parasole Rosanna1,Pession Andrea1,Santoro Nicola1,Testi Anna Maria1,Silvestri Daniela1,Basso Giuseppe1,Masera Giuseppe1,Conter Valentino1

Affiliation:

1. From the Pediatric Hematology Oncology, Ospedale dei Bambini G. Di Cristina, Palermo; Medical Statistics Unit and Department of Pediatrics, University of Milano-Bicocca, Milano; Ospedale San Gerardo, Monza; Pediatric Hematology Oncology, Torino; I Clinica Pediatrica, University of Napoli, Napoli; Pediatric Hematology Oncology, University of Pavia, Pavia; Pediatric Hematology Oncology, University of Catania, Catania; Pediatric Hematology, IRCCS Ospedale Bambino Gesù; Department of Hematology, University...

Abstract

Purpose Between May 1995 and August 2000 the Associazione Italiana di Ematologia Oncologia Pediatrica conducted the ALL-95 study for risk-directed, Berlin-Frankfurt-Muenster (BFM) –oriented therapy of childhood acute lymphoblastic leukemia, aimed at exploring treatment reduction in standard-risk patients (SR) and intensification during continuation therapy in intermediate-risk patients (IR) as randomized questions and treatment intensification in high-risk patients (HR). The prognostic value of DNA index was explored in this setting. Patients and Methods A total of 1,744 patients were enrolled (115, SR; 1,385, IR; and 244, HR). SR patients (DNA index ≥ 1.16 and < 1.60; age, 1 to 5 years; and WBC < 20,000, non–T-immunophenotype, with no high-risk features) received a reduced induction therapy (no anthracyclines); IR patients were randomly assigned to receive or not receive vincristine and dexamethasone pulses during maintenance; HR therapy was based on a conventional BFM schedule intensified with three chemotherapy blocks followed by a double reinduction phase. Results The event-free survival and overall survival probabilities at 10 years for the entire group were 72.5% (SE, 1.3) and 83.6% (SE, 0.9); 85.0% (SE, 3.4) and 95.5% (SE, 2.0) in SR, 75.1% (SE, 1.5) and 87.5% (SE, 0.9) in IR, and 51.0% (SE, 3.2) and 57.2% (SE, 3.3) in HR patients, respectively. Patients with a favorable DNA index had superior EFS in both IR (83.8% [2.7%] v 73.9% [1.7%]) and in HR (67.8% [9.4%] and 49.6% [3.5%]). Of the six patients with DNA index less than 0.8, only one remained in remission. Conclusion Favorable DNA index was associated with a better prognosis in IR and HR patients defined by presenting clinical criteria and treatment with a BFM-oriented chemotherapy.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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