TY - JOUR
T1 - 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
AU - Aricò, Maurizio
AU - Valsecchi, Maria Grazia
AU - Rizzari, Carmelo
AU - Barisone, Elena
AU - Biondi, Andrea
AU - Casale, Fiorina
AU - Locatelli, Franco
AU - Lo Nigro, Luca
AU - Luciani, Matteo
AU - Messina, Chiara
AU - Micalizzi, Concetta
AU - Parasole, Rosanna
AU - Pession, Andrea
AU - Santoro, Nicola
AU - Testi, Anna Maria
AU - Silvestri, Daniela
AU - Basso, Giuseppe
AU - Masera, Giuseppe
AU - Conter, Valentino
PY - 2008
Y1 - 2008
N2 - PurposeBetween 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 MethodsA 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.ResultsThe 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.ConclusionFavorable 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.
AB - PurposeBetween 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 MethodsA 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.ResultsThe 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.ConclusionFavorable 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.
KW - N/A
KW - N/A
UR - http://hdl.handle.net/10807/258455
U2 - 10.1200/JCO.2007.12.3927
DO - 10.1200/JCO.2007.12.3927
M3 - Article
SN - 0732-183X
VL - 26
SP - 283
EP - 289
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
ER -