Clinical Outcome of Children With Newly Diagnosed Philadelphia Chromosome–Positive Acute Lymphoblastic Leukemia Treated Between 1995 and 2005

Author:

Aricò Maurizio1,Schrappe Martin1,Hunger Stephen P.1,Carroll William L.1,Conter Valentino1,Galimberti Stefania1,Manabe Atsushi1,Saha Vaskar1,Baruchel André1,Vettenranta Kim1,Horibe Keizo1,Benoit Yves1,Pieters Rob1,Escherich Gabriele1,Silverman Lewis B.1,Pui Ching-Hon1,Valsecchi Maria Grazia1

Affiliation:

1. From the Azienda Ospedaliero Universitaria A. Meyer, Florence; Pediatria Ospedali Riuniti Bergamo, Bergamo; Pediatria Ospedale San Gerardo; University of Milan-Bicocca, Monza, Italy; University Medical Center Schleswig-Holstein, Kiel; University of Hamburg, Hamburg, Germany; The Children's Hospital and the University of Colorado School of Medicine, Aurora, CO; New York University Cancer Institute, New York, NY; Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA; St Jude Children's...

Abstract

Purpose In a previous analysis of 326 children with Philadelphia chromosome (Ph) –positive acute lymphoblastic leukemia (ALL) treated between 1986 and 1996, hematopoietic stem-cell transplantation from HLA-matched related donors, but not from unrelated donors, offered a superior outcome than chemotherapy alone. To evaluate the impact of recent improvements in chemotherapy and transplantation, we performed a similar analysis on patients treated in the following decade. Patients and Methods We analyzed 610 patients with Ph-positive ALL treated between 1995 and 2005 without tyrosine kinase inhibitor therapy. The median follow-up duration was 6.3 years. Results Complete remission was achieved in 89% of patients. The 7-year event-free survival and overall survival rates were superior in the present cohort compared with the previous cohort (32.0% ± 2.0% v 25.0% ± 3.0, respectively, P = .007; and 44.9% ± 2.2% v 36.0% ± 3.0%, respectively, P = .017). Compared with chemotherapy alone, transplantation with matched related donors or unrelated donors in first remission (325 patients) showed an advantage with increasing follow-up, suggesting greater protection against late relapses (hazard ratio at 5 years, 0.37; P < .001). In the multivariate Cox regression analysis accounting for treatment (transplantation v no transplantation), age, leukocyte count, and early response had independent impact on treatment outcome. Conclusion Clinical outcome of children and adolescents with Ph-positive ALL has improved with advances in transplantation and chemotherapy. Transplantations with matched related donors and unrelated donors were equivalent and offered better disease control compared with chemotherapy alone. Age, leukocyte count, and early treatment response were independent prognostic indicators. The results of this study will serve as a historical reference to evaluate the therapeutic impact of tyrosine kinase inhibitors on the outcome of Ph-positive ALL.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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