共 95 条
- [1] Bader P(2009)Prognostic value of minimal residual disease quantification before allogenic stem cell transplantation in related childhood acute lymphoblastic leukemia: the ALL-REZ BFM study group J Clin Oncol 27 377-384
- [2] Kreyenberg H(1998)Minimal residual disease status before allogenic bone marrow transplantation is an important determinant of successful outcome for children and adolescents with acute lymphoblastic leukemia Blood 92 4072-4079
- [3] Henze GH(2003)Level of minimal residual disease prior to hematopoietic transplantation predicts prognosis in pediatric patients with acute lymphoblastic leukemia: a report of the pre-BMT MRD study group Bone Marrow Transpl 32 849-851
- [4] Eckert C(2007)Detectable minimal residual disease before allogenic hematopoietic stem cell transplantation predicts extremely poor prognosis in children with acute lymphoblastic leukemia Pediatr Blood Cancer 48 93-100
- [5] Reising M(2003)Minimal residual disease detection after allogenic stem cell transplantation is correlated to relapse in patients with acute lymphoblastic leukemia Br J Haematol 122 788-794
- [6] Willasch A(2005)Chemotherapy versus allogenic hematopoietic stem cell transplantation for very high risk childhood acute lymphoblastic leukemia in first complete remission: comparison by genetic randomisation in an international prospective study Lancet 366 635-642
- [7] Knechtli CJ(2013)Hematopoietic stem cell transplantation for children with high risk acute lymphoblastic leukemia in first complete remission: a report from the AIEOP registry Haematologica 98 1273-1281
- [8] Goulden NJ(2001)Improved outcome for children with acute lymphoblastic leukemia: results of Dana Farber Consortium Protocol 91-01 Blood 97 1211-1218
- [9] Hancock JP(1998)Intensive BFM chemotherapy for childhood ALL: interim analysis of the AIEPO-ALL91 study Assoc Ital Ematol Oncol Pediatr Haematol 83 791-799
- [10] Grandage VI(1993)Improved therapy for children with acute lymphoblastic leukemia and unfavourable presenting features: a follow up report of the childrens cancer group study CCG-106J Clin Oncol 11 2234-2242