Philadelphia chromosome- positive (Ph+) acute lymphoblastic leukemia ( ALL) has a dismal prognosis. We prospectively evaluated minimal residual disease (MRD) by measuring BCR/ ABL levels with a quantitative real-time PCR procedure after induction and after consolidation in 45 adults with Ph+ ALL who obtained complete hematological remission after a high-dose daunorubicin induction schedule. At diagnosis, the mean BCR-ABL/GUS ratio was 1.55+/-1.78. A total of 42 patients evaluable for outcome analysis were operationally divided into two MRD groups: good molecular responders (GMRs; n = 28) with 42 log reduction of residual disease after induction and 43 log reduction after consolidation therapy, and poor molecular responders (PMRs; n = 14) who, despite complete hematological remission, had a higher MRD at both time points. In GMR, the actuarial probability of relapse- free, disease-free and overall survival at two years was 38, 27 and 48%, respectively, as compared to 0, 0 and 0% in PMR ( P = 0.0035, 0.0076 and 0.0026, respectively). Salvage therapy induced a second sustained complete hematological remission in three GMR patients, but in no PMR patient. Our data indicate that, as already shown in children, adult Ph+ ALL patients have a heterogeneous sensitivity to treatment, and that early quantification of residual disease is a prognostic parameter in this disease.

Significant reduction of the hybrid BCR/ABL transcripts after induction and consolidation therapy is a powerful predictor of treatment response in adult Philadelphia-positive acute lymphoblastic leukemia / F., Pane; Cimino, Giuseppe; B., Izzo; A., Camera; A., Vitale; C., Quintarelli; M., Picardi; G., Specchia; M., Mancini; A., Cuneo; C., Mecucci; G., Martinelli; G., Saglio; B., Rotoli; F., Mandelli; F., Salvatore; Foa, Roberto. - In: LEUKEMIA. - ISSN 0887-6924. - 19:4(2005), pp. 628-635. [10.1038/sj.leu.2403683]

Significant reduction of the hybrid BCR/ABL transcripts after induction and consolidation therapy is a powerful predictor of treatment response in adult Philadelphia-positive acute lymphoblastic leukemia

CIMINO, Giuseppe;FOA, Roberto
2005

Abstract

Philadelphia chromosome- positive (Ph+) acute lymphoblastic leukemia ( ALL) has a dismal prognosis. We prospectively evaluated minimal residual disease (MRD) by measuring BCR/ ABL levels with a quantitative real-time PCR procedure after induction and after consolidation in 45 adults with Ph+ ALL who obtained complete hematological remission after a high-dose daunorubicin induction schedule. At diagnosis, the mean BCR-ABL/GUS ratio was 1.55+/-1.78. A total of 42 patients evaluable for outcome analysis were operationally divided into two MRD groups: good molecular responders (GMRs; n = 28) with 42 log reduction of residual disease after induction and 43 log reduction after consolidation therapy, and poor molecular responders (PMRs; n = 14) who, despite complete hematological remission, had a higher MRD at both time points. In GMR, the actuarial probability of relapse- free, disease-free and overall survival at two years was 38, 27 and 48%, respectively, as compared to 0, 0 and 0% in PMR ( P = 0.0035, 0.0076 and 0.0026, respectively). Salvage therapy induced a second sustained complete hematological remission in three GMR patients, but in no PMR patient. Our data indicate that, as already shown in children, adult Ph+ ALL patients have a heterogeneous sensitivity to treatment, and that early quantification of residual disease is a prognostic parameter in this disease.
2005
minimal residual disease; ph-all; prognosis; real-time pcr
01 Pubblicazione su rivista::01a Articolo in rivista
Significant reduction of the hybrid BCR/ABL transcripts after induction and consolidation therapy is a powerful predictor of treatment response in adult Philadelphia-positive acute lymphoblastic leukemia / F., Pane; Cimino, Giuseppe; B., Izzo; A., Camera; A., Vitale; C., Quintarelli; M., Picardi; G., Specchia; M., Mancini; A., Cuneo; C., Mecucci; G., Martinelli; G., Saglio; B., Rotoli; F., Mandelli; F., Salvatore; Foa, Roberto. - In: LEUKEMIA. - ISSN 0887-6924. - 19:4(2005), pp. 628-635. [10.1038/sj.leu.2403683]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/238674
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