Forty-eight patients with chronic myeloid leukemia (CML) in chronic phase (CP) were treated by autologous stem cells transplantation (ASCT) and alpha Interferon (IFN) with three approaches: 1) ASCT at diagnosis followed by IFN, 2) ASCT post IFN with cells collected after an interval from IFN discontinuance, followed by IFN, 3) ASCT in patients selected by cytoconversion obtained with IFN, performed soon after IFN discontinuance. Following ASCT, a major karyotype response (more than 65% Ph1 negative cells, MKR) was observed at least once in 40%, 53% and 83% of patients from the three groups, respectively. At last follow-ups (median 39, 40 and 21 months, respectively) 19%, 13% and 67% of patients still present a MKR with 2 patients from group 1 and 4 patients from group 3 being 100% Ph' negative. Projected survival from diagnosis is 77% at 52 months for patients from group 1 and 47% at 75 months for patients from group 2. Present data indicate that 1) IFN can stabilize results obtained with ASCT, 2) ASCT can potentiate responses to IFN, 3) combined ASCT and IFN can improve survival. Longer follow-up of patients and randomized studies are required to define the real impact on disease outcome by these treatment approaches.

Alimena, G., Meloni, G., De Cuia, M., Rondinelli, M., LO COCO, F., Montefusco, E., et al. (1993). Management of chronic myeloid leukemia in chronic phase with autologous stem cell transplantation and alpha-2 interferon: Cytogenetic and clinical results. LEUKEMIA & LYMPHOMA, 11(s1), 281-291 [10.3109/10428199309047900].

Management of chronic myeloid leukemia in chronic phase with autologous stem cell transplantation and alpha-2 interferon: Cytogenetic and clinical results

LO COCO, FRANCESCO;
1993-01-01

Abstract

Forty-eight patients with chronic myeloid leukemia (CML) in chronic phase (CP) were treated by autologous stem cells transplantation (ASCT) and alpha Interferon (IFN) with three approaches: 1) ASCT at diagnosis followed by IFN, 2) ASCT post IFN with cells collected after an interval from IFN discontinuance, followed by IFN, 3) ASCT in patients selected by cytoconversion obtained with IFN, performed soon after IFN discontinuance. Following ASCT, a major karyotype response (more than 65% Ph1 negative cells, MKR) was observed at least once in 40%, 53% and 83% of patients from the three groups, respectively. At last follow-ups (median 39, 40 and 21 months, respectively) 19%, 13% and 67% of patients still present a MKR with 2 patients from group 1 and 4 patients from group 3 being 100% Ph' negative. Projected survival from diagnosis is 77% at 52 months for patients from group 1 and 47% at 75 months for patients from group 2. Present data indicate that 1) IFN can stabilize results obtained with ASCT, 2) ASCT can potentiate responses to IFN, 3) combined ASCT and IFN can improve survival. Longer follow-up of patients and randomized studies are required to define the real impact on disease outcome by these treatment approaches.
1993
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MED/15 - MALATTIE DEL SANGUE
English
Adult; Bone Marrow; Bone Marrow Purging; Bone Marrow Transplantation; Combined Modality Therapy; Female; Humans; Hydroxyurea; Immunologic Factors; Interferon-alpha; Italy; Karyotyping; Leukemia, Myelogenous, Chronic, BCR-ABL Positive; Leukemia, Myeloid, Chronic-Phase; Male; Middle Aged; Neoplastic Stem Cells; Prospective Studies; Recombinant Proteins; Remission Induction; Survival Rate; Treatment Outcome; Blood Component Transfusion; Blood Transfusion, Autologous; Hematopoietic Stem Cell Transplantation
Alimena, G., Meloni, G., De Cuia, M., Rondinelli, M., LO COCO, F., Montefusco, E., et al. (1993). Management of chronic myeloid leukemia in chronic phase with autologous stem cell transplantation and alpha-2 interferon: Cytogenetic and clinical results. LEUKEMIA & LYMPHOMA, 11(s1), 281-291 [10.3109/10428199309047900].
Alimena, G; Meloni, G; De Cuia, M; Rondinelli, M; LO COCO, F; Montefusco, E; Mancini, M; Pinto, R; Nanni, M; Cedrone, M; Fabritiis, P; Mandelli, F
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/161075
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