Background Autologous stem cell transplantation (ASCT) has gained growing consideration as a treatment option for favorable-risk acute myeloid leukemia (FR-AML) in first complete remission (CR1), compared with chemotherapy. Materials and Methods We report the long-term outcomes of 117 consecutive patients with FR-AML fit for intensive chemotherapy diagnosed in our center between 1999 and 2020, who underwent ASCT. Results Sixty-five of the 117 were eligible for intensive post-remission treatment, and 42 of those 65 received ASCT. Median follow up was 132 months. Overall survival (OS) and disease-free survival (DFS) were 75% and 76%. Higher doses of CD34 + stem cell infusions negatively impacted DFS in multivariate analysis. Core-binding factor (CBF) leukemia was an independent prognostic factor for improved DFS. No differences based on pre-transplant measurable residual disease (MRD) were observed. In CBF leukemia, 10-year DFS is 72% for MRD-positive patients versus 100% for MRD negative patients. Conclusions ASCT is effective and safe in FR-AML patients. In CBF leukemia, ASCT provides excellent results regardless of achievement of bone marrow MRD negativity. In NPM1-mutated/FLT3-wild type (mNPM1) AML, early molecular response seems to have more impact on prognosis. Prospective investigation of the role of gemtuzumab ozogamicin in this setting is ongoing.

Autologous stem cell transplantation in favorable-risk acute myeloid leukemia: single-center experience and current challenges / Capria, Saveria; Trisolini, Silvia Maria; Diverio, Daniela; Minotti, Clara; Breccia, Massimo; Cartoni, Claudio; Carmini, Daniela; Gozzer, Maria; La Rocca, Ursula; Shafii Bafti, Mahnaz; Martelli, Maurizio. - In: INTERNATIONAL JOURNAL OF HEMATOLOGY. - ISSN 0925-5710. - 116:4(2022), pp. 586-593. [10.1007/s12185-022-03370-4]

Autologous stem cell transplantation in favorable-risk acute myeloid leukemia: single-center experience and current challenges

Breccia, Massimo;La Rocca, Ursula;Martelli, Maurizio
2022

Abstract

Background Autologous stem cell transplantation (ASCT) has gained growing consideration as a treatment option for favorable-risk acute myeloid leukemia (FR-AML) in first complete remission (CR1), compared with chemotherapy. Materials and Methods We report the long-term outcomes of 117 consecutive patients with FR-AML fit for intensive chemotherapy diagnosed in our center between 1999 and 2020, who underwent ASCT. Results Sixty-five of the 117 were eligible for intensive post-remission treatment, and 42 of those 65 received ASCT. Median follow up was 132 months. Overall survival (OS) and disease-free survival (DFS) were 75% and 76%. Higher doses of CD34 + stem cell infusions negatively impacted DFS in multivariate analysis. Core-binding factor (CBF) leukemia was an independent prognostic factor for improved DFS. No differences based on pre-transplant measurable residual disease (MRD) were observed. In CBF leukemia, 10-year DFS is 72% for MRD-positive patients versus 100% for MRD negative patients. Conclusions ASCT is effective and safe in FR-AML patients. In CBF leukemia, ASCT provides excellent results regardless of achievement of bone marrow MRD negativity. In NPM1-mutated/FLT3-wild type (mNPM1) AML, early molecular response seems to have more impact on prognosis. Prospective investigation of the role of gemtuzumab ozogamicin in this setting is ongoing.
2022
Acute myeloid leukemia; Autologous stem cell transplantation; Minimal residual disease; Risk stratification
01 Pubblicazione su rivista::01a Articolo in rivista
Autologous stem cell transplantation in favorable-risk acute myeloid leukemia: single-center experience and current challenges / Capria, Saveria; Trisolini, Silvia Maria; Diverio, Daniela; Minotti, Clara; Breccia, Massimo; Cartoni, Claudio; Carmini, Daniela; Gozzer, Maria; La Rocca, Ursula; Shafii Bafti, Mahnaz; Martelli, Maurizio. - In: INTERNATIONAL JOURNAL OF HEMATOLOGY. - ISSN 0925-5710. - 116:4(2022), pp. 586-593. [10.1007/s12185-022-03370-4]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1664886
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