Abstract

Considerable progress has been made in the treatment of acute myeloid leukemia (AML). However, current therapeutic results are still unsatisfactory in untreated high-risk patients and poorer in those with primary refractory or relapsed disease. In older patients, reluctance by clinicians to treat unfit patients, higher AML cell resistance related to more frequent adverse karyotype and/or precedent myelodysplastic syndrome, and preferential involvement of chemorefractory early hemopoietic precursors in the pathogenesis of the disease further account for poor prognosis, with median survival lower than six months. A general agreement exists concerning the administration of aggressive salvage therapy in young adults followed by allogeneic stem cell transplantation; on the contrary, different therapeutic approaches varying in intensity, from conventional salvage chemotherapy based on intermediate–high-dose cytarabine to best supportive care, are currently considered in the relapsed, older AML patient population. Either patients’ characteristics or physicians’ attitudes count toward the process of clinical decision making. In addition, several new drugs with clinical activity described as “promising” in uncontrolled single-arm studies failed to improve long-term outcomes when tested in larger randomized clinical trials. Recently, new agents have been approved and are expected to consistently improve the clinical outcome for selected genomic subgroups, and research is in progress in other molecular settings. While relapsed AML remains a tremendous challenge to both patients and clinicians, knowledge of the molecular pathogenesis of the disease is fast in progress, potentially leading to personalized therapy in most patients.

Highlights

  • Acute myeloid leukemia (AML) occurs more commonly in elderly people

  • These results suggest that in patients with advanced IDH1-mutated relapsed or refractory acute myeloid leukemia (AML), IVO at a dose of 500 mg daily was associated with sustained clinical benefit, including transfusion independence, durable remissions, and molecular remissions in some patients with complete remission (CR)

  • A minority of patients over 65 years are eligible for stem cell transplantation (SCT) in CR1 and significantly less at relapse, new strategies are needed in order to improve therapeutic results

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Summary

Introduction

Acute myeloid leukemia (AML) occurs more commonly in elderly people. Median age at diagnosis is over 65 years, and incidence progressively increases with age, such that more than 40% of patients are currently diagnosed over the age of 70 [1,2,3]. Age over 65 represents a major adverse prognostic factor at the time of relapse This may be explained by excessive treatment toxicity resulting in reluctance by clinicians to treat very elderly or unfit patients, higher AML resistance related to more frequent adverse karyotype and/or precedent myelodysplastic syndrome (MDS), and preferential involvement of chemorefractory early hemopoietic precursors in the pathogenesis of the disease [22]. CR (CR2) followed by SCT to relapsed young-adult patients, the potential benefits—if any—deriving from the aggressive management of relapse of AML in elderly individuals are still unclear, and a remarkable uncertainty still impacts medical decisions This results in different strategies related to patients’ and physicians’ attitudes and ranging in intensity, from conventional salvage chemotherapy based on intermediate–high-dose ARA-C to BSC [19]. 2019, 11, x criteria are oftenCancers stringent and account for further exclusion

Survival from relapse
Intensive Salvage
FLT3 Inhibitors
IDH1 Inhibitors
Findings
Conclusions
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